Viewing Study NCT05899439



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Last Modification Date: 2024-10-26 @ 3:00 PM
Study NCT ID: NCT05899439
Status: RECRUITING
Last Update Posted: 2024-02-28
First Post: 2023-05-22

Brief Title: Immune Function and the Progression to T1D
Sponsor: University of Florida
Organization: University of Florida

Study Overview

Official Title: Immune Function and the Progression to Type 1 Diabetes
Status: RECRUITING
Status Verified Date: 2023-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To elucidate the mechanisms by which type 1 diabetes-associated genes IFIH1 TYK2 IKZF4 as well as total genetic risk impart functional immunoregulatory abnormalities that result in expansion of self-reactive adaptive immune cells defective regulatoryeffector mechanisms in T cells inflammatory antigen presenting cells and abnormal immune function in T cells and B cells
Detailed Description: Newly proposed studies will identify the inflammatory cues that draw immune cells into islets for disease initiation Project 1 probe the motility of immune cells through inflamed vasculature to the target organ and antigen priming sites within secondary lymphatics Project 2 and characterize the T1D-associated adaptive immune signatures in blood and immune tissues Project 3

The overall hypothesis of the renewed P01 states 1 the impact of T1D-risk variants will vary by tissue cell subset and activation state and 2 risk variants cellular stress and defects in immunologic pathways are key to engender the autoimmune destruction of pancreatic B-cells that results in T1D

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
P01AI042288 NIH University of Florida httpsreporternihgovquickSearchP01AI042288
PRO00043521 OTHER None None