Paulos Chrystal M, Suhoski Megan M, Plesa Gabriela, Jiang Tianying, Basu Samik, Golovina Tatiana N, Jiang Shuguang, Aqui Nicole A, Powell Daniel J, Levine Bruce L, Carroll Richard G, Riley James L, June Carl H
Abramson Family Cancer Research Institute, University of Pennsylvania, BRB II/III, Room 554, 421 Curie Boulevard, Philadelphia, PA, 19104-6160, USA.
Immunol Res. 2008;42(1-3):182-96. doi: 10.1007/s12026-008-8070-9.
Many recent advances in basic cell biology and immunology are a harbinger of progress in adoptive cell therapy (ACT) including (1) the finding that host lymphodepletion enhances engraftment and efficacy, (2) the recognition that in vitro T cell functions may not correlate with in vivo efficacy, and (3) the development of advanced ex vivo culture methods to expand lymphocytes to therapeutically effective numbers. In this article, we focus on the development of artificial antigen presenting cells (aAPCs) in our laboratory and their applicability to augment ACT protocols. We also describe how aAPCs can be used to broaden ACT to treat patients with a wide variety of cancers, chronic infectious diseases, and autoimmune manifestations.
基础细胞生物学和免疫学领域最近的许多进展预示着过继性细胞疗法(ACT)的进步,包括:(1)发现宿主淋巴细胞清除可增强植入和疗效;(2)认识到体外T细胞功能可能与体内疗效不相关;(3)开发先进的体外培养方法以将淋巴细胞扩增至治疗有效的数量。在本文中,我们重点介绍我们实验室中人工抗原呈递细胞(aAPC)的开发及其在增强ACT方案中的适用性。我们还描述了aAPC如何用于扩展ACT,以治疗患有多种癌症、慢性传染病和自身免疫表现的患者。