Development of T cell antigen-based human coronavirus vaccines SARS-CoV-2 variants

被引:3
作者
Zhou, Hao [1 ,2 ]
Leng, Ping [1 ,2 ]
Wang, Yang [1 ]
Yang, Kaiwen [1 ]
Li, Chen [3 ]
Ojcius, David M. [4 ]
Wang, Pengfei [3 ]
Jiang, Shibo [5 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Coll Med Technol, Chengdu 611137, Peoples R China
[2] Chongqing Tradit Chinese Med Hosp, Chongqing Key Lab Sichuan Chongqing Coconstruct Di, Chongqing 400016, Peoples R China
[3] Fudan Univ, Pudong Med Ctr, Shanghai Pudong Hosp, Shanghai Inst Infect Dis & Biosecur,Sch Life Sci, Shanghai, Peoples R China
[4] Univ Pacific, Arthur Dugoni Sch Dent, Dept Biomed Sci, San Francisco, CA 94115 USA
[5] Fudan Univ, Shanghai Inst Infect Dis & Biosecur, Chinese Acad Med Sci, Key Lab Med Mol Virol,Sch Basic Med Sci,Minist Hlt, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
COVID-19; Immune escape; Omicron variant; SARS-CoV-2; T cell antigen-based vaccine; MESSENGER-RNA VACCINES; RESIDENT MEMORY; DIFFERENTIATION; DURABILITY; PROTECTION; EPITOPES; CD4(+); VECTOR;
D O I
10.1016/j.scib.2024.02.041
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Currently approved vaccines have been successful in preventing the severity of COVID-19 and hospitalization. These vaccines primarily induce humoral immune responses; however, highly transmissible and mutated variants, such as the Omicron variant, weaken the neutralization potential of the vaccines, thus, raising serious concerns about their efficacy. Additionally, while neutralizing antibodies (nAbs) tend to wane more rapidly than cell-mediated immunity, long-lasting T cells typically prevent severe viral illness by directly killing infected cells or aiding other immune cells. Importantly, T cells are more cross-reactive than antibodies, thus, highly mutated variants are less likely to escape lasting broadly cross-reactive T cell immunity. Therefore, T cell antigen-based human coronavirus (HCoV) vaccines with the potential to serve as a supplementary weapon to combat emerging SARS-CoV-2 variants with resistance to nAbs are urgently needed. Alternatively, T cell antigens could also be included in B cell antigen-based vaccines to strengthen vaccine efficacy. This review summarizes recent advancements in research and development of vaccines containing T cell antigens or both T and B cell antigens derived from proteins of SARS-CoV-2 variants and/or other HCoVs based on different vaccine platforms. (c) 2024 Science China Press. Published by Elsevier B.V. and Science China Press. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
引用
收藏
页码:2456 / 2470
页数:15
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