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JOURNAL OF CLINICAL TRANSFUSION AND LABORATORY MEDICINE ›› 2026, Vol. 28 ›› Issue (1): 65-69.DOI: 10.3969/j.issn.1671-2587.2026.01.010

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Imbalance between Th17/Treg Cells and Associated Cytokines in Patients with Platelet Transfusion Refractoriness

LIU Wen1, WANG Wenxing2, FAN Na1, CHEN Wei3, LIANG Jing1   

  1. 1The Sixth Affiliated Hospital of Xinjiang Medical University, Blood Transfusion Department;
    2The Sixth Affiliated Hospital of Xinjiang Medical University;
    3People's Hospital of Xinjiang Uygur Autonomous Region, Blood Transfusion Department, Urumqi 830002
  • Received:2025-05-12 Published:2026-02-13

Abstract: Objective To investigate the changs and characteristics of regulatory T cells (Treg), helper T cells 17 (Th17) and related cytokines in the peripheral blood of patients with immune platelet transfusion refractoriness (IPTR). Methods A case-control study was conducted involving 20 patients with IPTR, 20 patients with effective platelet transfusion and 20 healthy controls. Flow cytometry was applied to detect the proportions of Treg (CD4+CD25+Foxp3+) and Th17 (CD4+IL-17A+) cells. Enzyme-linked immunosorbent assay (ELISA) was used to measure the serum levels of interleukin-6 (IL-6), interleukin-10 (IL-10), interleukin-17A (IL-17A) and transforming growth factor-β1 (TGF-β1). Results Compared with the healthy control group, the IPTR group showed a significantly decreased proportion of Treg (P<0.05), accompanied by a significantly increased proportion of Th17 cells and an elevated Th17/Treg ratio (both P<0.05). Meanwhile, the serum levels of pro-inflammatory cytokines IL-6 and IL-17A were significantly elevated (both P<0.05), while the levels of anti-inflammatory cytokines IL-10 and TGF-β1 were significantly reduced (both P<0.05). Conclusion Patients with IPTR have an imbalance in the Treg/Th17 axis and dysregulation of the pro-inflammatory and anti-inflammatory cytokine network. This finding suggests that the disruption of immune homeostasis may contribute to the pathogenesis of PTR by enhancing inflammatory responses and impairing immune tolerance.

Key words: Immune platelet transfusion refractoriness, Regulatory T cells, Helper T cells, Cytokines, Immune homeostasis

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