4.7 Article

Circulating Th2-biased T follicular helper cells impede antiviral humoral responses during chronic hepatitis B infection through upregulating CTLA4

Journal

ANTIVIRAL RESEARCH
Volume 216, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.antiviral.2023.105665

Keywords

T follicular helper cells; Hepatitis B virus; Cytotoxic T-lymphocyte associated antigen-4; T helper cell 2

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Failure to cure chronic hepatitis B virus (HBV) infection can impair B cell function. This study found that CTLA4 regulates B cell and T follicular helper (Tfh) cell differentiation, and that upregulation of CTLA4 in cTfh cells is associated with decreased HBsAg-specific resting memory B cells. Inhibition of CTLA4 restored HBsAb secretion and promoted plasma cell differentiation. These findings suggest that optimizing Tfh cell responses may lead to a functional cure for chronic HBV infection.
Failure in curing chronic hepatitis B (CHB) caused by hepatitis B virus (HBV) can lead to functional impairment of B cells. Cytotoxic T-lymphocyte associated antigen 4 (CTLA4) regulates B cell and T follicular helper (Tfh) cell differentiation. In addition, Tfh cells play a critical role in helping B cells generate antibodies upon pathogen exposure. Here, we analyzed the global and HBsAg-specific B cells and circulating Tfh (cTfh) cells using samples from treatment-naive and Peg-IFN-& alpha;-treated CHB patients and healthy subjects. Compared to healthy subjects, CTLA4 expression was significantly increased in cTfh cells, from CHB patients. The frequency of CTLA4+cTfh2 cells was negatively correlated with that of HBsAg-specific resting memory B cells. Importantly, inhibition of CTLA4 restored HBsAb secretion and promoted plasma cell differentiation. In addition, CTLA4+cTfh2 cells from CHB patients were ineffective in providing B cell help. Both expression of CTLA4 in cTfh and cTfh2 cells and ratios of CLTA4+cTfh and CTLA4+cTfh2 cells were significantly decreased in Peg-IFN-& alpha;-treated CHB patients who showed complete responses. Thus, our results highlighted that cTh2-biased T follicular helper cells could impede antiviral humoral responses during chronic HBV infection by upregulating CTLA4, suggesting that further optimizing potent Tfh cell responses may promote functional cure of CHB.

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