Immune Function and the Progression to T1D

Description

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 regulatory/effector mechanisms in T cells, inflammatory antigen presenting cells, and abnormal immune function in T cells and B cells.

Conditions

Type 1 Diabetes

Study Overview

Study Details

Study overview

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 regulatory/effector mechanisms in T cells, inflammatory antigen presenting cells, and abnormal immune function in T cells and B cells.

Immune Function and the Progression to Type 1 Diabetes:

Immune Function and the Progression to T1D

Condition
Type 1 Diabetes
Intervention / Treatment

-

Contacts and Locations

Gainesville

Kieran McGrail, Gainesville, Florida, United States, 32610

Columbus

The Ohio State University, Columbus, Ohio, United States, 43210

Houston

Baylor College of Medicine, Center for Research Advancement - Texas Children's Hospital, Houston, Texas, United States, 77030

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

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Eligibility Criteria

    Ages Eligible for Study

    0 Years to 100 Years

    Sexes Eligible for Study

    ALL

    Accepts Healthy Volunteers

    Yes

    Collaborators and Investigators

    University of Florida,

    Study Record Dates

    2085-01-01