FOXP3型
免疫系统
免疫学
免疫疗法
淋巴细胞
流式细胞术
RAR相关孤儿受体γ
生物
反复流产
医学
流产
怀孕
遗传学
作者
Lida Aslanian‐Kalkhoran,Amin Kamrani,Iraj Alipourfard,Forough Chakari-Khiavi,Aref Chakari-Khiavi,Leili Aghebati‐Maleki,Ali Akbar Shekarchi,Amir Mehdizadeh,Maryam Mojahedi,Shahla Danaii,Leila Roshangar,Javad Ahmadian Heris,Mohammad Ali Zolfaghari,Sanam Dolati,Mohammad Sadegh Soltani‐Zangbar,Mehdi Yousefi
标识
DOI:10.1016/j.intimp.2023.110326
摘要
In order to prevent miscarriage in RPL patients, the goal of this study was to determine how well lymphocyte immunotherapy (LIT) works in modifying immunological responses produced by cells, cytokines, transcription factors, and microRNAs. 200 RPL patients and 200 healthy controls were included in the study. Using flow cytometry, it was possible to compare the frequency of cells before and after lymphocyte treatment. Real-time PCR was used to assess the gene expression levels of transcription factors, cytokines, and microRNAs. ELISA method was used to evaluate the level of secretion of cytokines in the serum. Primary evaluation of the immune profile between healthy controls and RPL cases showed a higher frequency of Th17, NK, B cells and a lower frequency of Treg cells in RPL cases. Also, pro-inflammatory cytokines showed increased expression at mRNA and protein levels in the RPL group in comparison with the control group. Whereas, anti-inflammatory cytokines showed decreased expression in RPL patients. Decreased and increased frequency of Th17 and Treg lymphocytes observed in RPL cases following LIT, respectively. The same results obtained for RORγt and FoxP3 mRNA expression as transcription factor of Th17 and Treg cells, respectively. NK cell cytotoxicity decreased after LIT in RPL patients. miR-326a and miR-155 expression after LIT reduced, but miR-146a and miR-10a expression increased in RPL instances. LIT in RPL cases causes to elevation and modulation of anti-inflammatory and pro-inflammatory cytokines. Our data showed that lymphocyte therapy can be proposed as an effective therapeutic agent in RPL patients with immunological background by a modulating inflammatory condition.
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