肿瘤驱动的细胞因子免疫调节改善心功能并抑制纤维化

Heart failure remains a leading cause of morbidity and mortality worldwide, with limited progress in the development of novel therapies. It has been demonstrated that tumor growth improves cardiac function and reduces myocardial fibrosis in mouse models of heart failure. It is clear that cancer cell implantation is not a possible therapeutic strategy for heart failure.

Therefore, we further studied the underlying mechanism involved, with the objective of demonstrating its broad therapeutic applicability.

We show that a single intravenous injection of serum from tumor-bearing mice rapidly augments left-ventricular fractional shortening and suppresses fibrosis in the heart, diaphragm, and skeletal muscles. Cytokine profiling identified IFN and TNF as essential mediators secreted downstream of natural killer (NK) cell activation. Purified recombinant IFN and TNF mimic the serum effect, polarizing cardiac and skeletal macrophages toward an anti-inflammatory, reparative state.

We further show that macrophage depletion abrogates the observed beneficial effect, confirming their critical role.

Our findings define a novel NK cell-macrophage cytokine axis that reverses cardiac dysfunction and fibrosis in pressure-overload (transverse aortic constriction) and ATF3-transgenic heart failure models.

Together, these findings define a novel host-tumor microenvironment response through cytokine secretion, which leads to cardiac repair and dissolution of fibrosis. This work presents a novel therapeutic strategy for harnessing innate immune cells in the treatment of heart failure and fibrotic disease.