Current glycoconjugate vaccines are synthesized empirically, without scientifically based optimization of antigen presentation. We propose to establish a new generation of knowledge- based, target-specific, structurally designed, highly immunogenic and protective vaccines that can be produced at much lower cost, allowing for much wider use on a global scale. We anticipate that novel insights obtained from our proposed mechanistic studies on antigen processing and presentation, T cell responses, and glycoconjugate vaccine design will redefine the mechanisms by which vaccine design influences T cell activation, which in turn provides B cell help. As the model antigens for our studies, we will use group B streptococcal glycoconjugate vaccines. Our preliminary data show that, contrary to the traditional paradigm, complex glycoconjugate molecules are not handled by the endosomal compartment as previously believed. Consequently, the empirical construction of glycoconjugate vaccines, as presently undertaken by vaccine manufacturers and designers, fails to optimize immunogenic potential. More specifically, current glycoconjugate vaccines are designed without consideration of which epitopes should be presented to T cells for optimal immune responses. Our data show that glycopeptide epitopes of glycoconjugate vaccines, rather than peptide epitopes alone, are actually presented to T cells in the context of major histocompatibility complex class II (MHCII) on the surface of antigen-presenting cells (APCs). In the proposed studies, we will determine whether CD4+ T cells can differentiate glycopeptides from peptides and whether glycopeptide epitopes can induce IgM-to-IgG switching. With this information in hand, we can synthetically mimic optimal epitopes at optimal frequency and density, enhancing vaccine immunogenicity and protection through efficient processing and presentation by APCs and highly specific T cell recognition. On the basis of our data, we believe that, in terms of T cell help, these immunogenic epitopes are glycopeptides. By optimizing the use of the most immunogenic components, we will produce vaccines with greater immunogenicity;longer-lived immunity;lower dosage requirements (and therefore greater safety);and, in all probability, greater immunogenicity and protective capacity in elderly individuals and in children.

Public Health Relevance

The design of the current generation of vaccines is empirical and therefore does not make use of specific scientific knowledge to maximize stimulation of the immune cells involved in producing the antibodies needed for protection. Using small-molecular-sized carbohydrates coupled to small portions of proteins (peptides) as model vaccines, we will define precisely how these vaccines stimulate responses in critical cells of the immune system. On the basis of this information, we will create a new generation of knowledge-based, target-specific, structurally designed, highly immunogenic and protective vaccines that can be produced at much lower cost, allowing much wider use on a global scale.

National Institute of Health (NIH)
National Institute of Allergy and Infectious Diseases (NIAID)
Research Project (R01)
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Vaccines Against Microbial Diseases (VMD)
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Gondre-Lewis, Timothy A
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Harvard University
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Avci, Fikri Y; Li, Xiangming; Tsuji, Moriya et al. (2013) Carbohydrates and T cells: a sweet twosome. Semin Immunol 25:146-51
Chen, Vincent L; Avci, Fikri Y; Kasper, Dennis L (2013) A maternal vaccine against group B Streptococcus: past, present, and future. Vaccine 31 Suppl 4:D13-9
Avci, Fikri Y; Li, Xiangming; Tsuji, Moriya et al. (2012) Isolation of carbohydrate-specific CD4(+) T cell clones from mice after stimulation by two model glycoconjugate vaccines. Nat Protoc 7:2180-92
Surana, Neeraj K; Kasper, Dennis L (2012) The yin yang of bacterial polysaccharides: lessons learned from B. fragilis PSA. Immunol Rev 245:13-26
Avci, Fikri Y; Li, Xiangming; Tsuji, Moriya et al. (2011) A mechanism for glycoconjugate vaccine activation of the adaptive immune system and its implications for vaccine design. Nat Med 17:1602-9