Experimental Immunology Unit, Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milano, Italy.
Experimental Immunology Unit, Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milano, Italy.
Mol Immunol. 2018 Nov;103:200-208. doi: 10.1016/j.molimm.2018.09.025. Epub 2018 Oct 8.
Adoptive cell therapy (ACT) using tumor-specific "conventional" MHC-restricted T cells obtained from tumor-infiltrating lymphocytes, or derived ex vivo by either antigen-specific expansion or genetic engineering of polyclonal T cell populations, shows great promise for cancer treatment. However, the wide applicability of this therapy finds limits in the high polymorphism of MHC molecules that restricts the use in the autologous context. CD1 antigen presenting molecules are nonpolymorphic and specialized for lipid antigen presentation to T cells. They are often expressed on malignant cells and, therefore, may represent an attractive target for ACT. We provide a brief overview of the CD1-resticted T cell response in tumor immunity and we discuss the pros and cons of ACT approaches based on unconventional CD1-restricted T cells.
过继细胞疗法(ACT)使用肿瘤浸润淋巴细胞中获得的肿瘤特异性“常规”MHC 限制性 T 细胞,或通过抗原特异性扩增或多克隆 T 细胞群体的基因工程体外衍生,为癌症治疗带来了巨大希望。然而,这种疗法的广泛适用性受到 MHC 分子高度多态性的限制,限制了其在自体背景下的应用。CD1 抗原呈递分子是非多态性的,专门用于将脂质抗原呈递给 T 细胞。它们通常在恶性细胞上表达,因此可能代表 ACT 的一个有吸引力的靶点。我们简要概述了肿瘤免疫中的 CD1 限制性 T 细胞反应,并讨论了基于非传统 CD1 限制性 T 细胞的 ACT 方法的优缺点。