Evidence map›Paper›PMID 35231754›Full record

ArticleJournal of reproductive immunology2022

Decidual immune response following COVID-19 during pregnancy varies by timing of maternal SARS-CoV-2 infection.

Lillian J Juttukonda, Elisha M Wachman, Jeffery Boateng, Mayuri Jain, Yoel Benarroch, Elizabeth S Taglauer

Open access · greenAbstract read
In one paragraph

Article in Journal of reproductive immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

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  16. The Innate Defense in the Zika-Infected Placenta.Pathogens (Basel, Switzerland) · 2022
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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

6 authors at 3 institutions in 1 country.

Lillian J JuttukondaBoston Combined Residency Program, Boston Children's Hospital, 300 Longwood Avenue, Boston, MA 02115, USA; Department of Pediatrics, Boston Medical Center, 801 Albany Street, Boston, MA 02119, USA. Electronic address: Lillian.juttukonda@childrens.harvard.edu.
Elisha M WachmanDepartment of Pediatrics, Boston Medical Center, 801 Albany Street, Boston, MA 02119, USA. Electronic address: Elisha.Wachman@bmc.org.
Jeffery BoatengDepartment of Pediatrics, Boston Medical Center, 801 Albany Street, Boston, MA 02119, USA. Electronic address: Jeffery.Boateng@bmc.org.
Mayuri JainBoston University School of Public Health, 715 Albany Street, Boston, MA 02119, USA. Electronic address: jainm@bu.edu.
Yoel BenarrochBoston University School of Medicine, 72 East Concord Street, Boston, MA 02118, USA. Electronic address: ybena@bu.edu.
Elizabeth S TaglauerDepartment of Pediatrics, Boston Medical Center, 801 Albany Street, Boston, MA 02119, USA. Electronic address: Elizabeth.Taglauer@bmc.org.
Boston Medical Center · USBoston University · USBoston Children's Hospital · US

Funding

Project-005UL1TR001430 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BAIR-MERRITT, MEGAN H, CENTER, DAVID M. · 2015 to 2024
$52.3M
NCATS NIH HHS UL1 TR001430
6 · The paper itself

Abstract

While COVID-19 infection during pregnancy is common, fetal transmission is rare, suggesting that intrauterine mechanisms form an effective blockade against SARS-CoV-2. Key among these is the decidual immune environment of the placenta. We hypothesize that decidual leukocytes are altered by maternal SARS-CoV-2 infection in pregnancy and that this decidual immune response is shaped by the timing of infection during gestation. To address this hypothesis, we collected decidua basalis tissues at delivery from women with symptomatic COVID-19 during second (2nd Tri COVID, n = 8) or third trimester (3rd Tri COVID, n = 8) and SARS-CoV-2-negative controls (Control, n = 8). Decidual natural killer (NK) cells, macrophages and T cells were evaluated using quantitative microscopy, and pro- and anti-inflammatory cytokine mRNA expression was evaluated using quantitative reverse transcriptase PCR (qRT-PCR). When compared with the Control group, decidual tissues from 3rd Tri COVID exhibited significantly increased macrophages, NK cells and T cells, whereas 2nd Tri COVID only had significantly increased T cells. In evaluating decidual cytokine expression, we noted that IL-6, IL-8, IL-10 and TNF-α were significantly correlated with macrophage cell abundance. However, in 2nd Tri COVID tissues, there was significant downregulation of IL-6, IL-8, IL-10, and TNF-α. Taken together, these results suggest innate and adaptive immune responses are present at the maternal-fetal interface in maternal SARS-CoV-2 infections late in pregnancy, and that infections earlier in pregnancy show evidence of a resolving immune response. Further studies are warranted to characterize the full scope of intrauterine immune responses in pregnancies affected by maternal COVID-19.

Indexed as

COVID-19Pregnancy Complications, InfectiousCytokinesDeciduaFemaleHumansImmunityInterleukin-10Interleukin-6Interleukin-8PregnancySARS-CoV-2Tumor Necrosis Factor-alphaCytokinesInterleukin-10Interleukin-6Interleukin-8Tumor Necrosis Factor-alphaCOVID-19 in pregnancyCytokinesDecidual leukocytesSARS-CoV-2Vertical transmission

Identifiers

PMID35231754
PMCPMC8867981
OpenAlexW4225456980

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.