TNF signalling drives expansion of bone marrow CD4+ T cells responsible for HSC exhaustion in experimental visceral leishmaniasis

5 years ago

TNF signalling drives expansion of bone marrow CD4+ T cells responsible for HSC exhaustion in experimental visceral leishmaniasis

Paul M. Kaye, Helen Ashwin, Johannes S. P. Doehl, Olivier Preham, Ana Isabel Pinto, Najmeeyah Brown

by Ana Isabel Pinto, Najmeeyah Brown, Olivier Preham, Johannes S. P. Doehl, Helen Ashwin, Paul M. Kaye

Visceral leishmaniasis is associated with significant changes in hematological function but the mechanisms underlying these changes are largely unknown. In contrast to naïve mice, where most long-term hematopoietic stem cells (LT-HSCs; LSK CD150⁺ CD34^- CD48^- cells) in bone marrow (BM) are quiescent, we found that during Leishmania donovani infection most LT-HSCs had entered cell cycle. Loss of quiescence correlated with a reduced self-renewal capacity and functional exhaustion, as measured by serial transfer. Quiescent LT-HSCs were maintained in infected RAG2 KO mice, but lost following adoptive transfer of IFNγ-sufficient but not IFNγ-deficient CD4⁺ T cells. Using mixed BM chimeras, we established that IFNγ and TNF signalling pathways converge at the level of CD4⁺ T cells. Critically, intrinsic TNF signalling is required for the expansion and/or differentiation of pathogenic IFNγ⁺CD4⁺ T cells that promote the irreversible loss of BM function. These finding provide new insights into the pathogenic potential of CD4⁺ T cells that target hematopoietic function in leishmaniasis and perhaps other infectious diseases where TNF expression and BM dysfunction also occur simultaneously.

Publisher URL: http://journals.plos.org/plosone/article

DOI: 10.1371/journal.ppat.1006465