Evidence map›Paper›PMID 39681261›Full record

ReviewAnnals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology2025

Functional testing of humoral immunity in the Prevnar 20 era.

Jenna Zuzolo, Muhammad F Zulfiqar, Brian Spoelhof, Rebecca Revell, James T Patrie, Larry Borish, Monica G Lawrence

Abstract readReview
In one paragraph

Review in Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology, 2025. 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
–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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Jenna ZuzoloDepartment of Pediatrics, University of Virginia School of Medicine, Charlottesville, Virginia.
Muhammad F ZulfiqarUniversity of Virginia School of Medicine, Charlottesville, Virginia.
Brian SpoelhofPharmacy Services, University of Virginia Health, Charlottesville, Virginia.
Rebecca RevellDivision of Asthma, Allergy, and Immunology, Department of Medicine, University of Virginia School of Medicine, Charlottesville, Virginia.
James T PatrieDivision of Biostatistics, Department of Public Health Sciences, University of Virginia School of Medicine, Charlottesville, Virginia.
Larry BorishDivision of Asthma, Allergy, and Immunology, Department of Medicine, University of Virginia School of Medicine, Charlottesville, Virginia; Department of Microbiology, University of Virginia School of Medicine, Charlottesville, Virginia.
Monica G LawrenceDepartment of Pediatrics, University of Virginia School of Medicine, Charlottesville, Virginia; Division of Asthma, Allergy, and Immunology, Department of Medicine, University of Virginia School of Medicine, Charlottesville, Virginia. Electronic address: ml4nz@virginia.edu.

Funding

Defining the Role of Immunoglobulin G4 (IgG4) in Food-Induced Eosinophilic Esophagitis (EoE)R01AI175232 · NIAID · UNIVERSITY OF VIRGINIA · PI Emily Clarke McGowan · 2023 to 2026
$3.1M
Protracted clinical and inflammatory response to rhinovirus challenge in human asthmaticsR56AI158519 · NIAID · UNIVERSITY OF VIRGINIA · PI BORISH, LARRY C · 2022 to 2022
$323k
NIAID NIH HHS R01 AI175232NIAID NIH HHS R56 AI158519
6 · The paper itself

Abstract

Humoral immune disorders such as common variable immunodeficiency and specific antibody deficiency are prevalent in clinical practice and require accurate functional testing of humoral immunity for diagnosis and to guide treatment approach. Traditionally, the 23-valent pneumococcal polysaccharide vaccine (PPSV23) has been used to assess polysaccharide antibody responses by measuring pre- and post-vaccination pneumococcal titers. However, the recent introduction of pneumococcal conjugate vaccines (PCVs), such as PCV13, PCV15, and PCV20, into the childhood and adult vaccine schedules has significantly reduced the number of unique serotypes available for testing and in turn has complicated the evaluation process. We retrospectively analyzed serotype-specific antibody responses in patients aged 2 to 65 years who received PPSV23 at the University of Virginia Health System to compare diagnostic outcomes using all 23 serotypes vs the limited number of unique serotypes not included in previous PCVs-11 serotypes for PCV13 recipients and 4 for PCV20 recipients. Our findings reveal that although previous PCVs mean that there is a reduced number of serotypes available for interpretation, PPSV23 testing maintains diagnostic accuracy between 81% and 84%. Despite limitations, the use of PPSV23 remains a valuable tool for identifying patients with clinically significant humoral immune deficiencies. In the future, alternative diagnostic approaches such as Salmonella typhi polysaccharide vaccine response and opsonophagocytosis assays may become more frequently used as part of the evaluation of humoral immune disorders.

Indexed as

Antibodies, BacterialImmunity, HumoralPneumococcal InfectionsPneumococcal VaccinesStreptococcus pneumoniaeAdolescentAdultAgedChildChild, PreschoolFemaleHumansMaleMiddle AgedRetrospective StudiesSerogroup23-valent pneumococcal capsular polysaccharide vaccineAntibodies, BacterialPneumococcal Vaccines

Identifiers

PMID39681261
PMCPMC11885008

What OpenQuestion holds

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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.