Morandi Fabio, Horenstein Alberto Leonardo, Malavasi Fabio
Laboratorio Cellule Staminali Post-Natali e Terapie Cellulari, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Dipartimento Scienze Mediche, Università di Torino, Centro Ricerche Medicina Sperimentale (CeRMS) and Fondazione Ricerca Molinette Onlus, Torino, Italy.
Front Immunol. 2021 Apr 15;12:658263. doi: 10.3389/fimmu.2021.658263. eCollection 2021.
Nicotinamide adenine dinucleotide (NAD) is an important molecule that functions as a co-enzyme in numerous metabolic processes. Generated both through synthesis and salvage pathways, NAD is the substrate for a variety of NAD-consuming enzymes. Among them is CD38, a cell surface ecto-enzyme widely expressed on different types of cells and endowed with the function of cADP-ribose synthases/NAD glycohydrolase. Surface CD38 expression is increased in different hematological and solid tumors, where it cooperates with other ecto-enzymes to produce the immunosuppressive molecule adenosine (ADO). Few studies have explored the correlation of NAD levels with T-cell mediated anti-tumor response in preclinical models. We therefore discuss these novel findings, examining the possible contribution of NAD depletion, along with ADO production, in the immunosuppressive activities of CD38 in the context of human tumors. Lastly, we discuss the use of pharmacological inhibitors of CD38 and supplementation of different NAD precursors to increase NAD levels and to boost T cell responses. Such molecules may be employed as adjuvant therapies, in combination with standard treatments, for cancer patients.
烟酰胺腺嘌呤二核苷酸(NAD)是一种重要的分子,在众多代谢过程中作为辅酶发挥作用。NAD通过合成途径和补救途径生成,是多种消耗NAD的酶的底物。其中包括CD38,一种在不同类型细胞上广泛表达的细胞表面外切酶,具有cADP-核糖合酶/NAD糖水解酶的功能。在不同的血液系统肿瘤和实体瘤中,表面CD38表达增加,它与其他外切酶协同作用产生免疫抑制分子腺苷(ADO)。在临床前模型中,很少有研究探讨NAD水平与T细胞介导的抗肿瘤反应之间的相关性。因此,我们讨论这些新发现,研究在人类肿瘤背景下,NAD耗竭以及ADO产生在CD38免疫抑制活性中的可能作用。最后,我们讨论使用CD38的药理抑制剂以及补充不同的NAD前体来提高NAD水平并增强T细胞反应。这些分子可作为辅助疗法,与标准治疗联合用于癌症患者。