我国生殖免疫学发展的现状与未来

Chinese Journal of Practical Gynecology and Obstetrics ›› 2025, Vol. 41 ›› Issue (11) : 1057-1059.

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Chinese Journal of Practical Gynecology and Obstetrics ›› 2025, Vol. 41 ›› Issue (11) : 1057-1059. DOI: 10.19538/j.fk2025110101

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Colamatteo A, Fusco C, Micillo T, et al. Immunobiology of pregnancy:from basic science to translational medicine[J]. Trends Mol Med, 2023, 29(9):711-725. DOI:10.1016/j.molmed.2023.05.009.
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To investigate pregnancy outcomes in women with autoimmune rheumatic diseases (ARD) in the Italian prospective cohort study P-RHEUM.it.
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Wang Q, Zhang X, Li C, et al. Intracellular lipid accumulation drives the differentiation of decidual polymorphonuclear myeloid-derived suppressor cells via arachidonic acid metabolism[J]. Front Immuno, 2022, 13:868669. DOI:10.3389/fimmu.2022.868669.
Decidual polymorphonuclear myeloid-derived suppressor cells (PMN-MDSCs) are essential to immune tolerance during pregnancy. A reduction in the number of these cells is associated with unexplained recurrent pregnancy loss (URPL). In our previous study, we reported that PMN-MDSCs are a group of mature neutrophils that are activated by the decidua microenvironment. In the present study, we show that the decidua microenvironment induces substantial lipid accumulation in neutrophils during their differentiation to PMN-MDSCs. Lower levels of lipid accumulation are detected in PMN-MDSCs from URPL patients, and the amount of lipid in the PMN-MDSCs is positively correlated with the proportion of PMN-MDSCs. Next, we demonstrate that decidua-derived IL6 with the presence of arachidonic acid upregulates fatty acid-binding protein 5 (FABP5) via the phosphorylation of signal transducer and activator of transcription 3 (STAT3). Fy -60ABP5 then continuously stimulates intracellular lipid accumulation. Increased intracellular lipid accumulation mediates arachidonic acid metabolism, a pathway that is significantly activated by the induction of the decidua microenvironment, to stimulate the synthesis of prostaglandin E2 (PGE2) and finally induce the differentiation of PMN-MDSCs. To summarize, decidua-derived IL6 facilitates the differentiation of PMN-MDSCs from neutrophils via the pSTAT3/FABP5/PGE2 pathway. Defects in the process may result in impaired differentiation and dysfunction of PMN-MDSCs in URPL. These findings enhance our understanding of the physiological mechanisms of immune tolerance in pregnancy and provide therapeutic options for URPL.
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自然流产诊治中国专家共识编写组. 自然流产诊治中国专家共识(2020年版)[J]. 中国实用妇科与产科杂志, 2020, 36(11):1082-1090. DOI:10.19538/j.fk2020110113.
自然流产(spontaneous abortion,SA)是妇产科最常见的妊娠并发症之一。育龄期女性发生1次SA的风险为10%左右[1]。复发性流产(recurrent spontaneous abortion,RSA)的发生率为1%~5%[2],RSA的复发风险随着流产次数的增加而上升。曾有3次以上连续自然流产史的患者再次妊娠后胚胎丢失率为40%~80%[3]。如果不及时干预,不仅会给患者及其家庭带来严重的经济负担,而且还将对患者的身心健康造成极大的影响。浏览更多请关注本刊微信公众号及当期杂志。
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Liu T, Guo X, Liao Y, et al. Correlation between the presence of antinuclear antibodies and recurrent pregnancy loss:a mini review[J]. Front Endocrinol (Lausanne), 2022, 13:873286. DOI:10.3389/fendo.2022.873286.
In the past decade, the incidence of recurrent pregnancy loss (RPL) has increased significantly, and immunological disorders have been considered as one of the possible causes contributing to RPL. The presence of antinuclear antibodies (ANAs) is regarded as a typical antibody of autoimmunity. However, the relationship between the presence of ANAs and RPL, the underlying mechanism, and the possible role of immunotherapy is still controversial. The aim of this mini review is to assess the association between ANAs and RPL and the effects of immunotherapy on pregnancy outcomes in women with positive ANAs and a history of RPL from the available data and to provide a relevant reference basis for clinical application in this group of women.
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Could the risk of subsequent pregnancy loss be predicted based on the risk factors of recurrent pregnancy loss (RPL) patients?
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复发性流产合并风湿免疫病免疫抑制剂应用中国专家共识编写组. 复发性流产合并风湿免疫病免疫抑制剂应用中国专家共识[J]. 中华生殖与避孕杂志, 2020, 40(7):527-534. DOI:10.3760/cma.j.cn101441-20200419-00226.
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Li D, Du M, Liao A, et al. Editorial for the special issue on "Clinical reproductive immunology in China"[J]. Am J Reprod Immunol, 2023, 89(6):e13705. DOI:10.1111/aji.13705.

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Funding

National Natural Science Foundation of China—General Projects(82071725)
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