Evidence map›Paper›PMID 24954221›Full record

ReviewCellular & molecular immunology2014

Immune cells in term and preterm labor.

Nardhy Gomez-Lopez, Derek StLouis, Marcus A Lehr, Elly N Sanchez-Rodriguez, Marcia Arenas-Hernandez

Open access · hybridAbstract readReview
In one paragraph

Review in Cellular & molecular immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 281 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
281citing papers in PubMed, 6 pooled it
18.7field-weighted citation impact, top 1% 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

281 citing papers in PubMed, 6 syntheses or guidelines pooled it, 474 citations in OpenAlex.

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221 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 1 institution in 1 country.

Nardhy Gomez-Lopez1] Department of Obstetrics & Gynecology and Immunology & Microbiology, Wayne State University, Detroit, MI, USA [2] Perinatology Research Branch NICHD/NIH, School of Medicine, Wayne State University, Detroit, MI, USA.
Derek StLouisDepartment of Obstetrics & Gynecology and Immunology & Microbiology, Wayne State University, Detroit, MI, USA.
Marcus A LehrDepartment of Obstetrics & Gynecology and Immunology & Microbiology, Wayne State University, Detroit, MI, USA.
Elly N Sanchez-RodriguezDepartment of Obstetrics & Gynecology and Immunology & Microbiology, Wayne State University, Detroit, MI, USA.
Marcia Arenas-HernandezDepartment of Obstetrics & Gynecology and Immunology & Microbiology, Wayne State University, Detroit, MI, USA.
Wayne State University · US

Funding

Intramural NIH HHS
6 · The paper itself

Abstract

Labor resembles an inflammatory response that includes secretion of cytokines/chemokines by resident and infiltrating immune cells into reproductive tissues and the maternal/fetal interface. Untimely activation of these inflammatory pathways leads to preterm labor, which can result in preterm birth. Preterm birth is a major determinant of neonatal mortality and morbidity; therefore, the elucidation of the process of labor at a cellular and molecular level is essential for understanding the pathophysiology of preterm labor. Here, we summarize the role of innate and adaptive immune cells in the physiological or pathological activation of labor. We review published literature regarding the role of innate and adaptive immune cells in the cervix, myometrium, fetal membranes, decidua and the fetus in late pregnancy and labor at term and preterm. Accumulating evidence suggests that innate immune cells (neutrophils, macrophages and mast cells) mediate the process of labor by releasing pro-inflammatory factors such as cytokines, chemokines and matrix metalloproteinases. Adaptive immune cells (T-cell subsets and B cells) participate in the maintenance of fetomaternal tolerance during pregnancy, and an alteration in their function or abundance may lead to labor at term or preterm. Also, immune cells that bridge the innate and adaptive immune systems (natural killer T (NKT) cells and dendritic cells (DCs)) seem to participate in the pathophysiology of preterm labor. In conclusion, a balance between innate and adaptive immune cells is required in order to sustain pregnancy; an alteration of this balance will lead to labor at term or preterm.

Indexed as

Adaptive ImmunityAnimalsCervix UteriCytokinesFemaleHumansImmune ToleranceImmunity, InnateInflammation MediatorsLabor, ObstetricObstetric Labor, PrematurePregnancyCytokinesInflammation Mediators

Identifiers

PMID24954221
PMCPMC4220837
OpenAlexW1993271798

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.