Evidence map›Paper›PMID 40528087›Full record

ReviewNature protocols2026

Identification of immunogenic commensal antigens using phage display.

Sheenam Verma, Samantha Kimmel, Oliver J Harrison

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In one paragraph

Review in Nature protocols, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Sheenam VermaCenter for Fundamental Immunology, Benaroya Research Institute, Seattle, WA, USA.
Samantha KimmelCenter for Fundamental Immunology, Benaroya Research Institute, Seattle, WA, USA.
Oliver J HarrisonCenter for Fundamental Immunology, Benaroya Research Institute, Seattle, WA, USA. oharrison@benaroyaresearch.org.ORCID 0000-0003-1515-9586

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Humoral immunity plays a major role in the establishment and maintenance of host-microbiota commensalism and immunity to pathogenic microorganisms. However, identification of antigens eliciting adaptive immune responses within barrier and systemic tissues represents a significant hurdle to further understanding this host-microbe dialogue. Here, we provide a protocol to identify immunogenic protein antigens expressed by commensal and pathogenic microbes by using bacteriophage (phage) display-mediated antibody/antigen biopanning. The procedure entails generation of an M13-phagemid library, production of an ORFeome (totality of open reading frames) phage library followed by multiple rounds of affinity-based immunoprecipitation and subsequent antigen validation by ELISA, ELISPOT and/or B cell tetramer generation. The protocol is optimized to identify antigens eliciting both IgA and IgG isotype responses and can use either circulating or intestinal antibodies for antigen identification. Generation and isolation of monoclonal phage encoding putative protein antigens enable simple identification of immunogenic antigens by Sanger sequencing, often providing protein domain-level resolution of epitope-bearing regions. Our protocol can be carried out by a trained molecular biologist and enables antigen identification and validation in the timeframe of weeks.

Indexed as

AntigensAntigens, BacterialCell Surface Display TechniquesPeptide LibraryAnimalsBacteriophage M13BacteriophagesEnzyme-Linked Immunosorbent AssayMiceAntigensAntigens, BacterialPeptide Library

Identifiers

What OpenQuestion holds

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Registered trials

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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.