Cell Reports (Feb 2022)

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

  • 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

Journal volume & issue
Vol. 38, no. 6
p. 110345

Abstract

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Summary: 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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