Section of Rheumatology, Department of Medicine, University of Chicago, Chicago, IL 60637, USA.
Committee on Immunology, University of Chicago, Chicago, IL 60637, USA.
Viruses. 2021 May 22;13(6):965. doi: 10.3390/v13060965.
Antibodies are critical for providing protection against influenza virus infections. However, protective humoral immunity against influenza viruses is limited by the antigenic drift and shift of the major surface glycoproteins, hemagglutinin and neuraminidase. Importantly, people are exposed to influenza viruses throughout their life and tend to reuse memory B cells from prior exposure to generate antibodies against new variants. Despite this, people tend to recall memory B cells against constantly evolving variable epitopes or non-protective antigens, as opposed to recalling them against broadly neutralizing epitopes of hemagglutinin. In this review, we discuss the factors that impact the generation and recall of memory B cells against distinct viral antigens, as well as the immunological limitations preventing broadly neutralizing antibody responses. Lastly, we discuss how next-generation vaccine platforms can potentially overcome these obstacles to generate robust and long-lived protection against influenza A viruses.
抗体对于提供针对流感病毒感染的保护至关重要。然而,针对流感病毒的保护性体液免疫受到主要表面糖蛋白血凝素和神经氨酸酶的抗原漂移和转变的限制。重要的是,人们一生中都会接触到流感病毒,并倾向于重新利用先前暴露的记忆 B 细胞来产生针对新变体的抗体。尽管如此,人们往往会回忆起针对不断进化的可变表位或非保护性抗原的记忆 B 细胞,而不是针对血凝素的广泛中和表位来回忆它们。在这篇综述中,我们讨论了影响针对不同病毒抗原产生和回忆记忆 B 细胞的因素,以及阻止产生广泛中和抗体反应的免疫限制。最后,我们讨论了下一代疫苗平台如何克服这些障碍,针对甲型流感病毒产生强大和持久的保护。