Evidence map›Paper›PMID 37682072›Full record

ArticlemAbs

Rapid

Yoshiyuki Arata, Shigeki Motoyama, Mariko Yano, Tatsuya Ikuno, Shunsuke Ito, Tomochika Matsushita, Akira Takeiri, Yukari Nishito, Nami Yabuki, Hideaki Mizuno and 8 more

Open access · goldAbstract read
In one paragraph

Article in mAbs. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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

18 authors at 1 institution in 1 country.

Yoshiyuki ArataTranslational Research Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Shigeki MotoyamaResearch Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Mariko YanoTranslational Research Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Tatsuya IkunoTranslational Research Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Shunsuke ItoTranslational Research Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Tomochika MatsushitaTranslational Research Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Akira TakeiriTranslational Research Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Yukari NishitoTranslational Research Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Nami YabukiResearch Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Hideaki MizunoResearch Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Zenjiro SampeiResearch Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Masayuki MishimaTranslational Research Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Masaki HondaTranslational Research Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Jumpei KiyokawaTranslational Research Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Hiromi SuzukiTranslational Research Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Shuichi ChibaTranslational Research Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Mitsuyasu TaboResearch Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Chiyomi KuboTranslational Research Division, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Chugai Pharma (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapeutic antibodies sometimes elicit anti-drug antibodies (ADAs) that can affect efficacy and safety. Engineered antibodies that contain artificial amino acid sequences are potentially highly immunogenic, but this is currently difficult to predict. Therefore, it is important to efficiently assess immunogenicity during the development of complex antibody-based formats. Here, we present an in vitro peripheral blood mononuclear cell-based assay that can be used to assess immunogenicity potential within 3 days. This method involves examining the frequency and function of interleukin (IL)-2-secreting CD4

Indexed as

Interleukin-2T-LymphocytesCD4-Positive T-LymphocytesCytokinesLeukocytes, MononuclearCytokinesInterleukin-2antibody engineeringAnti-drug antibodybiotherapeuticsIL-2immunogenicityPBMCT cell activationT cell epitopes

Identifiers

PMID37682072
PMCPMC10494738
OpenAlexW4386530330

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.