Evidence map›Paper›PMID 25591581›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Seminal CD38 is a pivotal regulator for fetomaternal tolerance.

Byung-Ju Kim, Yun-Min Choi, So-Young Rah, Dae-Ryoung Park, Seon-Ah Park, Yun-Jo Chung, Seung-Moon Park, Jong Kwan Park, Kyu Yun Jang, Uh-Hyun Kim

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

27 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Targets for CAR Therapy in Multiple Myeloma.International journal of molecular sciences · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Memory regulatory T cells in pregnancy.Frontiers in immunology · 2023
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. The role of CD38 in HIV infection.AIDS research and therapy · 2021
    Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review
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

10 authors at 3 institutions in 3 countries.

Byung-Ju KimNational Creative Research Laboratory for Ca Signaling Network and Departments of Biochemistry.
Yun-Min ChoiNational Creative Research Laboratory for Ca Signaling Network and Departments of Biochemistry.
So-Young RahNational Creative Research Laboratory for Ca Signaling Network and Departments of Biochemistry.
Dae-Ryoung ParkNational Creative Research Laboratory for Ca Signaling Network and Departments of Biochemistry.
Seon-Ah ParkNational Creative Research Laboratory for Ca Signaling Network and.
Yun-Jo ChungNational Creative Research Laboratory for Ca Signaling Network and.
Seung-Moon ParkDivision of Biotechnology, College of Environmental and Bioresource Sciences, Chonbuk National University, Iksan, 570-752, Korea; and.
Jong Kwan ParkUrology, and.
Kyu Yun JangPathology, Chonbuk National University Medical School, Jeonju, 561-180, Korea;
Uh-Hyun KimNational Creative Research Laboratory for Ca Signaling Network and Departments of Biochemistry, Institute of Cardiovascular Research, Chonbuk National University, Jeonju, 561-180, Korea uhkim@chonbuk.ac.kr.
Creative Research · GBInstitute of Cytochemistry and Molecular Pharmacology · RUJeonbuk National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A successful pregnancy depends on a complex process that establishes fetomaternal tolerance. Seminal plasma is known to induce maternal immune tolerance to paternal alloantigens, but the seminal factors that regulate maternal immunity have yet to be characterized. Here, we show that a soluble form of CD38 (sCD38) released from seminal vesicles to the seminal plasma plays a crucial role in inducing tolerogenic dendritic cells and CD4(+) forkhead box P3(+) (Foxp3(+)) regulatory T cells (Tregs), thereby enhancing maternal immune tolerance and protecting the semiallogeneic fetus from resorption. The abortion rate in BALB/c females mated with C57BL/6 Cd38(-/-) males was high compared with that in females mated with Cd38(+/+) males, and this was associated with a reduced proportion of Tregs within the CD4(+) T-cell pool. Direct intravaginal injection of sCD38 to CBA/J pregnant mice at preimplantation increased Tregs and pregnancy rates in mice under abortive sonic stress from 48 h after mating until euthanasia. Thus, sCD38 released from seminal vesicles to the seminal plasma acts as an immunoregulatory factor to protect semiallogeneic fetuses from maternal immune responses.

Indexed as

Immune ToleranceMaternal-Fetal ExchangeADP-ribosyl Cyclase 1AnimalsDendritic CellsFemaleMaleMiceMice, Inbred C57BLMice, KnockoutPregnancySemenADP-ribosyl Cyclase 1CD38dendritic cellsfetomaternal toleranceregulatory T cellsseminal plasma

Identifiers

PMID25591581
PMCPMC4321276
OpenAlexW1983001605

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.