Cazzato Gerardo, Cascardi Eliano, Colagrande Anna, Lettini Teresa, Filosa Alessandra, Arezzo Francesca, Lupo Carmelo, Casatta Nadia, Loizzi Vera, Pellegrini Cristina, Fargnoli Maria Concetta, Maiorano Eugenio, Cicco Gerolamo, Tamma Roberto, Ingravallo Giuseppe
Section of Molecular Pathology, Department of Precision and Regenerative Medicine and Ionian Area (DiMePRe-J), University of Bari "Aldo Moro", 70124 Bari, Italy.
Department of Medical Sciences, University of Turin, 10124 Turin, Italy.
Cancers (Basel). 2023 Mar 10;15(6):1697. doi: 10.3390/cancers15061697.
T cell immunoglobulin and mucin domain 3 (TIM-3) is an inhibitory immunocheckpoint that belongs to the TIM gene family. Monney et al. first discovered it about 20 years ago and linked it to some autoimmune diseases; subsequent studies have revealed that some tumours, including melanoma, have the capacity to produce inhibitory ligands that bind to these receptor checkpoints on tumour-specific immune cells. We conducted a literature search using PubMed, Web of Science (WoS), Scopus, Google Scholar, and Cochrane, searching for the following keywords: "T cell immunoglobulin and mucin-domain containing-3", "TIM-3" and/or "Immunocheckpoint inhibitors" in combination with "malignant melanoma" or "human malignant melanoma" or "cutaneous melanoma". The literature search initially turned up 117 documents, 23 of which were duplicates. After verifying eligibility and inclusion criteria, 17 publications were ultimately included. A growing body of scientific evidence considers TIM-3 a valid inhibitory immuno-checkpoint with a very interesting potential in the field of melanoma. However, other recent studies have discovered new roles for TIM-3 that seem almost to contradict previous findings in this regard. All this demonstrates how common and valid the concept of 'pleiotropism' is in the TME field, in that the same molecule can behave completely or partially differently depending on the cell type considered or on temporary conditions. Further studies, large case series, and a special focus on the immunophenotype of TIM-3 are absolutely necessary in order to explore this highly promising topic in the near future.
T细胞免疫球蛋白和粘蛋白结构域3(TIM-3)是一种属于TIM基因家族的抑制性免疫检查点。大约20年前,莫尼等人首次发现了它,并将其与一些自身免疫性疾病联系起来;随后的研究表明,包括黑色素瘤在内的一些肿瘤能够产生抑制性配体,这些配体与肿瘤特异性免疫细胞上的这些受体检查点结合。我们使用PubMed、科学网(WoS)、Scopus、谷歌学术和考克兰进行了文献检索,搜索了以下关键词:“含T细胞免疫球蛋白和粘蛋白结构域-3”、“TIM-3”和/或“免疫检查点抑制剂”,并与“恶性黑色素瘤”或“人类恶性黑色素瘤”或“皮肤黑色素瘤”组合。文献检索最初找到了117篇文献,其中23篇是重复的。在核实入选标准和纳入标准后,最终纳入了17篇出版物。越来越多的科学证据认为TIM-3是一种有效的抑制性免疫检查点,在黑色素瘤领域具有非常有趣的潜力。然而,最近的其他研究发现了TIM-3的新作用,这似乎与之前在这方面的发现几乎相矛盾。所有这些都表明,“多效性”概念在肿瘤微环境领域是多么普遍和有效,即同一分子根据所考虑的细胞类型或临时条件可能表现出完全或部分不同的行为。为了在不久的将来探索这个极具前景的课题,进一步的研究、大型病例系列以及对TIM-3免疫表型的特别关注绝对必要。