European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Hinxton, Cambridgeshire CB10 1SD, UK.
Viruses. 2023 Apr 19;15(4):1008. doi: 10.3390/v15041008.
The genetic basis of antigenic drift of human A/H3N2 influenza virus is crucial to understanding the constraints of influenza evolution and determinants of vaccine escape. Amino acid changes at only seven positions near the receptor binding site of the surface hemagglutinin protein have been shown to be responsible for the major antigenic changes for over forty years. Experimental structures of HA are now available for the majority of the observed antigenic clusters of A/H3N2. An analysis of the HA structures of these viruses reveals the likely consequences of these mutations on the structure of HA and thus, provides a structural basis for the antigenic changes seen in human influenza viruses.
人类 A/H3N2 流感病毒抗原漂移的遗传基础对于了解流感进化的限制和疫苗逃逸的决定因素至关重要。四十多年来,已经证明表面血凝素蛋白受体结合位点附近仅七个位置的氨基酸变化是导致主要抗原变化的原因。目前已有大多数观察到的 A/H3N2 抗原簇的 HA 实验结构。对这些病毒的 HA 结构进行分析揭示了这些突变对 HA 结构的可能影响,从而为人类流感病毒中观察到的抗原变化提供了结构基础。