Evidence map›Paper›PMID 42221829›Full record

ArticleiScience2026

Development, validation, and implementation of the antibody-secreting cell maturity index: Universal prediction of human plasma cell maturity.

Tobit D Steinmetz, Guiyou Yang, Tessa de Nooijer, Nisha van der Meer, Naomi Karmi, Rick Wilbrink, Hendrika Bootsma, Gwenny M Verstappen, Frans G M Kroese

Abstract read
In one paragraph

Article in iScience, 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

9 authors.

Tobit D SteinmetzUniversity of Groningen, University Medical Center Groningen, Department of Rheumatology and Clinical Immunology, 9700RB Groningen, the Netherlands.
Guiyou YangUniversity of Groningen, University Medical Center Groningen, Department of Epidemiology, 9700RB Groningen, the Netherlands.
Tessa de NooijerUniversity of Groningen, University Medical Center Groningen, Department of Rheumatology and Clinical Immunology, 9700RB Groningen, the Netherlands.
Nisha van der MeerUniversity of Groningen, University Medical Center Groningen, Department of Oncology, 9700RB Groningen, the Netherlands.
Naomi KarmiUniversity of Groningen, University Medical Center Groningen, Department of Gastroenterology and Hepatology, 9700RB Groningen, the Netherlands.
Rick WilbrinkUniversity of Groningen, University Medical Center Groningen, Department of Rheumatology and Clinical Immunology, 9700RB Groningen, the Netherlands.
Hendrika BootsmaUniversity of Groningen, University Medical Center Groningen, Department of Rheumatology and Clinical Immunology, 9700RB Groningen, the Netherlands.
Gwenny M VerstappenUniversity of Groningen, University Medical Center Groningen, Department of Rheumatology and Clinical Immunology, 9700RB Groningen, the Netherlands.
Frans G M KroeseUniversity of Groningen, University Medical Center Groningen, Department of Rheumatology and Clinical Immunology, 9700RB Groningen, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Defining the maturity of long-lived antibody-secreting cells (ASCs) is important for vaccine optimization and research into autoimmune diseases, but current assessment of plasma cell maturity is limited. We developed a universal, robust method to define plasma cell maturity using a meta-analysis of public, human cytometry data, with harmonized expression of ASC maturity markers across samples. Vaccination or infection samples were selected to train a random forest-based machine learning prediction model (performance of r = 0.866). After evaluation (performance of r = 0.616), the final model, named the antibody-secreting cell maturity index (ASC-ME), was applied to compartments with long-term ASC survival niches, namely bone marrow and gut. Both compartments showed increased ASC maturity, biologically validating the ASC-ME model. Example analyses highlight the broad spectrum for model application, e.g., in vaccine research, clinical trials or in ASC-related autoimmune diseases. Overall, our ASC-ME model, accessible via an online platform, offers a robust approach in evaluating ASC maturity.

Indexed as

Artificial intelligenceComponents of the immune system

Identifiers

PMID42221829
PMCPMC13217880

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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.