Clinical Staphylococcus aureus inhibits human T-cell activity through interaction with the PD-1 receptor

临床金黄色葡萄球菌通过与PD-1受体相互作用抑制人T细胞活性

阅读:2
作者:Maiken Mellergaard # ,Sarah Line Skovbakke # ,Stine Dam Jepsen ,Nafsika Panagiotopoulou ,Amalie Bøge Rud Hansen ,Weihua Tian ,Astrid Lund ,Rikke Illum Høgh ,Sofie Hedlund Møller ,Romain Guérillot ,Ashleigh S Hayes ,Lise Tornvig Erikstrup ,Lars Andresen ,Anton Y Peleg ,Anders Rhod Larsen ,Timothy P Stinear ,Aase Handberg ,Christian Erikstrup ,Benjamin P Howden ,Steffen Goletz ,Dorte Frees ,Søren Skov

Abstract

Therapies that target and aid the host immune defense to repel cancer cells or invading pathogens are rapidly emerging. Antibiotic resistance is among the largest threats to human health globally. Staphylococcus aureus (S. aureus) is the most common bacterial infection, and it poses a challenge to the healthcare system due to its significant ability to develop resistance toward current available therapies. In long-term infections, S. aureus further adapt to avoid clearance by the host immune defense. In this study, we discover a new interaction that allows S. aureus to avoid elimination by the immune system, which likely supports its persistence in the host. Moreover, we find that blocking the specific receptor (PD-1) using antibodies significantly relieves the S. aureus-imposed inhibition. Our findings suggest that therapeutically targeting PD-1 is a possible future strategy for treating certain antibiotic-resistant staphylococcal infections.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。