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Does bone marrow-derived mesenchymal stem cell transfusion prevent antisperm antibody production after traumatic testis rupture?

机译:创伤性睾丸破裂后,骨髓间充质干细胞输注是否能阻止抗精子抗体的产生?

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Objective To determine whether transfusion of mesenchymal stem cells (MSCs) could prevent humoral immune response and autoimmunization against sperms after traumatic testis rupture. Methods Immunomodulatory properties of MSCs have been evaluated by a prospective cohort on 50 adult BALB/c mice. In each interventional arms of study, controlled testis rupture and surgical repair were exerted. In addition to tissue repair, single dose of 5 × 105 MSCs labeled by green fluorescent protein was delivered intravenously to 20 cases (cell therapy group). After euthanizing, seroconversion of antisperm antibody (ASA) was compared between 2 interventional groups as response of humoral immune system. Lung and testis tissues were examined for green fluorescent protein-positive cells to assess whether presence of stem cells is correlated with seroconversion rates. Results Six cases had been lost during the study. Fourteen of 16 mice in cell therapy control group formed ASA (87.5%) but 6 of 18 mice (33.3%) in cell therapy group were immunized and formed ASA (P =.002). Transplanted cells were traced in lungs of 55% (n = 10) of cell therapy group and none were found in trauma site. Small volume of mice blood was our main limitation to trace seroconversion or quantitative measurement of ASA in each case. Conclusion In this in vivo model of autoimmune infertility, bone marrow-derived MSC transfusion showed immunosuppressive effects on antibody production. Considering immunomodulatory properties of MSCs even in allogeneic settings, novel clinical application should be investigated further.
机译:目的探讨间充质干细胞(MSCs)的输注是否可以预防创伤性睾丸破裂后的体液免疫反应和针对精子的自身免疫。方法通过前瞻性队列评估了50只成年BALB / c小鼠的MSCs的免疫调节特性。在每个研究性干预领域,均进行了受控的睾丸破裂和手术修复。除组织修复外,还通过静脉注射单剂量5×105的绿色荧光蛋白标记的MSC,治疗20例(细胞治疗组)。安乐死后,比较两个干预组之间的抗精子抗体(ASA)的血清转化,作为体液免疫系统的反应。检查肺和睾丸组织中绿色荧光蛋白阳性细胞,以评估干细胞的存在是否与血清转化率相关。结果研究期间丢失6例。细胞治疗对照组的16只小鼠中有14只形成了ASA(87.5%),而细胞治疗组的18只小鼠中有6只(33.3%)被免疫并形成了ASA(P = .002)。在细胞治疗组的55%(n = 10)的肺中发现了被移植的细胞,而在创伤部位则没有发现。在每种情况下,少量的小鼠血液是我们进行微量血清转化或定量测定ASA的主要限制。结论在这种自身免疫性不育的体内模型中,骨髓源性MSC输注对抗体的产生具有免疫抑制作用。考虑到即使在同种异体环境中MSC的免疫调节特性,新的临床应用也应进一步研究。

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