Vaccine and immunotherapeutic approaches for the prevention of cryptococcosis: lessons learned from animal models
- 1 Department of Biology, The University of Texas at San Antonio, San Antonio, TX, USA
- 2 The South Texas Center for Emerging Infectious Diseases, The University of Texas at San Antonio, San Antonio, TX, USA
Cryptococcus neoformans and C. gattii, the predominant etiological agents of cryptococcosis, can cause life-threatening infections of the central nervous system in immunocompromised and immunocompetent individuals. Cryptococcal meningoencephalitis is the most common disseminated fungal infection in AIDS patients, and C. neoformans remains the third most common invasive fungal infection among organ transplant recipients. Current anti-fungal drug therapies are oftentimes rendered ineffective due to drug toxicity, the emergence of drug resistant organisms, and/or the inability of the host’s immune defenses to assist in eradication of the yeast. Therefore, there remains an urgent need for the development of immune-based therapies and/or vaccines to combat cryptococcosis. Studies in animal models have demonstrated the efficacy of various vaccination strategies and immune therapies to induce protection against cryptococcosis. This review will summarize the lessons learned from animal models supporting the feasibility of developing immunotherapeutics and vaccines to prevent cryptococcosis.
Cryptococcus neoformans and C. gattii, the etiological agents of cryptococcosis, are encapsulated fungal pathogens that cause fungal pneumonia and life-threatening infections of the central nervous system (CNS) (Mitchell and Perfect, 1995). Cryptococcal meningoencephalitis remains the most common disseminated fungal infection in AIDS patients (Powderly, 1993). Global estimates suggest that one million cases of cryptococcal meningitis due predominantly to C. neoformans occur each year resulting in approximately 620,000 deaths (Park et al., 2009). C. gattii primarily causes life-threatening fungal meningitis and infections of the lung and skin in otherwise healthy individuals (Jarvis and Harrison, 2008). The geographical distribution of C. gattii was believed to be limited to tropical and subtropical climates such as Australia, New Zealand, and Southeast Asia (Kwon-Chung and Bennett, 1984). However, C. gattii infections began to occur within animal and human populations on Vancouver Island, British Columbia, Canada, a temperate climate. Subsequently, C. gattii disseminated onto the mainland of British Columbia and proceeded throughout the Pacific Northwest of the United States (Datta et al., 2009a,b; Centers for Disease Control and Prevention, 2010; Galanis and Macdougall, 2010).
The administration of highly active antiretroviral therapy (HAART) has resulted in a decrease in the number of cases of AIDS-related cryptococcosis in developed countries, but in developing countries where HAART is not readily available, Cryptococcus is still a major problem (Dromer et al., 2004). Those who are successfully treated for AIDS-associated cryptococcal meningitis oftentimes require life-long anti-fungal therapy due to a high relapse rate (Bozzette et al., 1991; Vibhagool et al., 2003). C. neoformans also remains the third most common invasive fungal infection among organ transplant recipients (Husain et al., 2001; Singh et al., 2005; Pappas et al., 2010). Studies have shown that 2.8% of organ transplant recipients can develop cryptococcal infections resulting in an overall estimated death rate of 42% (Husain et al., 2001). Also, cryptococcosis accounted for 8% of the invasive fungal diseases in solid organ transplant recipients in the Transplant Associated Infection Surveillance Network database from March 2001 to March 2006 (Pappas et al., 2010). The acute mortality rate is between 10 and 25% in medically advanced countries (Powderly, 1993), and at least one third of patients with cryptococcal meningitis who receive appropriate therapy will undergo mycologic and/or clinical failure (Van Der Horst et al., 1997; Saag et al., 2000). Thus, there remains an urgent need for therapies and/or vaccines to combat cryptococcosis.
The current clinical picture of cryptococcosis suggests that immunosuppressed patients or individuals predicted to be at an exceptionally high risk for developing cryptococcosis are likely targets for vaccination to prevent the development of cryptococcal disease. Additional target populations for vaccination as a prophylactic measure include immune competent persons in high exposure areas as highlighted by the recent C. gattii outbreak in Vancouver Island, British Columbia, Canada, or those at high risk for exposure to HIV. Animal models of cryptococcosis have been important tools for elucidating the mechanisms of protection and for testing the efficacy of various antibody or antigen-based vaccine candidates. This review will focus on the lessons learned from animal models of cryptococcal disease that support efforts toward developing immunological therapies and/or vaccines against cryptococcosis.
Host Response to Cryptococcus
The consensus is that cell-mediated immunity (CMI) primarily by Th1-type CD4+ T cells directs the protective host immune response against C. neoformans (Huffnagle et al., 1991; Casadevall, 1995; Zhang et al., 2009), whereas a Th2-type immune response is considered detrimental to the host (Arora et al., 2005; Jain et al., 2009). A Th1-type response is characterized by the production of interleukin (IL)-2, IL-12, interferon-gamma (IFN-γ), and tumor necrosis factor-alpha (TNF-α) (Cherwinski et al., 1987). These cytokines induce granuloma formation in the lung to wall off the yeast and are responsible for initiating delayed-type hypersensitivity (DTH) reactions that lead to enhanced uptake, killing by neutrophils and dendritic cells, and the induction of classically activated macrophages (Cher and Mosmann, 1987; Zhang et al., 2009; Arora et al., 2011). A Th2-type response is characterized by the production of IL-4, IL-5, IL-9, IL-10, and IL-13 (Cherwinski et al., 1987), and is associated with eosinophilic inflammation and dissemination of cryptococci to the CNS (Huffnagle et al., 1994; Olszewski et al., 2001; Muller et al., 2007). A Th17-type response consisting of IL-17, IL-21, and IL-22 (reviewed in Onishi and Gaffen, 2010) has been suggested to be important in protection against C. neoformans, however, it seems to play a secondary role to the Th1-type response (Kleinschek et al., 2010). When a Th17-type response is blocked, there is no effect on survival of mice with experimental pulmonary C. neoformans infection (Wozniak et al., 2011a).
The predominant studies evaluating host immune responses to cryptococcal infections have been performed using C. neoformans as the model organism. However, several studies now suggest that the mechanism for mediating protection against C. neoformans infections differs from that which induces protection against C. gattii. Experimental studies suggest that C. gattii may thrive in immune competent hosts by suppressing host immune responses (Dong and Murphy, 1995; Wright et al., 2002; Cheng et al., 2009; Kronstad et al., 2011). C. gattii strain R265, the predominant isolate of the Vancouver Island outbreak, has been shown to be more suppressive in mice compared to those infected with C. neoformans. C. gattii infected mice had decreased neutrophil recruitment and decreased pro-inflammatory cytokine production (Dong and Murphy, 1995; Wright et al., 2002; Cheng et al., 2009).
While the patient population that historically develops cryptococcal infections includes individuals with defects in CMI, patients with defects in antibody-mediated immunity (AMI) such as hypogammaglobulinemia and hyper-IgM syndrome also have an increased probability of developing cryptococcosis (Gupta et al., 1987; Iseki et al., 1994; Tabone et al., 1994; Casadevall, 1995; Antachopoulos et al., 2007). The role of AMI in cryptococcal infections is complicated in that antibodies can be protective, non-protective, or can exacerbate the infection (Casadevall, 1995; Mukherjee et al., 1995a,b; Yuan et al., 1998). Antibody protection against cryptococcosis is dependent on the antibody isotype, concentration, and specificity (reviewed in Casadevall, 1995). Comparisons of variable-region-identical mAbs to the glucuronoxylomannan (GXM) component of the C. neoformans polysaccharide capsule of the murine IgG1, IgG2a, IgG2b, and IgG3 isotypes have consistently shown that all IgG isotypes, except IgG3 are protective against C. neoformans infection in mice (Yuan et al., 1995, 1998; Nussbaum et al., 1996). Resistance to disease may depend upon the proportion of protective anti-cryptococcal antibodies produced during infection. However, the efficacy of anti-cryptococcal antibodies of a protective isotype can be lost if induced or passively administered in excess creating a prozone-like effect (Taborda and Casadevall, 2001; Taborda et al., 2003). Other major determinants of the effectiveness of antibody isotype against C. neoformans infection include mouse genetics (Rivera and Casadevall, 2005; Zaragoza et al., 2007), T cell function (Yuan et al., 1997), and the presence of Th1- and Th2-related cytokines (Beenhouwer et al., 2001). Despite what we know from animal studies concerning protective antibody isotypes, the efficacy of various immunoglobulin isotypes against C. neoformans may vary between humans and mice (Beenhouwer et al., 2007) necessitating some caution in trying to translate findings in animal models to the clinic. Nevertheless, anti-cryptococcal antibodies can act as opsonins, participate in antibody-dependent cellular cytotoxicity, augment Th1-type polarization, and help to eliminate immunosuppressive polysaccharide antigen from serum and tissues. They also inhibit cryptococcal biofilm formation, alter lipid metabolism resulting in increased sensitivity to anti-fungal drugs, have direct anti-fungal activity, and modulate the immune response to prevent host damage (Martinez and Casadevall, 2005; Casadevall and Pirofski, 2007; Mcclelland et al., 2010; Brena et al., 2011). The role of antibodies in the host defense against fungal infection remains controversial; however, some recent studies continue to show a protective role of antibodies against cryptococcosis. For example, naturally occurring IgM (nIgM) is essential for the prevention of cryptococcosis in mice (Subramaniam et al., 2010). Cryptococcal disease is more severe in mice lacking serum IgM and in sIgM knockout mice. Experimental pulmonary C. neoformans infection of sIgM knockout mice results in increased mortality and higher blood and brain fungal burden compared to that observed in wild-type infected mice. While it is generally agreed that the protective host immune response to C. neoformans is dependent on inducing protective CMI, AMI certainly contributes in the protection against cryptococcosis.
Cryptococcal Protein Targets
Significant efforts have been made towards identification of cryptococcal antigens that induce Cryptococcus-specific Th1-type immune responses. This effort is based on the predominant role for CMI responses to mediate protection against C. neoformans infections. Protein antigens can induce T-dependent immune responses and thus be highly immunogenic. Additionally, proteins are biochemically defined, thus allowing for the production of large quantities of recombinant proteins. There is also no fear of protein “reversion” that could possibly occur using an attenuated strain to induce immunity. Immunization of mice with C. neoformans culture filtrate antigen (CneF), which contains secreted proteins as well as cell wall-associated proteins, resulted in the stimulation of DTH responses (Murphy et al., 1988). Fractionation of CneF revealed its mannoprotein (MP) fraction as the primary antigenic component responsible for DTH and T-dependent immune responses in mice (Murphy et al., 1988; Levitz and Specht, 2006). Mice given two immunizations of purified cryptococcal MP (MP98) experienced prolonged survival and had reduced CFUs in the organs when compared to the control mice receiving adjuvant alone (Mansour et al., 2002). Cryptococcal MP induced Th1-type responses in immunized mice upon infection with C. neoformans (Mansour et al., 2002). Four protective MP, one being a chitin deacetylase (MP98) (Levitz et al., 2001), one of unknown function (MP88) (Huang et al., 2002), and an additional two, MP84 and MP115 (Biondo et al., 2005) have been found.
In addition to the MP found in the cell wall, other potential targets include the heat shock protein (hsp) family (Kakeya et al., 1997; Nooney et al., 2005), fungal glucosylceramide (Rodrigues et al., 2007), and melanin (Rosas et al., 2001). MAbs to melanin have been shown to prolong the survival of and reduce fungal burden in lethally infected mice and reduce the growth rate of the fungus in vitro (Rosas et al., 2001). In the hsp family, hsp70 has been found to be highly immunogenic (Kakeya et al., 1997). Mycograb, a recombinant antibody targeting an epitope within the hsp90 of Candida albicans that is conserved in Cryptococcus, leads to enhanced fungicidal activity when combined with amphotericin B treatment of infected mice (Nooney et al., 2005). Targeting antigens common to multiple fungal species such as hsps or melanin may serve to extend protection to multiple disparate fungal pathogens.
Adaptive immunity against cryptococcosis is orchestrated via cytokine/chemokine production by Th1-type CD4+cells. Consequently, the historic objective of most immune-based therapies has been to skew the non-protective immune responses toward a protective Th1-type immune response. For example, IL-2 given along with a CD40 agonist antibody significantly prolonged the survival of C. neoformans-systemically infected mice (Zhou et al., 2006, 2007). In addition, mice depleted of CD4+ T cells were protected when stimulated with CD40 and IL-2 compared to depleted mice without these stimulations. This model also showed significant reduction of fungal burden in the organs and increased levels of IFN-γ and TNF-α (Zhou et al., 2006, 2007). Furthermore, mice treated with recombinant TNF-α experienced significantly prolonged survival times compared to non-treated control mice (Kawakami et al., 1996a). Additionally, treatment of mice with a TNF-α-expressing adenoviral vector after experimental challenge of C. neoformans resulted in a significant decrease in fungal burden, an increase in IFN-γ levels, and an increase in infiltration of macrophages and neutrophils (Milam et al., 2007). Treatment with IL-12 also led to significant increases in survival of mice with experimental cryptococcosis, but the timing of the treatment is important. Treating mice with IL-12 for 7 days post infection resulted in 90% survival, but delaying IL-12 treatment until day 7 post infection negated the effect of the IL-12, and the mice had similar survival rates compared to the untreated mice (Kawakami et al., 1996c). Administering IL-23, a cytokine necessary for the proliferation and stabilization of the Th17-type cells (reviewed in Onishi and Gaffen, 2010), significantly extended the survival of intraperitoneally infected mice (Kleinschek et al., 2010). However, when compared to their positive control group that received IL-12 and showed 100% survival at day 100, it was concluded that IL-23 may play only a limited role in the protection against C. neoformans (Kleinschek et al., 2010). Treating mice with IL-2 and anti-CD40, TNF-α, or IL-12 led to an increase in IFN-γ levels (Kawakami et al., 1996c; Zhou et al., 2006; Milam et al., 2007). Giving mice daily injections of IFN-γ prolonged their survival and reduced the fungal burden in the lungs and the brain (Kawakami et al., 1996b).
Studies in humans indicated that the cytokine profile at the site of infection determines the rate of clearance. Patients with higher IFN-γ at the site of infection had a faster rate of clearance compared to those with lower levels (Siddiqui et al., 2005), suggesting that the microenvironment at the site infection is more important than the macroenvironment. Considering this study, a highly virulent strain of C. neoformans, H99, was modified to produce murine IFN-γ. Mice given an experimental pulmonary infection with the IFN-γ producing C. neoformans strain, designated H99γ, were capable of completely resolving the infection and showed 100% protection upon re-challenge with wild-type cryptococci (Wormley et al., 2007). This protection was shown to be T cell dependent and B cell independent (Wozniak et al., 2009). T cell knock out (KO) mice succumbed to an experimental pulmonary infection with H99γ whereas B cell KO mice survived and showed 100% protection upon challenge with the wild-type C. neoformans strain H99 (Wozniak et al., 2009). Mice immunized with the H99γ strain and then depleted of either CD4+ or CD8+ T cells prior to and during subsequent challenge with wild-type C. neoformans, remained 100% protected (Wozniak et al., 2009). Remarkably, when the same experiment was performed with depletion of both CD4+ and CD8+ T cells during the challenge with wild-type cryptococci, there was still 80% survival (Wozniak et al., 2011b). These results suggest that if immune competent individuals are immunized against C. neoformans and then become T cell deficient they may still be protected. This system also produced high amounts of IL-17A, but when IL-17A deficient or IL-17A receptor KO mice were immunized with the H99γ strain there was no difference in protection compared to the wild-type mice (Hardison et al., 2010; Wozniak et al., 2011a). Thus, IL-17A may contribute to, but ultimately be dispensable for, protection against C. neoformans infection.
Cytokine treatment has also shown promising results when administered along with conventional anti-fungal drugs. In a systemic infection model, treating mice with IL-12 along with fluconazole significantly lowered the fungal burden in the brain compared to mice treated with fluconazole alone (Clemons et al., 1994). Administering IFN-γ along with amphotericin B during a lethal systemic infection model significantly lowered the fungal burden in the brain compared to amphotericin alone (Lutz et al., 2000). In a sub-lethal systemic infection model amphotericin B with IFN-γ led to complete clearance of the infection (Lutz et al., 2000). Fluconazole and IFN-γ significantly lowered the fungal burden in both the lethal and sub-lethal systemic infection models but failed to completely resolve the infection in any of the models (Lutz et al., 2000). Cytokine treatment may be necessary considering the immune suppressed status of the typical cryptococcosis patient. However, the possible induction of C. neoformans-related immune reconstitution inflammatory syndrome (IRIS) which is the induction of over-exuberant pro-inflammatory responses following the resolution of immune suppression necessitates caution when proceeding with such approaches.
Antibody-Mediated Immunotherapies and Antibody Vaccines
One of the main virulence factors of Cryptococcus is the polysaccharide capsule that is comprised primarily of the polysaccharides GXM and galactoxylomannan (GalXM) and to a much lesser extent, <1%, MP (Zaragoza et al., 2009). Cryptococcal polysaccharides such as GXM have profound suppressive effects on immune responses and elicit little to no antibody responses making it an unlikely choice as an antigen (reviewed in Zaragoza et al., 2009). GXM can bleb off the fungus and direct immune responses away from infection, while GXM and GalXM both can non-specifically diminish lymphocyte proliferation and induce apoptosis (Yauch et al., 2006; Cutler et al., 2007; Chow and Casadevall, 2011; Vecchiarelli et al., 2011). However, an entirely plausible strategy to induce protection against cryptococcosis may be to develop antibodies against specific capsular components. Mouse models have been utilized to investigate the efficacy of cryptococcal conjugate vaccines in which GXM or GalXM has been conjugated to protein carriers (Casadevall et al., 1992, 1998; Devi, 1996; Chow and Casadevall, 2011). GXM conjugated to the tetanus toxoid resulted in anti-GXM protective antibody responses and antibodies specific for GXM which help protect against cryptococcosis (Casadevall et al., 1992, 1998; Devi, 1996). Two GalXM conjugates where tested and found to be useful in generating high titers of anti-GalXM antibodies in the serum, but the responses were not protective (Chow and Casadevall, 2011). Casadevall developed an antibody to the capsule, 18B7, which was found to bind to all serotypes, enhance phagocytosis, and help with the clearance of the blebs of polysaccharide released by the fungus (Casadevall, 1995). Recently, MAb 18B7 has been conjugated to the therapeutic radioisotopes 188Rhenium or 213Bismuth (Dadachova et al., 2003; Bryan et al., 2010) and studied as a potential radioimmunotherapy (RIT) against C. neoformans. Administration of radiolabeled MAb 18B7 to lethally infected mice resulted in prolonged survival, reduced organ fungal burden, and was a more effective therapy compared to mice treated with amphotericin B alone.
A potential strategy to circumvent the immunosuppressant effects of GXM and GalXM may be to focus on specific epitopes within the polysaccharides that elicit protective antibody responses. An approach using small peptides that mimic defined GXM or GalXM epitopes may elicit protective antibody responses where using total polysaccharides has immunosuppressive effects. Peptides which are able to induce antibodies that are capable of binding to the native antigen when administered as immunogens are termed mimotopes. A peptide mimetic (P13) of GXM was developed that is recognized by human anti-GXM antibodies (Zhang et al., 1997). Vaccination with P13-protein conjugates in mice elicited an antibody response to GXM (Zhang et al., 1997). Additionally, mice immunized with the conjugates experienced prolonged survival after an otherwise lethal C. neoformans challenge compared to controls (Fleuridor et al., 2001) or following establishment of a chronic infection (Datta et al., 2008). Immunization with P13-protein conjugates also prolonged survival in mice transgenic for human immunoglobulin loci (Fleuridor et al., 2001) and passive immunization with serum from P13-conjugate vaccinated mice to naïve mice conferred partial protection to a lethal cryptococcal challenge (Maitta et al., 2004; Datta et al., 2008). Nonetheless, the therapeutic efficacy of conjugate vaccines containing a peptide mimotope of GXM appears to depend on the genetic background of the host and the carrier protein employed (Datta et al., 2008). Conjugation of P13 to keyhole limpet marine mollusk (KLH) elicited an anti-GXM response to non-protective epitopes possibly due to the generation of non-protective antibodies against an epitope within the carrier protein that is cross-reactive to GXM (May et al., 2003).
Development of antibodies targeting essential components within the fungal cell wall may be an additional method of antibody-mediated protection against cryptococcosis. Treatment with an anti-β-glucan antibody, MAb 2G8, which targets β(1,3) glucans of the brown algae, Laminaria digitata, was shown to inhibit capsule formation and growth of C. neoformans in vitro and mediate a significant reduction in fungal burden in mice given an experimental systemic cryptococcal infection (Rachini et al., 2007). Also, passive immunization with MAbs against melanin or glucosylceramide prolonged the survival of mice given a lethal infection with C. neoformans (Rosas et al., 2001; Rodrigues et al., 2007). Again, targeting fungal antigens that are common among multiple fungal pathogens is an appealing strategy toward generating cross-protection using one immune-therapy and/or vaccine.
The need for novel treatments to combat cryptococcosis is expected to rise. This is due to an increasing population of immune compromised patients, a high relapse rate, and increased percentage of patients predicted to experience mycologic and/or clinical failure. Animal models of cryptococcosis have been important tools for elucidating the mechanisms of protection against cryptococcosis and for testing the efficacy of various antibody or antigen-based vaccine candidates against cryptococcal infection. Overall, animal models have provided a means for studying strategies for modulating T helper responses and evaluating antibodies and radioimmunotherapies. They have also proved useful in developing approaches for inducing cell responses using peptide mimotopes and specific cryptococcal antigens. Perhaps a shift in approach from defining targets for anti-fungal drug development toward devising immune therapies and/or vaccines that enhance host anti-fungal immune responses is a direction requiring more focus. Such studies will concentrate more on the host and less on the pathogen. Still, Cryptococcus is a disease in which the host and pathogen are intimately intertwined. Consequently, animal models will surely be required to understand the relationship and devise plausible treatments and/or vaccines to prevent cryptococcal infections.
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.
Dr. Wormley and Mr. Hole are supported by the Army Research Office of the Department of Defense under Contract No. W911NF-11-1-0136 and grants RO1 AI071752-05 and R21 AI083718-02 from the National Institute of Allergy and Infectious Diseases (NIAID) of the National Institutes of Health (NIH). The content is solely the responsibility of the authors and does not necessarily represent the official views of the Department of Defense or NIAID of the NIH.
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Keywords: Cryptococcus neoformans, cryptococcosis, Cryptococcus, fungal pathogenesis, host-fungal interactions, fungal vaccines
Citation: Hole CR and Wormley FL Jr. (2012) Vaccine and immunotherapeutic approaches for the prevention of cryptococcosis: lessons learned from animal models. Front. Microbio. 3:291. doi: 10.3389/fmicb.2012.00291
Received: 25 May 2012; Accepted: 24 July 2012;
Published online: 28 August 2012.
Edited by:Joshua D. Nosanchuk, Albert Einstein College of Medicine, USA
Reviewed by:Marilene Henning Vainstein, Universidade Federal do Rio Grande do Sul, Brazil
Radames J. B. Cordero, Albert Einstein College of Medicine, USA
Copyright: © 2012 Hole and Wormley. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
*Correspondence: Floyd L. Wormley Jr., Department of Biology, The University of Texas at San Antonio, One UTSA Circle, San Antonio, TX 78249-0062, USA. e-mail: firstname.lastname@example.org