Evidence map›Paper›PMID 24427332›Full record

ArticleInternational journal of clinical and experimental pathology2014

Mouse endometrial stromal cells and progesterone inhibit the activation and regulate the differentiation and antibody secretion of mouse B cells.

Li Zhang, Kai-Kai Chang, Ming-Qing Li, Da-Jin Li, Xiao-Ying Yao

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

20 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Sex Steroid Hormone Regulation of T-Cell Function and Antitumor Immunity.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Review
  3. B Cell Tolerance and Obstetric Antiphospholipid Syndrome.Clinical reviews in allergy & immunology · 2025
    Review
  4. Article
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  15. Review
  16. Linking autoimmunity to the origin of the adaptive immune system.Evolution, medicine, and public health · 2018
    Article
  17. Review
  18. Review
  19. Article
  20. Observational
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

5 authors at 1 institution in 1 country.

Li ZhangLaboratory for Reproductive Immunology, Hospital and Institute of Obstetrics and Gynecology, Fudan University Shanghai Medical College, Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases Shanghai 200011, China.
Kai-Kai ChangLaboratory for Reproductive Immunology, Hospital and Institute of Obstetrics and Gynecology, Fudan University Shanghai Medical College, Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases Shanghai 200011, China.
Ming-Qing LiLaboratory for Reproductive Immunology, Hospital and Institute of Obstetrics and Gynecology, Fudan University Shanghai Medical College, Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases Shanghai 200011, China.
Da-Jin LiLaboratory for Reproductive Immunology, Hospital and Institute of Obstetrics and Gynecology, Fudan University Shanghai Medical College, Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases Shanghai 200011, China.
Xiao-Ying YaoLaboratory for Reproductive Immunology, Hospital and Institute of Obstetrics and Gynecology, Fudan University Shanghai Medical College, Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases Shanghai 200011, China.
Shanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The regulation mechanism for the B cells in the female reproductive tract (FRT) is unclear now. The aim of this study was to analysis the effect of progesterone and mouse endometrium stromal cells (ESCs) on B cells and explore it roles in modulating B cells-mediated immune responses. We primary isolated mouse ESCs from endometrium of BALB/c mice and B cells from spleen cells of BALB/c mice, and then constructed these two kind of cells co-culture system, and treated with or without progesterone. We found that both treatment with progesterone and co-culture with ESCs reduced the expression of co-stimulatory molecules CD80 and CD86 on mouse B cells from spleen cells. In addition, the expression of CD138 (syndecan-1) on B cells was increased after co-culture with ESCs, however, progesterone could partly reduce this effect. Unlike progesterone, ESCs alone promoted the proliferation and stimulated the secretion level of antibodies IgG and IgA of B cells. Our current results progesterone and ESCs could inhibit the activation of B cells through deceasing CD80 and CD86 expression, regulated the differentiation status of B cells by up-regulating the expression of CD138 together, and might further inhibit the antigen presentation function of B cells, which is beneficial to the establishment of fertilization and pregnancy. In addition, ESCs also promoted the proliferation and antibody secretion, which might participate in the resisting infections during non pregnancy and pregnancy.

Indexed as

AnimalsB-LymphocytesCell DifferentiationCoculture TechniquesEndometriumFemaleFlow CytometryImmunohistochemistryLymphocyte ActivationMiceMice, Inbred BALB CProgesteroneReal-Time Polymerase Chain ReactionStromal CellsProgesteroneactivationantibody secretionB cellsendometrium stromal cellsProgesteronethe female reproductive tract

Identifiers

PMID24427332
PMCPMC3885466
OpenAlexW2297921530

What OpenQuestion holds

Textmetadata
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.