Macrophage TNF-alpha licenses donor T cells in murine bone marrow failure and can be implicated in human aplastic anemia

摘要

Interferon-gamma (IFN-gamma) and tumor necrosis factor-alpha (TNF-alpha) have been implicated historically in the immune pathophysiology of aplastic anemia (AA) and other bone marrow (BM) failure syndromes. We recently defined the essential roles of IFN-gamma produced by donor T cells and the IFN-gamma receptor in the host in murine immune-mediated BM failure models. TNF-alpha has been assumed to function similarly to IFN-gamma. We used our murine models and mice genetically deficient in TNF-alpha or TNF-alpha receptors (TNF-alpha Rs) to establish an analogous mechanism. Unexpectedly, infusion of TNF-alpha(-/-) donor lymph node (LN) cells into CByB6F1 recipients or injection of FVB LN cells into TNF-alpha R-/- recipients both induced BM failure, with concurrent marked increases in plasma IFN-gamma and TNF-alpha levels. Surprisingly, in TNF-alpha(-/-) recipients, BM damage was attenuated, suggesting that TNF-alpha of host origin was essential for immune destruction of hematopoiesis. Depletion of host macrophages before LN injection reduced T-cell IFN-gamma levels and reduced BM damage, whereas injection of recombinant TNF-alpha into FVB-LN cell-infused TNF-alpha(-/-) recipients increased T-cell IFN-gamma expression and accelerated BM damage. Furthermore, infusion of TNF-alpha R-/- donor LN cells into CByB6F1 recipients reduced BM T-cell infiltration, suppressed T-cell IFN-gamma production, and alleviated BM destruction. Thus, TNF-alpha from host macrophages and TNF-alpha R expressed on donor effector T cells were critical in the pathogenesis of murine immune-mediated BM failure, acting by modulation of IFN-gamma secretion. In AA patients, TNF-alpha-producing macrophages in the BM were more frequent than in healthy controls, suggesting the involvement of this cytokine and these cells inhuman disease.