Academic Journal

Syphilitic infection impairs immunity by inducing both apoptosis and pyroptosis of CD4 and CD8 T lymphocytes

التفاصيل البيبلوغرافية
العنوان: Syphilitic infection impairs immunity by inducing both apoptosis and pyroptosis of CD4 and CD8 T lymphocytes
المؤلفون: Wei Xia, Jinxue Zhao, Bin Su, Yanmei Jiao, Wenjia Weng, Ming Zhang, Xiaodan Wang, Caiping Guo, Hao Wu, Tong Zhang, Yanqing Gao, Zaicun Li
المصدر: Innate Immunity, Vol 27 (2021)
بيانات النشر: SAGE Publishing, 2021.
سنة النشر: 2021
المجموعة: LCC:Immunologic diseases. Allergy
مصطلحات موضوعية: Immunologic diseases. Allergy, RC581-607
الوصف: Syphilis is an important health problem worldwide; however, few studies have probed the impact of syphilitic infection on T cell turnover. The mechanisms behind the frequency of T cell subset changes and the associations between these subsets during syphilitic infection remain unclear. Herein, we used a cell-staining method and flow cytometry to explore changes in T cell subpopulations and potential contribution of apoptosis and pyroptosis that triggered therein. We investigated caspase-1-mediated pyroptosis and caspase-3-mediated apoptosis of CD4 + and CD8 + T cells, the major effector lymphocytes with pivotal roles in the pathogenesis of infectious diseases. We found that the levels of caspase-1 and caspase-3 increased in both the circulation and intracellularly in CD4 + and CD8 + T cells. Caspase-1 showed a continual increase from early latent stage infection through to phase 2 disease, whereas caspase-3 increased through to phase 1 disease but declined during phase 2. In addition, serum levels and intracellular expression of caspase-1 and caspase-3 were positively correlated. Overall, this study increases our understanding of how syphilitic infection influences CD4 + and CD8 + T-cell turnover, which may help with designing novel and effective strategies to control syphilis infection and prevent its transmission.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1753-4259
1753-4267
17534259
Relation: https://doaj.org/toc/1753-4259; https://doaj.org/toc/1753-4267
DOI: 10.1177/1753425920952840
URL الوصول: https://doaj.org/article/1f67ca1a4be247a68d4a7885c2840ec0
رقم الانضمام: edsdoj.1f67ca1a4be247a68d4a7885c2840ec0
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:17534259
17534267
DOI:10.1177/1753425920952840