Evidence map›Paper›PMID 28662050›Full record

ArticlePloS one2017

Cord blood T cell subpopulations and associations with maternal cadmium and arsenic exposures.

Unni C Nygaard, Zhigang Li, Thomas Palys, Brian Jackson, Melanie Subbiah, Meena Malipatlolla, Vanitha Sampath, Holden Maecker, Margaret R Karagas, Kari C Nadeau

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
2.0field-weighted citation impact, top 15% 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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Toxic metal exposure as a possible risk factor for COVID-19 and other respiratory infectious diseases.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2020
    Pooled it
  3. Review
  4. Article
  5. Guardians under Siege: Exploring Pollution's Effects on Human Immunity.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Factors by which global warming worsens allergic disease.Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2023
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Effects of lead and cadmium on the immune system and cancer progression.Journal of environmental health science & engineering · 2020
    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

10 authors at 3 institutions in 2 countries.

Unni C NygaardSean N. Parker Center for Allergy and Asthma Research, Stanford University, Division of Pulmonary and Critical Care, Division of Immunology, Allergy, and Rheumatology, Departments of Medicine and Pediatrics, Stanford University School of Medicine, Stanford, California, United States of America.
Zhigang LiChildren's Environmental Health and Disease Prevention Research Center at Dartmouth, Lebanon, New Hampshire, United States of America.
Thomas PalysChildren's Environmental Health and Disease Prevention Research Center at Dartmouth, Lebanon, New Hampshire, United States of America.
Brian JacksonChildren's Environmental Health and Disease Prevention Research Center at Dartmouth, Lebanon, New Hampshire, United States of America.
Melanie SubbiahChildren's Environmental Health and Disease Prevention Research Center at Dartmouth, Lebanon, New Hampshire, United States of America.
Meena MalipatlollaInstitute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, California, United States of America.
Vanitha SampathSean N. Parker Center for Allergy and Asthma Research, Stanford University, Division of Pulmonary and Critical Care, Division of Immunology, Allergy, and Rheumatology, Departments of Medicine and Pediatrics, Stanford University School of Medicine, Stanford, California, United States of America.
Holden MaeckerInstitute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, California, United States of America.
Margaret R KaragasChildren's Environmental Health and Disease Prevention Research Center at Dartmouth, Lebanon, New Hampshire, United States of America.
Kari C NadeauSean N. Parker Center for Allergy and Asthma Research, Stanford University, Division of Pulmonary and Critical Care, Division of Immunology, Allergy, and Rheumatology, Departments of Medicine and Pediatrics, Stanford University School of Medicine, Stanford, California, United States of America.ORCID http://orcid.org/0000-0002-2146-2955
Dartmouth Psychiatric Research Center · USStanford University · USNorwegian Institute of Public Health · NO

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
NCI NIH HHS P30 CA023108
6 · The paper itself

Abstract

backgroundArsenic and cadmium are environmental pollutants, and although the evidence for adverse immune effects after prenatal arsenic and cadmium exposures is increasing, little is known about the underlying immunological mechanisms.

methodsWe investigated the relationship between prenatal arsenic and cadmium exposures and a variety of T cell subpopulations measured in cord blood for 63 participants in the New Hampshire Birth Cohort Study. Post-partum toenail concentrations of arsenic and cadmium were used as an estimate of maternal exposure during pregnancy. The characteristics of cord blood proportions of T lymphocytes and subpopulations (expression of markers for Th1, Th2, Th17, Th1Th17, induced and natural regulatory T cells and NKTs) are presented.

resultsIn regression analyses, maternal arsenic exposure levels were inversely associated with cord blood T helper memory cells (-21%, 95% CI: -36%, -3%) and the association was found to be stronger in females. They were also inversely associated with activated T helper memory cells, particularly in males (-26%, 95% CI: -43%, -3%). Similarly, inverse associations were observed between cadmium exposure levels and activated T helper memory cells (-16%, 95% CI: -30%, -1%) and also for T helper memory cells in females (-20%, 95% CI: -35%, -3%).

conclusionThe results suggest that prenatal exposures to relatively low levels of arsenic and cadmium may contribute to altered distribution of T cell populations at birth. These changes in theory, could have contributed to the previously reported immunosuppressive effects observed later in infancy/childhood.

Indexed as

Environmental ExposureAdultArsenicCadmiumFemaleFetal BloodHumansImmunophenotypingNailsPregnancyT-Lymphocyte SubsetsYoung AdultArsenicCadmium

Identifiers

PMID28662050
PMCPMC5491028
OpenAlexW2734029929

What OpenQuestion 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 OpenQuestion graph.