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Immunoregulatory gene GIMAP6 suppresses lethal atherosclerotic vasculopathy and ischemic heart failure

Xiang, C.; Arusha, K.; Springer, D.; Nakamori, S.; Jiang, P. D.; Yang, Z.-H.; Cui, J.; Zhang, Y.; Jing, H.; Park, A. Y.; Zhu, M. H.; Weber, S. E.; Cagdas, D.; Abolhassan, H.; Behniafard, N.; Smelkinson, M. G.; Liang, Q.; Everest, E.; Kun, J. F.; Grogan, A.; Treat, J. D.; Zerbe, C. S.; Holland, S. M.; Virmani, R.; Remaley, A. T.; Su, H. C.; Zheng, L.; Lenardo, M. J.

2026-01-28 immunology
10.64898/2026.01.26.701509 bioRxiv
Show abstract

Controlling hyperlipidemia has reduced but not eliminated atherosclerotic cardiovascular disease as a predominant cause of human mortality. Here, we report that loss of the immunoregulatory gene GTPase of immunity-associated protein 6 (GIMAP6), causes an inflammatory vasculopathy and accelerated atherosclerosis in the absence of hyperlipidemia. These pathologic changes in turn result in progressive cardiac ischemia, myocardial infarction, and heart failure, culminating in early death. In humans, rare deleterious GIMAP6 variants are associated with premature severe cardiovascular disease. These findings reveal GIMAP6 to play an important protective role against atherosclerotic cardiovascular disease whose identification offers opportunities for improved risk management and a target for new therapies.

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