Evidence map›Paper›PMID 33679787›Full record

ReviewFrontiers in immunology2021

Malaria and Early Life Immunity: Competence in Context.

Perri C Callaway, Lila A Farrington, Margaret E Feeney

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. 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.

Perri C CallawayInfectious Diseases and Immunity Graduate Group, University of California, Berkeley, Berkeley, CA, United States.
Lila A FarringtonDepartment of Medicine, University of California, San Francisco, San Francisco, CA, United States.
Margaret E FeeneyDepartment of Medicine, University of California, San Francisco, San Francisco, CA, United States.

Funding

The role of γδ T cells in fetal and infant immune defense against malariaR01AI093615 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FEENEY, MARGARET E · 2011 to 2025
$9.1M
Mentoring Translational Researchers for Careers in Pediatric Global HealthK24AI113002 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FEENEY, MARGARET E · 2014 to 2023
$1.9M
NIAID NIH HHS K24 AI113002NIAID NIH HHS R01 AI093615
6 · The paper itself

Abstract

Childhood vaccines have been the cornerstone tool of public health over the past century. A major barrier to neonatal vaccination is the "immaturity" of the infant immune system and the inefficiency of conventional vaccine approaches at inducing immunity at birth. While much of the literature on fetal and neonatal immunity has focused on the early life propensity toward immune tolerance, recent studies indicate that the fetus is more immunologically capable than previously thought, and can, in some circumstances, mount adaptive B and T cell responses to perinatal pathogens

Indexed as

ImmunocompetenceAdaptive ImmunityAge FactorsAntibodies, ProtozoanAntigen-Presenting CellsFemaleFetusHumansImmune ToleranceImmunity, InnateImmunization ScheduleInfant, NewbornLymphocytesMalariaMalaria VaccinesMaternal-Fetal ExchangeAntibodies, ProtozoanMalaria Vaccinesfetal immunitymalarianeonatal immunityneonatal vaccinationplasmodium

Identifiers

PMID33679787
PMCPMC7933008

What OpenQuestion holds

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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.