Fujimura Taku, Kakizaki Aya, Furudate Sadanori, Kambayashi Yumi, Aiba Setsuya
Department of Dermatology, Tohoku University Graduate School of Medicine, Seiryo-machi 1-1, Aoba-ku, Sendai, 980-8574, Japan.
Department of Dermatology, Tohoku University Graduate School of Medicine, Seiryo-machi 1-1, Aoba-ku, Sendai, 980-8574, Japan.
J Dermatol Sci. 2016 Sep;83(3):167-73. doi: 10.1016/j.jdermsci.2016.05.015. Epub 2016 May 25.
Immunosuppressive tumor-associated macrophages (TAMs) promote an immunosuppressive environment in the tumor-bearing host, together with regulatory T cells (Tregs). TAMs compose cancer stroma in skin cancers including melanomas and non-melanomas. The majority of tumor-associated macrophages (TAMs) are alternatively activated M2 macrophages that favor tumor development, and they comprise one of the main populations of inflammatory cells in skin cancers. On the other hand, TAMs could be modulated into M1-type macrophages that suppress tumor growth by stimulating and recruiting Th1 and effector cells in the tumor sites. Therefore, TAMs are a target for immunotherapy in various cancers. In this review, we discuss the definition and suppressive mechanisms of TAMs, as well as their biological activities in tumor-bearing hosts to assess potential therapeutic strategies.
免疫抑制性肿瘤相关巨噬细胞(TAM)与调节性T细胞(Treg)一起,在荷瘤宿主中促进免疫抑制环境的形成。TAM构成包括黑色素瘤和非黑色素瘤在内的皮肤癌中的癌基质。大多数肿瘤相关巨噬细胞(TAM)是偏向于促进肿瘤发展的替代性活化M2巨噬细胞,它们是皮肤癌中炎症细胞的主要群体之一。另一方面,TAM可被调节为M1型巨噬细胞,通过在肿瘤部位刺激和募集Th1细胞及效应细胞来抑制肿瘤生长。因此,TAM是各种癌症免疫治疗的靶点。在本综述中,我们讨论了TAM的定义和抑制机制,以及它们在荷瘤宿主中的生物学活性,以评估潜在的治疗策略。