Evidence map›Paper›PMID 41957528›Full record

ArticleFEBS open bio2026

Development of human monoclonal antibodies against TARM1 by yeast display.

Rikio Yabe, Mayumi Saeki, Masaaki Hashiguchi, Sayaka Ono, Kazuhisa Aoki, Hidetaka Tanno

Abstract read
In one paragraph

Article in FEBS open bio, 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

6 authors.

Rikio YabeCancer Immunology Project, Tokyo Metropolitan Institute of Medical Science, Setagaya, Japan.ORCID https://orcid.org/0000-0001-7542-8819
Mayumi SaekiCancer Immunology Project, Tokyo Metropolitan Institute of Medical Science, Setagaya, Japan.
Masaaki HashiguchiCancer Immunology Project, Tokyo Metropolitan Institute of Medical Science, Setagaya, Japan.
Sayaka OnoCancer Immunology Project, Tokyo Metropolitan Institute of Medical Science, Setagaya, Japan.
Kazuhisa AokiCancer Immunology Project, Tokyo Metropolitan Institute of Medical Science, Setagaya, Japan.
Hidetaka TannoCancer Immunology Project, Tokyo Metropolitan Institute of Medical Science, Setagaya, Japan.

Funding

Astellas Foundation for Research on Metabolic DisordersChugai Foundation for Innovative Drug Discovery Science: 2024-II-07Japan Agency for Medical Research and Development JP24ck0106965Japan Society for the Promotion of Science JP20K23383Japan Society for the Promotion of Science JP24K10099Mochida Memorial Foundation for Medical and Pharmaceutical ResearchNakatani Foundation for Advancement of Measuring Technologies in Biomedical Engineering
6 · The paper itself

Abstract

TARM1, a leukocyte immunoglobulin-like receptor expressed on myeloid cells, functions as a costimulatory receptor promoting proinflammatory cytokine secretion. Recent studies have revealed the involvement of TARM1 in immune-mediated diseases. Despite its biological importance, research tools for elucidating human TARM1 function have been limited. Here, we generated monoclonal antibodies (mAbs) against human TARM1 by a yeast display platform combined with a human single-chain variable fragment (scFv) library. Two scFv clones were isolated and converted into IgG1 antibodies, both of which bound recombinant TARM1 with high affinity and cell-surface TARM1. Importantly, these antibodies induced activation signals into Jurkat NFAT-GFP reporter cells expressing TARM1-CD28-4-1BB-CD3ζ chimera, indicating agonistic activity. These mAbs provide valuable tools for dissecting TARM1-mediated function and represent a potential approach for therapeutic strategies in inflammatory diseases and cancer.

Indexed as

Antibodies, MonoclonalHumansJurkat CellsSingle-Chain AntibodiesYeastsAntibodies, MonoclonalSingle-Chain Antibodiesfully human monoclonal antibodyTARM1yeast display

Identifiers

PMID41957528
PMCPMC13327005

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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.