Evidence map›Paper›PMID 36302840›Full record

ArticleScientific reports2022

A novel anti-TNF-α drug ozoralizumab rapidly distributes to inflamed joint tissues in a mouse model of collagen induced arthritis.

Shohei Oyama, Kosuke Ebina, Yuki Etani, Makoto Hirao, Masanao Kyuuma, Yasuyuki Fujii, Katsuya Iwata, Bunichiro Ogawa, Tomoya Hasegawa, Sasagu Kawano and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.4field-weighted citation impact, top 3% of its field
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

15 citing papers in PubMed, 36 citations in OpenAlex.

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  15. Next-Generation Anti-TNFα Agents: The Example of Ozoralizumab.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2024
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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

13 authors at 2 institutions in 1 country.

Shohei OyamaDepartment of Musculoskeletal Regenerative Medicine, Osaka University Graduate School of Medicine, Osaka, Japan.
Kosuke EbinaDepartment of Musculoskeletal Regenerative Medicine, Osaka University Graduate School of Medicine, Osaka, Japan. k-ebina@ort.med.osaka-u.ac.jp.
Yuki EtaniDepartment of Orthopaedic Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Makoto HiraoDepartment of Orthopaedic Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Masanao KyuumaTaisho Pharmaceutical Co., Ltd., Saitama, Japan.
Yasuyuki FujiiTaisho Pharmaceutical Co., Ltd., Saitama, Japan.
Katsuya IwataTaisho Pharmaceutical Co., Ltd., Saitama, Japan.
Bunichiro OgawaTaisho Pharmaceutical Co., Ltd., Saitama, Japan.
Tomoya HasegawaTaisho Pharmaceutical Co., Ltd., Saitama, Japan.
Sasagu KawanoTaisho Pharmaceutical Co., Ltd., Saitama, Japan.
Yutaka NakanishiTaisho Pharmaceutical Co., Ltd., Saitama, Japan.
Seiji OkadaDepartment of Orthopaedic Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Ken NakataDepartment of Medicine for Sports and Performing Arts, Osaka University Graduate School of Medicine, Osaka, Japan.
Taisho Pharmaceutical (Japan) · JPOsaka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In clinical studies, the next-generation anti-tumor necrosis factor-alpha (TNF-α) single domain antibody ozoralizumab showed high clinical efficacy shortly after the subcutaneous injection. To elucidate the mechanism underlying the rapid onset of the effects of ozoralizumab, we compared the biodistribution kinetics of ozoralizumab and adalimumab after subcutaneous injection in an animal model of arthritis. Alexa Fluor 680-labeled ozoralizumab and adalimumab were administered by subcutaneous injection once (2 mg/kg) at five weeks after induction of collagen-induced arthritis (CIA) in an animal arthritis model. The time-course of changes in the fluorescence intensities of the two compounds in the paws and serum were evaluated. The paws of the CIA mice were harvested at four and eight hours after the injection for fluorescence microscopy. Biofluorescence imaging revealed better distribution of ozoralizumab to the joint tissues than of adalimumab, as early as at four hours after the injection. Fluorescence microscopy revealed a greater fluorescence intensity of ozoralizumab in the joint tissues than that of adalimumab at eight hours after the injection. Ozoralizumab showed a significantly higher absorption rate constant as compared with adalimumab. These results indicate that ozoralizumab enters the systemic circulation more rapidly and is distributed to the target tissues earlier and at higher levels than conventional IgG antibodies. Our investigation provides new insight into the mechanism underlying the rapid onset of the effects of ozoralizumab in clinical practice.

Indexed as

Arthritis, ExperimentalAdalimumabAnimalsAntibodies, MonoclonalDisease Models, AnimalMiceTissue DistributionTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsAdalimumabAntibodies, MonoclonalTumor Necrosis Factor-alphaTumor Necrosis Factor Inhibitors

Identifiers

PMID36302840
PMCPMC9613905
OpenAlexW4307777211

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.