人羊膜上皮细胞对复发性自然流产妇女自然杀伤细胞和T细胞的免疫调节作用

IF 0.2 Q4 IMMUNOLOGY Turkish Journal of Immunology Pub Date : 2019-01-01 DOI:10.25002/TJI.2019.991
Fahimeh Khadem, N. Esmaeil, A. Rezaei, Hossein Motadayen, B. Khani
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引用次数: 6

摘要

不明原因复发性自然流产(URSA)是妊娠期最常见的免疫并发症。人羊膜上皮细胞(hAECs)等细胞在体内体外均具有调节免疫应答的作用。在本研究中,我们评估了haec对URSA女性NK细胞和T细胞的免疫调节作用。材料与方法:取14例URSA患者外周血单个核细胞(PBMC),与分离的haec共培养。NK细胞和T细胞用抗cd56和抗cd3单克隆抗体(mAb)进行鉴定。用特异性单抗检测NK细胞和T细胞上活化受体CD69和脱颗粒标志物CD107a的表达,并用流式细胞术分析。结果:我们发现,与hAECs孵育后,NK细胞和T细胞上CD69激活受体的表达呈剂量依赖性显著降低(p=0.049)。此外,与hAEC孵育后,NK细胞和T细胞上的脱颗粒标志物CD107a显著下调(p=0.003)。结论:hAECs对NK细胞和T细胞的活化和细胞毒性具有免疫调节作用。heec在治疗NK和T细胞免疫失调方面的潜在应用有待进一步研究。
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Immunoregulatory Effects of Human Amnion Epithelial Cells on Natural Killer and T Cells in Women with Recurrent Spontaneous Abortion (RSA)
Introduction: Unexplained Recurrent Spontaneous Abortion (URSA) is the most common immunological complication during pregnancy. It has been found that the cells such as human amnion epithelial cells (hAECs) have the potency to modulate immune responses in vitro and in vivo. In the present study, we assessed the immunomodulatory effect of hAECs on NK cells and T cells in women with URSA. Materials and Methods: Peripheral Blood mononuclear cells (PBMC) were obtained from 14 URSA patients and co-cultured with isolated hAECs. NK cells and T cells were identified using anti-CD56 and anti-CD3 monoclonal antibodies (mAb). The expression of the activating receptor CD69 and the degranulation marker CD107a on NK cells and T cells were detected using specific mAb and analyzed by flow cytometry. Results: We found that CD69 activating receptor expression on NK cells and T cells was significantly decreased by incubation with hAECs in a dose-dependent manner (p=0.049). Also, the degranulation marker CD107a was significantly downregulated on NK cells and T cells following incubation with hAEC (p=0.003). Conclusion: Our results suggest hAECs have immune regulatory effects on activation and cytotoxicity of NK and T cells. Potential therapeutic application of hAECs for dysregulated NK and T cells immunity should be investigated in the future.
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