Proportional change of CD4+ CD25+ regulatory T cells after lymphocyte therapy in unexplained recurrent spontaneous abortion patients

Objective To investigate the proportional changes of CD4+ CD25+ regulatory T cells in peripheral blood after lymphocyte therapy in unexplained recurrent spontaneous abortion (URSA) patients. Design Prospective cohort study. Setting University Hospital. Patient(s) Twenty-five URSA patients. Intervent...

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Veröffentlicht in:Fertility and sterility 2009-07, Vol.92 (1), p.301-305
Hauptverfasser: Yang, Hui, M.D., Ph.D, Qiu, Lihua, M.D., Ph.D, Di, Wen, M.D., Ph.D, Zhao, Aiming, M.D., Ph.D, Chen, Guangjie, Ph.D, Hu, Ke, M.D., Ph.D, Lin, Qide, M.D
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Sprache:eng
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Zusammenfassung:Objective To investigate the proportional changes of CD4+ CD25+ regulatory T cells in peripheral blood after lymphocyte therapy in unexplained recurrent spontaneous abortion (URSA) patients. Design Prospective cohort study. Setting University Hospital. Patient(s) Twenty-five URSA patients. Intervention(s) Measurements of CD4+ CD25+ regulatory T cells in peripheral blood before and after paternal or third-party lymphocyte immunization. Main Outcome Measure(s) The proportion of CD4+ CD25bright regulatory T cells and the percentage of CD25bright cells in the CD4+ T-cell population. Result(s) The proportion of CD4+ CD25bright T cells in peripheral blood from URSA patients was increased significantly after paternal or third-party lymphocyte immunization therapy, whereas the percentage of CD4+ CD25dim cells were decreased significantly. The percentage of CD4+ CD25bright cells in the CD4+ T-cell population was significantly increased, and the proportion of CD4+ CD25bright T cells was significantly higher in successfully pregnant women than in those with pregnancy loss after lymphocyte therapy. Conclusion(s) Allogeneic lymphocyte therapy can enhance the percentage of CD4+ CD25bright regulatory T cells in peripheral blood, therefore CD4+ CD25+ regulatory T cells may serve as a novel biomarker for monitoring allogeneic lymphocyte therapy in URSA patients.
ISSN:0015-0282
1556-5653
DOI:10.1016/j.fertnstert.2008.04.068