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Kexiao Zheng

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Review Open access Jul 2026

Cardiac regeneration and repair: the emerging mechanisms and therapeutic approaches

Myocardial infarction, characterized by irreversible cardiomyocyte loss, progressive cardiac fibrosis and subsequent deteriorated heart function, constitute an intractable global health burden. Promoting endogenous cardiomyocyte proliferation to achieve functional cardiac regeneration represents an available foreground for combatting heart failure. Based on extensive preclinical evidence, researchers have characterized the cellular and molecular mechanisms governing cardiomyocyte proliferation and elucidated the modulatory influence of the metabolic factors and extracellular matrix. Insights from various studies have facilitated the development of regenerative approaches that reprogramming terminally differentiated cardiomyocytes toward a more metabolic plastic and fetal-like state, thereby enhancing the proliferative and reparative potential. Integration of metabolic and mechanical signals has emerged as a critical determinant of successful cardiomyocyte reactivation, providing a mechanistic rationale for combinatorial therapeutic strategies. Nevertheless, despite remarkable progression in mechanistic understanding and proof-of-concept studies, cardiac regeneration protocols advanced to robust clinical validation or pharmacal application have yet to be developed. This review provides a historical and biologically grounded synthesis of preclinical advances in cardiac repair, regeneration and cardiomyocyte reprogramming, with particular emphasis on translational feasibility and clinical applicability. Current strategies and preclinical trial outcomes are summarized to construct a readiness framework that maps the developmental maturity of each approach. Finally, the review highlights existing biological and technical barriers, as well as emerging opportunities poised to shape the future of cardiac regenerative medicine.

Yilong Li, Kexiao Zheng, Yinghua Liu et al. · 0 citations
Review Open access Aug 2026

Regulatory T cells in cardiac allograft vasculopathy: from mechanistic insights to clinical tolerance

Cardiac allograft vasculopathy (CAV) is the primary impairment that influences the long-term prognosis of transplanted hearts. CAV is characterized by diffuse intimal hyperplasia of the coronary arteries, which is mediated by chronic inflammation, the alloimmune response, and vascular remodeling. Current immunosuppressive regimens effectively control acute rejection but have limited efficacy in preventing CAV and are associated with significant adverse effects upon long-term use. Regulatory T cells (Tregs) are essential for preserving immunological homeostasis and facilitating transplantation tolerance. They are pivotal in suppressing the activation of effector T cells (Teffs), modulating local inflammation, and postponing the progression of CAV. This review comprehensively elucidates the pathophysiology of and diagnostic advancements in CAV, emphasizes the phenotypic heterogeneity, immunosuppressive mechanisms, and protective role of Tregs in heart transplantation, and thoroughly discuss the interplay of PD-1/PD-L1, IL-33, IL-6, CTLA-4, fatty acid oxidation (FAO), and other signaling pathways in modulating Treg function and CAV pathogenesis. In terms of the translational medicine, the adoptive infusion of in vitro-expanded autologous Tregs has demonstrated the ability to postpone CAV in preclinical models; nonetheless, its clinical use is limited by cell stability, challenging preparation processes, and the lack of efficacy biomarkers. Therefore, this review seeks to establish a theoretical foundation and research viewpoint to comprehensively understand the immunological mechanisms of CAV and the advancement of novel Treg-targeted therapies.

Buyan Li, Yu-Ling Su, Yanglin Hao et al. · 0 citations

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