Evidence map›Paper›PMID 33552052›Full record

ReviewFrontiers in immunology2020

Understanding Early-Life Adaptive Immunity to Guide Interventions for Pediatric Health.

Eleanor C Semmes, Jui-Lin Chen, Ria Goswami, Trevor D Burt, Sallie R Permar, Genevieve G Fouda

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed, 4 pooled it
11.5field-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

108 citing papers in PubMed, 4 syntheses or guidelines pooled it, 141 citations in OpenAlex.

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  5. Article
  6. Maternal Influenza Vaccine Reduces the Risk of Respiratory Syncytial Virus and Related Respiratory Hospitalizations in Early Infancy: An Epidemiological Study.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026
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48 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

6 authors at 1 institution in 1 country.

Eleanor C SemmesDuke Human Vaccine Institute, Duke University, Durham, NC, United States.
Jui-Lin ChenDuke Human Vaccine Institute, Duke University, Durham, NC, United States.
Ria GoswamiDuke Human Vaccine Institute, Duke University, Durham, NC, United States.
Trevor D BurtChildren's Health and Discovery Initiative, Department of Pediatrics, Duke University, Durham, NC, United States.
Sallie R PermarDuke Human Vaccine Institute, Duke University, Durham, NC, United States.
Genevieve G FoudaDuke Human Vaccine Institute, Duke University, Durham, NC, United States.
Duke University · US

Funding

Project 2: RNA vaccination in early life to induce potent and broad HIV Env-specific antibody responsesP01AI117915 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI DE PARIS, KRISTINA, PERMAR, SALLIE R. · 2015 to 2024
$21.2M
Medical Scientist Training Program Training GrantT32GM145449 · NIGMS · DUKE UNIVERSITY · PI Christopher D Kontos · 2022 to 2026
$6.6M
Functional profile to HIV vaccine elicited antibodies in infantsR01AI131978 · NIAID · DUKE UNIVERSITY · PI POLLARA, JUSTIN JOSEPH · 2017 to 2021
$2.0M
NIAID NIH HHS P01 AI117915NIAID NIH HHS R01 AI131978NIGMS NIH HHS T32 GM145449
6 · The paper itself

Abstract

Infants are capable of mounting adaptive immune responses, but their ability to develop long-lasting immunity is limited. Understanding the particularities of the neonatal adaptive immune system is therefore critical to guide the design of immune-based interventions, including vaccines, in early life. In this review, we present a thorough summary of T cell, B cell, and humoral immunity in early life and discuss infant adaptive immune responses to pathogens and vaccines. We focus on the differences between T and B cell responses in early life and adulthood, which hinder the generation of long-lasting adaptive immune responses in infancy. We discuss how knowledge of early life adaptive immunity can be applied when developing vaccine strategies for this unique period of immune development. In particular, we emphasize the use of novel vaccine adjuvants and optimization of infant vaccine schedules. We also propose integrating maternal and infant immunization strategies to ensure optimal neonatal protection through passive maternal antibody transfer while avoiding hindering infant vaccine responses. Our review highlights that the infant adaptive immune system is functionally distinct and uniquely regulated compared to later life and that these particularities should be considered when designing interventions to promote pediatric health.

Indexed as

Adaptive ImmunityInfant HealthB-LymphocytesHumansInfantT-Lymphocytesadaptive immunityadjuvantsinfant immunitymaternal antibody transferneonatal B cellsneonatal T cellspediatric infectious diseasesvaccines

Identifiers

PMID33552052
PMCPMC7858666
OpenAlexW3125433020

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.