Evidence map›Paper›PMID 40622550›Full record

ReviewAdvances in experimental medicine and biology2025

Innate Immune Mechanisms in Normal and Adverse Pregnancy.

Shanmuga Priyaa Madhukaran, Hadida Yasmin, Uday Kishore

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

3 authors.

Shanmuga Priyaa MadhukaranCecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA. Shanmugapriyaa.madhukaran@utsouthwestern.edu.
Hadida YasminCellular and Molecular Immunology Laboratory, Department of Zoology, Cooch Behar Panchanan Barma University, Cooch Behar, India.
Uday KishoreDepartment of Veterinary Medicine, United Arab Emirates University, Al Ain, United Arab Emirates.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The innate immune system's recognition of microorganisms through pattern recognition receptors (PRRs) is a fundamental aspect of host defense and microbial symbiosis. During pregnancy, this system is finely tuned to accommodate the fetal allograft while still protecting against infections. Dysregulation in the recognition and response to commensal microorganisms can lead to pathological conditions, which may have implications for both maternal and fetal health. PRRs play a critical role in maintaining a balanced immune response, which is essential during pregnancy to prevent excessive inflammation that could affect pregnancy outcomes. They are involved in the regulation of immune cell proliferation and the integrity of mucosal barriers, which are vital for the protection of the maternal-fetal interface. The signaling pathways of PRRs are also key in the initiation and modulation of inflammation in response to microbial invasion. Changes in PRR function, as observed in certain animal models, indicate that the outcome of immune responses can be significantly altered by the specific signaling pathways activated in immune cells, and by the nature of the microbial environment. This is particularly relevant in pregnancy, where an altered PRR response may influence the risk of developing inflammatory conditions that could impact gestation and labor. In light of these considerations, understanding the role of PRR signaling in pregnancy is crucial for elucidating the mechanisms of maternal immune tolerance and the maintenance of a healthy pregnancy, as well as for identifying potential therapeutic targets for pregnancy-related complications arising from immune system dysregulation.

Indexed as

Immunity, InnatePregnancy ComplicationsReceptors, Pattern RecognitionAnimalsFemaleHumansImmune ToleranceInflammationPregnancySignal TransductionReceptors, Pattern RecognitionFemale reproductive tractImmune cellsInfertilityMacrophagesNatural killer cellsNeutrophilsPattern recognition receptorsPregnancyPregnancy lossPreterm birthT cells

Identifiers

PMID40622550

What Socratic 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 Socratic graph.