Abstract
Type 1 diabetes (T1D) patients might experience a transient partial remission (PR) stage. However, the immunological mechanisms responsible for the PR stage still need to be elucidated. Here, we have applied single-cell RNA sequencing to delineate the immune underpinnings of peripheral immune cells among healthy individuals, new-onset T1D patients, and T1D patients in the PR phase. Combined with cohort validation and functional assays, the expansion of TIGIT+ CCR7− Tregs as well as the decrease of CD226+ CCR7− CD8+ T cells helps to maintain a window in which to transit the immune balance in the remission stage via the TGF-β signal. These findings, especially the identified cell subsets may provide novel mechanism for future therapeutic interventions. Disclosure X.Li: None. T.Zhong: None. X.Li: None. L.Kang: None. R.Tang: None.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
