Evidence map›Paper›PMID 35773120›Full record

ArticleVaccine2022

Kinetics of pneumococcal antibodies among HIV-exposed, uninfected infants in Botswana.

Emilie A Uffman, Shuk Hang Li, Jui-Lin Chen, Noel Allen, Sefelani Boiditswe, Genevieve G Fouda, Jillian H Hurst, Mohamed Z Patel, Andrew P Steenhoff, Coleen K Cunningham and 3 more

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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

13 authors at 6 institutions in 2 countries.

Emilie A UffmanDuke Human Vaccine Institute, Duke University Medical Center, Durham, NC, USA.
Shuk Hang LiDuke Human Vaccine Institute, Duke University Medical Center, Durham, NC, USA; Department of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, NC, USA.
Jui-Lin ChenDuke Human Vaccine Institute, Duke University Medical Center, Durham, NC, USA.
Noel AllenDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, USA.
Sefelani BoiditsweBotswana-UPenn Partnership, Gaborone, Botswana.
Genevieve G FoudaDuke Human Vaccine Institute, Duke University Medical Center, Durham, NC, USA; Division of Pediatric Infectious Diseases, Duke University Medical Center, Durham, NC, USA.
Jillian H HurstDivision of Pediatric Infectious Diseases, Duke University Medical Center, Durham, NC, USA.
Mohamed Z PatelUniversity of Botswana School of Medicine, Gaborone, Botswana.
Andrew P SteenhoffBotswana-UPenn Partnership, Gaborone, Botswana; Global Health Center, Children's Hospital of Philadelphia, Philadelphia, PA, USA; Division of Pediatric Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Coleen K CunninghamDivision of Pediatric Infectious Diseases, University of California-Irvine and Children's Hospital of Orange County, Orange, CA, USA.
Emily QinDivision of Pediatric Infectious Diseases, Duke University Medical Center, Durham, NC, USA.
Clemontina A DavenportDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, USA.
Matthew S KellyDivision of Pediatric Infectious Diseases, Duke University Medical Center, Durham, NC, USA. Electronic address: matthew.kelly@duke.edu.
Duke Medical Center · USDuke University · USBotswana Open University · BWChildren's Hospital of Orange County · USChildren's Hospital of Philadelphia · USUniversity of Botswana · BW

Funding

Virus & Reservoirs CoreP30AI045008 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI DAVID S METZGER · 1999 to 2026
$78.6M
Nasopharyngeal Microbiome and Risk of Bacterial Pathogen Colonization in InfantsK23AI135090 · NIAID · DUKE UNIVERSITY · PI KELLY, MATTHEW SCOTT · 2018 to 2022
$860k
Rational identification of Corynebacterium strains for use as probioticsR21AI154081 · NIAID · LURIE CHILDREN'S HOSPITAL OF CHICAGO · PI KELLY, MATTHEW SCOTT, SEED, PATRICK C. · 2022 to 2023
$439k
NIAID NIH HHS K23 AI135090NIAID NIH HHS P30 AI045008NIAID NIH HHS R21 AI154081
6 · The paper itself

Abstract

backgroundStreptococcus pneumoniae is a leading cause of severe infections among children. Despite vaccination, HIV-exposed, uninfected (HEU) children have a higher incidence of invasive pneumococcal disease than HIV-unexposed, uninfected (HUU) children. We sought to compare the immunogenicity of 13-valent pneumococcal conjugate vaccine (PCV-13) in HEU and HUU infants.

methodsWe conducted a prospective cohort study of 134 mother-infant dyads in Botswana. Infants received PCV-13 doses at 2, 3, and 4 months through routine clinical care. We measured IgG antibodies specific to vaccine serotypes in sera collected from infants at 0, 5, and 12 months of age. We calculated the proportion of infants with protective IgG levels (≥0.35 µg/mL) to specific pneumococcal serotypes.

resultsAt birth, fewer than half of infants had protective IgG levels to serotypes 1 (38%), 3 (46%), 4 (33%), 5 (23%), 6B (40%), 7F (44%), 9 V (44%), and 23F (46%). Compared to HUU infants (n = 97), HEU infants (n = 37) had lower antibody concentrations at birth to serotypes 5 (p = 0.046) and 19A (p = 0.008) after adjustment for maternal age and infant birth weight. More than 80% of HEU and HUU infants developed protective antibody levels to each of the 13 vaccine serotypes following PCV-13 vaccination. Median concentrations of antibodies to pneumococcal serotypes declined by 55-93% between 5 and 12 months of age, with fewer than half of infants having protective antibody levels to serotypes 1 (47%), 3 (28%), 9 V (44%), 18C (24%), and 23F (49%) at 12 months of age.

conclusionsBoth HEU and HUU infants developed protective antibody responses to PCV-13 administered in a 3 + 0 schedule. However, antibody concentrations to many pneumococcal serotypes waned substantially by 12 months of age, suggesting that a PCV-13 booster dose in the second year of life may be needed to maintain protective pneumococcal antibody levels in older infants and young children.

Indexed as

HIV InfectionsPneumococcal InfectionsAgedAntibodies, BacterialBotswanaChildChild, PreschoolHumansImmunoglobulin GInfantInfant, NewbornKineticsPneumococcal VaccinesProspective StudiesVaccines, ConjugateAntibodies, BacterialImmunoglobulin GPneumococcal VaccinesVaccines, Conjugate13-valent pneumococcal conjugate vaccineHIV-exposed uninfected childrenimmunization-induced immune responsesStreptococcus pneumoniaesub-Saharan Africa

Identifiers

PMID35773120
PMCPMC9912097
OpenAlexW4283772636

What OpenQuestion holds

Textmetadata
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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.