| Autor: |
Jing Guo, Chowdhury, Roshni Roy, Mallajosyula, Vamsee, Jianming Xie, Dubey, Megha, Yuanyuan Liu, Jing Li, Yu-ling Wei, Palanski, Brad A., Conghua Wang, Lingfeng Qiu, Ohanyan, Mané, Kask, Oliver, Sola, Elsa, Kamalyan, Lilit, Lewis, David B., Scriba, Thomas J., Davis, Mark M., Dodd, Dylan, Xun Zeng |
| Předmět: |
|
| Zdroj: |
Proceedings of the National Academy of Sciences of the United States of America; 1/23/2024, Vol. 121 Issue 4, p1-11, 32p |
| Abstrakt: |
γδ T cells are essential for immune defense and modulating physiological processes. While they have the potential to recognize large numbers of antigens through somatic gene rearrangement, the antigens which trigger most γδ T cell response remain unidentified, and the role of antigen recognition in γδ T cell function is contentious. Here, we show that some γδ T cell receptors (TCRs) exhibit polyspecificity, recognizing multiple ligands of diverse molecular nature. These ligands include haptens, metabolites, neurotransmitters, posttranslational modifications, as well as peptides and proteins of microbial and host origin. Polyspecific γδ T cells are enriched among activated cells in naive mice and the responding population in infection. They express diverse TCR sequences, have different functional potentials, and include the innate-like γδ T cells, such as the major IL-17 responders in various pathological/physiological conditions. We demonstrate that encountering their antigenic microbiome metabolite maintains their homeostasis and functional response, indicating that their ability to recognize multiple ligands is essential for their function. Human γδ T cells with similar polyspecificity also respond to various immune challenges. This study demonstrates that polyspecificity is a prevalent feature of γδ T cell antigen recognition, which enables rapid and robust T cell responses to a wide range of challenges, highlighting a unique function of γδ T cells. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
|
