IL-15-producing splenic B cells play pathogenic roles in the development of autoimmune hepatitis.

ABSTRACT:

Background & aims

B-cell depletion therapy with an anti-CD20 is an effective treatment strategy for patients with refractory autoimmune hepatitis (AIH). However, the mechanisms underlying B-cell action are unclear.

Methods

Herein, we used the adeno-associated virus IL-12 model, in which hepatic IL-12 expression triggers liver injuries characteristic of AIH. We also analysed the clinical samples of patients with AIH.

Results

B-cell depletion using anti-CD20 or splenectomy was found to improve liver functions and decrease the cytotoxic CD8⁺ T-cell (cytotoxic T lymphocyte [CTL]) count in the liver. This improvement was reversed by the adoptive transfer of splenic B cells derived from AAV IL-12-treated mice to splenectomised mice as it caused the hepatic CTL count to increase. RNA-sequencing analysis identified IL-15 as a key factor in pathogenic B cells, which promotes CTL expansion and subsequent migration to the liver via the CXCL9/CXCR3 axis. Indeed, IL-15 neutralisation ameliorated hepatitis by suppressing splenic and hepatic CTLs in vivo. The close distribution of B220⁺ B cells and CD8⁺ T cells in the spleen of AIH mice suggested mutual interactions. Mechanistically, IFNγ and CD40L/CD40 signalling were indispensable for the expression of IL-15 in B cells, and in vitro co-culture experiments revealed that splenic CD40L⁺CD8⁺ T cells promoted IL-15 production in B cells, which led to CTL expansion. In patients with AIH, high serum IL-15 concentration and IL-15⁺ B-cell counts, positively correlating with serum alanine aminotransferase levels, support translation and potential therapeutic targeting in human AIH.

Conclusions

This investigation elucidated the roles of IL-15-producing splenic B cells that occur in concert with pathogenic CD8⁺ T cells during the development of AIH.

Impact and implications

IL-15-producing B cells were shown to exacerbate experimental AIH via cytotoxic T lymphocyte expansion. CD40L⁺CD8⁺ T cells promoted IL-15 expression in B cells, indicating the mutual interaction of both cells. High serum IL-15 concentrations, IL-15⁺ B-cell counts, and CD40L⁺IL-15Rα⁺CD8⁺ T-cell counts were confirmed in the blood of patients with AIH.

SUBMITTER: Fujimori S 

PROVIDER: S-EPMC10251155 | biostudies-literature | 2023 Jul

REPOSITORIES: biostudies-literature