Sarter Kerstin, Leimgruber Elisa, Gobet Florian, Agrawal Vishal, Dunand-Sauthier Isabelle, Barras Emmanuèle, Mastelic-Gavillet Béatris, Kamath Arun, Fontannaz Paola, Guéry Leslie, Duraes Fernanda do Valle, Lippens Carla, Ravn Ulla, Santiago-Raber Marie-Laure, Magistrelli Giovanni, Fischer Nicolas, Siegrist Claire-Anne, Hugues Stéphanie, Reith Walter
Department of Pathology and Immunology, Faculty of Medicine, University of Geneva, 1211 Geneva, Switzerland.
Department of Pathology and Immunology, Faculty of Medicine, University of Geneva, 1211 Geneva, Switzerland Department of Pediatrics, World Health Organization Collaborating Center for Vaccinology and Neonatal Immunology, University of Geneva, 1211 Geneva, Switzerland.
J Exp Med. 2016 Feb 8;213(2):177-87. doi: 10.1084/jem.20150435. Epub 2016 Jan 25.
Evidence has recently emerged that butyrophilins, which are members of the extended B7 family of co-stimulatory molecules, have diverse functions in the immune system. We found that the human and mouse genes encoding butyrophilin-2A2 (BTN2A2) are regulated by the class II trans-activator and regulatory factor X, two transcription factors dedicated to major histocompatibility complex class II expression, suggesting a role in T cell immunity. To address this, we generated Btn2a2-deficient mice. Btn2a2(-/-) mice exhibited enhanced effector CD4(+) and CD8(+) T cell responses, impaired CD4(+) regulatory T cell induction, potentiated antitumor responses, and exacerbated experimental autoimmune encephalomyelitis. Altered immune responses were attributed to Btn2a2 deficiency in antigen-presenting cells rather than T cells or nonhematopoietic cells. These results provide the first genetic evidence that BTN2A2 is a co-inhibitory molecule that modulates T cell-mediated immunity.
最近有证据表明,作为共刺激分子扩展B7家族成员的嗜乳脂蛋白在免疫系统中具有多种功能。我们发现,编码嗜乳脂蛋白-2A2(BTN2A2)的人类和小鼠基因受II类反式激活因子和调节因子X调控,这两种转录因子专门负责主要组织相容性复合体II类分子的表达,提示其在T细胞免疫中发挥作用。为了对此进行研究,我们构建了Btn2a2基因缺陷小鼠。Btn2a2(-/-)小鼠表现出效应性CD4(+)和CD8(+) T细胞反应增强、CD4(+)调节性T细胞诱导受损、抗肿瘤反应增强以及实验性自身免疫性脑脊髓炎加剧。免疫反应的改变归因于抗原呈递细胞中Btn2a2的缺陷,而非T细胞或非造血细胞。这些结果提供了首个遗传学证据,证明BTN2A2是一种调节T细胞介导免疫的共抑制分子。