Ex vivo-expanded human CD19 ⁺TIM-1 ⁺ regulatory B cells suppress immune responses in vivo and are dependent upon the TIM-1/STAT3 axis

Abstract

Regulatory B cells (Breg) are a heterogenous population with immune-modulating functions. The rarity of human IL-10 ⁺ Breg makes translational studies difficult. Here we report ex vivo expansion of human B cells with in vivo regulatory function (expBreg). CD154-stimulation of human CD19 ⁺ B cells drives >900-fold expansion of IL-10 ⁺ B cells that is maintained in culture for 14 days. Whilst expBreg-mediated suppressive function is partially dependent on IL-10 expression, CRISPR-mediated gene deletions demonstrate predominant roles for TIM-1 and CD154. TIM-1 regulates STAT3 signalling and modulates downstream suppressive function. In a clinically relevant humanised mouse model of skin transplantation, expBreg prolongs human allograft survival. Meanwhile, CD19 ⁺CD73 ^-CD25 ⁺CD71 ⁺TIM-1 ⁺CD154 ⁺ Breg cells are enriched in the peripheral blood of human donors with cutaneous squamous cell carcinoma (SCC). TIM-1 ⁺ and pSTAT3 ⁺ B cells are also identified in B cell clusters within histological sections of human cutaneous SCC tumours. Our findings thus provide insights on Breg homoeostasis and present possible targets for Breg-related therapies.

Abstract

Human regulatory B (Breg) cells have been difficult to study due to their scarcity and heterogeneity. Here the authors expand human B cells to exert immunosuppressive function in vitro and in vivo, and to implicate the TIM-1/STAT3 axis for the regulation of their homoeostasis and function.