Institute of Immunology, Hannover Medical School, 30625 Hannover, Germany.
Cells. 2020 Mar 18;9(3):743. doi: 10.3390/cells9030743.
Right after the discovery of γδ T-cells in 1984, people started asking how γδ T-cells interact with other immune cells such as B-cells. Early reports showed that γδ T-cells are able to help B-cells to produce antibodies and to sustain the production of germinal centers. Interestingly, the presence of γδ T-cells seems to promote the generation of antibodies against "self" and less against challenging pathogens. More recently, these hypotheses were supported using γδ T-cell-deficient mouse strains, in different mouse models of systemic lupus erythematous, and after induction of epithelial cell damage. Together, these studies suggest that the link between γδ T-cells and the production of autoantibodies may be more relevant for the development of autoimmune diseases than generally acknowledged and thus targeting γδ T-cells could represent a new therapeutic strategy. In this review, we focus on what is known about the communication between γδ T-cells and B-cells, and we discuss the importance of this interaction in the context of autoimmunity.
γδ T 细胞于 1984 年被发现后,人们开始研究 γδ T 细胞与 B 细胞等其他免疫细胞之间的相互作用。早期研究表明,γδ T 细胞能够帮助 B 细胞产生抗体,并维持生发中心的产生。有趣的是,γδ T 细胞的存在似乎促进了针对“自身”的抗体产生,而对挑战病原体的抗体产生则较少。最近,使用缺乏 γδ T 细胞的小鼠品系,在系统性红斑狼疮的不同小鼠模型中,以及在诱导上皮细胞损伤后,这些假设得到了支持。这些研究表明,γδ T 细胞与自身抗体产生之间的联系可能与自身免疫性疾病的发展比人们普遍认为的更为相关,因此靶向 γδ T 细胞可能代表一种新的治疗策略。在这篇综述中,我们重点关注 γδ T 细胞与 B 细胞之间的通信,以及在自身免疫背景下这种相互作用的重要性。