IL-32 positively regulates the AEBP1-IκBα-NF-κB-TNF-α axis to inhibit Mycobacterium tuberculosis infection in human macrophages.

IL-32 positively regulates the AEBP1-IκBα-NF-κB-TNF-α axis to inhibit Mycobacterium tuberculosis infection in human macrophages.

Publication date: Nov 01, 2025

Mycobacterium tuberculosis (MTB), the causative agent of tuberculosis, survives in host macrophages, the primary effector and antigen-presenting cells involved in the host immune response. We previously showed that Interleukin-32 (IL-32) is significantly increased in the peripheral blood plasma of tuberculosis patients, can act as an anti-MTB agent. However, the underlying molecular mechanism for its effect remains unknown. Here, we showed that inhibiting IL-32 with monoclonal antibody increases MTB loads that was positively correlated with higher antibody concentrations and longer exposure times. RNA-Sequencing result indicated that 3797 genes were shown to be up-regulated in response to IL-32 inhibition, while 1365 genes were down-regulated. GO and KEGG analysis indicated that classical signaling pathways, including TNF, cell cycle, and Wnt were significantly enriched. Consistent expression trends were observed in NF-_705B pathway-related antibacterial factors that are functionally capable of inhibiting MTB. Using differentially expressed gene and protein-protein interaction analysis, AEBP1 was the gene with the most significant difference in expression and regulated by IL-32. These findings suggest a dynamic molecular and cellular mechanism by which IL-32 positively regulates the AEBP1-I_705Bα-NF-_705B-TNF-α axis to inhibit MTB infection in human macrophages.

Concepts Keywords
Antibody AEBP1
Classical Antibodies, Monoclonal
Mycobacterium Antibodies, Monoclonal
Tuberculosis Gene Expression Regulation
Host-Pathogen Interactions
Humans
IL-32
IL32 protein, human
Interleukins
Interleukins
Macrophage
Macrophages
Mycobacterium tuberculosis
Mycobacterium tuberculosis
NF-kappa B
NF-kappa B
NF-KappaB Inhibitor alpha
NF-KappaB Inhibitor alpha
RNA-Seq
Signal Transduction
TNF pathway
Tuberculosis
Tumor Necrosis Factor-alpha
Tumor Necrosis Factor-alpha

Semantics

Type Source Name
disease MESH Mycobacterium tuberculosis infection
pathway KEGG Tuberculosis
disease IDO host
disease IDO immune response
pathway REACTOME Cell Cycle
disease IDO protein
disease MESH infection
disease IDO pathogen
pathway REACTOME Signal Transduction

Original Article

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