Self-powered rapid antigen-specific T-cell response assay for Mycobacterium tuberculosis infections.

Publication date: Jun 27, 2025

Interferon-gamma release assays (IGRAs) that evaluate an individual’s T-cell activation response to Mycobacterium tuberculosis (M. tb)-specific peptides serve an important role in diagnosing tuberculosis (TB). However, there are substantial challenges to the use of IGRAs in resource-limited settings. Further, IGRA diagnostic performance can also be compromised in anergic individuals. Here we describe a microfluidic chip-based antigen-specific T-cell response assay (ASTRA) that automates the detection of M. tb-specific T-cell activation responses to facilitate screening for latent M. tb infection and TB. We observe that ASTRA demonstrates high specificity for M. tb infection in independent patient cohorts. Compared with IGRA, ASTRA shows greater diagnostic sensitivity in individuals with HIV-1 co-infections (93. 8% versus 67%), comparable diagnostic sensitivity in HIV-negative individuals (92. 8%) and faster detection (4 h versus 24-48 h). We also find that a self-powered ASTRA chip that analysed microsample (~25 μl) whole-blood samples produced comparable results. ASTRA holds the potential to facilitate efforts to control the global TB epidemic and serve as a versatile platform for analysing T-cell responses across various infectious diseases and immunotherapeutic interventions.

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Concepts Keywords
Faster Antigen
Immunotherapeutic Assay
Mycobacterium Astra
Tuberculosis Cell
Diagnostic
Individuals
Infections
Mycobacterium
Powered
Self
Specific
Tb
Tuberculosis

Semantics

Type Source Name
disease IDO cell
disease IDO assay
disease MESH Mycobacterium tuberculosis infections
pathway REACTOME Release
disease IDO role
pathway KEGG Tuberculosis
disease MESH infection
disease MESH co-infections
disease IDO blood
disease MESH infectious diseases
disease MESH COVID 19 pandemic
drug DRUGBANK BCG vaccine
disease MESH measles
pathway KEGG Measles
disease MESH smallpox
disease IDO immunodeficiency
disease MESH HIV infection
pathway REACTOME HIV Infection
disease IDO production
drug DRUGBANK Coenzyme M
drug DRUGBANK Saquinavir
disease IDO history

Original Article

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