Wiemer David F, Wiemer Andrew J
Department of Chemistry, University of Iowa, Iowa City, IA 52245, United States.
Department of Pharmaceutical Sciences, University of Connecticut, Storrs, CT 06269, United States.
Biochem Pharmacol. 2014 Jun 1;89(3):301-12. doi: 10.1016/j.bcp.2014.03.009. Epub 2014 Mar 26.
In contrast to T cells that express the more prevalent αβ T cell receptor and respond to peptide antigens, T cells that express the Vγ9Vδ2 T cell receptor detect and respond to non-peptide phosphorous-containing small molecules known as phosphoantigens. Because γδ T cells are early responders to infections and malignancies, it has been suggested that stimulation of their activity with small molecule phosphoantigen drugs may hold promise for therapeutic interventions. Recent studies have greatly advanced our knowledge of phosphoantigens as well as their cellular receptors. At the same time, clinical trials of phosphoantigens have suggested that development of these Vγ9Vδ2 T cell agonists has met unexpected challenges. In this commentary, we summarize the biology that underlies phosphoantigen activity and discuss the structural features of synthetic phosphoantigens that affect both their ability to stimulate Vγ9Vδ2 T cells and their potential as therapeutic agents.
与表达更为普遍的αβT细胞受体并对肽抗原作出反应的T细胞不同,表达Vγ9Vδ2 T细胞受体的T细胞能够检测并对被称为磷酸抗原的含磷小分子非肽作出反应。由于γδT细胞是感染和恶性肿瘤的早期应答者,因此有人提出,用小分子磷酸抗原药物刺激其活性可能为治疗干预带来希望。最近的研究极大地推进了我们对磷酸抗原及其细胞受体的认识。与此同时,磷酸抗原的临床试验表明,这些Vγ9Vδ2 T细胞激动剂的开发遇到了意想不到的挑战。在这篇评论中,我们总结了磷酸抗原活性背后的生物学原理,并讨论了合成磷酸抗原的结构特征,这些特征既影响其刺激Vγ9Vδ2 T细胞的能力,也影响其作为治疗剂的潜力。