Maintenance of broad neutralizing antibodies and memory B cells 1 year post-infection is predicted by SARS-CoV-2-specific CD4+ T cell responses

SARS-CoV-2特异性CD4+ T细胞反应可预测感染后1年内广谱中和抗体和记忆B细胞的维持情况。

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作者:Harikrishnan Balachandran ,Chansavath Phetsouphanh ,David Agapiou ,Anurag Adhikari ,Chaturaka Rodrigo ,Mohamed Hammoud ,Lok Bahadur Shrestha ,Elizabeth Keoshkerian ,Money Gupta ,Stuart Turville ,Daniel Christ ,Cecile King ,Sarah C Sasson ,Adam Bartlett ,Branka Grubor-Bauk ,William Rawlinson ,Anupriya Aggarwal ,Alberto Ospina Stella ,Vera Klemm ,Michael M Mina ,Jeffrey J Post ,Bernard Hudson ,Nicky Gilroy ,Pam Konecny ,Golo Ahlenstiel ,Dominic E Dwyer ,Tania C Sorrell ,Anthony Kelleher ,Nicodemus Tedla ,Andrew R Lloyd ,Marianne Martinello ,Rowena A Bull

Abstract

Understanding the long-term maintenance of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) immunity is critical for predicting protection against reinfection. In an age- and gender-matched cohort of 24 participants, the association of disease severity and early immune responses on the maintenance of humoral immunity 12 months post-infection is examined. All severely affected participants maintain a stable subset of SARS-CoV-2 receptor-binding domain (RBD)-specific memory B cells (MBCs) and good neutralizing antibody breadth against the majority of the variants of concern, including the Delta variant. Modeling these immune responses against vaccine efficacy data indicate a 45%-76% protection against symptomatic infection (variant dependent). Overall, these findings indicate durable humoral responses in most participants after infection, reasonable protection against reinfection, and implicate baseline antigen-specific CD4+ T cell responses as a predictor of maintenance of antibody neutralization breadth and RBD-specific MBC levels at 12 months post-infection.

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