Cobey Sarah, Hensley Scott E
Department of Ecology & Evolution, The University of Chicago, Chicago, IL 19104, USA.
Department of Microbiology, Perelman School of Medicine, The University of Pennsylvania, Philadelphia, PA 19104, USA.
Curr Opin Virol. 2017 Feb;22:105-111. doi: 10.1016/j.coviro.2016.12.004. Epub 2017 Jan 12.
Antibody responses to influenza viruses are critical for protection, but the ways in which repeated viral exposures shape antibody evolution and effectiveness over time remain controversial. Early observations demonstrated that viral exposure history has a profound effect on the specificity and magnitude of antibody responses to a new viral strain, a phenomenon called 'original antigenic sin.' Although 'sin' might suppress some aspects of the immune response, so far there is little indication that hosts with pre-existing immunity are more susceptible to viral infections compared to naïve hosts. However, the tendency of the immune response to focus on previously recognized conserved epitopes when encountering new viral strains can create an opportunity cost when mutations arise in these conserved epitopes. Hosts with different exposure histories may continue to experience distinct patterns of infection over time, which may influence influenza viruses' continued antigenic evolution. Understanding the dynamics of B cell competition that underlie the development of antibody responses might help explain the low effectiveness of current influenza vaccines and lead to better vaccination strategies.
对流感病毒的抗体反应对于保护机体至关重要,但随着时间的推移,反复接触病毒塑造抗体进化和效力的方式仍存在争议。早期观察表明,病毒接触史对针对新病毒株的抗体反应的特异性和强度有深远影响,这一现象称为“原始抗原罪”。尽管“罪”可能会抑制免疫反应的某些方面,但到目前为止,几乎没有迹象表明与未接触过病毒的宿主相比,已有免疫力的宿主更容易受到病毒感染。然而,当遇到新病毒株时,免疫反应倾向于聚焦先前识别的保守表位,这可能会在这些保守表位发生突变时产生机会成本。随着时间的推移,具有不同接触史的宿主可能会持续经历不同的感染模式,这可能会影响流感病毒的持续抗原进化。了解抗体反应发展背后的B细胞竞争动态,可能有助于解释当前流感疫苗效果不佳的原因,并导致更好的疫苗接种策略。