γδ T Cells’ Role in Donor-Specific Antibody Generation: Insights From Transplant Recipients and Experimental Models

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Charmetant, Xavier | Rigault, Guillaume | Chen, Chien-Chia | Kaminski, Hannah | Visentin, Jonathan | Taton, Benjamin | Marseres, Gabriel | Mathias, Virginie | Koenig, Alice | Barba, Thomas | Merville, Pierre | Graff-Dubois, Stéphanie | Morelon, Emmanuel | Déchanet-Merville, Julie | Dubois, Valérie | Duong van Huyen, Jean-Paul | Couzi, Lionel | Thaunat, Olivier

Edité par CCSD ; Frontiers Media -

International audience. The generation of donor-specific antibodies (DSA) requires that alloreactive B cells receive help from follicular helper T (T FH ) cells. Recent works have suggested that γδ T cells could contribute to T cell-dependent humoral responses, leading us to investigate their role in DSA generation. Analysis of a cohort of 331 kidney transplant recipients found no relation between the number of circulating γδ T cells and the risk to develop DSA. Coculture models demonstrated that activated γδ T cells were unable to promote the differentiation of B cells into plasma cells, ruling out that they can be “surrogate” T FH . In line with this, γδ T cells preferentially localized outside the B cell follicles, in the T cell area of lymph nodes, suggesting that they could instead act as “antigen-presenting cell” (APC) to prime αβ T FH . This hypothesis was proven wrong since γδ T cells failed to acquire APC functions in vitro . These findings were validated in vivo by the demonstration that following transplantation with an allogeneic Balb/c (H2 d ) heart, wild-type and TCRδKO C57BL/6 (H2 b ) mice developed similar DSA responses, whereas TCRαKO recipients did not develop DSA. We concluded that the generation of DSA is unfazed by the absence of γδ T cells.

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