George W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA.
Parker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA.
J Immunol. 2024 Jan 15;212(2):199-207. doi: 10.4049/jimmunol.2300488.
Adoptively transferred T cells constitute a major class of current and emergent cellular immunotherapies for the treatment of disease, including but not limited to cancer. Although key advancements in molecular recognition, genetic engineering, and manufacturing have dramatically enhanced their translational potential, therapeutic potency remains limited by poor homing and infiltration of transferred cells within target host tissues. In vitro microengineered homing assays with precise control over micromechanical and biological cues can address these shortcomings by enabling interrogation, screening, sorting, and optimization of therapeutic T cells based on their homing capacity. In this article, the working principles, application, and integration of microengineered homing assays for the mechanistic study of biophysical and biomolecular cues relevant to homing of therapeutic T cells are reviewed. The potential for these platforms to enable scalable enrichment and screening of next-generation manufactured T cell therapies for cancer is also discussed.
过继转移的 T 细胞是目前和新兴的细胞免疫疗法治疗疾病的主要类型,包括但不限于癌症。尽管在分子识别、基因工程和制造方面取得了重大进展,极大地提高了它们的转化潜力,但治疗效果仍然受到转移细胞在靶宿主组织中归巢和浸润不良的限制。体外微工程化归巢测定通过精确控制微机械和生物线索,可以通过基于归巢能力对治疗性 T 细胞进行询问、筛选、分类和优化,从而解决这些缺点。本文综述了用于研究与治疗性 T 细胞归巢相关的生物物理和生物分子线索的微工程化归巢测定的工作原理、应用和整合。还讨论了这些平台在实现下一代用于癌症的制造 T 细胞疗法的可扩展富集和筛选方面的潜力。