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September 3, 2026Journal of Cellular and Molecular MedicineOpen Access

Single‐Cell Immune Profiling Suggests Non‐Classical Monocyte Is Associated Immunodepression in Tuberculosis Treatment Non‐Responders

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Authors

YXYiqun XiongNingbo No. 2 HospitalYQYahong QuNingbo No. 2 HospitalYWYing WangNingbo No. 2 Hospital

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Implication

Observational single-cell study reveals non-classical monocyte enrichment and immunosuppressive signaling in tuberculosis treatment non-responders, suggesting potential biomarkers of early failure.

Key Points

  • To characterize the immune cell landscape and molecular signaling pathways associated with 2-month sputum culture conversion status in tuberculosis patients.
  • Conducted single-cell RNA sequencing on peripheral blood mononuclear cells from eight patients with tuberculosis (N=8).
  • Stratified patients by 2-month sputum culture conversion status and applied CellChat analysis to model intercellular communications.
  • Non-responders exhibited relative enrichment of non-classical monocytes, higher tuberculosis progression risk scores, and altered IL16 and TRAIL signaling.
  • CD4+ regulatory T cells in non-responders demonstrated elevated LGALS9 expression with inferred GALECTIN signaling toward cytotoxic lymphocytes, alongside correlated HAVCR2 and TIGIT co-expression.
  • Mature natural killer cell subclusters showed distinct enrichment patterns between responders and non-responders.

Cite This Study

Xiong et al. (2026) studied this question.

synapsesocial.com/papers/6a993586636c6408cfa7dcachttps://doi.org/10.1111/jcmm.71345
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