Evidence map›Paper›PMID 38732104›Full record

ReviewInternational journal of molecular sciences2024

The Role of Regulatory T Cells and Their Therapeutic Potential in Hypertensive Disease of Pregnancy: A Literature Review.

Kyle Headen, Vaidile Jakaite, Vita Andreja Mesaric, Cristiano Scotta, Giovanna Lombardi, Kypros H Nicolaides, Panicos Shangaris

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Insights into Reproductive Immunology and Placental Pathology, 2nd Edition.International journal of molecular sciences · 2026
    Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Insights into Reproductive Immunology and Placental Pathology.International journal of molecular sciences · 2024
    Article
  8. 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

7 authors.

Kyle HeadenDepartment of Women and Children's Health, School of Life Course Sciences, Faculty of Life Sciences & Medicine, King's College London, London SE5 8AF, UK.
Vaidile JakaiteHarris Birthright Research Centre for Fetal Medicine, King's College Hospital, London SE5 8BB, UK.ORCID 0000-0002-4688-5751
Vita Andreja MesaricHarris Birthright Research Centre for Fetal Medicine, King's College Hospital, London SE5 8BB, UK.ORCID 0000-0003-1214-344X
Cristiano ScottaPeter Gorer Department of Immunobiology, School of Immunology & Microbial Sciences, Faculty of Life Sciences & Medicine, King's College London, London SE1 1UL, UK.ORCID 0000-0003-3942-5201
Giovanna LombardiPeter Gorer Department of Immunobiology, School of Immunology & Microbial Sciences, Faculty of Life Sciences & Medicine, King's College London, London SE1 1UL, UK.
Kypros H NicolaidesDepartment of Women and Children's Health, School of Life Course Sciences, Faculty of Life Sciences & Medicine, King's College London, London SE5 8AF, UK.
Panicos ShangarisDepartment of Women and Children's Health, School of Life Course Sciences, Faculty of Life Sciences & Medicine, King's College London, London SE5 8AF, UK.ORCID 0000-0003-2750-8405

Funding

Fetal Medicine Foundation n/a
6 · The paper itself

Abstract

Hypertensive disorders of pregnancy (HDP), including preeclampsia (PE) and gestational hypertension (GH), are major causes of maternal and foetal morbidity and mortality. This review elucidates the role of regulatory T cells (Tregs) in the immunological aspects of HDP and explores their therapeutic potential. Tregs, which play a critical role in maintaining immune homeostasis, are crucial in pregnancy to prevent immune-mediated rejection of the foetus. The review highlights that Tregs contribute to immunological adaptation in normal pregnancy, ensuring foetal acceptance. In contrast, HDP is associated with Treg dysfunction, which is marked by decreased numbers and impaired regulatory capacity, leading to inadequate immune tolerance and abnormal placental development. This dysfunction is particularly evident in PE, in which Tregs fail to adequately modulate the maternal immune response against foetal antigens, contributing to the pathophysiology of the disorder. Therapeutic interventions aiming to modulate Treg activity represent a promising avenue for HDP management. Studies in animal models and limited clinical trials suggest that enhancing Treg functionality could mitigate HDP symptoms and improve pregnancy outcomes. However, given the multifactorial nature of HDP and the intricate regulatory mechanisms of Tregs, the review explores the complexities of translating in vitro and animal model findings into effective clinical therapies. In conclusion, while the precise role of Tregs in HDP is still being unravelled, their central role in immune regulation during pregnancy is indisputable. Further research is needed to fully understand the mechanisms by which Tregs contribute to HDP and to develop targeted therapies that can safely and effectively harness their regulatory potential for treating hypertensive diseases of pregnancy.

Indexed as

Hypertension, Pregnancy-InducedT-Lymphocytes, RegulatoryAnimalsFemaleHumansImmune TolerancePre-EclampsiaPregnancyhypertensive disordersimmune tolerancepreeclampsiasemi-allogeneic foetusTregs

Identifiers

PMID38732104
PMCPMC11084408

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.