Evidence map›Paper›PMID 42454041›Full record

ArticleFrontiers in immunology2026

The immunogenicity database collaborative: a standardized, publicly available database for clinical immunogenicity observations and insights.

Sudhanshu Agnihotri, Bruno Gonzalez-Nolasco, Brinda Monian, Sofie Pattijn, Chloé Ackaert, Patrick Wu, Hubert Kettenberger, Sophie Tourdot, Timothy Hickling, Zicheng Hu and 2 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 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

12 authors.

Sudhanshu AgnihotriDepartment of Pharmaceutical Sciences, University at Buffalo, The State University of New York, Buffalo, NY, United States.
Bruno Gonzalez-NolascoEarly Development Services, Lonza Biologics Inc., Cambridge, MA, United States.
Brinda MonianGenerate Biomedicines, Somerville, MA, United States.
Sofie PattijnIn Vitro Immunology, IQVIA Laboratories, Gosselies, Belgium.
Chloé AckaertIn Vitro Immunology, IQVIA Laboratories, Gosselies, Belgium.
Patrick WuDepartment of Translational Pharmacokinetics and Pharmacodynamics, Genentech Inc, South San Francisco, CA, United States.
Hubert KettenbergerLarge Molecule Research, Roche Pharma Research and Early Development, Roche Innovation Center Munich, Penzberg, Germany.
Sophie TourdotPharmacokinetics, Dynamics and Metabolism, Pfizer Inc., Andover, MA, United States.
Timothy HicklingPharma Research and Early Development, Roche Innovation Centre Welwyn, Roche, Welwyn Garden City, United Kingdom.
Zicheng HuDepartment of Translational Pharmacokinetics and Pharmacodynamics, Genentech Inc, South San Francisco, CA, United States.
Richard E HiggsEli Lilly and Company, Indianapolis, IN, United States.
Daniel S LeventhalGenerate Biomedicines, Somerville, MA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anti-drug antibodies (ADAs) against biotherapeutics remain difficult to predict, limiting efforts to assess and mitigate immunogenicity risk prior to clinical development. Existing immunogenicity data are fragmented across disparate sources and reported using inconsistent definitions, creating a major barrier to understanding the drivers of ADA formation. To address this challenge, we established the Immunogenicity Database Collaborative (IDC), launched its public website (https://www.immunogenicitydb.org), and developed the first release of the Immunogenicity Dataset (IDC DS V1), a structured clinical immunogenicity dataset integrating therapeutic characteristics, amino acid sequence information, and patient cohort-level clinical data curated from publicly available sources. The IDC DS V1 contains 4,146 ADA-related datapoints spanning 1,788 cohorts, 727 clinical trials, and 218 therapeutics. Analysis of the dataset highlights trends in ADA frequency, reveals important sources of variability across clinical contexts, and identifies key factors associated with immunogenicity risk. The IDC provides a foundational resource to standardize clinical immunogenicity data and support immunogenicity risk assessment across the biopharmaceutical industry. In addition to the current dataset release, it establishes an extensible data architecture and framework for future community-driven expansion into additional areas of immunogenicity research.

Indexed as

AntibodiesDatabases, FactualBiocurationHumansAntibodiesanti-drug antibodiesbiologicsdatabaseimmunogenicityimmunogenicity risk assessment

Identifiers

PMID42454041
PMCPMC13365037

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.