Evidence map›Paper›PMID 35649416›Full record

ArticleImmunity2022

Phage display of environmental protein toxins and virulence factors reveals the prevalence, persistence, and genetics of antibody responses.

Julia W Angkeow, Daniel R Monaco, Athena Chen, Thiagarajan Venkataraman, Sahana Jayaraman, Cristian Valencia, Brandon M Sie, Thomas Liechti, Payam N Farhadi, Gabriela Funez-dePagnier and 17 more

Open access · greenAbstract read
In one paragraph

Article in Immunity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 38 citations in OpenAlex.

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  18. PhIP-Seq: methods, applications and challenges.Frontiers in bioinformatics · 2024
    Review
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  20. 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

27 authors at 8 institutions in 2 countries.

Julia W AngkeowInstitute for Cell Engineering, Division of Immunology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Daniel R MonacoInstitute for Cell Engineering, Division of Immunology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Athena ChenDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Thiagarajan VenkataramanInstitute for Cell Engineering, Division of Immunology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Sahana JayaramanInstitute for Cell Engineering, Division of Immunology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Cristian ValenciaDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Brandon M SieInstitute for Cell Engineering, Division of Immunology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Thomas LiechtiImmunoTechnology Section, Vaccine Research Center, NIAID, NIH, Bethesda, MD, USA.
Payam N FarhadiEnvironmental Autoimmunity Group, Clinical Research Branch, National Institute of Environmental Health Sciences, NIH, Bethesda, MD, USA.
Gabriela Funez-dePagnierJill Roberts Institute for Research in IBD, Division of Gastroenterology and Hepatology, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
Cheryl A Sherman-BaustLaboratory of Molecular Biology and Immunology, NIH/National Institute on Aging, Baltimore, MD, USA.
May Q WongBC Children's Hospital Research Institute, Vancouver, BC, Canada.
Ingo RuczinskiDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Patrizio CaturegliDivision of Immunology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Cynthia L SearsDepartments of Medicine and Oncology, Johns Hopkins University School of Medicine, and Department of Molecular Microbiology & Immunology, Bloomberg School of Public Health, Baltimore, MD, USA.
Patricia J SimnerDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
June L RoundDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, UT, USA.
Priya DuggalDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Uri LasersonDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Theodore S SteinerBC Children's Hospital Research Institute, Vancouver, BC, Canada.
Ranjan SenLaboratory of Molecular Biology and Immunology, NIH/National Institute on Aging, Baltimore, MD, USA.
Thomas E LloydDepartment of Neurology, Solomon H. Snyder Department of Neuroscience, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Mario RoedererImmunoTechnology Section, Vaccine Research Center, NIAID, NIH, Bethesda, MD, USA.
Andrew L MammenMuscle Disease Unit, Laboratory of Muscle Stem Cells and Gene Regulations, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, MD, USA.
Randy S LongmanJill Roberts Institute for Research in IBD, Division of Gastroenterology and Hepatology, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
Lisa G RiderEnvironmental Autoimmunity Group, Clinical Research Branch, National Institute of Environmental Health Sciences, NIH, Bethesda, MD, USA.
H Benjamin LarmanInstitute for Cell Engineering, Division of Immunology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA. Electronic address: hlarman1@jhmi.edu.
Johns Hopkins University · USBC Children's Hospital · CACornell University · USNational Institute of Environmental Health Sciences · USNational Institute on Aging · USIcahn School of Medicine at Mount Sinai · USNational Institute of Arthritis and Musculoskeletal and Skin Diseases · USUniversity of Utah · US

Funding

Muscle Disease UnitZIAAR041203 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI MAMMEN, ANDREW · 2015 to 2025
$19.7M
Medical Scientist Training ProgramT32GM136577 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI ANDREA L COX · 2020 to 2026
$13.4M
Age-associated alterations in pro-inflammatory gene expression in humansZIAAG000386 · NIA · NATIONAL INSTITUTE ON AGING · PI SEN, RANJAN · 2009 to 2025
$4.8M
Pathogenesis of Early Onset Colorectal Cancer: Microbiome Contributions and MechanismsR01CA264217 · NCI · JOHNS HOPKINS UNIVERSITY · PI SEARS, CYNTHIA · 2021 to 2025
$2.3M
Host-Microbiota Interactions in Crohn's Disease-associated SpondyloarthritisR01DK114252 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI LONGMAN, RANDY S · 2018 to 2022
$1.9M
Design and Analysis of Displayed PeptidomesR01GM136724 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI LARMAN, HARRY BENJAMIN, RUCZINSKI, INGO · 2020 to 2023
$1.9M
Immune and inflammatory interactions in Alzheimer's disease-related dementiasZIAAG000525 · NIA · NATIONAL INSTITUTE ON AGING · PI SEN, RANJAN · 2020 to 2025
$1.3M
NCI NIH HHS R01 CA264217NIDDK NIH HHS R01 DK114252NIGMS NIH HHS R01 GM136724NIGMS NIH HHS T32 GM136577Wellcome Trust
6 · The paper itself

Abstract

Microbial exposures are crucial environmental factors that impact healthspan by sculpting the immune system and microbiota. Antibody profiling via Phage ImmunoPrecipitation Sequencing (PhIP-Seq) provides a high-throughput, cost-effective approach for detecting exposure and response to microbial protein products. We designed and constructed a library of 95,601 56-amino acid peptide tiles spanning 14,430 proteins with "toxin" or "virulence factor" keyword annotations. We used PhIP-Seq to profile the antibodies of ∼1,000 individuals against this "ToxScan" library. In addition to enumerating immunodominant antibody epitopes, we studied the age-dependent stability of the ToxScan profile and used a genome-wide association study to find that the MHC-II locus modulates bacterial epitope selection. We detected previously described anti-flagellin antibody responses in a Crohn's disease cohort and identified an association between anti-flagellin antibodies and juvenile dermatomyositis. PhIP-Seq with the ToxScan library is thus an effective tool for studying the environmental determinants of health and disease at cohort scale.

Indexed as

BacteriophagesPeptide LibraryAmino Acid SequenceAntibodiesAntibody FormationGenome-Wide Association StudyHumansImmunodominant EpitopesPrevalenceVirulence FactorsAntibodiesImmunodominant EpitopesPeptide LibraryVirulence Factorsantibody epitoe profilingCrohn'sdiseasehumoral immunityimmunogeneticsjuvenile dermatomyositismicrobiomeToxScan

Identifiers

PMID35649416
PMCPMC9203978
OpenAlexW4281646402

What OpenQuestion holds

Textmetadata
LicenceTDM
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.