Laboratory of Immuno-Genetics and Human Pathologies, Faculty of Medicine and Pharmacy of Casablanca, Hassan II University, Casablanca 20000, Morocco.
Mohammed VI Center of Oncology, CHU Ibn Rochd, Faculty of Medicine and Pharmacy of Casablanca, Hassan II University, Casablanca 20000, Morocco.
Int J Mol Sci. 2022 Nov 3;23(21):13424. doi: 10.3390/ijms232113424.
Butyrophilin-3A (BTN3A) subfamily members are a group of immunoglobulins present on the surface of different cell types, including innate and cancer cells. Due to their high similarity with the B7 family members, different studies have been conducted and revealed the involvement of BTN3A molecules in modulating T cell activity within the tumor microenvironment (TME). However, a great part of this research focused on γδ T cells and how BTN3A contributes to their functions. In this review, we will depict the roles and various aspects of BTN3A molecules in distinct tumor microenvironments and review how BTN3A receptors modulate diverse immune effector functions including those of CD4+ (Th1), cytotoxic CD8+ T cells, and NK cells. We will also highlight the potential of BTN3A molecules as therapeutic targets for effective immunotherapy and successful cancer control, which could represent a bright future for patient treatment.
但钛素蛋白 3A(BTN3A)亚家族成员是一组存在于不同细胞类型表面的免疫球蛋白,包括先天免疫细胞和癌细胞。由于其与 B7 家族成员的高度相似性,不同的研究已经进行,并揭示了 BTN3A 分子在调节肿瘤微环境(TME)内 T 细胞活性中的作用。然而,这项研究的很大一部分集中在 γδ T 细胞上,以及 BTN3A 如何促进其功能。在这篇综述中,我们将描述 BTN3A 分子在不同肿瘤微环境中的作用和各个方面,并综述 BTN3A 受体如何调节各种免疫效应功能,包括 CD4+(Th1)、细胞毒性 CD8+ T 细胞和 NK 细胞。我们还将强调 BTN3A 分子作为有效的免疫治疗和成功的癌症控制的治疗靶点的潜力,这为患者治疗带来了光明的前景。