Evidence map›Paper›PMID 41085630›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

MHC II MAPPs for High-Confident Immunogenicity Risk Assessment of Biotherapeutics.

Elise Pepermans, Zuben E Sauna, Sofie Pattyn

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Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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.

Elise PepermansImmuneSpec, Niel, Belgium. Elise.Pepermans@ImmuneSpec.com.
Zuben E SaunaDivision of Hemostasis, Office of Plasma Protein Therapeutics, Center for Biologics Evaluation and Research (CBER), Food and Drug Administration (FDA), Silver Spring, MD, USA.
Sofie PattynIQVIA Laboratories (Formerly known as ImmunXperts, a Q2 Solutions Company), Gosselies, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biotherapeutics can provoke unwanted immunogenicity, which can affect the safety and/or efficacy of the drug. Consequently, immunogenicity risk assessments are carried out during drug development. Further, immunogenicity is evaluated during clinical trials prior to licensure. Most therapeutic proteins are either purified from plasma or, increasingly, manufactured using recombinant DNA technology. The immune response to these protein therapies involves internalization of the protein into antigen-presenting cells (APCs), enzymatic processing of the protein into peptides, and presentation of peptides on major histocompatibility class II (MHC II) proteins (HLA class II in humans). The MHC II-peptide complex if recognized by T cell receptors (TCRs) engages with CD4+ T helper cells, which ultimately results in formation of anti-drug antibodies (ADAs). The MHC-associated peptide proteomics (MAPPs) is an assay that in principle can identify the peptides derived from the therapeutic protein that are associated with an individual subject's MHC variants. The MAPPs assay is the only assay that provides information about both protein processing in APCs and peptide presentation by MHC proteins. This is important because not all possible peptides from a protein can be generated during protein processing in APCs. Here we describe a highly robust protocol for MHC II MAPPs.

Indexed as

Biological ProductsHistocompatibility Antigens Class IIPeptidesProteomicsAntigen PresentationAntigen-Presenting CellsHumansRisk AssessmentBiological ProductsHistocompatibility Antigens Class IIPeptidesAntigen presentationBiotherapeutic developmentImmunogenicityMAPPsMHC-associated peptide proteomicsMHC IIRisk assessmentT cell epitopeUnwanted immunogenicity

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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.