Frontiers in Immunology (Jun 2024)

Coordinated expansion of memory T follicular helper and B cells mediates spontaneous clearance of HCV reinfection

  • Mohamed Eisa,
  • Elsa Gomez-Escobar,
  • Elsa Gomez-Escobar,
  • Nathalie Bédard,
  • Nourtan F. Abdeltawab,
  • Nourtan F. Abdeltawab,
  • Nourtan F. Abdeltawab,
  • Nicol Flores,
  • Nicol Flores,
  • Sabrina Mazouz,
  • Sabrina Mazouz,
  • Alizée Fieffé-Bédard,
  • Patrick Sakayan,
  • John Gridley,
  • Mohamed S. Abdel-Hakeem,
  • Mohamed S. Abdel-Hakeem,
  • Mohamed S. Abdel-Hakeem,
  • Julie Bruneau,
  • Julie Bruneau,
  • Arash Grakoui,
  • Naglaa H. Shoukry,
  • Naglaa H. Shoukry

DOI
https://doi.org/10.3389/fimmu.2024.1403769
Journal volume & issue
Vol. 15

Abstract

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IntroductionFollicular helper T cells are essential for helping in the maturation of B cells and the production of neutralizing antibodies (NAbs) during primary viral infections. However, their role during recall responses is unclear. Here, we used hepatitis C virus (HCV) reinfection in humans as a model to study the recall collaborative interaction between circulating CD4 T follicular helper cells (cTfh) and memory B cells (MBCs) leading to the generation of NAbs.MethodsWe evaluated this interaction longitudinally in subjects who have spontaneously resolved primary HCV infection during a subsequent reinfection episode that resulted in either another spontaneous resolution (SR/SR, n = 14) or chronic infection (SR/CI, n = 8).ResultsBoth groups exhibited virus-specific memory T cells that expanded upon reinfection. However, early expansion of activated cTfh (CD4+CXCR5+PD-1+ICOS+FoxP3−) occurred in SR/SR only. The frequency of activated cTfh negatively correlated with time post-infection. Concomitantly, NAbs and HCV-specific MBCs (CD19+CD27+IgM−E2-Tet+) peaked during the early acute phase in SR/SR but not in SR/CI. Finally, the frequency of the activated cTfh1 (CXCR3+CCR6−) subset correlated with the neutralization breadth and potency of NAbs.ConclusionThese results underscore a key role for early activation of cTfh1 cells in helping antigen-specific B cells to produce NAbs that mediate the clearance of HCV reinfection.

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