Ragon Institute of MGH, MIT and Harvard, Cambridge, MA 02139, USA.
Ragon Institute of MGH, MIT and Harvard, Cambridge, MA 02139, USA.
Curr Opin Virol. 2021 Apr;47:52-67. doi: 10.1016/j.coviro.2021.01.001. Epub 2021 Feb 10.
Pathogen-specific immunity evolves in the context of the infected tissue. However, current immune correlates analyses and vaccine efficacy metrics are based on immune functions from peripheral cells. Less is known about tissue-resident mechanisms of immunity. While antibodies represent the primary correlate of immunity following most clinically approved vaccines, how antibodies interact with localized, compartment-specific immune functions to fight infections, remains unclear. Emerging data demonstrate a unique community of immune cells that reside within different tissues. These tissue-specific immunological communities enable antibodies to direct both expected and unexpected local attack strategies to control, disrupt, and eliminate infection in a tissue-specific manner. Defining the full breadth of antibody effector functions, how they selectively contribute to control at the site of infection may provide clues for the design of next-generation vaccines able to direct the control, elimination, and prevention of compartment specific diseases of both infectious and non-infectious etiologies.
病原体特异性免疫是在感染组织的背景下进化的。然而,目前的免疫相关性分析和疫苗效力衡量标准是基于外周细胞的免疫功能。关于组织驻留免疫机制知之甚少。虽然抗体是大多数临床批准疫苗后免疫的主要相关物,但抗体如何与局部、特定部位的免疫功能相互作用以抵抗感染尚不清楚。新出现的数据表明,存在一个独特的免疫细胞群体,存在于不同的组织中。这些组织特异性免疫群落使抗体能够针对预期和意外的局部攻击策略进行定向,以特定于组织的方式控制、破坏和消除感染。定义抗体效应功能的全部范围,以及它们如何有选择地有助于控制感染部位,可能为设计能够定向控制、消除和预防传染病和非传染病病因的特定部位疾病的下一代疫苗提供线索。