Young infants exhibit robust functional antibody responses and restrained IFN-γ production to SARS-CoV-2

婴幼儿对SARS-CoV-2表现出强大的功能性抗体反应和抑制的IFN-γ产生。

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作者:Anu Goenka ,Alice Halliday ,Michaela Gregorova ,Emily Milodowski ,Amy Thomas ,Maia Kavanagh Williamson ,Holly Baum ,Elizabeth Oliver ,Anna E Long ,Lea Knezevic ,Alistair J K Williams ,Vito Lampasona ,Lorenzo Piemonti ,Kapil Gupta ,Natalie Di Bartolo ,Imre Berger ,Ashley M Toye ,Barry Vipond ,Peter Muir ,Jolanta Bernatoniene ,Mick Bailey ,Kathleen M Gillespie ,Andrew D Davidson ,Linda Wooldridge ,Laura Rivino ,Adam Finn

Abstract

Severe COVID-19 appears rare in children. This is unexpected, especially in young infants, who are vulnerable to severe disease caused by other respiratory viruses. We evaluate convalescent immune responses in 4 infants under 3 months old with confirmed COVID-19 who presented with mild febrile illness, alongside their parents, and adult controls recovered from confirmed COVID-19. Although not statistically significant, compared to seropositive adults, infants have high serum levels of IgG and IgA to SARS-CoV-2 spike protein, with a corresponding functional ability to block SARS-CoV-2 cellular entry. Infants also exhibit robust saliva anti-spike IgG and IgA responses. Spike-specific IFN-γ production by infant peripheral blood mononuclear cells appears restrained, but the frequency of spike-specific IFN-γ- and/or TNF-α-producing T cells is comparable between infants and adults. On principal-component analysis, infant immune responses appear distinct from their parents. Robust functional antibody responses alongside restrained IFN-γ production may help protect infants from severe COVID-19.

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