Adaptive immune response to bordetella pertussis during vaccination and infection: emerging perspectives and unanswered questions

被引:0
|
作者
Kim, A-Reum [1 ]
Sette, Alessandro [1 ,2 ]
Antunes, Ricardo da Silva [1 ]
机构
[1] La Jolla Inst Immunol LJI, Ctr Vaccine Innovat, 9420 Athena Circle, La Jolla, CA 92037 USA
[2] Univ Calif San Diego UCSD, Dept Med, Div Infect Dis & Global Publ Hlth, La Jolla, CA USA
关键词
Adaptive responses; asymptomatic; B; pertussis; colonization; infection; T cells; transmission; vaccination; whooping cough; REAL-TIME PCR; WHOLE-CELL PERTUSSIS; ANTIBODY-RESPONSES; ADULT PERTUSSIS; BABOON MODEL; VACCINES; TRANSMISSION; IMMUNIZATION; CHILDREN; SEROPREVALENCE;
D O I
10.1080/14760584.2024.2383745
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IntroductionWhooping cough, also known as pertussis, remains a significant challenge as a vaccine-preventable disease worldwide. Since the switch from the whole-cell Pertussis (wP) vaccine to the acellular Pertussis vaccine (aP), cases of whooping cough have increased in countries using the aP vaccine. Understanding the immune system's response to pertussis vaccines and infection is crucial for improving current vaccine efficacy.Areas coveredThis review of the literature using PubMed records offers an overview of the qualitative differences in antibody and T cell responses to B. pertussis (BP) in vaccination and infection, and their potential association with decreased efficacy of the aP vaccine in preventing infection and subclinical colonization. We further discuss how asymptomatic infections and carriage are widespread among vaccinated human populations, and explore methodologies that can be employed for their detection, to better understand their impact on adaptive immune responses and identify key features necessary for protection against the disease.Expert opinionAn underappreciated human BP reservoir, stemming from the decreased capacity of the aP vaccine to prevent subclinical infection, offers an alternative explanation for the increased incidence of clinical disease and recurrent outbreaks.
引用
收藏
页码:705 / 714
页数:10
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