MYCOBACTERIUM TUBERCULOSIS PROTEOME-WIDE EPITOPE DISCOVERY AND HOST TRANSCRIPTOME-WIDE T CELL PHENOTYPING IN HIGH DISEASE BURDEN POPULATIONS

NIH RePORTER · NIH · N01 · $1,504,937 · view on reporter.nih.gov ↗

Abstract

The contractor will apply innovative, highly-multiplexed DNA-barcoded antigen assays to comprehensively discover and validate 100,000s of CD4 T cell epitopes across the entire proteome of Mycobacterium Tuberculosis (Mtb) – together with their HLA restrictions, cognate paired TCR α:βs, and corresponding T cell transcriptomes . The Assays will focus on a large panel of HLA proteins that include alleles prevalent in sub-Saharan African populations with high disease burdens but that remain vastly understudied at the epitope level. By comparing cohorts with different disease states across a large two-dimensional space defined by the pathogen genome and host transcriptome, the contractor will identify novel T cell features associated with protection from disease.

Key facts

NIH application ID
11201171
Project number
75N93024C00054-0-9999-1
Recipient
TRANSLATIONAL GENOMICS RESEARCH INST
Principal Investigator
John Altin
Activity code
N01
Funding institute
NIH
Fiscal year
2024
Award amount
$1,504,937
Award type
—
Project period
2024-09-30 → 2025-09-29