Evidence map›Paper›PMID 31921098›Full record

ReviewFrontiers in immunology2019

The Dual Role of HLA-C in Tolerance and Immunity at the Maternal-Fetal Interface.

Henrieta Papúchová, Torsten B Meissner, Qin Li, Jack L Strominger, Tamara Tilburgs

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 1 pooled it
7.5field-weighted citation impact, top 2% 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

77 citing papers in PubMed, 1 synthesis or guideline pooled it, 131 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Shared Genetics of Hypertension and Preeclampsia Converges on Immune Regulation.medRxiv : the preprint server for health sciences · 2026
    Article
  6. Article
  7. Article
  8. Review
  9. Decidual CD4 Effector Memory and Resident Memory T Cells Respond to Cord Blood Allo-Antigens.American journal of reproductive immunology (New York, N.Y. : 1989) · 2026
    Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. The Placenta as an Immunological Environment.British journal of biomedical science · 2025
    Review

17 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Henrieta PapúchováDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, United States.
Torsten B MeissnerDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, United States.
Qin LiDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, United States.
Jack L StromingerDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, United States.
Tamara TilburgsDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, United States.
Harvard University · USCincinnati Children's Hospital Medical Center · US

Funding

Regulation of HLA-C in Human Trophoblasts and its Impact on Preterm BirthR21AI138019 · NIAID · HARVARD UNIVERSITY · PI STROMINGER, JACK L · 2019 to 2020
$465k
NIAID NIH HHS R21 AI138019
6 · The paper itself

Abstract

To establish a healthy pregnancy, maternal immune cells must tolerate fetal allo-antigens and remain competent to respond to infections both systemically and in placental tissues. Extravillous trophoblasts (EVT) are the most invasive cells of extra-embryonic origin to invade uterine tissues and express polymorphic Human Leucocyte Antigen-C (HLA-C) of both maternal and paternal origin. Thus, HLA-C is a key molecule that can elicit allogeneic immune responses by maternal T and NK cells and for which maternal-fetal immune tolerance needs to be established. HLA-C is also the only classical MHC molecule expressed by EVT that can present a wide variety of peptides to maternal memory T cells and establish protective immunity. The expression of paternal HLA-C by EVT provides a target for maternal NK and T cells, whereas HLA-C expression levels may influence how this response is shaped. This dual function of HLA-C requires tight transcriptional regulation of its expression to balance induction of tolerance and immunity. Here, we critically review new insights into: (i) the mechanisms controlling expression of HLA-C by EVT, (ii) the mechanisms by which decidual NK cells, effector T cells and regulatory T cells recognize HLA-C allo-antigens, and (iii) immune recognition of pathogen derived antigens in context of HLA-C.

Indexed as

Immune ToleranceImmunityAllelesDeciduaFemaleGene Expression RegulationHLA-A AntigensHLA-B AntigensHLA-C AntigensHumansImmunomodulationKiller Cells, NaturalMaternal-Fetal ExchangePlacentaPregnancyPromoter Regions, GeneticHLA-A AntigensHLA-B AntigensHLA-C Antigensdeciduadecidual NK cellseffector T cellsHLA-Ghumanpregnancyregulatory T cellstrophoblast

Identifiers

PMID31921098
PMCPMC6913657
OpenAlexW2996329464

What Socratic holds

Textmetadata
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 Socratic graph.