Frontiers in Immunology (Dec 2024)

Reduced durability of hybrid immunity to SARS-CoV-2 in immunocompromised children

  • Youjia Zhong,
  • Youjia Zhong,
  • Youjia Zhong,
  • Amuthavalli Kottaiswamy,
  • Chen Xiang Ang,
  • Hui’ En Li,
  • Gaik Chin Yap,
  • Carina J. X. Tay,
  • Nurul Elyana Osman,
  • Siti Namirah Binte Roslan,
  • Chee Wah Tan,
  • Wee Chee Yap,
  • Elizabeth Y. Ang,
  • Pauline P. L. Chan Ng,
  • Pauline P. L. Chan Ng,
  • Hui Kim Yap,
  • Hui Kim Yap,
  • Liangjian Lu,
  • Marion M. Aw,
  • Marion M. Aw,
  • Sivaraman V. Karthik,
  • Seng Hock Quak,
  • Thuan Chong Quah,
  • Elizabeth H. Tham,
  • Elizabeth H. Tham,
  • Lynette P. Shek,
  • Lynette P. Shek,
  • Eng Eong Ooi,
  • Eng Eong Ooi,
  • Eng Eong Ooi

DOI
https://doi.org/10.3389/fimmu.2024.1502598
Journal volume & issue
Vol. 15

Abstract

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BackgroundIn endemic COVID-19, immunocompromised children are vulnerable until vaccinated but the optimal primary vaccination regime and need for booster doses remains uncertain.MethodsWe recruited 19 immunocompromised children (post-solid organ transplantation, have autoimmune disease or were on current or recent chemotherapy for acute lymphoblastic leukemia), and followed them from the start of primary vaccination with BNT162b2 mRNA SARS-CoV-2 until 1-year post-vaccination. We investigated the quality of vaccine immunogenicity, and longevity of hybrid immunity, in comparison to healthy children.ResultsImmunocompromised children failed to produce T cell and memory B cell (MBC) responses reaching thresholds of protection after 2 doses; a third dose however improved both responses. Initially robust hybrid immunity demonstrated significantly more decline in T cell and MBC responses in immunocompromised compared to healthy children, to levels below the protective threshold by month 12.DiscussionImmunocompromised children may benefit from a 3-dose primary vaccination regime, with yearly or twice-yearly booster doses for sustained immunity.

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