免疫系统
多效性
生物
免疫学
T细胞
移植
癌症研究
细胞生物学
医学
遗传学
基因
表型
外科
作者
Luigina Romani,Silvia Moretti,Francesca Fallarino,Silvia Bozza,Loredana Ruggeri,Andrea Casagrande,Franco Aversa,Francesco Bistoni,Andrea Velardi,Enrico Garaci
标识
DOI:10.1111/j.1749-6632.2012.06716.x
摘要
Thymosin α1 (Tα1), a thymosin‐related 28‐mer synthetic amino‐terminal acetylated peptide, has gained increasing interest in recent years, due to its pleiotropy. The peptide has been used worldwide as an adjuvant or immunotherapeutic agent to treat disparate human diseases, including viral infections, immunodeficiencies, and malignancies. The peptide can enhance T cell, dendritic cell (DC), and antibody responses, modulate cytokine and chemokine production, and block steroid‐induced apoptosis of thymocytes. Its central role in modulating DC function and activating multiple signaling pathways that contribute to different functions may offer a plausible explanation for its pleiotropic action. Additionally, the ability of Tα1 to activate the indoleamine 2,3‐dioxygenase enzyme—which confers immune tolerance during transplantation and restrains the vicious circle of chronic inflammation—has been a turning point, suggesting a potential, specific function in immunity. Accordingly, Tα1 has recently been shown to promote immune reconstitution and improve survival of recipients of HLA‐matched sibling T cell–depleted stem cell transplants in a phase I/II clinical trial. Thus, Tα1 continues to live up to its promises.
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