T cell reactivity to Bordetella pertussis is highly diverse regardless of childhood vaccination

被引:9
作者
Antunes, Ricardo da Silva [1 ]
Garrigan, Emily [1 ]
Quiambao, Lorenzo G. [1 ]
Dhanda, Sandeep Kumar [1 ]
Marrama, Daniel [1 ]
Westernberg, Luise [1 ]
Wang, Eric [1 ]
Abawi, Adam [1 ]
Sutherland, Aaron [1 ]
Armstrong, Sandra K. [2 ]
Brickman, Timothy J. [2 ]
Sidney, John [1 ]
Frazier, April [1 ]
Merkel, Tod J. [3 ]
Peters, Bjoern [1 ,4 ]
Sette, Alessandro [1 ,4 ]
机构
[1] La Jolla Inst Immunol LJI, Ctr Infect Dis & Vaccine Res, La Jolla, CA 92037 USA
[2] Univ Minnesota, Med Sch, Dept Microbiol & Immunol, Minneapolis, MN 55455 USA
[3] US FDA, Ctr Biol Evaluat & Res, Div Bacterial Parasit & Allergen Prod, Silver Spring, MD 20993 USA
[4] Univ Calif San Diego UCSD, Dept Med, Div Infect Dis & Global Publ Hlth, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
ADENYLATE-CYCLASE TOXIN; ANTIBODY-RESPONSES; WHOLE-CELL; SEROLOGIC RESPONSE; IMMUNE-RESPONSES; VACCINES; INFECTION; ADULTS; IMMUNIZATION; SEROPREVALENCE;
D O I
10.1016/j.chom.2023.06.015
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The incidence of whooping cough due to Bordetella pertussis (BP) infections has increased recently. It is believed that the shift from whole-cell pertussis (wP) vaccines to acellular pertussis (aP) vaccines may be contributing to this rise. While T cells are key in controlling and preventing disease, nearly all knowledge relates to antigens in aP vaccines. A whole-genome mapping of human BP-specific CD4+ T cell responses was performed in healthy vaccinated adults and revealed unexpected broad reactivity to hundreds of antigens. The overall pattern and magnitude of T cell responses to aP and non-aP vaccine antigens are similar regardless of childhood vaccination, suggesting that asymptomatic infections drive the pattern of T cell reactivity in adults. Lastly, lack of Th1/Th2 polarization to non-aP vaccine antigens suggests these antigens have the potential to counteract aP vaccination Th2 bias. These findings enhance our insights into human T cell responses to BP and identify potential targets for next-generation pertussis vaccines.
引用
收藏
页码:1404 / 1416.e4
页数:18
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