Evidence map›Paper›PMID 35180876›Full record

ArticleJournal of nanobiotechnology2022

Human placental exosomes induce maternal systemic immune tolerance by reprogramming circulating monocytes.

Kunfeng Bai, Cheuk-Lun Lee, Xiaofeng Liu, Jianlin Li, Dandan Cao, Li Zhang, Duanlin Hu, Hong Li, Yanqing Hou, Yue Xu and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

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  13. Maternal Immune Characteristics at Mid and Late Pregnancy Are Mostly Independent of Fetal Allogeneity in Mice.American journal of reproductive immunology (New York, N.Y. : 1989) · 2025
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  19. The Placenta as an Immunological Environment.British journal of biomedical science · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 2 countries.

Kunfeng Bai *Department of Obstetrics and Gynaecology, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong S.A.R., China.
Cheuk-Lun Lee *Department of Obstetrics and Gynaecology, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong S.A.R., China. kcllee@hku.hk.
Xiaofeng LiuThe University of Hong Kong Shenzhen Key Laboratory of Fertility Regulation, Shenzhen, China.
Jianlin LiDepartment of Obstetrics and Gynaecology, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong S.A.R., China.
Dandan CaoThe University of Hong Kong Shenzhen Key Laboratory of Fertility Regulation, Shenzhen, China.
Li ZhangDepartment of Obstetrics and Gynaecology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Duanlin HuDepartment of Obstetrics and Gynaecology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Hong LiDepartment of Obstetrics and Gynaecology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Yanqing HouDepartment of Obstetrics and Gynaecology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Yue XuDepartment of Obstetrics and Gynaecology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Anita S Y KanDepartment of Obstetrics and Gynaecology, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong S.A.R., China.
Ka-Wang CheungDepartment of Obstetrics and Gynaecology, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong S.A.R., China.
Ernest H Y NgDepartment of Obstetrics and Gynaecology, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong S.A.R., China.
William S B YeungThe University of Hong Kong Shenzhen Key Laboratory of Fertility Regulation, Shenzhen, China.
Philip C N ChiuDepartment of Obstetrics and Gynaecology, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong S.A.R., China. pchiucn@hku.hk.ORCID http://orcid.org/0000-0001-6217-1970
University of Hong Kong - Shenzhen Hospital · CNChinese University of Hong Kong · HKUniversity of Hong Kong · HK

Funding

Health and Medical Research Fund 09202056National Natural Science Foundation of China 81971396Research Grant Councils of Hong Kong 17115320Research Grant Councils of Hong Kong 17115619Research Grant Councils of Hong Kong 17118917
6 · The paper itself

Abstract

backgroundThe maternal immune system needs to tolerate the semi-allogeneic fetus in pregnancy. The adaptation occurs locally at the maternal-fetal interface as well as systemically through the maternal circulation. Failure to tolerate the paternal antigens may result in pregnancy complications, such as pregnancy loss and pre-eclampsia. However, the mechanism that regulates maternal immune tolerance, especially at the systemic level, is still an enigma. Here we report that the first-trimester placenta-derived exosomes (pEXOs) contribute to maternal immune tolerance by reprogramming the circulating monocytes.

resultspEXOs predominantly target monocytes and pEXO-educated monocytes exhibit an immunosuppressive phenotype as demonstrated by reduced expression of marker genes for monocyte activation, T-cell activation and antigen-process/presentation at the transcriptomic level. They also have a greater propensity towards M2 polarization when compared to the monocytes without pEXO treatment. The inclusion of pEXOs in a monocyte-T-cell coculture model significantly reduces proliferation of the T helper cells and cytotoxic T cells and elevates the expansion of regulatory T cells. By integrating the microRNAome of pEXO and the transcriptomes of pEXO-educated monocytes as well as various immune cell functional assays, we demonstrate that the pEXO-derived microRNA miR-29a-3p promotes the expression of programmed cell death ligand-1, a well-known surface receptor that suppresses the adaptive immune system, by down-regulation of phosphatase and tensin homolog in monocytes.

conclusionsThis is the first report to show how human pEXO directly regulates monocyte functions and its molecular mechanism during early pregnancy. The results uncover the importance of pEXO in regulating the maternal systemic immune response during early pregnancy by reprogramming circulating monocytes. The study provides the basis for understanding the regulation of maternal immune tolerance to the fetal allograft.

Indexed as

ExosomesMonocytesCoculture TechniquesFemaleHumansImmune TolerancePlacentaPregnancyMaternal immune toleranceMonocytePD-L1Placental exosomePTENT cell

Identifiers

PMID35180876
PMCPMC8857816
OpenAlexW4213288902

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.