Evidence map›Paper›PMID 24325967›Full record

ArticleThe Journal of infectious diseases2014

Cord blood Vγ2Vδ2 T cells provide a molecular marker for the influence of pregnancy-associated malaria on neonatal immunity.

Cristiana Cairo, Nyaradzo Longinaker, Giulia Cappelli, Rose G F Leke, Manuel Mve Ondo, Rosine Djokam, Josephine Fogako, Robert J Leke, Bertrand Sagnia, Samuel Sosso and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Trial
  2. Review
  3. Frontiers in immunology · 2026
    Article
  4. Article
  5. Article
  6. Observational
  7. Review
  8. Microbial exposure drives polyclonal expansion of innate γδ T cells immediately after birth.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  9. Review
  10. The immune response to malaria in utero.Immunological reviews · 2020
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Effector Vγ9Vδ2 T cells dominate the human fetal γδ T-cell repertoire.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  18. Article
  19. 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

12 authors at 5 institutions in 4 countries.

Cristiana CairoInstitute of Human Virology.
Nyaradzo Longinaker
Giulia Cappelli
Rose G F Leke
Manuel Mve Ondo
Rosine Djokam
Josephine Fogako
Robert J Leke
Bertrand Sagnia
Samuel Sosso
Vittorio Colizzi
C David Pauza
Centre International De Reference Chantal Biya · CMUniversité de Yaoundé I · CMInstitute of Human Virology · NGCentral Hospital of Yaoundé · CMUniversity of Maryland, Baltimore · US

Funding

EXPAND PARTICIPATION BY MINORITIES IN BIOMEDICAL SCIENCER25GM055036 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI SUMMERS, MICHAEL FINLEY · 1996 to 2021
$16.9M
Mechanisms for SIV evasion of vaccine immunity: Role of FasL-mediated cell deathR01AI068508 · NIAID · UNIVERSITY OF MD BIOTECHNOLOGY INSTITUTE · PI PAUZA, C. DAVID · 2006 to 2009
$2.0M
Antigen exposure in utero: impacts on newborn immunity and infectious diseasesR01AI104702 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI CAIRO, CRISTIANA · 2013 to 2016
$1.5M
NIAID NIH HHS 1R01AI104702NIAID NIH HHS AI068508NIAID NIH HHS R01 AI068508NIAID NIH HHS R01 AI104702NIGMS NIH HHS R25 GM055036
6 · The paper itself

Abstract

backgroundPlasmodium falciparum placental infection primes the fetal immune system and alters infant immunity. Mechanisms leading to these outcomes are not completely understood. We focused on Vγ2Vδ2 cells, which are part of the immune response against many pathogens, including P. falciparum. These unconventional lymphocytes respond directly to small, nonpeptidic antigens, independent of major histocompatibility complex presentation. We wondered whether placental malaria, which may increase fetal exposure to P. falciparum metabolites, triggers a response by neonatal Vγ2Vδ2 lymphocytes that can be a marker for the extent of fetal exposure to malarial antigens.

methodsCord blood mononuclear cells were collected from 15 neonates born to mothers with P. falciparum infection during pregnancy (8 with placental malaria) and 25 unexposed neonates. Vγ2Vδ2 cell phenotype, repertoire, and proliferative responses were compared between newborns exposed and those unexposed to P. falciparum.

resultsPlacental malaria-exposed neonates had increased proportions of central memory Vγ2Vδ2 cells in cord blood, with an altered Vγ2 chain repertoire ex vivo and after stimulation.

conclusionOur results suggest that placental malaria affects the phenotype and repertoire of neonatal Vγ2Vδ2 lymphocytes. Placental malaria may lower the capacity for subsequent Vγ2Vδ2 cell responses and impair the natural resistance to infectious diseases or the response to pediatric vaccination.

Indexed as

Immunity, Maternally-AcquiredBiomarkersFemaleFetal BloodGene Expression RegulationHumansImmunoglobulin gamma-ChainsInfant, NewbornMalaria, FalciparumPregnancyPregnancy Complications, ParasiticT-Lymphocyte SubsetsBiomarkersImmunoglobulin gamma-Chainsaminobisphosphonatecord bloodgammadeltainnateneonatalphosphoantigenplacental malariaPlasmodiumrepertoire

Identifiers

PMID24325967
PMCPMC4007110
OpenAlexW2152150928

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.