| Literature DB >> 35149193 |
Amy B Hont1, Allison B Powell1, Danielle K Sohai1, Izabella K Valdez2, Maja Stanojevic3, Ashley E Geiger1, Kajal Chaudhary1, Ehsan Dowlati3, Catherine M Bollard1, Conrad Russell Y Cruz4.
Abstract
Immunotherapy with antigen-specific T cells is a promising, targeted therapeutic option for patients with cancer as well as for immunocompromised patients with virus infections. In this review, we characterize and compare current manufacturing protocols for the generation of T cells specific to viral and non-viral tumor-associated antigens. Specifically, we discuss: (1) the different methodologies to expand virus-specific T cell and non-viral tumor-associated antigen-specific T cell products, (2) an overview of the immunological principles involved when developing such manufacturing protocols, and (3) proposed standardized methodologies for the generation of polyclonal, polyfunctional antigen-specific T cells irrespective of donor source. Ex vivo expanded cells have been safely administered to treat numerous patients with virus-associated malignancies, hematologic malignancies, and solid tumors. Hence, we have performed a comprehensive review of the clinical trial results evaluating the safety, feasibility, and efficacy of these products in the clinic. In summary, this review seeks to provide new insights regarding antigen-specific T cell technology to benefit a rapidly expanding T cell therapy field.Entities:
Keywords: adoptive immunotherapy; antigen-specific T cells; cancer; manufacturing protocols; virus infection
Mesh:
Substances:
Year: 2022 PMID: 35149193 PMCID: PMC9171249 DOI: 10.1016/j.ymthe.2022.02.002
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 12.910