Evidence map›Paper›PMID 42827951›Full record

ArticleFrontiers in immunology2026

Ozoralizumab, a trivalent anti-TNFα NANOBODY

Mai Morimoto, Yukihisa Sawa, Chihiro Ishiwatari-Ogata, Naoki Kojima, Yasuyuki Fujii

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

5 authors.

Mai MorimotoResearch Headquarters, Taisho Pharmaceutical Co., Ltd., Saitama, Japan.
Yukihisa SawaResearch Headquarters, Taisho Pharmaceutical Co., Ltd., Saitama, Japan.
Chihiro Ishiwatari-OgataResearch Headquarters, Taisho Pharmaceutical Co., Ltd., Saitama, Japan.
Naoki KojimaResearch Headquarters, Taisho Pharmaceutical Co., Ltd., Saitama, Japan.
Yasuyuki FujiiResearch Headquarters, Taisho Pharmaceutical Co., Ltd., Saitama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid factor (RF), an autoantibody targeting IgG, is a key diagnostic marker of autoimmune diseases, especially rheumatoid arthritis (RA). In patients with RA, high RF titers have been reported to be associated with disease severity and may influence the pharmacological behavior and clinical response of certain biologic agents, including tumor necrosis factor (TNF) inhibitors. TNF inhibitors are widely used biologic agents in RA treatment and include two structure types: the fragment crystallizable (Fc)-containing protein (e.g. IgG) and the Fc-free protein. Clinical studies have suggested that in RA patients with high RF titers, sufficient circulating drug concentrations are more likely to be maintained with Fc-free TNF inhibitors than with Fc-containing TNF inhibitors. To clarify the mechanisms underlying this clinical observation, we investigated whether RF differentially alters FcRn-dependent recycling and macrophage uptake of the Fc-containing antibody adalimumab and the Fc-free, human serum albumin (HSA)-binding NANOBODY

Indexed as

Antibodies, Monoclonal, HumanizedAntigen-Antibody ComplexHistocompatibility Antigens Class IReceptors, FcRheumatoid FactorTumor Necrosis Factor-alphaAdalimumabAnimalsArthritis, RheumatoidHumansMacrophagesMicePhagocytosisAdalimumabAntibodies, Monoclonal, HumanizedAntigen-Antibody ComplexFc receptor, neonatalHistocompatibility Antigens Class IReceptors, FcRheumatoid FactorTumor Necrosis Factor-alphaanti-TNFα antibodyFcRn recyclingimmune complexphagocytosisrheumatoid arthritisrheumatoid factortumor necrosis factorVHH

Identifiers

PMID42827951
PMCPMC13631012

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.