Target intelligence / Profile preview

ESAT-6-like protein EsxH (TB10.4 / EsxH)

Target
TB10.4 / EsxH
Molecular classification
Antigen, Immunodominant protein, Member of the ESAT-6 family, Small secreted protein
01

Overview

TB10.4 antigen (EsxH) is a small, secreted immunodominant protein from *Mycobacterium tuberculosis*, belonging to the ESAT-6 family and encoded by the gene Rv0288[1][3][6]. It is highly recognized by CD4+ and CD8+ T cells in humans and mice following infection or BCG vaccination, with specific epitopes inducing robust type 1 helper and cytotoxic responses[1][3][4][6]. Polymorphisms in TB10.4 can impact antigenicity and alter immune recognition, contributing to immune evasion strategies by *M. tuberculosis*[2]. TB10.4 has emerged as a promising subunit vaccine candidate, with research demonstrating its value in eliciting protection in experimental vaccine models, though successful implementation depends on adjuvant use and host genetic factors[3][4]. It does not have direct interactions with conventional drugs but is a target for vaccine design and immunodiagnostics[3][4][6]. The protein presents diverse epitopes, with the immunodominance and T-cell response patterns varying between infection, vaccination, and recombinant protein exposure[3][4][6].

Other names
EsxHRv0288TB10.4 proteinESAT-6 family antigenTB10.4 antigen
02

Mechanism of action

Vaccines targeting TB10.4 induce strong Th1-polarized CD4+ and CD8+ T-cell responses. Experimental vectors (e.g., CyaA toxoid, adenylate cyclase) are used. This mechanism is not applicable for small-molecule drug action.

03

Biological functions

Immune response modulation (stimulates T-cell responses)Antigenic variation and immune evasionCytotoxic T-cell activation (CD4 and CD8 epitopes)Vaccine candidate
04

Disease associations

Infection (mainly tuberculosis)Biomarker for Mycobacterium tuberculosis exposure
05

Safety considerations

Vaccine development challenges: adjuvant necessity and epitope presentation uncertaintyVariable immune response dependent on host geneticsImmune evasion potential via polymorphisms in TB10.4 (relevance for immune escape)
06

Interacting drugs

Subunit vaccines incorporating TB10.4

3 more in the full profile.

07

Biomarkers

TB10.4-specific T-cell responses (e.g., CD4+ and CD8+ reactive against TB10.4 epitopes)Measurement of IFN-γ production after TB10.4 stimulation in diagnostic assays (IGRA)

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