Tsai Ching-Yi, Lee Chih-Yuan, Chen Jia-Huang, Chiang Chih-Kang
Graduate Institute of Toxicology, College of Medicine, National Taiwan University, Taipei 100233, Taiwan.
Department of Medical Research, National Taiwan University Hospital, Taipei 100225, Taiwan.
Int J Mol Sci. 2025 Mar 18;26(6):2711. doi: 10.3390/ijms26062711.
Chronic alloantibody-mediated rejection (cAMR) remains a major challenge in transplant immunology, with no FDA-approved targeted therapies currently available. Despite advancements in cellular immunosuppression, effective strategies to mitigate alloantibody-mediated rejection are still lacking. This review provides a comprehensive overview of transplant rejection with a particular focus on the pathophysiology and therapeutic landscape of cAMR. We highlight the role of plasma cell-driven alloantibody production and its susceptibility to endoplasmic reticulum (ER) stress, a pathway with potential for therapeutic intervention. Special attention is given to calcineurin inhibitors (CNIs), which, beyond their well-established T-cell inhibitory effects, exhibit differential impacts on ER stress and plasma cell viability. By delineating the mechanistic differences between cyclosporine and tacrolimus in regulating ER stress responses, we propose potential therapeutic implications for optimizing cAMR management. This review underscores the need for innovative strategies targeting plasma cell biology to improve long-term transplant outcomes.
慢性同种异体抗体介导的排斥反应(cAMR)仍然是移植免疫学中的一项重大挑战,目前尚无FDA批准的靶向治疗方法。尽管细胞免疫抑制取得了进展,但减轻同种异体抗体介导的排斥反应的有效策略仍然缺乏。本综述全面概述了移植排斥反应,特别关注cAMR的病理生理学和治疗前景。我们强调浆细胞驱动的同种异体抗体产生的作用及其对内质网(ER)应激的敏感性,这是一条具有治疗干预潜力的途径。特别关注钙调神经磷酸酶抑制剂(CNIs),它们除了具有公认的T细胞抑制作用外,还对ER应激和浆细胞活力表现出不同的影响。通过阐述环孢素和他克莫司在调节ER应激反应方面的机制差异,我们提出了优化cAMR管理的潜在治疗意义。本综述强调了针对浆细胞生物学的创新策略对于改善长期移植结果的必要性。