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Front. Immunol., 23 March 2021
Sec. Vaccines and Molecular Therapeutics

Single-Arm, Multicenter Phase I/II Clinical Trial for the Treatment of Envenomings by Massive Africanized Honey Bee Stings Using the Unique Apilic Antivenom

Alexandre Naime Barbosa&#x;Alexandre Naime Barbosa1†Rui Seabra Ferreira Jr,,,*&#x;Rui Seabra Ferreira Jr1,2,3,4*†Francilene Capel Tavares de Carvalho,Francilene Capel Tavares de Carvalho2,3Fabiana Schuelter-Trevisol,&#x;Fabiana Schuelter-Trevisol5,6†Mnica Bannwart MendesMônica Bannwart Mendes1Bruna Cavecci Mendona,Bruna Cavecci Mendonça2,3Jos Nixon BatistaJosé Nixon Batista5Daisson Jos Trevisol,Daisson José Trevisol5,6Leslie BoyerLeslie Boyer7Jean-Philippe Chippaux,Jean-Philippe Chippaux8,9Natlia Bronzatto MedolagoNatália Bronzatto Medolago10Claudia Vilalva Cassaro,Claudia Vilalva Cassaro2,3Mrcia Tonin Rigotto CarneiroMárcia Tonin Rigotto Carneiro10Ana Paola Piloto de OliveiraAna Paola Piloto de Oliveira10Daniel Carvalho Pimenta,Daniel Carvalho Pimenta2,11Luís Eduardo Ribeiro da CunhaLuís Eduardo Ribeiro da Cunha12Lucilene Delazari dos Santos,,,&#x;Lucilene Delazari dos Santos1,2,3,4†Benedito Barraviera,,,&#x;Benedito Barraviera1,2,3,4†
  • 1Department of Infectology, Dermatology, Imaging Diagnosis and Radiotherapy, Botucatu Medical School (FMB), São Paulo State University (UNESP – Univ Estadual Paulista), Botucatu, Brazil
  • 2Graduate Program in Tropical Diseases, Botucatu Medical School (FMB), São Paulo State University (UNESP—Univ Estadual Paulista), Botucatu, Brazil
  • 3Center for the Study of Venoms and Venomous Animals (CEVAP), São Paulo State University (UNESP—Univ Estadual Paulista), Botucatu, Brazil
  • 4Graduate Program in Clinical Research, Center for the Study of Venoms and Venomous Animals (CEVAP) and Botucatu Medical School (FMB), São Paulo State University (UNESP—Univ Estadual Paulista), Botucatu, Brazil
  • 5Clinical Research Center, Nossa Senhora da Conceição Hospital, Tubarão, Brazil
  • 6Graduate Program in Health Sciences, University of Southern Santa Catarina at Tubarão, Tubarão, Brazil
  • 7VIPER Institute, University of Arizona College of Medicine, Tucson, AZ, United States
  • 8MERIT, IRD, Université Paris 5, Sorbonne Paris Cité, Paris, France
  • 9CRT, Institut Pasteur, Paris, France
  • 10Clinical Research Unit (UPECLIN), Botucatu Medical School, São Paulo State University (UNESP—Univ Estadual Paulista), Botucatu, Brazil
  • 11Biochemistry and Biophysics Laboratory, Butantan Institute, São Paulo, Brazil
  • 12Antivenom Production Laboratory, Vital Brazil Institute, Rio de Janeiro, Brazil

We evaluated the safety, optimal dose, and preliminary effectiveness of a new-approach Africanized honeybee (Apis mellifera) Antivenom (AAV) in a phase I/II, multicenter, non-randomized, single-arm clinical trial involving 20 participants with multiple stings. Participants received 2 to 10 vials of AAV depending on the number of stings they suffered, or a predefined adjuvant, symptomatic, and complementary treatment. The primary safety endpoint was the occurrence of early adverse reactions within the first 24 h of treatment. Preliminary efficacy based on clinical evolution, including laboratory findings, was assessed at baseline and at various time points over the four following weeks. ELISA assays and mass spectrometry were used to estimate venom pharmacokinetics before, during, and after treatment. Twenty adult participants, i.e., 13 (65%) men and 7 (35%) women, with a median age of 44 years and a mean body surface area of 1.92 m2 (median = 1.93 m2) were recruited. The number of stings ranged from 7 to > 2,000, with a median of 52.5. Symptoms of envenoming were classified as mild, moderate, or severe in 80% (16), 15% (3), and 5% (1) of patients, respectively; patients with mild, moderate, or severe envenoming received 2, 6, and 10 vials of AAV as per the protocol. None of the patients had late reactions (serum sickness) within 30 d of treatment. There was no discontinuation of the protocol due to adverse events, and there were no serious adverse events. One patient had a moderate adverse event, transient itchy skin, and erythroderma. All participants completed the intravenous antivenom infusion within 2 h, and there was no loss to follow-up after discharge. ELISA assays showed venom (melittin and PLA2) concentrations varying between 0.25 and 1.479 ng/mL prior to treatment. Venom levels decreased in all patients during the hospitalization period. Surprisingly, in nine cases (45%), despite clinical recovery and the absence of symptoms, venom levels increased again during outpatient care 10 d after discharge. Mass spectrometry showed melittin in eight participants, 30 d after treatment. Considering the promising safety results for this investigational product in the treatment of massive Africanized honeybee attack, and its efficacy, reflected in the clinical improvements and corresponding immediate decrease in blood venom levels, the AAV has shown to be safe for human use. Clinical Trial Registration: UTN: U1111-1160-7011, identifier [RBR-3fthf8].


In 1956, African honeybees of the subspecies, Apis mellifera scutellata, were introduced from Tanganyika and South Africa to Brazil because they were more productive and resistant to pests (1). They incidentally escaped and crossed with the existing European bees of the subspecies, Apis mellifera mellifera, resulting in an Africanized hybrid. These presented marked defensive and swarming capacities, and easily adapted to different climates and environments. In addition, these capacities made it possible for them to expand throughout Brazil and several other countries in the Western Hemisphere, including the United States (24). When threatened, these honeybees massively attack the target; consequently, the number of accidents involving humans and animals has increased (3, 5, 6).

Bee venom is composed of a complex mixture of biogenic amines, proteins, enzymes, and peptides. Among these are proteins of low allergenic importance and intense pharmacological action such as melittin, phospholipase A2, apamine, hyaluronidase, and several low molecular weight peptides, which constitute approximately 50–60%, 11–12%, 3%, 1–2%, and 1% of the gross weight, respectively, and water, and mineral salts.

Melittin and phospholipase A2 are the two most toxic components of the bee venom and may act synergistically to induce a variety of pathophysiological effects (710).

Envenoming by venomous snakes is a serious public health problem in tropical countries and is one of the most neglected health problems according to the World Health Organization’s (WHO) classification (11, 12). Health effects become more serious when the envenoming is caused by the injection of fairly large amounts of venom, such as that caused by the bites of adult specimens of Bothrops jararaca. Similarly, A. mellifera attacks massively, and thousands of bees can inject up to half a gram of venom. The expansion of Africanized honeybees (AHB) throughout the Americas (3, 4, 13), and consequently, the severity of the accidents they provoke, led health authorities to classify such accidents as objects of health surveillance in Brazil (Figure 1) (14).


Figure 1 Annual distribution of the number of accidents and deaths caused by AHB in Brazil between 2006 and 2019 (14).

These accidents show different magnitudes of clinical manifestation depending mainly on the number of stings and the individual’s sensitivity. The most frequent accident is that involving individuals not sensitized to the venom, affected by a few stings. In these cases, the clinical presentation is limited to a local inflammatory reaction, which manifests as erythematous papules, pain, and heat. In most cases, this situation is resolved without medical intervention. Another clinical form is that involving individuals sensitized to one or more components of the venom; they exhibit an immediate type I hypersensitivity reaction, as defined by Coombs and Gell (15). This serious event can be triggered by a single sting, and requires immediate medical intervention. Generally, the clinical manifestations include glottal edema, angioedema, and bronchospasm associated with anaphylactic shock (3, 5, 6).

The third presentation is that caused by multiple stings occurring when an individual is attacked by a swarm of honeybees. Here, a large amount of venom is inoculated, usually caused by hundreds or thousands of honeybees (3, 5, 6). These patients present with generalized pain, intense itching, and agitation, which may progress to numbness, associated with severe acute respiratory and kidney failure. Patients who die present on pathological examination acute tubular necrosis, with the presence of heme and/or myoglobin casts inside the renal tubules or glomeruli. There is usually intense proteolysis in skeletal muscles, with the release of myoglobin and creatine kinase (CK) into the blood. The heart may be affected, in which case a sub-endocardial lesion with infarction is observed. The liver may show signs of hydropic degeneration in cases of severe envenoming (1618).

Laboratory findings change rapidly and the blood cell count may show leukocytosis with neutrophilia and a staggered leftward shift, and type I urinalysis usually reveals proteinuria, glycosuria, and the presence of heme pigments. Serum urea and creatinine levels may increase due to kidney damage. Levels of CK and aspartate aminotransferase (AST) are usually elevated due to severe rhabdomyolysis. Alanine aminotransferase (ALT) levels may increase over time, indicating liver failure. Finally, levels of acute-phase proteins, including the C-reactive protein (CRP) and fibrinogen, are usually altered, indicating a severe systemic inflammatory response syndrome (3, 5, 6, 18).

Until recently, the treatment of patients who suffered from both smaller and larger numbers of stings was symptomatic and relied on antihistamines, corticosteroids, and even epinephrine in case of anaphylactic shock. The search for a specific treatment based on heterologous antivenoms has been a challenge for many researchers (19, 20). In 2000, Ferreira Jr. et al. (3) initiated the development of a new antivenom constituted only of antibodies against the two main toxins, melittin and phospholipase A2 (8, 9, 21). In 2017, Barbosa et al. (22) published a clinical protocol for the treatment of patients with multiple stings, which was applied in the present clinical study. Recently, Teixeira-Cruz et al. (23) published preclinical results, focusing mainly on the neutralization of biochemical and pharmacological activities of bee venom by apilic antivenom and they have concluded that this specific antivenom emerges as a new promising immunobiological product for the treatment of massive AHB attacks.

This clinical study was performed to assess the safety, establish the optimal minimum dose, and evaluate the preliminary effectiveness of the novel Apilic Antivenom (AAV).

Patients and Methods

Ethical Approval and Consent to Participate

The clinical protocol was approved by the Brazilian National Commission on Ethics in Research (CONEP, Certificate of Presentation of Ethical Appreciation No. 19006813.4.1001.5411, v7, approved on 06/07/2016), and the Brazilian National Health Surveillance Agency (ANVISA), which approved the Apis Study on 02/05/2016; No. 0907532142; Proc. No. 25361611582201493. This trial RBR-3FTHF8 was registered in 2015 in the Brazilian Clinical Trials Registry (ReBEC) (24). The first participant was recruited on 08/22/2016; Universal Trial Number (UTN): U1111-1160-7011; Register Number: RBR-3fthf8; Public access URL: The clinical trial protocol was published by Barbosa et al. (22).

Study Design

This was a phase I/II, multicenter, non-randomized, single-arm clinical trial study, involving 20 AHB multiple-sting participants treated with the new Apilic Antivenom “batch 155804 R” (Figure 2), performed from 08/22/2016 to 07/27/2018, in which 1 mL of AAV neutralized 1.25 mg of whole honeybee venom (23). Two clinical research units of the Brazilian National Clinical Research Network (RNPC) were used for this study; these were the Botucatu Medical School, São Paulo State University, São Paulo, Brazil, and the Clinical Research Center of the Nossa Senhora da Conceição Hospital (HNSC), Tubarão, Santa Catarina, Brazil. All participants provided informed consent by signing the free and informed consent form (FICF).


Figure 2 New Apilic Antivenom.


The primary endpoints were to assess the safety of AAV, based on the occurrence of adverse events, in participants exposed to multiple Africanized honeybees’ stings, and to estimate the proportion of participants showing improvements with respect to their initial clinical state, by monitoring symptoms and laboratory test results.

The secondary endpoint was to determine the correlation between the number of stings and the severity of the initial clinical presentation using the AHB score, adapted for this envenoming, based on APACHE II (25).

In addition, an exploratory endpoint was included in the study to estimate the pharmacokinetic profile of the AHB venom using ELISA tests carried out on blood samples collected at different time points (before AVV administration and 2, 6, 12, and 24 h after AAV administration). Furthermore, we aimed to assess the acute-phase reaction profile of AAV, by monitoring variations in C-reactive protein (CRP) and fibrinogen levels.

Inclusion, Exclusion, and Discontinuation Criteria

All participants who presenting with AHB stings were screened for eligibility by the clinical staff (Table 1). People aged over 18 years were eligible to receive AAV with respect to the number of stings, as described below. Each participant or his/her relative signed the FICF. Supplementary Video 1 - Stringer Video shows the procedure for removing the sting of Africanized bees in one of the patients.


Table 1 Inclusion, exclusion, and discontinuation criteria.

Antivenom Doses and Adjuvant Treatments

Before treatment, height in centimeters (cm), body weight in kilograms (kg), body mass index in Kg/m2; and body surface area in square meters (m2) were measured, as described by Madden and Smith (26). Then, all participants received a single intravenous administration of the AAV, diluted in a solution of 250 mL of 0.9% sodium chloride intravenously over two h, according to the protocol, and based on the number of stings as described below:

● Up to 5 stings: Specific treatment with AAV was not indicated. Here, only adjuvant, symptomatic, and complementary treatments were administered.

● Between 5 and 200 stings: Two vials (20 mL) of AAV;

● Between 201 and 600 stings: Six vials (60 mL) of AAV;

● Above 600 stings: Ten vials (100 mL) of AAV.

The adjuvant, symptomatic, and complementary treatments were described and published in detail by Barbosa et al. (22) at http://www.doi:10.1186/s40409-017-0106-y.

Criteria for Measuring the Severity and Clinical Outcomes in the Participants

An AHB score was assigned based on APACHE II, which is a validated system for classifying disease severity (25). The proposed AHB score varied between 1 and 15 according to the severity criteria, which included eight clinical and seven strategic laboratory alterations, based on medical literature, assessed at the time of the first examination (4, 7, 1618). These criteria, except for those that did not change throughout the treatment period (i.e., age > 60 years, body mass index over 30 kg/m2, time elapsed between the accident and medical care, and number of stings) were evaluated and monitored throughout the course of the treatment to verify clinical outcomes, and the normalization of laboratory parameters upon discharge from the hospital and during follow-up visits, 10, 20, and 30 d later was also monitored.

AHB Score Proposed for Clinical and Laboratory Assessments

-Age > 60 years: Score 1

-Body mass index > 30 kg/m2: Score 1

-Time elapsed between the accident and medical care (over 24 hours): Score 1

-Number of stings

● 5–200 stings: Score 1

● 201–600 stings: Score 2

● More than 600 stings: Score 3

-Hemodynamic disorders (tachycardia, arterial hypotension, shock): Score 1

-Respiratory disorders (bradypnea, bronchospasm, wheezing, and/or dyspnea): Score 1

-Neurological disorders (mental confusion and/or intense headache): Score 1

-Acute kidney injury (anuria and/or oliguria): Score 1

-Increased CK levels: Score 1

-Increased ALT levels: Score 1

-Increased creatinine levels: Score 1

-Increased CRP levels: Score 1

-Increased fibrinogen levels: Score 1

-Increased leukocyte levels: Score 1

-Decreased platelet count: Score 1

Subsidiary and Strategic Laboratory Tests

Laboratory tests (CK, ALT, creatinine, CRP, fibrinogen, leukocytes, and platelets) were used to assess safety parameters before treatment (hospital admission), on the day of discharge, and at follow-up (10, 20, and 30 d after discharge from the hospital). All procedures and protocols for laboratory tests are presented in Data Sheet 1-Tables-1-2 (27, 28).

Classification of Early and Late Adverse Reactions to Antivenom

Adverse reactions to AAV were defined as mild, moderate, or severe based on the international classification of anaphylactic reactions described in Table 2 (29, 30). During the outpatient evaluations (10, 20, and 30 d), a clinical history focused on serum sickness (a type III hypersensitivity reaction) was taken. Thus, the patient was asked if in the 10 d prior to the consultation he had had any type of cutaneous rash, fever, lymphadenopathy, facial and periorbital edema, changes in urine color, and/or arthralgia.


Table 2 Classification of acute adverse reactions to antivenoms (29, 30).

ELISA Assays for the Estimation of Venom Pharmacokinetics

F(ab’)2-type immunoglobulin fractions prepared from the blood of hyperimmunized horses against melittin and PLA2, found in the venom of A. mellifera [Anti-melittin F(ab’)2, and Anti-PLA2 F(ab’)2], were obtained from the AAV using a modified version of the single affinity chromatographic step described by Chávez-Olórtegui et al. (31).

Crude venom (32 mg) from A. mellifera was immobilized with 3 g of CNBr-Sepharose resin and prepared according to the manufacturer’s instructions (Cytiva GE Healthcare Life Sciences - USA) for the aforementioned affinity chromatography assay. Anti-melittin F(ab’)2 and Anti-PLA2 F(ab’)2 were conjugated to peroxidase (HRP - Sigma) according to the method described by Nakane and Kawoi (32). The conjugate was titrated as described by Chávez-Olórtegui et al. (31), modified with the conjugate diluted at ratios of 1:20, 1:2,000, 1:5,000, and 1:10,000, and its viability was evaluated for 30 min.

Then, an ELISA assay was performed to quantify the melittin and PLA2 fractions in the blood of participants by the method described by Bucaretchi et al. (33). For this, 96-well plates were sensitized with 100 μL of an anti-melittin F(ab’)2 and anti- PLA2 F(ab’)2 mixture at a concentration of 20 μg/mL. The conjugate was used at a dilution of 1:2,000; both in the calibration curve of the A. mellifera crude venom and that of the blood samples of the participants. Calculations were performed using the Microsoft Excel software v.16, using linear regression analysis and dose-response curves. The results were expressed in ng/mL.

Mass Spectrometry Analyses

The participants’ sera (50 µL) were added to 5% DMSO, 0.1% acetic acid (50 µL), and vortexed for 30 min. Then, the solution was centrifuged for 3 min at 3000 × g. The supernatant was collected for further processing. Purified melittin from crude A. mellifera venom (8) was used as a standard for method development.

Samples were analyzed by liquid chromatography-tandem mass spectrometry in an ESI-IT-TOF instrument coupled to a UFLC 20A Prominence (Shimadzu, Kyoto, Japan). Samples (15 μL) were injected into a C18 column (Kinetex C18 2.6 µm 100 Å, 100 × 4.6 mm), and analyzed using a binary gradient, employing the following solvents: (A) water:DMSO:acetic acid (949:50:1) and (B) ACN:DMSO:water:acetic acid (850:50:99:1). Optimal detection conditions for melittin were achieved at an elution gradient of 25–50% B for 20 min at a constant flow of 0.7 mL.min-1, after initial isocratic elution for 5 min. Eluates were monitored using a Shimadzu SPD-M20A PDA detector (Shimadzu, Kyoto, Japan) before being injected into the mass spectrometer.

The interface was maintained at 4.5 kV and 275°C. The detection voltage was 1.95 kV, and fragmentation was induced using argon collision, with 55 ‘energy’ parameters. MS spectra were acquired in positive mode in the 700–730 m/z range, and MS/MS spectra were obtained in the 50–1400 m/z range, according to the previous optimization with purified melittin. The m/z ion, 712.15 (M+4H+), was selected for fragmentation, and the [y13]2+ ion (811.95, the tallest peak) was monitored at MS2 (Data Sheet 2 - Figures 1-5).

Statistical Analysis

Statistical analyses, and the choice comparison tests used among the research participants, were carried out with respect to presuppositions determined by the results, characteristics, and course of the variables in the study. Binomial variables were compared using the chi-squared and Fisher’s exact tests. Numerical values were compared using the Student’s t-test or the Mann–Whitney U test. Statistical analyses of the pharmacokinetic assays were performed using the GraphPad Prism software version 8.3.0, with differences considered to be statistically significant when p < 0.05. The results obtained were compared using the ANOVA test for repeated measures, followed by Tukey’s test. The data are represented as the mean ± standard error of the mean (34, 35).


Description of Participants

Twenty participants were included, i.e., 13 males (65%) and 7 females (35%). Participants’ ages varied between 22 and 77 years, with a median age of 44 years. Nineteen patients were white-skinned, and one was brown-skinned. Sixteen of them were from the Botucatu region (SP) and four from Tubarão (SC). The number of stings varied from 7 to more than 2,000. The number of vials of AAV administered, based on the clinical protocol, was as follows: mild cases (two vials), 16 participants; moderate cases (six vials), 3 participants; and severe cases (10 vials), 1 participant. The time elapsed between the accident and the clinical care varied as follows: less than 24 h, 5 cases; 1 d, 5 cases; and between 2 and 6 d, 8 cases. One participant was attended 10 and another 19 days after the accident (Table 3).


Table 3 Description of participants; study protocol number, age, sex, clinical care location, occupation, the estimated number of stings, number of AVV vials administered, and the time elapsed between the accident and medical care in days.

As shown in Table 4, height varied between 151 and 190 cm, body mass index (BMI) ranged from 19.3 to 32.8 kg/m2 (mean: 26.4; median: 26.1), and body surface area (BSA) varied from 1.54 to 2.30 m2 (mean: 1.92 m2; median: 1.93 m2).


Table 4 Description of participants; study protocol number, height in centimeters (cm), weight in kilograms (Kg), body mass index in Kg/m2, body surface area (m2), and estimated number of stings.

Participant 302, aged 77, received 150 stings and was attended to at the hospital in Tubarão (SC) 1 h after the accident. Figure 3A shows a bee inside the ocular conjunctiva of the participant, demonstrating the aggressiveness of this accident. Figure 3B shows an Africanized honeybee.


Figure 3 (A) Participant 302 with A. mellifera Africanized honeybee inside the ocular conjunctiva. (B) Apis mellifera Africanized honeybee.

Clinical Outcomes

Adverse Events Not Related to the Investigational Product

Participant 103 developed an abscess on the lower-left flank (hypogastric region); participant 105 had inflammation of the right eye; participant 115 had strong-smelling urine, and pain in the testicular and lumbar regions (kidney); participant 113 had tachycardia and edema in the lower limbs (chronic hypertensive patient), and participant 111 had bronchospasms.

At follow-up visits, especially 10 d after treatment, all four participants, with moderate to severe cases, complained of intense itching in the lesions. This complaint was also mentioned by one of the participants who suffered a mild accident.

Adverse Events Related to the Investigational Product

During the AAV infusion, participant 110 presented with numb lips and itchy head; and participant 117 had pruritus and urticarial reactions. All AEs related to the product were adequately treated, and AAV infusion was completed. All adverse events, whether related or unrelated to the study, are described in Data Sheet 3 - Clinical aspects.

Clinical and Laboratory Outcomes

According to Table 1 from Data Sheet 4 Tables-1-21, from a clinical perspective, only one patient had hemodynamic alterations, whereas two presented with respiratory disorders. From a laboratory perspective, 15 had elevated CK levels, nine showed increased CRP levels, eight had leukocytosis, seven showed increased fibrinogen levels, and four showed increased ALT levels. All laboratory findings for CK, CRP, ALT, and complete blood count, including platelets count, fibrinogen, and creatinine levels, are available in the Supplementary Materials in Data Sheet 5 -Laboratory exams.

The AHB scores assigned to the participants before the administration of AVV were 7, 6, and 5 or below 5, for 2, 5, and 13 participants, respectively (Table 2, Data Sheet 4 -table 1-21). The participant with the most severe case had a score of 7, and the 3 participants whose cases were considered to be of moderate severity had scores of 7 and 6, for 1 and 2 of them, respectively. All 16 participants whose cases were considered to be of mild severity had a score of 5 or less.

Laboratory tests showed an increase in CK, CRP, leukocytosis, fibrinogen, and ALT levels in 15, 9, 8, 7, and 4 participants, respectively. The biological AHB score, excluding clinical parameters, assigned to participants before the administration of AVV, was 5 in one, 4 in two, 3 in six, and score 2 or 1 in 11 participants respectively (Table 6, Data Sheet 4 -Tables-1-21).

As shown in Table 18 of the Data Sheet 4 -Tables-1-21, none of the participants showed clinical alterations 30 d after the administration of AAV. However, CRP, fibrinogen, CK, and ALT and leukocytosis, were altered in 4, 3, 2, and 1 of them, respectively.

As shown in Table 21 of the Data Sheet 4 -Tables-1-21, eight participants still had changes in the laboratory AHB score 30 d after AAV administration, with 1, 2, and 5 participants at scores 3, 2, and 1, respectively. Four participants, including 3 considered to have moderate cases and 1 considered to have a severe case, presented a laboratory AHB score of zero. Finally, Table 5 shows the comparison between AHB scores before and 30 d after AAV treatment.


Table 5 Comparison between AHB scores before and 30 days after AAV treatment.

Melittin and Phospholipase A2 Pharmacokinetics—ELISA Assays

All participants were monitored at 0, 2, 6, 12, 24, and 48 h of hospitalization, and at 10, 20, and 30 d of outpatient follow-up. Of the 20 participants, 6 had missed at least one of the scheduled sample collection sessions, and the ELISA test was not performed for 2 participants (301 and 303).

Fourteen participants had a complete follow-up, and all their blood samples for the different collection periods were obtained. Concentrations of melittin + phospholipase A2 varied between 0.03 ng/mL and 587.35 ng/mL during the hospitalization and follow-up period; despite the excellent clinical states of all the participants, melittin + phospholipase A2 concentrations ranged between 0 and 1.479 ng/mL.

Figure 4 shows the time-course of melittin + phospholipase A2 levels in eighteen participants at admission, 2, 6, 12, 24, and 48 h after admission, and at 10, 20, and 30 d during the outpatient follow-up period. It is possible to observe that the blood concentration of melittin and PLA2 rises again especially after 10 days of admission, but without any clinical symptoms.


Figure 4 Time-course of melittin + phospholipase A2 levels (ng/mL) by ELISA test in eighteen participants at admission, 2, 6, 12, 24, and 48 h after admission and AAV administration, and at 10, 20, and 30 d during the outpatient follow-up period.

All the results of the ELISA assays are available in Data Sheet 6-Elisa assays.

Mass Spectrometry

Analyses of the TIC chromatograms (Figures 5A, B) indicated that the 712.15 ion [M+4H4+], as well as the MS2 profiles, particularly that of the [y13]2+ fragment, made it possible to determine the presence and relative levels of melittin in the participants, as shown in Table 6. The relative quantity of melittin in the serum was determined based on the graphical interpretation of the spectra, as presented in the Supplementary Materials, in Data Sheet 2 –Figures-15.


Figure 5 Representative mass spectrometry profile for the qualitative assessment of the presence of melittin in the serum of participant 115, considered positive (+++): (A) Melittin [M+4H]4+ MS profile and (B) MS2 interpreted profile, annotated for the larger b and y ions, as well as internal fragments (*).


Table 6 Qualitative melittin detection in 19 participants 30 days after the AAV treatment.


Antivenom therapy was discovered in 1894 in France by Césaire Auguste Phisalix and Gabriel Bertrand (36), and Albert Calmette (37, 38). In Brazil, the discovery of this therapy had a profound impact on the work of Vital Brazil Mineiro da Campanha, a researcher has known worldwide for his scientific discoveries and for providing evidence of the specificity of antivenoms (3941).

Since the 2000s, CEVAP has initiated different strategies to develop new antivenoms and therapies named “next antivenom approach”, including the development of a new Apilic antivenom (AAV), based on the association between a robust clinical protocol and an antivenom that strategically neutralizes only toxic molecules, i.e., melittin and phospholipase A2 (21). Then, allergens and nociceptive components were removed from the crude venom, significantly reducing suffering in the serum-producing animals; this directed the immune response of the herd toward the actual toxic and harmful compounds in envenomated humans. After the validation of the drug candidate, researchers from two Brazilian antivenom producers, the Vital Brazil Institute (VBI) and the Butantan Institute (BI), joined the CEVAP team to produce a new AAV for clinical and pre-clinical trials.

In 2017, the Brazilian National Health Surveillance Agency (ANVISA), through Resolution RDC N ° 187 of November 8, 2017, established the minimum requirements for the registration of hyperimmune sera, with the aim of guaranteeing the quality, safety, and efficacy of these products. It also established that the request for the registration of these immunobiological must include the results of clinical trial studies. This is because, until then, Brazilian antivenoms were not validated through clinical trials (42). Therefore, this phase I/II clinical trial on the use of the AAV for the treatment of massive Africanized honeybee (A. mellifera) attacks, the clinical protocol of which was published in 2017 by Barbosa et al. (22), is the first to follow this new guideline.

The certainty diagnosis of envenoming by Africanized honey bees was made by the signs, symptoms, and by the clinical history of the patients, such as walking near an apiary, beekeepers handling swarms without the personal protective equipment (PPE), and, accidentally, when the people walked or played sports on the field (3, 5, 6). Second, according to the patient’s behavior in relation to the swarm because these bees attack victims and chase them for up to 400 meters (43, 44), moving at an average height of 1.62 m. Therefore, the head, trunk, and upper limbs are the parts of the human body most affected (13). Third, due to the presence of the stinger at the bee sting site - the only Hymenoptera in the world that dies after the bee sting (3, 45). Finally, due to the presence of melittin in the patients’ blood, evaluated by the Elisa assay and mass spectrometry - melittin is a peptide found only in the Apis genus (46). The main differential diagnosis was made with envenoming by social wasps common in Brazil (Polybia spp, Polistes spp, and Solenopsis spp). In this case, there would be no massive attack, no stinger at the bite site, and no melittin in the patient blood (10, 47).

According to WHO guidelines (48), clinical trials on antivenoms are designed to address three main issues: (a) the optimal initial dose; (b) efficacy, i.e., the ability of the antivenom to control the main clinical manifestations of envenoming; and (c) safety, i.e., the incidence and severity of early and late adverse reactions. Dose-finding studies are usually followed by randomized, controlled trials in which the new antivenom is compared to another antivenom already used, or in its absence, two doses of the new antivenom are compared (49).

As AAV was designed to specifically neutralize the two main toxic compounds of the venom, the clinical effects of low molecular mass proteins and peptides, that cause manifestation such as intense pruritus, flushing, hyperthermia, papules, urticarial plaques, hypotension, tachycardia, headache, nausea, vomiting, abdominal colic, bronchospasms, and psychomotor agitation, were neutralized by symptomatic medications such as antihistamines, corticosteroids, adrenaline (when the anaphylactic shock was suspected), and pethidine hydrochloride (for severe pain). In case of the occurrence of bronchospasms, oxygen (O2) catheters associated with β-2-agonist-type inhaled bronchodilators (salbutamol, fenoterol, or terbutaline) were used at the usual recommended doses (22). As the main objective of this study was to assess the safety of AAV, including the severity of acute adverse events, and to confirm its lowest effective dose when confronted with different amounts of inoculated venom, the main adverse events caused by equine-heterologous antivenom therapy were studied.

Safety was assessed mainly through early adverse events, particularly, IgE-mediated anaphylactic reactions type I, non-IgE-mediated anaphylactic reactions, pyrogenic reactions (endotoxin contamination), and late adverse reactions (type III hypersensitivity, such as serum sickness) (5053).

Regarding adverse events unrelated to the product, the persistence of itching the sting sites at the first follow-up outpatient, i.e., 10 d after AAV administration, was highlighted. This clinical manifestation and its persistence at the sting site or in the subcutaneous cellular tissue are related to envenoming (4, 6, 7, 18). Since the clinical protocol recommended the use of antihistamines only during the hospitalization period, this point should be revised and the use of this medication should be extended to at least 15 days after discharge.

Regarding the adverse events related to this product, only two participants (10%) experienced mild and early adverse reactions, such as numbness of the lips, itchy head, pruritus, and urticarial reactions. Recently, Mendonça-da-Silva et al. (54) evaluated the safety and efficacy of a freeze-dried trivalent antivenom for snakebites in the Brazilian Amazon, with 112 participants treated in an open-label, randomized controlled phase IIb clinical trial. Twenty-three (19.8%) participants experienced early adverse events after antivenom therapy. The most common symptoms were urticaria (13.8%), pruritus (11.2%), facial flushing (3.4%), and vomiting (3.4%). Our results are similar to those of Mendonça-da-Silva et al. (54), and those of other studies in the literature (5053). None of the participants developed serum sickness. AAV appears to be a safe investigational product for clinical use.

It should be emphasized that in the event of an accident involving AHB, classically described adverse reactions due to antivenoms may be confused with adverse events of the envenoming itself. Therefore, it becomes difficult to determine whether they are caused by the venom or AAV (4, 6, 7, 18). Despite these limitations, it was possible to conclude that adverse events related to the investigational product were similar to those caused by common antivenoms used in other types of envenomings (4549); thus, confirming the safety of AAV for clinical use.

As concerns clinical and laboratory outcomes, the authors proposed a new AHB score to assess the severity of the participants’ cases at the time of the first visit, in addition to the evolutive outcome. The use of the AHB score proved to be simple and showed proportionality to the severity of the envenoming, and the normalization of clinical and biological signs. As it combines clinical and biological criteria, the score appears to be both sensitive and accurate, particularly with respect to biological variables, for the characterization of the severity and course of envenoming. This allowed us to confirm clinical remission in all participants 30 d after AAV administration. However, biological alterations persisted in some participants (8/20) even though they did not present with particularly severe envenomings. Surprisingly, the two participants with the most severe cases of envenoming, who received 500 and 2,000 stings, and were assigned an AHB score of 7, had a score of zero 30 d after AAV administration. In addition, all the 5 participants who had an AHB score of 6 at inclusion, had a score of zero 30 d after discharge; but one remained at 1 because of a CRP level slightly above the limit (1.1 mg/dL). It should also be emphasized that envenoming caused by venomous animals triggers a systemic inflammatory response syndrome described by several authors since the 1990s (5559). This constitutes an acute phase reaction with a massive release of pro-inflammatory cytokines (particularly, IL-1, IL-6, and TNF alpha), and acute-phase proteins, especially CRP. These acute-phase reactions are in accordance with previous clinical studies performed on other antivenoms (4, 6, 5560).

ELISA tests, standardized to assess the presence of melittin and phospholipase A2 in this study, showed the reappearance of these two fractions 10, 20, and 30 d after treatment in most participants.

In a study using an ovine model to evaluate the interactions between the venom produced by Micrurus fulvius and a F(ab’)2 antivenom administered intravenously, Paniagua et al. (61) observed an immediate neutralization of the venom in the bloodstream. Antivenom appears not to be able to neutralize the residual venom deposited at the site of the sting; so, the venom can remain active, with slow-release into the bloodstream and consequently be distributed systemically (61). However, as long as the antivenom remains in the plasma compartment, the venom is captured and eliminated until the plasma antivenom concentration is no longer sufficient to neutralize the released venom (6264). This phenomenon is well illustrated by the use of Fab, which has a short half-life of approximately 10-15 h (62), in the treatment of envenoming caused by Crotalidae; this treatment requires constant re-administration of the Fab antivenom (65, 66). Under these conditions, the renewal of the administration of the antivenom serum must be planned based on the half-life of the F(ab’)2 antibodies, which is approximately 50 h (62), and the quantity of bee venom in circulation, which is more difficult to determine.

We hypothesize that, in consonance with the findings of Paniagua et al. (61), multiple bee stings occur in many parts of the human body, depositing the venom in the subcutaneous tissue from where it is slowly released to the bloodstream. In addition to the clearance of the F(ab’)2 molecule, the latter remains in the plasma compartment without entering the tissues, preventing the neutralization of the venom in the subcutaneous cellular tissue (62). Surprisingly, participants who received only two vials of AAV were those who still presented with a systemic inflammatory response syndrome 30 d after treatment, i.e., an inflammatory response based on increased CRP levels (4 participants), fibrinogen levels (3 participants), and leukocyte count (1 participant) (4, 5459). This can be explained by a lower F(ab’)2 concentration, which is eliminated more quickly, permitting the venom, even in small quantities, to stay longer in the body. This clearly raises the question of renewing AAV administration in participants who suffered multiple AHB stings a week after the first dose or increasing the number of vials at the first administration, even if the initial symptoms were mild.

Finally, qualitative mass spectrometry (8) showed the presence of melittin in the blood of participants with mild (five), moderate (two), and severe (one) cases 30 d after AAV administration. It should be emphasized that participant 115, who received 2 vials of AAV after being stung by approximately 100 honeybees, experienced a particular increase in circulating melittin 30 d after treatment. Thus, the clinical response of the participants, laboratory test results from the acute-phase response, ELISA tests, and mass spectrometry allowed us to infer that although the investigational product is safe (which was the main objective of this study), it would be necessary to revise the clinical protocol, especially concerning the number of vials of AAV to be administered. A multicenter phase III clinical trial should be performed to confirm these hypotheses and adjust the doses of this new antivenom.


AAV proved to be safe, as related adverse events were observed in only two (10%) participants, corroborating reports on heterologous antivenom use. No late adverse events were observed on d 10, 20, or 30 during clinical surveillance. Preliminary efficacy was observed by clinical improvement in participants, a decrease in acute-phase-reaction markers, and a reduction in circulating melittin and phospholipase A2 levels, measured using ELISA. The doses recommended in the clinical protocol should be reassessed and increased, given that melittin was founding the blood of eight participants 30 d after the specific treatment, through mass spectrometry. It should be noted that these issues were expected, as accidents involving AHB are peculiar and different from all other venomous animal accidents described. A phase III clinical trial should be performed to confirm these observations, adjust the recommended doses, and assess the efficacy of the product.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics Statement

The clinical protocol has been previously approved by the Brazilian National Commission on Ethics in Research (CONEP, Certificate of Presentation of Ethical Appreciation No. 19006813.4.1001.5411, v7, approved in 06/07/2016) and the Brazilian National Health Surveillance Agency (ANVISA) whose Consent Record of Apis Study was approved on 02/05 2016 by No. 0907532142, Proc. No. 25361611582201493. This trial RBR-3FTHF8 was registered in 2015 in the Brazilian Clinical Trials Registry (ReBEC) (24). The first participant was included in 08/22/2016, the Universal Trial Number (UTN) is U1111-1160-7011, the Register Number is RBR-3fthf8 and the public access URL is available at The patients/participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.

Author Contributions

AB, FS-T, and MM were the principal investigators. FC, BM, and LS standardized the ELISA assay. RF and LC produced and performed quality control on the Apilic Antivenom. JB, DT, NM, CC, MC, and AO recruited the participants. DP developed the mass spectrometry assay. RF, LB, J-PC, and BB discussed the proposal and corrected the manuscript. All authors contributed to the article and approved the submitted version.


This study was supported by the National Council of Technological and Scientific Development (CNPq) under Grant No. 437089/2018-5 (LS), 563582/2010-3 (BB), and 401170/2013-6 (BB), and in part by grants from the Coordination for the Improvement of Higher Education Personnel (CAPES) [AUX-PE Toxinology Proc. No. 23,038.000823/201121]. RF is a CNPq PQ1C fellow researcher [303224/2018-5]. DP is a CNPq fellow researcher [301974/2019-5]. BB is a CNPq PQ-2 fellow researcher [306339/2020-0]. FAPESP Grant No. 2020/09819-6 and No. 2020/16747-1 (BM, LS, RF). PROPG/UNESP Edital 01/2021. DECIT/MS No. 841906/2016-SICONV and No.841904/2016- SICONV (RF).

Conflict of Interest

RF is a CNPq PQ1C fellow researcher, process number 303224/2018-5.

RF, BB, LC, and DP participated as authors in patent application BR10201502630. Deposit: 10/16/2015. PCT deposit number: 10201502630. PCT deposit date: 10/16/2015 “Process of obtaining anti-apilic equine serum and its uses” INPI: National Institute of Industrial Property, Brazil.

The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.


We are grateful to the Center for the Study of Venoms and Venomous Animals (CEVAP) of the São Paulo State University (UNESP), Brazil; Pasqual Barretti, Rodrigo Bazan, Carlos Antonio Caramori, and Patricia Carvalho Garcia from the Botucatu Medical School, São Paulo State University (UNESP), Brazil; André Balbi and the emergency room team of the Botucatu Medical School Clinical Hospital (HCFMB), São Paulo, Brazil; Sergio Muller of the São Paulo State Department of Health; Camile Giaretta Sachetti, Patricia de Souza Boaventura, and Felipe Nunes Bonifácio from the Department of Science and Technology of the Brazilian Ministry of Health; and Ricardo de Oliveira Orsi from the Botucatu School of Veterinary Medicine and Zootechnics (UNESP), Brazil.

Supplementary Material

The Supplementary Material for this article can be found online at:


1. Scott Schneider S, DeGrandi-Hoffman G, Smith DR. The African honey bee: factors contributing to a successful biological invasion. Annu Rev Entomol (2004) 49:351–76. doi: 10.1146/annurev.ento.49.061802.123359

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Oliveira GP, Kadri SM, Benaglia BGE, Ribolla PEM, Orsi RO. Energetic supplementation for maintenance or development of Apis mellifera L. colonies. J Venom Anim Toxins incl Trop Dis (2020) 26:e20200004. doi: 10.1590/1678-9199-jvatitd-2020-0004

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Ferreira RS Jr, Almeida R, Barraviera SRS, Barraviera B. Historical perspective and human consequences of Africanized bee stings in the Americas. J Toxicol Environ Health Part B (2012) 15:97–108. doi: 10.1080/10937404.2012.645141

CrossRef Full Text | Google Scholar

4. United States Department of Agriculture, Agricultural Research Service. ARS Honey Bee Health (2021). Available at: (Accessed January 7, 2021).

Google Scholar

5. Pucca MB, Cerni FA, Oliveira IS, Jenkins TP, Argemí L, Sørensen CV, et al. Bee updated: Current knowledge on bee venom and bee envenoming therapy. Front Immunol (2019) 10:2090. doi: 10.3389/fimmu.2019.02090

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Almeida R, Olivo T, Mendes RP, Barraviera SRCS, Souza LR, Martins JG, et al. Africanized honeybee stings: How to treat them. Rev Soc Bras Med Trop (2011) 44(6):755–61. doi: 10.1590/S0037-86822011000600020

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Ownby CL, Powell JR, Jiang M, Fletcher JE. Melittin and phospholipase A2 from bee (Apis mellifera) venom cause necrosis of murine skeletal muscle in vivo. Toxicon (1997) 35(1):67–80. doi: 10.1016/s0041-0101(96)00078-5

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Ferreira RS Jr, Sciani JM, Marques-Porto R, Junior AL, Orsi RO, Barraviera B, et al. Africanized honey bee (Apis mellifera) venom profiling: Seasonal variation of melittin and phospholipase A2 levels. Toxicon (2010) 56(3):355–62. doi: 10.1016/j.toxicon.2010.03.023

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Sciani JM, Marques-Porto R, Lourenço A, Orsi RO, Ferreira RS Jr, Barraviera B, et al. Identification of a novel melittin isoform from Africanized Apis mellifera venom. Peptides (2010) 31(8):1473–9. doi: 10.1016/j.peptides.2010.05.001

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Santos LD, Pieroni M, Menegasso ARS, Pinto JRAS, Palma MS. A new scenario of bioprospecting of Hymenoptera venoms through proteomic approach. J Venom Anim Toxins incl Trop Dis (2011) 17(4):364–77. doi: 10.1590/S1678-91992011000400003

CrossRef Full Text | Google Scholar

11. World Health Organization (WHO). Report of the tenth meeting of the WHO: Strategic and Technical Advisory Group for Neglected Tropical Diseases (2017). Geneva: WHO. Available at: (Accessed January 7, 2021).

Google Scholar

12. Chippaux JP. Snakebite envenomation turns again into a neglected tropical disease! J Venom Anim Toxins incl Trop Dis (2017) 23:38. doi: 10.1186/s40409-017-0127-6

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Oliveira SK, Trevisol DJ, Parma GC, Ferreira RS Jr, Barbosa AN, Barraviera B, et al. Honey bee envenoming in Santa Catarina, Brazil, 2007 through 2017: an observational, retrospective cohort study. Rev Soc Bras Med Trop (2019) 52:e20180418. doi: 10.1590/0037-8682-0418-2018

PubMed Abstract | CrossRef Full Text | Google Scholar

14. BRAzIL – Ministry of Health (MS). Epidemiological situation - Health Information (TABNET), Accidents by Venomous Animals, Bee (2020). Available at: (Accessed January 7, 2021).

Google Scholar

15. Coombs RRA, Gell PGH. “Classification of allergic reactions responsible for clinical hypersensitivity and disease”. In: Gell PHG, Coombs RRA, editors. Clinical aspects of immunology, 2nd edition. Oxford and Edinburgh: Blackwell Scientific Publ. (1968). p. 575–96.

Google Scholar

16. Caldas SA, Graça FA, Barros JS, Rolim MF, Peixoto TC, Peixoto PV. Lesions caused by Africanized honeybee stings in three cattle in Brazil. J Venom Anim Toxins incl Trop Dis (2013) 19:18. doi: 10.1186/1678-9199-19-18

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Silva GBD Jr, Vasconcelos AG Jr, Rocha AMT, Vasconcelos VR, Barros JN, Fujishima JS, et al. Acute kidney injury complicating bee stings - a review. Rev Inst Med Trop Sao Paulo (2017) 59:e25. doi: 10.1590/S1678-9946201759025

PubMed Abstract | CrossRef Full Text | Google Scholar

18. França FO, Benvenuti LA, Fan HW, Santos DR, Hain SH, Picchi-Martins FR, et al. Severe and fatal mass attacks by ‘killer’ bees (Africanized honey bees - Apis mellifera scutellata) in Brazil: clinicopathological studies with measurement of serum venom concentrations. Q J Med (1994) 87(5):269–82. doi: 10.1093/oxfordjournals.qjmed.a068927

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Santos KS, Stephano MA, Marcelino JR, Ferreira VM, Rocha T, Caricati C, et al. Production of the first effective hyperimmune equine serum antivenom against Africanized bees. PLoS One (2013) 8(11):e79971. doi: 10.1371/journal.pone.0079971

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Ferreira RS Jr, Anderlini RP, Sant’Anna OABE, Pimenta DC, Orsi RO, Barraviera B. New nanostructured silica adjuvant (SBA-15) employed to produce antivenom in young sheep using Crotalus durissus terrificus and Apis mellifera venoms detoxified by cobalt-60. J Toxicol Environ Health Part A (2010) 73(13-14):926–33. doi: 10.1080/15287391003745069

CrossRef Full Text | Google Scholar

21. Africanized Honeybee Antivenom. Movie (2015). Available at: (Accessed January 7, 2021).

Google Scholar

22. Barbosa AN, Boyer L, Chippaux JP, Medolago NB, Caramori CA, Paixão AG, et al. A clinical trial protocol to treat massive Africanized honeybee (Apis mellifera) attack with a new apilic antivenom. J Venom Anim Toxins incl Trop Dis (2017) 23:14. doi: 10.1186/s40409-017-0106-y

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Teixeira-Cruz JM, Strauch MA, Monteiro-Machado M, Tavares-Henriques MS, Moraes JA, Cunha LER, et al. A novel apilic antivenom to treat massive, Africanized honeybee attacks: a preclinical study from the lethality to some biochemical and pharmacological activities neutralization. Toxins (2021) 13(1):30. doi: 10.3390/toxins13010030

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Brazilian Clinical Trials Registry (ReBEC). Available at: (Accessed January 7, 2021).

Google Scholar

25. Knaus WA, Draper EA, Wagner DP, Zimmerman JE. APACHE II: a severity of disease classification system. Crit Care Med (1985) 13(10):818–29. doi: 10.1097/00003246-198510000-00009

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Madden AM, Smith S. Body composition and morphological assessment of nutritional status in adults: a review of anthropometric variables. J Hum Nutr Diet (2016) 29(1):7–25. doi: 10.1111/jhn.12278

PubMed Abstract | CrossRef Full Text | Google Scholar

27. McPherson RA, Pincus MR. Henry"s Clinical Diagnosis and Management by Laboratory Methods. USA: Elsevier Missouri (2017). p. 1584, ISBN: 978-0-323-29568-0.

Google Scholar

28. Kidney Disease: Improving Global Outcomes (KDIGO) CKD Work Group. KDIGO 2017 clinical practice guideline update for the diagnosis, evaluation, prevention, and treatment of Chronic Kidney Disease - Mineral and Bone Disorder (CKD-MBD). Kidney Int Suppl (2017) 7(1):1–59. doi: 10.1016/j.kisu.2017.04.001

CrossRef Full Text | Google Scholar

29. Brown SGA. Clinical features and severity grading of anaphylaxis. J Allergy Clin Immunol (2004) 114:371–6. doi: 10.1016/j.jaci.2004.04.029

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Silva HA, Pathmeswaran A, Ranasinha CD, Jayamanne S, Samarakoon SB, Hittharage A, et al. Low-dose adrenaline, promethazine, and hydrocortisone in the prevention of acute adverse reactions to antivenom following snakebite: a randomized, double-blind, placebo-controlled trial. PloS Med (2011) 8(5):e1000435. doi: 10.1371/journal.pmed.1000435

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Chávez-Olórtegui C, Fonseca SCG, Campolina D, Amaral CFS, Diniz CR. ELISA for the detection of toxic antigens in experimental and clinical envenoming by Tityus serrulatus scorpion venom. Toxicon (1994) 32(12):1649–56. doi: 10.1016/0041-0101(94)90323-9

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Nakane PK, Kawoi A. Peroxidase-labeled antibody. A new method of conjugation. J Histochem Cytochem (1974) 22(12):1084–91. doi: 10.1177/22.12.1084

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Bucaretchi F, Mello SM, Vieira RJ, Mamoni RL, Blotta MHSL, Antunes E, et al. Systemic envenomation caused by the wandering spider Phoneutria nigriventer, with quantification of circulating venom. Clin Toxicol (2008) 46(9):885–9. doi: 10.1080/15563650802258524

CrossRef Full Text | Google Scholar

34. Hackshaw A. A concise guide to clinical trials. Oxford: Wiley-Blackwell (2009). p. 224, ISBN: 978-1-405-16774-1.

Google Scholar

35. Zar JH. Bioestatistical analysis. New Jersey: Prentice Hall (2010). p. 944, ISBN: 978-8-178-08965-2.

Google Scholar

36. Bochner R. Paths to the discovery of antivenom serotherapy in France. J Venom Anim Toxins incl Trop Dis (2016) 22:20. doi: 10.1186/s40409-016-0074-7

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Phisalix C, Bertrand G. Sur la propriété antitoxique du sang des animaux vaccinés contre le venin de vipère. C R Soc Biol (1894) 46:111–3.

Google Scholar

38. Calmette A. L’immunisation artificielle des animaux contre le venin des serpents, et la thérapeutique expérimentale des morsures venimeuses. C R Soc Biol (1894) 46:120–4.

Google Scholar

39. Lucas SM. The history of venomous spider identification, venom extraction methods and antivenom production: a long journey at the Butantan Institute, São Paulo, Brazil. J Venom Anim Toxins incl Trop Dis (2015) 21:21. doi: 10.1186/s40409-015-0020-0

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Pucca MB, Cerni FA, Janke R, Bermúdez-Méndez E, Ledsgaard L, Barbosa JE, et al History of envenoming therapy and current perspectives. Front Immunol (2019) 10:1598. doi: 10.3389/fimmu.2019.01598

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Grego KF, Vieira SEM, Vidueiros JP, Serapicos EO, Barbarini CC, da Silveira GPM, et al Maintenance of venomous snakes in captivity for venom production at Butantan Institute from 1908 to the present: a scoping history. J Venom Anim Toxins Incl Trop Dis (2021) 27:e20200068. doi: 10.1590/1678-9199-JVATITD-2020-0068

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Collins AM, Rinderer TE, Tucker KW. Colony defence of two honeybee types and their hybrid 1. Naturally mated queens. J Apic Res (1988) 27(3):137–40. doi: 10.1080/00218839.1988.11100793

CrossRef Full Text | Google Scholar

44. Silveira DC, Maracajá PB, Silva RA, Sousa RM, Sotoblanco B. Diurnal and seasonal changes of defensive behavior of Africanized bees (“Apis mellifera” L.). Rev Bras Saúde Prod Anim (2015) 16(4):925–34. doi: 10.1590/S1519-99402015000400016

CrossRef Full Text | Google Scholar

45. Fitzgerald KT, Flood AA. Hymenoptera stings. Clin Tech Small Anim Pract (2006) 21(4):194–204. doi: 10.1053/j.ctsap.2006.10.002

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Moreno M, Giralt E. Three valuable peptides from bee and wasp venoms for therapeutic and biotechnological use: melittin, apamin and mastoparan. Toxins (2015) 7(4):1126–50. doi: 10.3390/toxins7041126

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Souza MM, Teofilo-Guedes GS, Bueno ET, Milani LR, Souza ASB. Social wasps (Hymenoptera, Polistinae) from the Brazilian savanna – review. Sociobiology (2020) 67(2):129–38. doi: 10.13102/sociobiology.v67i2.4958

CrossRef Full Text | Google Scholar

48. World Health Organization. WHO Guidelines for the Production, Control and Regulation of Snake Antivenom Immunoglobulins. Geneva, Switzerland: World Health Organization (2018). Available at: (Accessed January 7, 2021).

Google Scholar

49. Gutiérrez JM, Solano G, Pla D, Herrera M, Segura Á, Vargas M, et al. Preclinical evaluation of the efficacy of antivenoms for snakebite envenoming: State-of-the-art and challenges ahead. Toxins (2017) 9(5):163. doi: 10.3390/toxins9050163

CrossRef Full Text | Google Scholar

50. Morais V. Antivenom therapy: efficacy of premedication for the prevention of adverse reactions. J Venom Anim Toxins incl Trop Dis (2018) 24:7. doi: 10.1186/s40409-018-0144-0

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Gutiérrez JM. Global availability of antivenoms: The relevance of Public Manufacturing Laboratories. Toxins (2018) 11(1):5. doi: 10.3390/toxins11010005

CrossRef Full Text | Google Scholar

52. León G, Herrera M, Segura Á, Villalta M, Vargas M, Pathogenic GJM. Mechanisms underlying adverse reactions induced by intravenous administration of snake antivenoms. Toxicon (2013) 76:63–76. doi: 10.1016/j.toxicon.2013.09.010

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Silva HA, Ryan NM, de Silva HJ. Adverse reactions to snake antivenom, and their prevention and treatment. Br J Clin Pharmacol (2016) 81(3):446–52. doi: 10.1111/bcp.12739

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Mendonça-da-Silva I, Magela-Tavares A, Sachett J, Sardinha JF, Zaparolli L, Gomes-Santos MF, et al. Safety and efficacy of a freeze-dried trivalent antivenom for snakebites in the Brazilian Amazon: An open randomized controlled phase IIb clinical trial. PloS Negl Trop Dis (2017) 11(11):e0006068. doi: 10.1371/journal.pntd.0006068

PubMed Abstract | CrossRef Full Text | Google Scholar

55. Lomonte B, Tarkowski A, Hanson LÅ. Host response to Bothrops asper snake venom: analysis of edema formation, inflammatory cells, and cytokine release in a mouse model. Inflammation (1993) 17:93–105. doi: 10.1007/BF00916097

PubMed Abstract | CrossRef Full Text | Google Scholar

56. Barraviera B, Lomonte B, Tarkowski A, Hanson LÅ, Meira DA. Acute-phase reactions, including cytokines, in patients bitten by Bothrops and Crotalus snakes in Brazil. J Venom Anim Toxins (1995) 1(1):11–22. doi: 10.1590/S0104-79301995000100003

CrossRef Full Text | Google Scholar

57. Sofer S. Scorpion envenomation. Intensive Care Med (1995) 21:626–8. doi: 10.1007/BF01711538

PubMed Abstract | CrossRef Full Text | Google Scholar

58. Paolino G, Di Nicola MR. Letter to the Editor: Acute-phase response fever in Viperidae as a potential and additional clinical sign. Toxicon (2020) 184:229–30. doi: 10.1016/j.toxicon.2020.07.008

PubMed Abstract | CrossRef Full Text | Google Scholar

59. Voronov E, Apte RN, Sofer S. The systemic inflammatory response syndrome related to the release of cytokines following severe envenomation. J Venom Anim Toxins (1999) 5(1):5–33. doi: 10.1590/S0104-79301999000100002

CrossRef Full Text | Google Scholar

60. Slevin M, Molins B. Editorial: C-Reactive protein in age-related disorders. Front Immunol (2018) 9:2745. doi: 10.3389/fimmu.2018.02745

PubMed Abstract | CrossRef Full Text | Google Scholar

61. Paniagua D, Vergara I, Román R, Romero C, Benard-Valle M, Calderón A, et al. Antivenom effect on lymphatic absorption and pharmacokinetics of coral snake venom using a large animal model. Clin Toxicol (2019) 57(8):727–34. doi: 10.1080/15563650.2018.1550199

CrossRef Full Text | Google Scholar

62. Rivière G, Choumet V, Audebert F, Sabouraud A, Debray M, Scherrmann JM, et al. Effect of antivenom on venom pharmacokinetics in experimentally envenomed rabbits: toward an optimization of antivenom therapy. J Pharmacol Exp Ther (1997) 281(1):1–8.

PubMed Abstract | Google Scholar

63. Rivière G, Choumet V, Saliou B, Debray M, Bon C. Absorption and elimination of viper venom after antivenom administration. J Pharmacol Exp Ther (1998) 285(2):490–5.

PubMed Abstract | Google Scholar

64. Barraviera B, Sartori A, Silva MFP, Kaneno R, Peraçoli MTS. Use of an ELISA assay to evaluate venom, antivenom, IgG and IgM human antibody levels in serum and cerebrospinal fluid from patients bitten by Crotalus durissus terrificus in Brazil. J Venom Anim Toxins (1996) 2(1):14–27. doi: 10.1590/S0104-79301996000100003

CrossRef Full Text | Google Scholar

65. Boyer LV, Seifert SA, Clark RF, McNally JT, Williams SR, Nordt SP, et al. Recurrent and persistent coagulopathy following pit viper envenomation. Arch Intern Med (1999) 159:706–10. doi: 10.1001/archinte.159.7.706

PubMed Abstract | CrossRef Full Text | Google Scholar

66. Boyer LV, Seifert SA, Cain JS. Recurrence phenomena after immunoglobulin therapy for snake envenomations: Part 2. Guidelines for clinical management with crotaline Fab antivenom. Ann Emerg Med (2001) 37(2):196–201. doi: 10.1067/mem.2001.113134

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: antivenom, Apis mellifera (Africanized), clinical trial, safety assessment, enzyme-linked immunosorbent assay (ELISA)

Citation: Barbosa AN, Ferreira RS Jr, de Carvalho FCT, Schuelter-Trevisol F, Mendes MB, Mendonça BC, Batista JN, Trevisol DJ, Boyer L, Chippaux J-P, Medolago NB, Cassaro CV, Carneiro MTR, de Oliveira APP, Pimenta DC, da Cunha LER, Santos LDd and Barraviera B (2021) Single-Arm, Multicenter Phase I/II Clinical Trial for the Treatment of Envenomings by Massive Africanized Honey Bee Stings Using the Unique Apilic Antivenom. Front. Immunol. 12:653151. doi: 10.3389/fimmu.2021.653151

Received: 13 January 2021; Accepted: 05 March 2021;
Published: 23 March 2021.

Edited by:

Choo Hock Tan, University of Malaya, Malaysia

Reviewed by:

José María Gutiérrez, University of Costa Rica, Costa Rica
Anjana Silva, Rajarata University of Sri Lanka, Sri Lanka

Copyright © 2021 Barbosa, Ferreira, de Carvalho, Schuelter-Trevisol, Mendes, Mendonça, Batista, Trevisol, Boyer, Chippaux, Medolago, Cassaro, Carneiro, de Oliveira, Pimenta, da Cunha, Santos and Barraviera. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Rui Seabra Ferreira Jr,

These authors have contributed equally to this work and share first authorship

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