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子宫内膜异位症患者外周血和腹腔液中 CD4+T 细胞的变化:系统评价和荟萃分析。

The deviations of CD4 + T cells during peripheral blood and peritoneal fluid of endometriosis: a systematic review and meta-analysis.

机构信息

Department of Gynecology, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, 519000, China.

出版信息

Arch Gynecol Obstet. 2023 Nov;308(5):1431-1446. doi: 10.1007/s00404-023-06964-3. Epub 2023 Feb 25.

DOI:10.1007/s00404-023-06964-3
PMID:36840769
Abstract

OBJECTIVE

To assess whether endometriosis (EMs) was related to systematic and/or local deviations of cluster of differentiation (CD)4 + T cells.

METHODS

Until November 2022, we enrolled a total of 1363 EMs and 1564 healthy women from 32 studies who met the inclusion criteria.

RESULTS

After systematically retrieving the literature, we identified 1086 citations and 32 case-control studies were enrolled. Cumulative results suggested that there were insignificant deviations of CD4 + T cells during peripheral blood (PB) between EMs and healthy women (RR: - 0.83, I = 99%, p = 0.65), also no statistically significant difference was found between mild and severe EMs (RR: 3.19, I = 94%, p = 0.19). We also found insignificant deviations of CD4 + /CD8 + during PB between EMs and healthy women (RR: 0.09, I = 99%, p = 0.39), and between mild and severe EMs (RR: - 0.16, I = 99%, p = 0.29). The results might suggest that there was no significant correlation between EMs and systematic deviations of CD4 + T cells. When it came to local deviation during peritoneal fluid (PF), the polled results suggested that the frequency of CD4 + T cells during EMs was significantly lower than healthy women (RR: - 5.38, I = 93%, p = 0.01), and the ratio of CD4 + /CD8 + during EMs was significantly lower than healthy women (RR: - 0.13, I = 0%, p < 0.0001). However, there were insignificant deviations of CD4 + during PF between mild and severe EMs (RR: 1.65, I = 53%, p = 0.15), also there was an insignificant difference of CD4 + /CD8 + between mild and severe EMs (RR: - 0.09, I = 14%, p = 0.19). EMs might be closely related to local deviations of CD4 + T cells.

CONCLUSION

There was no obvious correlation between EMs and systematic deviations of CD4 + T cells, EMs might be closely related to local deviations of CD4 + T cells. Further study on the functional deviations and subpopulation distribution of CD4 + T cells is urgently needed.

摘要

目的

评估子宫内膜异位症(EMs)是否与 CD4+T 细胞的系统性和/或局部偏差有关。

方法

截至 2022 年 11 月,我们共纳入了 32 项研究中的 1363 例 EMs 患者和 1564 例健康女性,这些研究均符合纳入标准。

结果

通过系统检索文献,我们共识别出 1086 篇引文,纳入了 32 项病例对照研究。累积结果表明,EMs 患者和健康女性的外周血(PB)中 CD4+T 细胞无明显偏差(RR:-0.83,I=99%,p=0.65),轻度和重度 EMs 之间也无统计学差异(RR:3.19,I=94%,p=0.19)。我们还发现,EMs 患者和健康女性的 PB 中 CD4+/CD8+无明显偏差(RR:0.09,I=99%,p=0.39),轻度和重度 EMs 之间也无统计学差异(RR:-0.16,I=99%,p=0.29)。这可能表明 EMs 与 CD4+T 细胞的系统性偏差之间没有显著相关性。当涉及到腹膜液(PF)中的局部偏差时,汇总结果表明,EMs 患者的 CD4+T 细胞频率明显低于健康女性(RR:-5.38,I=93%,p=0.01),并且 EMs 患者的 CD4+/CD8+比值明显低于健康女性(RR:-0.13,I=0%,p<0.0001)。然而,轻度和重度 EMs 之间的 PF 中 CD4+的偏差无统计学意义(RR:1.65,I=53%,p=0.15),并且轻度和重度 EMs 之间的 CD4+/CD8+也无统计学差异(RR:-0.09,I=14%,p=0.19)。EMs 可能与 CD4+T 细胞的局部偏差密切相关。

结论

EMs 与 CD4+T 细胞的系统性偏差之间没有明显的相关性,EMs 可能与 CD4+T 细胞的局部偏差密切相关。需要进一步研究 CD4+T 细胞的功能偏差和亚群分布。

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本文引用的文献

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Endometriosis and cardiovascular disease.子宫内膜异位症与心血管疾病。
Eur Heart J Open. 2022 Feb 2;2(1):oeac001. doi: 10.1093/ehjopen/oeac001. eCollection 2022 Jan.
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Immunopathogenesis of endometriosis - a novel look at an old problem.子宫内膜异位症的免疫发病机制——对一个老问题的新视角
Cent Eur J Immunol. 2022;47(1):109-116. doi: 10.5114/ceji.2022.113830. Epub 2022 Mar 6.
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The Role of Peritoneal Macrophages in Endometriosis.腹膜巨噬细胞在子宫内膜异位症中的作用。
免疫细胞与子宫内膜异位症的因果关联:一项孟德尔随机化研究
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Exploring the link: Systemic immune-inflammation index as a marker in endometriosis-Insights from the NHANES 2001-2006 cross-sectional study.探讨关联:系统性免疫炎症指数作为子宫内膜异位症的标志物——来自 NHANES 2001-2006 横断面研究的见解。
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The role of CD8+ T cells in endometriosis: a systematic review.CD8+T 细胞在子宫内膜异位症中的作用:系统评价。
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Endometrial stem/progenitor cells and their roles in immunity, clinical application, and endometriosis.子宫内膜干细胞/祖细胞及其在免疫、临床应用和子宫内膜异位症中的作用。
Stem Cell Res Ther. 2021 Aug 23;12(1):474. doi: 10.1186/s13287-021-02526-z.
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