Evidence map›Paper›PMID 41206008›Full record

ArticleThe Journal of infectious diseases2026

Adenovirus 40 and 41 Antibodies Associated With Protection From Infection in a Bangladeshi Birth Cohort.

Jennifer Hendrick, Jennie Z Ma, Vu Huynh, Jozelyn V Pablo, Andy A Teng, Amit Oberai, Joseph J Campo, David Camerini, William A Petri

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Jennifer HendrickDepartment of Medicine, University of Virginia Health System, Charlottesville, Virginia, USA.ORCID 0000-0001-7352-2596
Jennie Z MaDepartment of Public Health Sciences, University of Virginia School of Medicine, Charlottesville, Virginia, USA.ORCID 0000-0002-5839-2882
Vu HuynhAntigen Discovery Incorporated (ADI), Irvine California, USA.
Jozelyn V PabloAntigen Discovery Incorporated (ADI), Irvine California, USA.ORCID 0000-0002-7286-7688
Andy A TengAntigen Discovery Incorporated (ADI), Irvine California, USA.
Amit OberaiAntigen Discovery Incorporated (ADI), Irvine California, USA.ORCID 0009-0006-2384-8890
Joseph J CampoAntigen Discovery Incorporated (ADI), Irvine California, USA.ORCID 0000-0002-8652-0917
David CameriniAntigen Discovery Incorporated (ADI), Irvine California, USA.ORCID 0000-0001-9429-5951
William A PetriDepartment of Medicine, University of Virginia Health System, Charlottesville, Virginia, USA.

Funding

The integrated Translational Health Research Institute of Virginia (iTHRIV): Using Data to Improve HealthUL1TR003015 · NCATS · UNIVERSITY OF VIRGINIA · PI BROWN, DONALD E, JOHNSTON, KAREN C. · 2019 to 2023
$20.3M
FIELD STUDIES OF IMMUNITY TO AMEBIASIS IN BANGLADESHR01AI043596 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI CAROL A GILCHRIST, William A Petri · 1998 to 2026
$7.7M
Institutional Career Development CoreKL2TR003016 · NCATS · UNIVERSITY OF VIRGINIA · PI PAPIN, JASON, WORRALL, BRADFORD B · 2019 to 2023
$3.9M
Active and passive humoral immunity to enteric adenovirus infection in Bangladeshi childrenK23AI187708 · NIAID · UNIVERSITY OF VIRGINIA · PI Jennifer Marie Hendrick · 2025 to 2026
$384k
National Institutes of Allergy and Infectious Diseases K23AI187708NCATS NIH HHSNCATS NIH HHS KL2 TR003016NCATS NIH HHS UL1 TR003015NIAID NIH HHS K23 AI187708NIAID NIH HHS R01 AI043596NIH HHS KL2TR003016NIH HHS UL1TR003015
6 · The paper itself

Abstract

backgroundAdenovirus (AdV) 40/41 is a major cause of pediatric acute gastroenteritis (AGE), leading to significant morbidity and mortality worldwide. As little is known about clinical correlates of protection, we analyzed AdV-specific antibody reactivities using a multi-AdV protein microarray and serum from a Bangladeshi birth cohort surveilled for diarrhea during the first 2 years of life.

methodsArrays contained a comprehensive set of proteins from AdV 40 and 41, in addition to respiratory AdVs 4, 5, and 26. Children were split into four groups according to AdV 40/41 infection occurrence during year 1 (Y1) and year 2 (Y2) of life. One-year array antibody reactivity levels were analyzed from 119 children using principal component analysis (PCA). Top antibody reactivities were evaluated for associations with AdV 40/41 disease severity and protection in Year 2 using logistic regression.

resultsEight principal components (PCs) were identified from PCA. Top targets contributing to the leading PCs included external AdV 40/41 antigens that function in host cell entry, particularly penton base (PB) proteins. AdV 41 PB antibody reactivity at Year 1 is significantly associated with reduced risk of AdV 40/41 infection in Year 2 (OR = 0.36, 95% CI: 0.16-0.80, P = .013, adjusted P = .003). Additionally, those with mild to moderate infections in Year 2 had higher reactivities to AdV 40 and 41 PB compared to severe infections (P = .008 and .032, respectively).

conclusionsHigher antibody reactivity to AdV PB was associated with improved Year 2 AdV 40/41 outcomes, elevating it as a promising vaccine or monoclonal antibody target.

Indexed as

Adenoviridae InfectionsAdenoviruses, HumanAdenovirus Infections, HumanAntibodies, ViralGastroenteritisBangladeshBirth CohortChild, PreschoolCohort StudiesDiarrheaFemaleHumansInfantMalePrincipal Component AnalysisProtein Array AnalysisAntibodies, Viraladenovirus 40/41antibody responsepediatric gastroenteritis

Identifiers

PMID41206008
PMCPMC12776611

What Socratic 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 Socratic graph.