Communications medicine · 2026
Birth imprinting effects on the antibody responses of H7N9 patients from 2013-2018 in China.
СтатьяНазвание и аннотация: Перевод в очереди
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Lin Xia, Guan Wenda, Chen Liping, Su Yin, Liang Zaolan, Xiao Cheng, Bai Yaqin, Lei Hui, Lin Fangmei, Huang Zhenting, Chow Isaac Cheuk Long, Yang Bingyi, Tsang Tim K, Weng Yunceng, Bhandari Nisha, Varadarajan Raghavan, Peiris Malik, Cowling Benjamin, Li Tang, McGargill Maureen, Thomas Paul G, Zhong Nanshan, Webby Richard, Yang Zifeng, Zanin Mark, Wong Sook-San
Аннотация
BACKGROUND: There is an urgent need to understand the immune correlates of protection against avian influenza viruses (AIV), where pre-existing immunity may be limited.
METHODS: Here, we characterized the antibody response in 12 severely ill A(H7N9) patients and examined its association with early-life imprinting and clinical outcome.
RESULTS: We find that A(H7N9) patients imprinted with A(H2N2) during early life show minimal H7-IgM and a rapid IgG response across diverse hemagglutinin subtypes. They also have more high avidity H7-antibodies compared to older or younger patients. Early antibody titers against seasonal H1, H3, and conserved stalk domains trend negatively with clinical severity in A(H7N9) infection, while an inverse pattern is observed following severe A(H1N1) infection, potentially suggesting a different mechanism of immune regulation between seasonal and avian influenza virus infections.
CONCLUSIONS: These data provide direct serological evidence that birth imprinting profoundly shapes the humoral immune landscape during zoonotic influenza infection and may influence subsequent disease outcome.
METHODS: Here, we characterized the antibody response in 12 severely ill A(H7N9) patients and examined its association with early-life imprinting and clinical outcome.
RESULTS: We find that A(H7N9) patients imprinted with A(H2N2) during early life show minimal H7-IgM and a rapid IgG response across diverse hemagglutinin subtypes. They also have more high avidity H7-antibodies compared to older or younger patients. Early antibody titers against seasonal H1, H3, and conserved stalk domains trend negatively with clinical severity in A(H7N9) infection, while an inverse pattern is observed following severe A(H1N1) infection, potentially suggesting a different mechanism of immune regulation between seasonal and avian influenza virus infections.
CONCLUSIONS: These data provide direct serological evidence that birth imprinting profoundly shapes the humoral immune landscape during zoonotic influenza infection and may influence subsequent disease outcome.