Vaccine adjuvants to engage the cross-presentation pathway

被引:51
作者
Lee, Woojong [1 ]
Suresh, M. [1 ]
机构
[1] Univ Wisconsin Madison, Dept Pathobiol Sci, Madison, WI 53706 USA
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
关键词
adjuvants; cross-presentation; immunity; memory; CD8 T cells; vaccines; MHC CLASS-I; PLASMACYTOID DENDRITIC CELLS; CD8(+) T-CELLS; EXOGENOUS ANTIGEN-PRESENTATION; ANTIBODY-RESPONSES; ALUMINUM-HYDROXIDE; ADAPTIVE IMMUNITY; PRESENTING CELLS; TARGETING CLEC9A; POTENT ADJUVANT;
D O I
10.3389/fimmu.2022.940047
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Adjuvants are indispensable components of vaccines for stimulating optimal immune responses to non-replicating, inactivated and subunit antigens. Eliciting balanced humoral and T cell-mediated immunity is paramount to defend against diseases caused by complex intracellular pathogens, such as tuberculosis, malaria, and AIDS. However, currently used vaccines elicit strong antibody responses, but poorly stimulate CD8 cytotoxic T lymphocyte (CTL) responses. To elicit potent CTL memory, vaccines need to engage the cross-presentation pathway, and this requirement has been a crucial bottleneck in the development of subunit vaccines that engender effective T cell immunity. In this review, we focus on recent insights into DC cross-presentation and the extent to which clinically relevant vaccine adjuvants, such as aluminum-based nanoparticles, water-in oil emulsion (MF59) adjuvants, saponin-based adjuvants, and Toll-like receptor (TLR) ligands modulate DC cross-presentation efficiency. Further, we discuss the feasibility of using carbomer-based adjuvants as next generation of adjuvant platforms to elicit balanced antibody- and T-cell based immunity. Understanding of the molecular mechanism of DC cross-presentation and the mode of action of adjuvants will pave the way for rational design of vaccines for infectious diseases and cancer that require balanced antibody- and T cell-based immunity.
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页数:20
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