Dexamethasone reduces autoantibody levels in MRL/lpr mice by inhibiting Tfh cell responses.

ABSTRACT: Previous studies have shown that dexamethasone (Dex) reduces the levels of anti-nuclear (ANA) and anti-dsDNA antibodies in MRL/lpr mice (a mouse model of SLE). However, the effect of Dex on T follicular helper (Tfh) cells is less documented. Here, using the MRL/lpr mouse model, we investigated the influence of Dex on Tfh cells and potential underlying mechanisms. The data showed that the proportion of Tfh cells, identified as CD4⁺ CXCR5⁺ ICOS⁺ , CD4⁺ CXCR5⁺ PD-1⁺ or CD4⁺ BCL-6⁺ cells, markedly decreased after treatment with the Dex, in both Balb/c mice and MRL/lpr mice. Dex significantly inhibited IL-21 expression at both the mRNA and the protein levels. Dex also significantly reduced the proportion of germinal centre B cells and decreased serum IgG, IgG2a/b and IgA levels. Moreover, a positive correlation between the proportion of Tfh cells (CD4⁺ CXCR5⁺ ICOS⁺ , CD4⁺ CXCR5⁺ PD-1⁺ or CD4⁺ BCL-6⁺ ) and autoantibodies was observed. Dex significantly increased the Prdm1 and Stat5b mRNA expression and decreased the Bcl-6 and c-Maf mRNA expression of CD4⁺ T cells. In brief, Dex inhibited the Tfh development, which relies on many other transcription factors in addition to Bcl-6. Our data indicate that Dex can be used as a Tfh cell inhibitor in SLE.

SUBMITTER: Shen C 

PROVIDER: S-EPMC8419171 | biostudies-literature |

REPOSITORIES: biostudies-literature