Determining antigen recognition in systemic sclerosis

NIH RePORTER · NIH · U19 · $112,950 · view on reporter.nih.gov ↗

Abstract

PROJECT SUMMARY This project focuses on the identification of specific self-antigens that activate CD4+ T cells in systemic sclerosis. Cytotoxic CD4+T cells may directly contribute to cell death in tissues and secrete cytokines that lead to fibrosis. They likely receive help from activated B cells in tissues that in turn are induced by T follicular helper cells. Our goal is to use an unbiased approach to identify self antigens that activate clonally expanded cytotoxic CD4+T cells and/or T follicular helper cells from patients with diffuse systemic sclerosis who specifically have inherited HLA-DPB1*1301. Single cell cloning of CD4+ T cells will be used to identify matched T cell receptor alpha and beta chains from the most expanded cytotoxic CD4+ T cells and T follicular helper cells. Soluble T cell receptors will be generated. These soluble receptors will be used to screen a library of all human self peptides fused to HLA-DPB1*1301 and expressed in yeast.

Key facts

NIH application ID
9915867
Project number
5U19AI110495-07
Recipient
MASSACHUSETTS GENERAL HOSPITAL
Principal Investigator
Michael Birnbaum
Activity code
U19
Funding institute
NIH
Fiscal year
2020
Award amount
$112,950
Award type
5
Project period
— → —