Evidence map›Paper›PMID 33656624›Full record

ArticleJournal of clinical immunology2021

Serum IgG Profiling of Toddlers Reveals a Subgroup with Elevated Seropositive Antibodies to Viruses Correlating with Increased Vaccine and Autoantigen Responses.

Patricia Pichilingue-Reto, Prithvi Raj, Quan-Zhen Li, Igor Dozmorov, David R Karp, Edward K Wakeland, Morgan Nelson, Rebecca S Gruchalla, M Teresa de la Morena, Nicolai S C van Oers

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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

10 authors at 4 institutions in 1 country.

Patricia Pichilingue-Reto *Department of Immunology, The University of Texas Southwestern Medical Center, NA2.200, 6000 Harry Hines Blvd., Dallas, TX, 75390-9093, USA.
Prithvi Raj *Department of Immunology, The University of Texas Southwestern Medical Center, NA2.200, 6000 Harry Hines Blvd., Dallas, TX, 75390-9093, USA.
Quan-Zhen LiDepartment of Immunology, The University of Texas Southwestern Medical Center, NA2.200, 6000 Harry Hines Blvd., Dallas, TX, 75390-9093, USA.
Igor DozmorovDepartment of Immunology, The University of Texas Southwestern Medical Center, NA2.200, 6000 Harry Hines Blvd., Dallas, TX, 75390-9093, USA.
David R KarpDepartment of Internal Medicine, The University of Texas Southwestern Medical Center, NA2.200, 6000 Harry Hines Blvd., Dallas, TX, 75390-9093, USA.
Edward K WakelandDepartment of Immunology, The University of Texas Southwestern Medical Center, NA2.200, 6000 Harry Hines Blvd., Dallas, TX, 75390-9093, USA.
Morgan NelsonChildren's Health, Dallas, TX, 75235, USA.
Rebecca S GruchallaDepartment of Pediatrics, The University of Texas Southwestern Medical Center, NA2.200, 6000 Harry Hines Blvd., Dallas, TX, 75390-9093, USA.
M Teresa de la MorenaDepartment of Pediatrics, Division of Immunology, University of Washington and Seattle Children's Hospital, Seattle, WA, 98105, USA.
Nicolai S C van OersDepartment of Immunology, The University of Texas Southwestern Medical Center, NA2.200, 6000 Harry Hines Blvd., Dallas, TX, 75390-9093, USA. Nicolai.vanoers@utsouthwestern.edu.ORCID 0000-0002-6545-8405
The University of Texas Southwestern Medical Center · USSeattle Children's Hospital · USSouthwestern Medical Center · USSt. Jude Children's Research Hospital · US

Funding

Long noncoding RNAs and their contribution to 22q11.2 deletion syndromeR01AI114523 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI VAN OERS, NICOLAI STANISLAS CYRILLE · 2015 to 2024
$4.1M
NIAID NIH HHS AI114523NIAID NIH HHS R01 AI114523
6 · The paper itself

Abstract

purposeThe human antibody repertoire forms in response to infections, the microbiome, vaccinations, and environmental exposures. The specificity of such antibody responses was compared among a cohort of toddlers to identify differences between seropositive versus seronegative responses.

methodsAn assessment of the serum IgM and IgG antibody reactivities in 197 toddlers of 1- and 2-years of age was performed with a microfluidic array containing 110 distinct antigens. Longitudinal profiling was done from years 1 to 2. Seropositivity to RNA and DNA viruses; bacteria; live attenuated, inactive, and subunit vaccines; and autoantigens was compared. A stratification was developed based on quantitative variations in the IgG responses. Clinical presentations and previously known genetic risk alleles for various immune system conditions were investigated in relation to IgG responses.

resultsIgG reactivities stratified toddlers into low, moderate, and high responder groups. The high group (17%) had elevated IgG responses to multiple RNA and DNA viruses (e.g., respiratory syncytial virus, Epstein-Barr virus, adenovirus, Coxsackievirus) and this correlated with increased responses to live attenuated viral vaccines and certain autoantigens. This high group was more likely to be associated with gestational diabetes and an older age. Genetic analyses identified polymorphisms in the IL2RB, TNFSF4, and INS genes in two high responder individuals that were associated with their elevated cytokine levels and clinical history of eczema and asthma.

conclusionSerum IgG profiling of toddlers reveals correlations between the magnitude of the antibody responses towards viruses, live attenuated vaccines, and certain autoantigens. A low responder group had much weaker responses overall, including against vaccines. The serum antibody screen also identifies individuals with IgG responses to less common infections (West Nile virus, parvovirus, tuberculosis). The characterization of the antibody responses in combination with the identification of genetic risk alleles provides an opportunity to identify children with increased risk of clinical disease.

Indexed as

Antibodies, ViralAutoantigensBacteriaChild, PreschoolCytokinesDNA VirusesFemaleGenotypeHumansImmunoglobulin GImmunoglobulin MInfantMaleMicrofluidic Analytical TechniquesRNA VirusesVaccinesAntibodies, ViralAutoantigensCytokinesImmunoglobulin GImmunoglobulin MVaccinesantigen arraysIgGsserum antibody responsestoddler immune responsesvaccines

Identifiers

PMID33656624
PMCPMC7927113
OpenAlexW3135501461

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.