Delfanti Gloria, Dellabona Paolo, Casorati Giulia, Fedeli Maya
Experimental Immunology Unit, Division of Immunology, Transplantation, and Infectious Diseases, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) San Raffaele Scientific Institute, Milan, Italy.
Vita-Salute San Raffaele University, Milan, Italy.
Front Med (Lausanne). 2022 May 9;9:897750. doi: 10.3389/fmed.2022.897750. eCollection 2022.
Invariant Natural Killer T (iNKT) cells are T lymphocytes expressing a conserved semi-invariant TCR specific for lipid antigens (Ags) restricted for the monomorphic MHC class I-related molecule CD1d. iNKT cells infiltrate mouse and human tumors and play an important role in the immune surveillance against solid and hematological malignancies. Because of unique functional features, they are attractive platforms for adoptive cells immunotherapy of cancer compared to conventional T cells. iNKT cells can directly kill CD1d-expressing cancer cells, but also restrict immunosuppressive myelomonocytic populations in the tumor microenvironment (TME) CD1d-cognate recognition, promoting anti-tumor responses irrespective of the CD1d expression by cancer cells. Moreover, iNKT cells can be adoptively transferred across MHC barriers without risk of alloreaction because CD1d molecules are identical in all individuals, in addition to their ability to suppress graft vs. host disease (GvHD) without impairing the anti-tumor responses. Within this functional framework, iNKT cells are successfully engineered to acquire a second antigen-specificity by expressing recombinant TCRs or Chimeric Antigen Receptor (CAR) specific for tumor-associated antigens, enabling the direct targeting of antigen-expressing cancer cells, while maintaining their CD1d-dependent functions. These new evidences support the exploitation of iNKT cells for donor unrestricted, and possibly off the shelf, adoptive cell therapies enabling the concurrent targeting of cancer cells and suppressive microenvironment.
不变自然杀伤T(iNKT)细胞是表达一种保守的半不变T细胞受体(TCR)的T淋巴细胞,该受体对受单态性MHC I类相关分子CD1d限制的脂质抗原(Ag)具有特异性。iNKT细胞浸润小鼠和人类肿瘤,并在针对实体和血液系统恶性肿瘤的免疫监视中发挥重要作用。由于其独特的功能特性,与传统T细胞相比,它们是癌症过继性细胞免疫治疗的有吸引力的平台。iNKT细胞可以直接杀死表达CD1d的癌细胞,还可以通过CD1d同源识别限制肿瘤微环境(TME)中的免疫抑制性骨髓单核细胞群体,促进抗肿瘤反应,而不考虑癌细胞的CD1d表达。此外,iNKT细胞可以跨越MHC屏障进行过继转移而没有同种异体反应的风险,因为CD1d分子在所有个体中都是相同的,此外它们还具有在不损害抗肿瘤反应的情况下抑制移植物抗宿主病(GvHD)的能力。在这个功能框架内,iNKT细胞通过表达针对肿瘤相关抗原的重组TCR或嵌合抗原受体(CAR)成功地进行工程改造以获得第二种抗原特异性,从而能够直接靶向表达抗原的癌细胞,同时保持其CD1d依赖性功能。这些新证据支持利用iNKT细胞进行供体无限制且可能现成可用的过继性细胞疗法,从而能够同时靶向癌细胞和抑制性微环境。