Department of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Front Immunol. 2020 Feb 28;11:257. doi: 10.3389/fimmu.2020.00257. eCollection 2020.
Minor histocompatibility antigens (mHAgs) in allogeneic hematopoietic stem cell transplantation are highly immunogenic as they are foreign antigens and cause polymorphism between donors and recipients. Adoptive cell therapy with mHAg-specific T cells may be an effective option for therapy against recurring hematological malignancies following transplantation. Genetically modified T cells with T cell receptors (TCRs) specific to mHAgs have been developed, but formation of mispaired chimeric TCRs between endogenous and exogenous TCR chains may compromise their function. An alternative approach is the development of chimeric antigen receptor (CAR)-T cells with TCR-like specificity whose CAR transmembrane and intracellular domains do not compete with endogenous TCR for CD3 complexes and transmit their own activation signals. However, it has been shown that the recognition of low-density antigens by high-affinity CAR-T cells has poor sensitivity and specificity. This mini review focuses on the potential for and limitations of TCR-like CAR-T cells in targeting human leukocyte antigen-bound peptide antigens, based on their recognition mechanisms and their application in targeting mHAgs.
次要组织相容性抗原(mHAgs)在异基因造血干细胞移植中具有高度免疫原性,因为它们是外来抗原,并且在供体和受者之间引起多态性。用 mHAg 特异性 T 细胞进行过继细胞治疗可能是移植后针对复发性血液恶性肿瘤的有效治疗选择。已经开发了针对 mHAgs 的 T 细胞受体(TCR)特异性的基因修饰 T 细胞,但是内源性和外源性 TCR 链之间形成错配嵌合 TCR 可能会影响其功能。另一种方法是开发具有 TCR 样特异性的嵌合抗原受体(CAR)-T 细胞,其 CAR 跨膜和细胞内结构域不会与内源性 TCR 竞争 CD3 复合物并传递其自身的激活信号。然而,已经表明,高亲和力 CAR-T 细胞对低密度抗原的识别具有较差的灵敏度和特异性。本综述重点介绍了 TCR 样 CAR-T 细胞在靶向人白细胞抗原结合肽抗原方面的潜力和局限性,基于其识别机制及其在靶向 mHAgs 中的应用。