Original Research ARTICLE
Assessing the Diversity and Stability of Cellular Immunity Generated in Response to the Candidate Live-Attenuated Dengue Virus Vaccine TAK-003
- 1Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, MA, United States
- 2Department of Medicine, Upstate Medical University of New York, Syracuse, NY, United States
The development of an efficacious DENV vaccine has been a long-standing public health priority. However, this effort has been complicated significantly due to the hazard presented by incomplete humoral immunity in mediating immune enhancement of infection and disease severity. Therefore, there is a significant need for DENV vaccine platforms capable of generating broad immune responses including durable cellular immunity, as well as novel analytical tools to assess the magnitude, diversity, and persistence of vaccine-elicited immunity. In this study, we demonstrate that a single dose of the recombinant, tetravalent, live-attenuated DENV vaccine TAK-003 elicits potent and durable cellular immunity against both the structural and non-structural proteins of all four DENV serotypes, which is maintained for at least 4 months post-immunization. Although not contained within the vaccine formulation, significant reactivity against the non-structural (NS) proteins of DENV-1,-3, and-4 is observed following vaccination, to an extent directly proportional to the magnitude of responses to the corresponding vaccine (DENV-2) components. Distinct, quantifiable, and durable patterns of DENV antigen reactivity can be observed in individuals following vaccination. Detailed epitope mapping of T cell reactivity against the DENV-2 proteome using a matrix of overlapping peptide pools demonstrated that TAK-003 elicits a broad response directed across the DENV-2 proteome, with focused reactivity against NS1 and NS3. We conclude that, as measured by an IFN-γ ELISPOT assay, a single dose of TAK-003 generates potent T cell-mediated immunity which is durable in magnitude and breadth through 4 months post-vaccination.
Dengue virus (DENV) is the causative agent of an acute febrile illness in humans and is a significant source of global morbidity (1). It is an arthropod-borne virus that is transmitted predominantly by the mosquito vectors of the genus Aedes (2). DENV is a single-stranded positive sense RNA virus that belongs to the family Flaviviridae, genus Flavivirus, and consists of four genetically and immunologically distinct serotypes: DENV-1; DENV-2; DENV-3; and DENV-4. DENV infects between 280 and 550 million people worldwide every year with as many as 100 million infection resulting in clinical presentation (any severity of disease) (1, 3). Infection with DENV is subclinical in the majority of cases, but it may also cause dengue fever, a debilitating flu-like illness that lasts for up to 2 weeks. Approximately 500,000 cases per year develop into severe dengue, dengue hemorrhagic fever/dengue shock syndrome (DHF/DSS), which has a mortality rate of up to 20% (4–7). Dengue is endemic in south and south-east Asia, the western Pacific, sub-Saharan Africa, and Central and South America, and hence at least 40% of the world's population is at risk of infection (1). Extensive globalization of DENV and increases in regional endemic serotype make-up and complexity continue to occur (1). As a result, developing a protective, durable, and safe vaccine product to counter the global threat of DENV infection is a public health priority. However, the difficulty in inducing immunity to all four DENV serotypes, the lack of a validated animal model for vaccine testing, and the lack of defined immune correlates of protective immunity represent significant obstacles to this effort. These challenges are further highlighted by the recent revelation that the only currently available DENV vaccine (Dengvaxia®) not only fails to protect previously DENV naïve individuals from infection, but can increase the risk of hospitalization with virologically confirmed dengue (8, 9). Therefore, there is significant need for new DENV vaccine candidates, as well as new tools and approaches to assess DENV vaccine safety, efficacy, durability, and immunogenicity.
To date, much focus has been placed on measuring neutralizing antibodies (NAb) as an immune correlate of protection against subsequent dengue infection (10–14). However, data from Phase IIb and Phase III trials of the Sanofi-Pasteur vaccine product (Dengvaxia®) demonstrated a discordance between vaccine efficacy and NAb titers (15–17). In addition, while DENV-elicited humoral immunity undoubtedly contributes to protection against homotypic and heterotypic reinfection, the same humoral milieu may play a more pathologic role upon heterotypic infection. While the pathogenesis of DHF/DSS is mechanistically complex and may involve some degree of genetic predisposition (18, 19), waning humoral immunity following infection and partial antibody-mediated cross-recognition of heterotypic DENV is one potential explanation for the increased incidence of severe disease in the setting of secondary infection (5, 20, 21). Antibody-dependent enhancement (ADE) of DENV infection has been demonstrated in numerous in vitro experimental models and in vivo adoptive transfer animal models (5, 10, 22–24), although these models have not translated to human disease, and definitive in vivo evidence of ADE in humans has been elusive.
In light of gaps in knowledge about the relationship between humoral immunity and outcome of DENV infection, there is the need to investigate the contribution of other immune response parameters, particularly cell mediated immunity (CMI)—especially T cell-mediated immunity—to the outcome of DENV infection (25–27). Recent studies suggest that the expression of certain HLA alleles—and the nature/magnitude of the T cell responses they facilitate—correspond to susceptibility or resistance to disease, and potential DENV vaccine efficacy (28, 29). Human T cell responses to DENV were first characterized over 30 years ago, and many of the general principles originally described have remained consistent (25, 27). Infection with one DENV induces both CD4+ and CD8+ memory T cells specific for DENV epitopes, with a small number of epitopes dominating the response in each individual (28, 29). Epitopes are located throughout the DENV polyprotein, although several regions, especially non-structural protein 3 (NS3) and the capsid protein, appear to have a concentration of immunodominant epitopes targeted by CD8+ T cells and CD4+ T cells, respectively (30–32). The amino acid homology across the four DENV serotypes varies for each epitope; however, most epitopes are well-conserved among strains within the same serotype and differ at relatively few positions (1–3 of 9 residues) from the corresponding epitopes of other DENV serotypes (and other flaviviruses) (33, 34). As is observed in DENV-elicited humoral immunity, the overall T cell response induced by a primary DENV infection is strongest to the serotype to which the subject was exposed, but variable degrees of cross-reactivity are usually observed to one or more of the other serotypes (35, 36).
TAK-003 is a tetravalent, recombinant DENV vaccine candidate based on the attenuated PDK-53 DENV-2 virus strain that is currently undergoing phase III testing with a two-dose vaccine schedule (37). The PDK-53 strain was initially derived from the WT DENV-2 16,681 isolate, and attenuated by serial passage in primary dog kidney (PDK) cells. Key attenuation mutations have been identified in the 5′ UTR, NS1, and NS3 regions of the viral genome (38). This DENV-2 backbone virus was previously shown to be safe, immunogenic, and capable of stimulating durable cellular and humoral immunity (39–43). To create a vaccine capable of eliciting an immune response against all four DENV serotypes, recombinant viruses were created using the PDK-53 DENV-2 genetic backbone and the prM and E genes from DENV-1,-3, and-4 (44). The tetravalent TAK-003 formulation was also shown to be safe, immunogenic, and protective against lethal DENV challenge in both rodent models and non-human primates (37, 44, 45). In clinical trials, TAK-003 is well-tolerated and capable of generating significant humoral immunity against all four DENV serotypes in both children and adults, regardless of previous dengue serostatus (46–51). Previous analysis of the T cell cytokine production profile generated by TAK-003 administration in flavivirus-naïve recipients demonstrated that this product generates a pool of NS1, NS3, and NS5 reactive CD8+ T cells capable of producing IFN-γ, TNF-α, and to a lesser extent IL-2 upon ex vivo restimulation (52). However, the magnitude, stability, and antigen specificity of cell-mediated immunity generated in response to a TAK-003 vaccination has not previously been described in detail.
In this study, we demonstrate that a single dose of TAK-003 elicits a potent T cell response as assessed by IFN-γ ELISPOT 28- and 120-days post vaccination. Reactivity against the structural genes of DENV-1,-2,-3, and-4 contained within the vaccine formulation was observed to be significantly elevated over pre-vaccination levels 28 days post vaccination, with reactivity against the structural proteins of DENV-2 and-4 maintained for at least 120 days. However, reactivity against the structural regions of DENV represented only 13–20% of the total T cell response observed, with the rest of the T cell response directed against the non-structural DENV proteins. As the PDK-53-derived DENV-2 backbone is the only source of non-structural DENV antigen in TAK-003, a significant amount of reactivity against these gene products is observed, with reactivity against DENV-2 NS1, NS3, and NS5 dominating. While there are no DENV-1,-3, and-4 non-structural antigens present in TAK-003, a significant amount of T cell cross-reactivity against these antigens was observed 28- and 120-days post vaccination. The magnitude of cross-reactivity observed was directly proportional to the strength of the response directed against the DENV-2 non-structural antigens contained within TAK-003. While the overall response rate to vaccination as measured by IFN-γ ELISPOT was very high in this study (85% at day 120), significant individual-to-individual variability was observed in antigen immunodominance hierarchy. Dimensional-reduction visualization (tSNE projection) and hierarchal cluster analysis of ELISPOT reactivity data revealed the presence of 7 distinct patterns of DENV-2 reactivity following TAK-003 vaccination. Individuals falling within these distinct clusters of reactivity maintained their relative cluster localization between 28- and 120-days post vaccination, suggesting that these designations represent stable outcomes of vaccination. Finally, detailed epitope mapping of T cell reactivity against the DENV-2 proteome using a matrix of overlapping peptide pools demonstrated that TAK-003 elicits a broad response directed across the DENV-2 proteome.
Materials and Methods
The samples used in this study were collected during a Phase 1 trial in US adults of a tetravalent, live-attenuated dengue virus vaccine candidate, TAK-003 (“Impact of Subcutaneous vs. Intramuscular Administration of Inviragen's Live Attenuated Dengue Vaccine on Safety and Immunogenicity” NCT01728792; WRAIR #1987). Subjects received one dose of TAK-003 either subcutaneously or intramuscularly and whole blood was collected at day of vaccination (day 0) and at days 14, 28, and 120 post-vaccination. Individuals were not stratified by route of vaccination in subsequent analysis. Whole blood was collected in Cell Preparation Tubes (BD Vacutainer) for isolation of PBMC. Cells were cryopreserved at ~107 per mL and stored in vapor-phase liquid nitrogen until use. Vaccine administration and PBMC collection were performed after written informed consent in accordance with the Declaration of Helsinki. The studies and protocols were approved by the institutional review boards at the State University of New York Upstate Medical University and the Human Subjects Research Review Board for the Commanding General of the U.S. Army Medical Research and Material Command. Exclusion criteria for participation in this study include history of dengue fever, Japanese Encephalitis, West Nile or Yellow Fever disease, and history of travel to dengue endemic areas including the Caribbean, Mexico, Central America, South America or Southeast Asia during the month prior to screening, or planned travel to a dengue endemic area during the study period. All subjects were screened to be seronegative to dengue or West Nile at the time of study initiation.
T Cell ELISPOT Assay
Cryopreserved PBMC were thawed and placed in RPMI 1640 medium supplemented with 10% heat-inactivated normal human serum (100–318, Gemini Bio-Products), L-glutamine, penicillin, and streptomycin. After an overnight rest at 37°C, the PBMC were washed, resuspended in serum free medium (SFM; X-VIVO 15, Lonza), cellular viability assessed by trypan blue exclusion, and 1–2 × 105 viable cells were plated per well of a 96-well Millipore MAIPSWU plate coated with anti-IFN-γ antibody according to the manufacturer's instructions (3420-2HW-Plus, Mabtech Inc.). Peptide pools were added to the cells at a final concentration of 1 μg/mL/peptide prior to incubation at 37°C overnight. Controls included SFM plus 0.5% DMSO (negative) and anti-CD3 (positive). The ELISPOT plates were developed using TMB substrate and read using a CTL-ImmunoSpot® S6 Ultimate-V Analyzer (Cellular Technology Limited). All peptide pools were tested in duplicate, and the mean value of the duplicate wells utilized as the reported value. Individuals were considered reactive to a peptide pool when the response was >50 SFC/106 PBMC and was 4-fold over the corresponding negative control. For matrix ELISPOT analysis, positive wells were defined as those with a signal 5-fold over the negative (no stimulation) control, and >5 spots per well after subtracting the negative (no stimulation) control. All data were normalized based on the number of cells plated per well and are presented herein as SFC/106 PBMC values.
Overlapping peptide pools corresponding to the full-length envelop (E), non-structural 1 (NS1), NS3, and NS5 proteins for DENV-1-4 and NS2a/b and NS4a/b proteins for DENV-2 were obtained through the NIH Biodefense and Emerging Infections Research Resources Repository, NIAID, NIH (Supplemental Table 4). Additional overlapping peptide pools covering the capsid (C) and precursor membrane (prM) proteins of DENV-1-4, were purchased from JPT Peptide Technologies (Supplemental Table 4). Peptide pool stocks were reconstituted in DMSO at a concentration of 200 μg/mL/peptide and stored at −80°C.
TSNE projection, hierarchical clustering, and visualization of multidimensional IFN-γ ELISPOT data was performed in R (v3.5.2). tSNE projection and hierarchical clustering was calculated using the package rtsne utilizing background-subtracted data, a perplexity value of 30 and theta value of 0.5. Hierarchical clustering was performed using a cluster value of 7. The resulting two-dimensional dataset was visualized using the package ggplot2. All code is available upon request from the corresponding author. All other statistical analyses were performed using GraphPad Prism v6 Software (GraphPad Software, La Jolla, CA). A p-value <0.05 was considered significant.
TAK-003 Elicits Significant Cellular Immunity Against the Structural Proteins of DENV-1,-2,-3, and -4
TAK-003 is a recombinant, tetravalent, live-attenuated dengue vaccine candidate derived from the attenuated PDK-53 DENV-2 strain. To generate a vaccine product which contains the structural proteins from all four DENV serotypes, the structural genes (CprM/E) from the parental DENV-2 backbone were sequentially replaced with those from DENV-1, DENV-3, or DENV-4 to create three additional recombinant DENV strains (Figure 1A). These four live-attenuated viruses were co-formulated for simultaneous vaccine administration.
Figure 1. Cell-mediated reactivity against DENV-1,-2,-3, and-4 structural proteins following TAK-003 administration. (A) Schematic representation of the genetic structure of the tetravalent TAK-003 vaccine platform. Key attenuating mutations in the 5′ UTR, NS1, and NS3 are indicated by the yellow stars. (B) Frequency of IFN-γ producing cells as quantified by ELISPOT following DENV-1 CprM/E peptide stimulation at the indicated time points following vaccination. (C) Frequency of IFN-γ producing cells as quantified by ELISPOT following DENV-2 CprM/E peptide stimulation at the indicated time points following vaccination. (D) Frequency of IFN-γ producing cells as quantified by ELISPOT following DENV-3 CprM/E peptide stimulation at the indicated time points following vaccination. (E) Frequency of IFN-γ producing cells as quantified by ELISPOT following DENV-4 CprM/E peptide stimulation at the indicated time points following vaccination. (F) Frequency of IFN-γ producing cells as quantified by ELISPOT following DENV-1,-2,-3, and-4 CprM/E peptide stimulation at day 120 post vaccination. n = 60 for days 0 and 28, n = 54 for day 120. *p < 0.05, **p < 0.01, ****p < 0.0001, ns, not significant Paired two-tailed t-test. Bars indicate group mean ± SEM. Zero values were superimposed on the logarithmic graph.
Vaccination with TAK-003 resulted in a significant increase in the number of circulating IFN-γ producing cells at day 28 post vaccination responding to the structural proteins (CprM/E) from DENV 1 (Figure 1B, Table 1), DENV-2 (Supplemental Figure 1, Figure 1C, Table 1), DENV-3 (Figure 1D, Table 1), and DENV-4 (Figure 1E, Table 1) as assessed by IFN-γ ELISPOT. However, while the number of circulating IFN-γ producing cells reacting to the structural proteins (CprM/E) of DENV-2 and DENV-4 remained significantly elevated on day 120 post vaccination relative to pre-vaccination (Figures 1C,E), the number of circulating DENV-1 CprM/E and DENV-3 CprM/E reactive cells on day 120 post vaccination was returning to baseline (pre-vaccination) levels when assessed as a group (Figures 1B,D). Therefore, despite significant reactivity against CprM/E derived from all serotypes at 28-days post vaccination, there were significantly more DENV-2 and DENV-4 reactive T cells on day 120 than DENV-1 and DENV-3 reactive cells (Figure 1F).
TAK-003 Elicits Significant and Broad Cellular Immunity Against the Non-structural Proteins of DENV-2
While the majority of the protective humoral immunity generated by DENV infection or vaccination is canonically thought to be directed against the DENV envelope protein (53–56), a significant fraction of the cell-mediated immune response to DENV infection is directed against the non-structural proteins (NS1, NS2a/b, NS3, NS4a/b, and NS5) (33, 34). As the only non-structural DENV proteins contained within the TAK-003 formulation originate from the DENV-2 backbone (Figure 1A), we assessed the magnitude and breadth of the T cell response generated against all five DENV-2 NS proteins on days 28 and 120 post vaccination.
Immunization with TAK-003 resulted in a significant increase in the number of circulating IFN-γ producing T cells at day 28 post vaccination responding to DENV-2 NS1 (Supplemental Figure 1, Figure 2A, Table 2), DENV-2 NS2a/b (Supplemental Figure 1, Figure 2B, Table 2), DENV-2 NS3 (Supplemental Figure 1, Figure 2C, Table 2), DENV-2 NS4a/b (Supplemental Figure 1, Figure 2D, Table 2), and DENV-2 NS5 (Supplemental Figure 1, Figure 2E, Table 2). These responses persisted for at least 120 days post vaccination, some of which increased moderately from day 28 to day 120 (Figures 2A–E). Responses to non-structural proteins accounted for ~85% of the total reactivity against DENV-2, with NS1, NS3, and NS5 contributing a combined ~75% of the overall DENV-2 response (Figure 2F). While the total number of IFN-γ producing DENV-2 reactive T cells increased from day 28 to day 120 post vaccination, the relative distribution of the responses to individual DENV-2 structural and non-structural proteins remained consistent.
Figure 2. Cell-mediated reactivity against DENV2 non-structural proteins following TAK-003 administration. (A) Frequency of IFN-γ producing cells as quantified by ELISPOT following DENV-2 NS1 peptide stimulation at the indicated time points following vaccination. (B) Frequency of IFN-γ producing cells as quantified by ELISPOT following DENV-2 NS2a/b peptide stimulation at the indicated time points following vaccination. (C) Frequency of IFN-γ producing cells as quantified by ELISPOT following DENV-2 NS3 peptide stimulation at the indicated time points following vaccination. (D) Frequency of IFN-γ producing cells as quantified by ELISPOT following DENV-2 NS4a/b peptide stimulation at the indicated time points following vaccination. (E) Frequency of IFN-γ producing cells as quantified by ELISPOT following DENV-2 NS5 peptide stimulation at the indicated time points following vaccination. (F) Relative distribution and magnitude of DENV2 reactivity at day 28 and 120 post vaccination. Numbers at the top of each bar indicate average number of Spot Forming Cells (SFCs) per million PBMCs observed in response to DENV-2 stimulation in all subjects at the relevant time points. n = 60 for days 0 and 28, n = 54 for day 120. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 Paired two-tailed t-test. Bars indicate group mean ± SEM. Zero values were superimposed on the logarithmic graph.
TAK-003 Elicits DENV Serotype Cross-Reactive Responses Against the Non-structural Proteins of DENV-1,-3, and -4
While the only non-structural DENV genes contained within TAK-003 are DENV-2 in origin, a significant cellular immune response to the non-structural proteins (NS1, NS3, NS5) of DENV-1,-3, and-4 was observed 28- and 120-days post TAK-003 administration as assessed by IFN-γ ELISPOT (Supplemental Figure 2, Table 3). The only exception to this trend was the cross-reactive response observed against DENV-1 NS1. While some individuals did have a detectible DENV-1 NS1 response (Table 3) the overall magnitude of all subjects failed to reach significance at either 28- or 120-days post vaccination (Supplemental Figure 1). While the overall magnitude of the observed cross-reactive response against most non-structural proteins of DENV-1,-3, and-4 was significantly elevated relative to baseline following TAK-003 administration, the relative responses to NS1 (Figure 3A), NS3 (Figure 3B), and NS5 (Figure 3C) from DENV-1,-3, and-4 were significantly lower than the responses observed against the corresponding proteins from DENV-2. These data suggest that any reactivity against the non-structural proteins of DENV-1, -3, and-4 is dependent on a strong response against the non-structural proteins of DENV-2. This hypothesis is supported by the observation that the magnitude of TAK-003-stimulated DENV-1 (Figure 3D), DENV-3 (Figure 3E) and DENV-4 (Figure 3F) non-structural protein cross-reactivity is directly proportional to the magnitude of the corresponding DENV-2 non-structural protein response. Therefore, while multi-serotype cellular immunity against DENV non-structural proteins can be generated in response to what is essentially a monovalent exposure, the magnitude of cross-reactivity is significantly lower and directly proportional to the magnitude of the vaccine-directed response.
Figure 3. Cross-reactivity of T cell responses following TAK-003 administration. (A) Frequency of IFN-γ producing cells as quantified by ELISPOT upon DENV-1,-2,-3, and-4 NS1 peptide stimulation at day 120 post vaccination. (B) Frequency of IFN-γ producing cells as quantified by ELISPOT upon DENV-1,-2,-3, and-4 NS3 peptide stimulation at day 120 post vaccination. (C) Frequency of IFN-γ producing cells as quantified by ELISPOT upon DENV-1,-2,-3, and-4 NS5 peptide stimulation at day 120 post vaccination. (D) Relative frequency of IFN-γ producing cells activated in response to DENV-1 NS1, NS3, and NS5 vs. DENV-2 NS1, NS3, and NS5 peptide stimulation at day 120 post vaccination. (E) Relative frequency of IFN-γ producing cells activated in response to DENV-3 NS1, NS3, and NS5 vs. DENV-2 NS1, NS3, and NS5 peptide stimulation at day 120 post vaccination. (F) Relative frequency of IFN-γ producing cells activated in response to DENV-4 NS1, NS3, and NS5 vs. DENV-2 NS1, NS3, and NS5 peptide stimulation at day 120 post vaccination. n = 54. ***p < 0.001, ****p < 0.0001 Paired two-tailed t-test. R2 calculated by linear regression. Bars indicate group mean ± SEM. Zero values were superimposed on the logarithmic graph.
Distinct Patterns of Antigen Reactivity Following TAK-003 Administration
Although administration of TAK-003 resulted in a significant and fairly uniform overall increase in total DENV-2 reactivity 28- and 120-days post vaccination (Table 2), there was significant individual-to-individual variation in the pattern of DENV-2 protein reactivity. As has been observed following natural DENV infection or vaccination with other DENV vaccine candidates, individuals often exhibit differences in antigen immunodominance hierarchy (33, 34). This variation in individual DENV epitope reactivity can be partially attributed to differences in host HLA genotype, which dictates which DENV-derived epitopes can be efficiently presented by infected cells or professional antigen presenting cells to putative DENV-reactive T cells (28).
In an attempt to capture and quantify the unique individual patterns of DENV reactivity elicited by TAK-003 administration in an unsupervised fashion—and to potentially define statistically unique patterns of reactivity that might eventually correlate with vaccine efficacy or durability—we utilized dimensional compression analysis to display the magnitude and specificity of the IFN-γ ELISPOT response directed against the DENV-2 proteome (CprM, E, NS1, NS2a/b, NS3, NS4a/b, and NS5) on days 0, 28, and 120 post vaccination in 2-dimensional space. We used t-Distributed Stochastic Neighbor Embedding (tSNE) visualization and hierarchical cluster analysis to visualize and group 174 data points generated during this study. Each data point corresponds to one time point for one subject, and reflects the cumulative reactivity against both the structural and non-structural proteins of DENV-2.
Using these tools, we were able to identity 7 statistically distinct clusters of DENV-2 reactivity in TAK-003 recipients on days 0, 28, or 120 post vaccination (Figures 4A,B). Data points falling in cluster 1 possess little-or-no DENV reactivity, and overwhelmingly correspond to pre-vaccination samples (Figure 4C). Cluster 2 contains a mix of day 0, 28, and 120 post vaccination samples. While exhibiting slightly higher DENV-2 reactivity than cluster 1, cluster 2 does not exhibit a distinct pattern of reactivity and contains those individuals who responded poorly to vaccination or whose response to vaccination did not persist (Figure 4D). Data points falling in clusters 3 and 4 are from primarily day 28 and day 120 post vaccination samples and exhibit a strong NS1 or NS2a/b biased response, respectively (Figures 4E,F). Cluster 5 is characterized by a dominant NS5 response (Figure 4G), while clusters 6 and 7 have dual NS3 and NS5 reactivity of differing magnitudes (Figures 4H,I).
Figure 4. Unsupervised dimensional reduction and hierarchal clustering of DENV-2 antigen reactivity. (A) tSNE projection and hierarchal clustering of 7-dimentional DENV-2 reactivity data (C/M, E, NS1, NS2a/b, NS3, NS4a/b, and NS5 stimulation) as assessed by IFN-γ ELISPOT in all samples from days 0, 28, and 120 post TAK-003 administration. Average frequency of IFN-γ producing cells as assessed by ELISPOT in response to stimulation with the indicated peptide pools in (B) all data points, (C) cluster 1 data points, (D) cluster 2 data points, (E) cluster 3 data points, (F) cluster 4 data points, (G) cluster 5 data points, (H) cluster 6 data points, or (I) cluster 7 data points. Bars indicate group mean ± SEM. tSNE clustering was performed with a perplexity value of 30 and theta of 0.5. Hierarchical clustering analysis was performed using a cluster value of 7.
Since our analysis contained multiple time points for each individual post vaccination, we were able to assess the stability of our statistically defined clusters as TAK-003-elicted immunity matured over time, and how localization in a given cluster corresponded to an individual's long-term DENV reactivity. Only two individuals fell within cluster 1 at day 28 post vaccination and either remained in cluster 1 on day 120 post vaccination or moved to the poorly-responsive cluster 2 (Supplemental Figure 3, Supplemental Table 1), suggesting that these individuals are true non-responders to vaccination from the perspective of T cell immunity. As predicted by the low-level and relatively non-specific DENV-2 reactivity that characterizes cluster 2, this cluster is highly unstable between days 28 and 120 post vaccination and likely represents a “transition” state between more stable outcomes of vaccination (Supplemental Figure 3, Supplemental Table 1). Individuals falling within cluster 3 and cluster 4 on day 28 post vaccination (NS1 or NS2a/b reactive) are highly stable, with 82% of individuals staying within the same cluster between days 28 and 120 post vaccination (Supplemental Figure 3, Supplemental Table 1). There is significant movement of individuals between clusters 5, 6 and 7 between days 28 and 120, but little movement of individuals out of this “super-group.” As clusters 5, 6, and 7 are characterized by different magnitudes of reactivity against the same antigens (NS3 and/or NS5), movement between these clusters might be predicted as immunity stabilizes after vaccination. No information is currently available on how these clusters may correspond to protection against subsequent challenge or infection, but these data demonstrate a novel method to assess the diversity and stability of vaccine-elicited cellular immunity.
Epitope Mapping of DENV-2 Reactivity Day-120 Post Vaccination
In light of the complex—yet restricted—pattern of DENV-2 reactivity observed following TAK-003 administration, we endeavored to define the exact DENV-2 derived epitopes recognized by the immune system following vaccination. To this end, we performed a matrix ELISPOT analysis of PBMC samples from 40 individuals obtained 120 days post TAK-003 vaccination using a library of 532 overlapping peptides spanning the entire DENV-2 proteome. The peptides used were 15-20 AA in length, overlapping by 10–14 AA, and were derived from the DENV-2 NGC strain.
A total of 221 peptides from the library of 532 possible candidates were recognized as reactive across all 40 individuals screened in this assay (Figure 5A, Supplemental Table 2). Of these immunogenic peptides, 109 were recognized by 5% or more of subjects analyzed (Supplemental Table 3), while 17 peptides were recognized by more than 10% of subjects (Figure 5B). The frequency of observed reactivity was highest for peptides derived from NS3, with 79.5% of all peptides derived from this protein eliciting a positive response in at least one subject, and with each peptide being recognized by 4.7% of subjects on average (Supplemental Table 2). In contrast, only 13.4% of peptides derived from E were recognized as immunogenic in TAK-003 immunized individuals, with each peptide being recognized by 0.48% of subjects on average. While proportionally the majority of the immunogenic peptides identified in this analysis were derived from NS3 (18.5% of all positive peptides), the most commonly recognized peptide screened in this analysis was derived from NS1, with 30% of subjects exhibiting reactivity against this single peptide. Notably, 90% of subjects falling into the previously described NS1-reactive “cluster 3” (Figure 4A) exhibited reactivity against this single dominant NS1-derived peptide or its adjacent neighbor (with which it shares 10 of 16 AA), suggesting that responsiveness to this epitope may be a significant driving factor in determining NS1- biased reactivity following vaccination.
Figure 5. Fine epitope mapping of DENV-2 T cell responses following TAK-003 administration. Magnitude and distribution of DENV-2 reactivity in TAK-003 recipients 120 days post vaccination. (A) Schematic representation of DENV-2 epitope reactivity following TAK-003 vaccination across the DENV-2 proteome. Bar height indicates the percentage of subjects responding to the indicated peptide at the corresponding genomic location. (B) Immunodominant DENV-2 epitopes identified in this analysis, defined as peptides eliciting a response in 10% or more of study participants following vaccination. Conservation of identified immunodominant DENV-2 peptides shown relative to DENV-1 (Singapore/S275/1990), DENV-3 (Philippines/H87/1956), and DENV-4 (Singapore/8976/1995). Conservation calculated as percent identify at the amino acid level. n = 40 subjects.
On average, amino acid level sequence conservation (identity) is 70% between all DENV serotypes (57). However, there is variation in the extent of sequence conservation in the various DENV protein subunits, including regions compatible with HLA presentation (33, 34). This fact is reflected in the relative amino acid level conservation of the 17 dominant immunogenic peptides identified in our screen. For those peptides derived from DENV-2 NS1 identified as immunogenic in this analysis, the average amino-acid level conservation (identity) between DENV-2 and the other 3 DENV serotypes is only 58%. In contrast, the immunogenic peptides derived from DENV-2 NS3 shared on-average 76% amino-acid level identity with NS3 from the other 3 DENV serotypes. These values offer a potential mechanistic explanation for the weak DENV-1 NS1 cross-reactivity observed in TAK-003 recipients, as well as the correspondingly robust NS3 cross-reactivity (Supplemental Figure 2).
In this study, we demonstrate that a single dose of the candidate tetravalent DENV vaccine TAK-003 elicits DENV-specific T cell responses in humans as assessed by IFN-γ ELISPOT at both 28- and 120-days post immunization. These responses were directed against all the antigens contained within the formulation, including the structural regions of DENV-1 to-4, as well as the non-structural regions of the DENV-2 derived vaccine backbone. In addition, significant cross-reactivity against the non-structural gene products (NS1, NS3, and NS5) of DENV-1,-3, and-4 was observed, with the magnitude of the cross-reactivity dictated by the magnitude of the response generated by the non-structural gene products of the vaccine's DENV-2 backbone. While the fraction of individuals responding to TAK-003 vaccination as assessed by IFN-γ ELISPOT was very high (85% at day 28), significant individual-to-individual variation in the pattern of antigenic reactivity was observed. We were able to categorize individuals into statistically distinct clusters based on their pattern of antigen reactivity using unsupervised dimensional reduction projection/visualization and hierarchical clustering of the IFN-γ ELISPOT data. Finally, we performed fine-epitope mapping of the DENV-2 T cell responses generated by TAK-003 vaccination using a matrix of 532 overlapping peptides representing the entire DENV-2 proteome. This approach identified 221 potential T cell epitopes spread across the DENV-2 proteome, of which 109 were found to be immunogenic in 5% or more study-subjects following vaccination, while 17 peptides were found to be immunogenic in 10% or more study-subjects.
Assessing and leveraging cell-mediated immunity in the setting of dengue vaccine design is increasing in relevance and urgency in light of the weak correlation observed between NAb titers and protective immunity following vaccination with Dengvaxia®) (15–17). While neutralizing antibodies are necessary and sufficient to provide sterile immunity to viral infection in animal models (58), growing evidence suggests that they are not sufficient to provide complete protection from infection in humans (15–17). Vaccine-directed cell-mediated immunity can in theory restrict viral replication and dissemination following DENV infection without risking the development of severe dengue via antibody-mediated immune enhancement during waning immunity. Furthermore, the development of stable, diverse, and mature humoral immunity is dependent on T cell help during B cell germinal center maturation (59). All vaccine products can reasonably be expected to induce some form of cell-mediated immunity—whether it is direct effector cells such as classical CTL, or NK cells, helper T cells which modulate the antibody and CTL responses, or more likely some combination of these. However, ensuring and confirming that the antigen-specific cellular immune response (T cell mediated) is directed against antigens that can enable lysis of infected cells or facilitate maturation of nascently activated B cells has not always been a focus in immunogenicity studies of candidate dengue vaccines.
In addition to producing durable and functional immunity, a key consideration for DENV vaccine design is generating immunity against four immunologically distinct viruses in a balanced and simultaneous manner. There is significant amino acid level homology between the four DENV serotypes (~70%), meaning that immunological cross-reactivity is readily achieved for both humoral and cell-mediated immunity, albeit with varying degrees of balance. However, the role that cross-reactive T cells play in facilitating DENV immunity and/or pathology is complex and incompletely understood. Severe dengue is often associated with significant peripheral T cell activation and expansion, including a significant number of serotype cross-reactive T cells (35, 60–62). Prior DENV exposure appears to have little impact on the number and frequency of DENV cross-reactive cells activated in response to acute infection, although the timing of their expansion and circulation differs between primary and secondary infection. However, as clinical symptoms of severe dengue (plasma leakage, etc) occur with or after defervescence and viral clearance, severe dengue is a consequence of dysregulated immunity following symptomatic viral infection (63). Therefore, categorizing cross-reactive T cells as either pathogenic or protective based on their presence during severe dengue is potentially problematic, and may misconstrue cause-and-effect. As there are currently no data available on the relationship between the generation of cross-reactive T cells following vaccination and protection from infection or severe disease, the precise role these cells play in protective immunity—especially in previously flavivirus-naïve individuals—remains unclear.
In addition to quantifying the cellular immunogenicity of the candidate DENV vaccine TAK-003, this study highlights two important features of DENV cellular immunity which can help refine approaches for functionally assessing future vaccines. Firstly, caution should be exercised when down-selecting epitopes or antigens to assess cellular immunity following vaccination or natural exposure to DENV. While NS3-derived peptides dominate the list of immunogenic epitopes identified in this analysis and NS3 responses exhibit the most cross-reactivity (presumably due to NS3 sequence conservation between serotypes), a significant fraction of vaccinated individuals in this trial exhibited little-or-no reactivity against NS3, and instead exhibited monotypic reactivity against NS1, NS2a/b, or NS4a/b. These distinct and stable patterns of individual reactivity are most likely attributable to differences in host HLA genotype. Whether or not these unique patterns of reactivity correlate with protection following vaccination is still unclear, but the observation underlines the prudence of assessing the immunogenicity of a broad panel of vaccine-derived antigens. Secondly, due to the unique design of the TAK-003 vaccine product, this study is among the first to directly assess the magnitude and persistence of vaccine-elicited DENV serotype-cross-reactivity in previously flavivirus-naïve individuals. We observed that the magnitude of serotype cross-reactivity for any given antigen is directly proportional to the magnitude of the response elicited by the corresponding vaccine-component. This observation provides mechanistic insight into the pattern of vaccine-driven immunity, and can also guide future vaccine design. Notably, while reactivity against the structural regions of DENV-1 and DENV-3 (antigens contained within the vaccine formulation) wanes by 120-days post vaccination, significant reactivity against the non-structural regions of DENV-1,-3, and-4 can still be observed at 120-days, despite the fact that these antigens are not contained within the vaccine formulation. The persistence of this cross-reactive response is attributable to the fact that the non-structural regions of the TAK-003 DENV-2 backbone accounts for the majority of the cellular immune response observed following vaccination. While the cross-reactive immune response directed against the non-structural regions of DENV-1,-3, and-4 is significantly lower than the vaccine-elicited response to the same regions of DENV-2, the relative magnitude of these responses still means that cross-reactive cellular immunity can persist even when responsiveness to other vaccine components wanes.
The investigators have adhered to the policies for protection of human subjects as prescribed in AR 70–25. The studies were approved by the institutional review boards at the State University of New York Upstate Medical University and the Human Subjects Research Review Board for the Commanding General of the U.S. Army Medical Research and Material Command.
MG and AK generated the data. JC conceived of the analysis, designed the experiments, and analyzed the data. RJ provided project oversite and secured funding. TE and ST conceived and designed the clinical trial. MP executed and oversaw the clinical trial and collected samples. HF designed and executed experiments and analyzed the data. AW analyzed the data and wrote the manuscript.
The opinions or assertions contained herein are the private views of the authors and are not to be construed as reflecting the official views of the US Army or the US Department of Defense. Material has been reviewed by the Walter Reed Army Institute of Research. There is no objection to its presentation and/or publication. The investigators have adhered to the policies for protection of human subjects as prescribed in AR 70–25.
Conflict of Interest Statement
The 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.
This work was supported by the Military Infectious Disease Research Program (MIDRP), the Congressionally Directed Medical Research Program (CDMRP), and MILVAX program. We wish to acknowledge Steven M. Taffet for his role in executing and overseeing the clinical trial associated with this study.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2019.01778/full#supplementary-material
2. Gubler DJ. Aedes aegypti and aedes aegypti-borne disease control in the 1990s: top down or bottom up. Charles franklin craig lecture. Am J Trop Med Hyg. (1989) 40:571–8. doi: 10.4269/ajtmh.1989.40.571
5. Sangkawibha N, Rojanasuphot S, Ahandrik S, Viriyapongse S, Jatanasen S, Salitul V, et al. Risk factors in dengue shock syndrome: a prospective epidemiologic study in Rayong, Thailand. I. the 1980 outbreak. Am J Epidemiol. (1984) 120:653–69. doi: 10.1093/oxfordjournals.aje.a113932
7. Yoon IK, Srikiatkhachorn A, Hermann L, Buddhari D, Scott TW, Jarman RG, et al. Characteristics of mild dengue virus infection in thai children. Am J Trop Med Hyg. (2013) 89:1081–7. doi: 10.4269/ajtmh.13-0424
8. Hadinegoro SR, Arredondo-García JL, Capeding MR, Deseda C, Chotpitayasunondh T, Dietze R, et al. Efficacy and long-term safety of a dengue vaccine in regions of endemic disease. N Engl J Med. (2015) 373:1195–206. doi: 10.1056/NEJMoa1506223
9. Sridhar S, Luedtke A, Langevin E, Zhu M, Bonaparte M, Machabert T, et al. Effect of dengue serostatus on dengue vaccine safety and efficacy. N Engl J Med. (2018) 379:327–40. doi: 10.1056/NEJMoa1800820
11. Halstead SB, Scanlon JE, Umpaivit P, Udomsakdi S. Dengue and chikungunya virus infection in man in Thailand, 1962-1964. IV. Epidemiologic studies in the Bangkok metropolitan area. Am J Trop Med Hyg. (1969) 18:997–1021. doi: 10.4269/ajtmh.1969.18.997
14. Putnak JR, de la Barrera R, Burgess T, Pardo J, Dessy F, Gheysen D, et al. Comparative evaluation of three assays for measurement of dengue virus neutralizing antibodies. Am J Trop Med Hyg. (2008) 79:115–22. doi: 10.4269/ajtmh.2008.79.115
15. Capeding MR, Tran NH, Hadinegoro SR, Ismail HI, Chotpitayasunondh T, Chua MN, et al. Clinical efficacy and safety of a novel tetravalent dengue vaccine in healthy children in Asia: a phase 3, randomised, observer-masked, placebo-controlled trial. Lancet. (2014) 384:1358–65. doi: 10.1016/S0140-6736(14)61060-6
16. Dayan GH, Garbes P, Noriega F, Izoton de Sadovsky AD, Rodrigues PM, Giuberti C, et al. Immunogenicity and safety of a recombinant tetravalent dengue vaccine in children and adolescents ages 9–16 years in Brazil. Am J Trop Med Hyg. (2013) 89:1058–65. doi: 10.4269/ajtmh.13–0304
17. Sabchareon A, Wallace D, Sirivichayakul C, Limkittikul K, Chanthavanich P, Suvannadabba S, et al. Protective efficacy of the recombinant, live-attenuated, CYD tetravalent dengue vaccine in thai schoolchildren: a randomised, controlled phase 2b trial. Lancet. (2012) 380:1559–67. doi: 10.1016/S0140–6736(12)61428–7
20. Katzelnick LC, Gresh L, Halloran ME, Mercado JC, Kuan G, Gordon A, et al. Antibody-dependent enhancement of severe dengue disease in humans. Science. (2017) 358:929–932. doi: 10.1126/science.aan6836
21. Wang TT, Sewatanon J, Memoli MJ, Wrammert J, Bournazos S, Bhaumik SK, et al. IgG antibodies to dengue enhanced for FcgammaRIIIA binding determine disease severity. Science. (2017) 355:395–8. doi: 10.1126/science.aai8128
23. Kliks SC, Nisalak A, Brandt WE, Wahl L, Burke DS. Antibody-dependent enhancement of dengue virus growth in human monocytes as a risk factor for dengue hemorrhagic fever. Am J Trop Med Hyg. (1989) 40:444–51. doi: 10.4269/ajtmh.1989.40.444
24. Zellweger RM, Prestwood TR, Shresta S. Enhanced infection of liver sinusoidal endothelial cells in a mouse model of antibody-induced severe dengue disease. Cell Host Microbe. (2010) 7:128–39. doi: 10.1016/j.chom.2010.01.004
28. Weiskopf D, Angelo MA, de Azeredo EL, Sidney J, Greenbaum JA, Fernando AN, et al. Comprehensive analysis of dengue virus-specific responses supports an hla-linked protective role for CD8+ T cells. Proc Natl Acad Sci USA. (2013) 110:E2046–53. doi: 10.1073/pnas.1305227110
30. Zivna I, Green S, Vaughn DW, Kalayanarooj S, Stephens HA, Chandanayingyong D, et al. T cell responses to an HLA-B*07-restricted epitope on the dengue NS3 protein correlate with disease severity. J Immunol. (2002) 168:5959–65. doi: 10.4049/jimmunol.168.11.5959
31. Duangchinda T, Dejnirattisai W, Vasanawathana S, Limpitikul W, Tangthawornchaikul N, Malasit P, et al. Immunodominant T-cell responses to dengue virus NS3 are associated with DHF. Proc Natl Acad Sci USA. (2010) 107:16922–7. doi: 10.1073/pnas.1010867107
32. Rivino L, Kumaran EA, Jovanovic V, Nadua K, Teo EW, Pang SW, et al. Differential targeting of viral components by CD4+ versus CD8+ T lymphocytes in dengue virus infection. J Virol. (2013) 87:2693–706. doi: 10.1128/JVI.02675–12
33. Olsen LR, Zhang GL, Keskin DB, Reinherz EL, Brusic V. Conservation analysis of dengue virus T-cell epitope-based vaccine candidates using peptide block entropy. Front Immunol. (2011) 2:69. doi: 10.3389/fimmu.2011.00069
34. Khan AM, Miotto O, Nascimento EJ, Srinivasan KN, Heiny AT, Zhang GL, et al. Conservation and variability of dengue virus proteins: implications for vaccine design. PLoS Negl Trop Dis. (2008) 2:e272. doi: 10.1371/journal.pntd.0000272
35. Friberg H, Burns L, Woda M, Kalayanarooj S, Endy TP, Stephens HA, et al. Memory CD8+ T cells from naturally acquired primary dengue virus infection are highly cross-reactive. Immunol Cell Biol. (2011) 89:122–9. doi: 10.1038/icb.2010.61
36. Mongkolsapaya J, Dejnirattisai W, Xu XN, Vasanawathana S, Tangthawornchaikul N, Chairunsri A, et al. Original antigenic sin and apoptosis in the pathogenesis of dengue hemorrhagic fever. Nat Med. (2003) 9:921–7. doi: 10.1038/nm887
37. Osorio JE, Brewoo JN, Silengo SJ, Arguello J, Moldovan IR, Tary-Lehmann M, et al. Efficacy of a tetravalent chimeric dengue vaccine (DENVax) in cynomolgus macaques. Am J Trop Med Hyg. (2011) 84:978–87. doi: 10.4269/ajtmh.2011.10–0592
38. Butrapet S, Huang CY, Pierro DJ, Bhamarapravati N, Gubler DJ, Kinney RM. Attenuation markers of a candidate dengue type 2 vaccine virus, strain 16681 (PDK-53), are defined by mutations in the 5' noncoding region and nonstructural proteins 1 and 3. J Virol. (2000) 74:3011–9. doi: 10.1128/JVI.74.7.3011–3019.2000
39. Vaughn DW, Hoke CH, Yoksan S, Lachance R, Innis BL, Rice RM, et al. Testing of a dengue 2 live-attenuated vaccine (Strain 16681 PDK 53) in ten American volunteers. Vaccine. (1996) 14:329–36. doi: 10.1016/0264–410X(95)00167-Y
40. Sabchareon A, Lang J, Chanthavanich P, Yoksan S, Forrat R, Attanath P, et al. Safety and immunogenicity of tetravalent live-attenuated dengue vaccines in thai adult volunteers: role of serotype concentration, ratio, and multiple doses. Am J Trop Med Hyg. (2002) 66:264–72. doi: 10.4269/ajtmh.2002.66.264
41. Kanesa-thasan N, Sun W, Kim-ahn G, Van Albert S, Putnak JR, King A, et al. Safety and immunogenicity of attenuated dengue virus vaccines (Aventis Pasteur) in human volunteers. Vaccine. (2001) 19:3179–88. doi: 10.1016/S0264–410X(01)00020–2
42. Dharakul T, Kurane I, Bhamarapravati N, Yoksan S, Vaughn DW, Hoke CH, et al. Dengue virus-specific memory T cell responses in human volunteers receiving a live attenuated dengue virus type 2 candidate vaccine. J Infect Dis. (1994) 170:27–33. doi: 10.1093/infdis/170.1.27
43. Rothman AL, Kanesa-thasan N, West K, Janus J, Saluzzo JF, Ennis FA. Induction of T lymphocyte responses to dengue virus by a candidate tetravalent live attenuated dengue virus vaccine. Vaccine. (2001) 19:4694–9. doi: 10.1016/S0264–410X(01)00236–5
44. Huang CY, Butrapet S, Tsuchiya KR, Bhamarapravati N, Gubler DJ, Kinney RM. Dengue 2 PDK-53 virus as a chimeric carrier for tetravalent dengue vaccine development. J Virol. (2003) 77:11436–47. doi: 10.1128/JVI.77.21.11436–11447.2003
45. Huang CY, Butrapet S, Pierro DJ, Chang GJ, Hunt AR, Bhamarapravati N, et al. Chimeric dengue type 2 (vaccine strain PDK-53)/dengue type 1 virus as a potential candidate dengue type 1 virus vaccine. J Virol. (2000) 74:3020–8. doi: 10.1128/JVI.74.7.3020–3028.2000
46. Sáez-Llorens X, Tricou V, Yu D, Rivera L, Jimeno J, Villarreal AC, et al. Immunogenicity and safety of one versus two doses of tetravalent dengue vaccine in healthy children aged 2–17 years in Asia and Latin America: 18-month interim data from a phase 2, randomised, placebo-controlled study. Lancet Infect Dis. (2018) 18:162–170. doi: 10.1016/S1473–3099(17)30632–1
47. Osorio JE, Velez ID, Thomson C, Lopez L, Jimenez A, Haller AA, et al. Safety and immunogenicity of a recombinant live attenuated tetravalent dengue vaccine (DENVax) in flavivirus-naive healthy adults in Colombia: a randomised, placebo-controlled, phase 1 study. Lancet Infect Dis. (2014) 14:830–8. doi: 10.1016/S1473–3099(14)70811–4
48. George SL, Wong MA, Dube TJ, Boroughs KL, Stovall JL, Luy BE, et al. Safety and immunogenicity of a live attenuated tetravalent dengue vaccine candidate in flavivirus-naive adults: a randomized, double-blinded phase 1 clinical trial. J Infect Dis. (2015) 212:1032–41. doi: 10.1093/infdis/jiv179
49. Rupp R, Luckasen GJ, Kirstein JL, Osorio JE, Santangelo JD, Raanan M, et al. Safety and immunogenicity of different doses and schedules of a live attenuated tetravalent dengue vaccine (TDV) in healthy adults: a phase 1b randomized study. Vaccine. (2015) 33:6351–9. doi: 10.1016/j.vaccine.2015.09.008
50. Sirivichayakul C, Barranco-Santana EA, Esquilin-Rivera I, Oh HM, Raanan M, Sariol CA, et al. Safety and immunogenicity of a tetravalent dengue vaccine candidate in healthy children and adults in dengue-endemic regions: a randomized, placebo-controlled phase 2 study. J Infect Dis. (2016) 213:1562–72. doi: 10.1093/infdis/jiv762
51. Sáez-Llorens X, Tricou V, Yu D, Rivera L, Tuboi S, Garbes P, et al. Safety and immunogenicity of one versus two doses of takeda's tetravalent dengue vaccine in children in Asia and Latin America: interim results from a phase 2, randomised, placebo-controlled study. Lancet Infect Dis. (2017) 17:615–25. doi: 10.1016/S1473–3099(17)30166–4
52. Chu H, George SL, Stinchcomb DT, Osorio JE, Partidos CD. CD8+ T-cell responses in flavivirus-naive individuals following immunization with a live-attenuated tetravalent dengue vaccine candidate. J Infect Dis. (2015) 212:1618–28. doi: 10.1093/infdis/jiv258
54. Beltramello M, Williams KL, Simmons CP, Macagno A, Simonelli L, Quyen NT, et al. The human immune response to dengue virus is dominated by highly cross-reactive antibodies endowed with neutralizing and enhancing activity. Cell Host Microbe. (2010) 8:271–83. doi: 10.1016/j.chom.2010.08.007
55. Friberg H, Jaiswal S, West K, O'Ketch M, Rothman AL, Mathew A. Analysis of human monoclonal antibodies generated by dengue virus-specific memory B cells. Viral Immunol. (2012) 25:348–59. doi: 10.1089/vim.2012.0010
56. Smith SA, de Alwis AR, Kose N, Jadi RS, de Silva AM, Crowe JE. Isolation of dengue virus-specific memory B cells with live virus antigen from human subjects following natural infection reveals the presence of diverse novel functional groups of antibody clones. J Virol. (2014) 88:12233–41. doi: 10.1128/JVI.00247–14
60. Friberg H, Bashyam H, Toyosaki-Maeda T, Potts JA, Greenough T, Kalayanarooj S, et al. Cross-reactivity and expansion of dengue-specific T cells during acute primary and secondary infections in humans. Sci Rep. (2011) 1:51. doi: 10.1038/srep00051
61. Bashyam HS, Green S, Rothman AL. Dengue virus-reactive CD8+ T cells display quantitative and qualitative differences in their response to variant epitopes of heterologous viral serotypes. J Immunol. (2006) 176:2817–24. doi: 10.4049/jimmunol.176.5.2817
62. Chandele A, Sewatanon J, Gunisetty S, Singla M, Onlamoon N, Akondy RS, et al. Characterization of human CD8 T cell responses in dengue virus-infected patients from India. J Virol. (2016) 90:11259–11278. doi: 10.1128/JVI.01424–16
Keywords: dengue, vaccine, T cell, cellular immunity, epitope discovery
Citation: Waickman AT, Friberg H, Gargulak M, Kong A, Polhemus M, Endy T, Thomas SJ, Jarman RG and Currier JR (2019) Assessing the Diversity and Stability of Cellular Immunity Generated in Response to the Candidate Live-Attenuated Dengue Virus Vaccine TAK-003. Front. Immunol. 10:1778. doi: 10.3389/fimmu.2019.01778
Received: 01 February 2019; Accepted: 15 July 2019;
Published: 31 July 2019.
Edited by:Daniela Weiskopf, La Jolla Institute for Immunology (LJI), United States
Reviewed by:David Koelle, University of Washington, United States
Lázaro Gil, Center for Genetic Engineering and Biotechnology (CIGB), Cuba
Copyright © 2019 Waickman, Friberg, Gargulak, Kong, Polhemus, Endy, Thomas, Jarman and Currier. 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: Adam T. Waickman, firstname.lastname@example.org