Evidence map›Paper›PMID 35207448›Full record

ArticleLife (Basel, Switzerland)2022

A Novel Anti-B7-H3 × Anti-CD3 Bispecific Antibody with Potent Antitumor Activity.

Yan Feng, Kun Xie, Yanxin Yin, Bingyu Li, Chenyu Pi, Xiaoqing Xu, Tao Huang, Jingming Zhang, Bo Wang, Hua Gu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-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

14 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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  5. Review
  6. B7 homolog 3 in pancreatic cancer.World journal of gastroenterology · 2024
    Review
  7. Article
  8. Article
  9. Review
  10. Article
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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

11 authors at 1 institution in 1 country.

Yan FengSchool of Life Sciences and Technology, Tongji University, Shanghai 200092, China.
Kun XieSchool of Life Sciences and Technology, Tongji University, Shanghai 200092, China.
Yanxin YinSchool of Life Sciences and Technology, Tongji University, Shanghai 200092, China.
Bingyu LiSchool of Life Sciences and Technology, Tongji University, Shanghai 200092, China.
Chenyu PiSchool of Life Sciences and Technology, Tongji University, Shanghai 200092, China.
Xiaoqing XuSchool of Life Sciences and Technology, Tongji University, Shanghai 200092, China.ORCID 0000-0001-8294-6307
Tao HuangSchool of Life Sciences and Technology, Tongji University, Shanghai 200092, China.
Jingming ZhangSchool of Life Sciences and Technology, Tongji University, Shanghai 200092, China.
Bo WangSchool of Life Sciences and Technology, Tongji University, Shanghai 200092, China.
Hua GuSchool of Life Sciences and Technology, Tongji University, Shanghai 200092, China.
Jianmin FangSchool of Life Sciences and Technology, Tongji University, Shanghai 200092, China.
Tongji University · CN

Funding

the National Basic Research Program of China 2015CB553706the National Natural Science Foundation of China NSFC82172604
6 · The paper itself

Abstract

B7-H3 plays an important role in tumor apoptosis, proliferation, adhesion, angiogenesis, invasion, migration, and evasion of immune surveillance. It is overexpressed in various human solid tumor tissues. In patients, B7-H3 overexpression correlates with advanced stages, poor clinical outcomes, and resistance to therapy. The roles of B7-H3 in tumor progression make it a potential candidate for targeted therapy. Here, we generated a mouse anti-human B7-H3 antibody and demonstrated its binding activity via Tongji University Suzhou Instituteprotein-based and cell-based assays. We then developed a novel format anti-B7-H3 × anti-CD3 bispecific antibody based on the antibody-binding fragment of the anti-B7-H3 antibody and single-chain variable fragment structure of anti-CD3 antibody (OKT3) and demonstrated that this bispecific antibody mediated potent cytotoxic activities against various B7-H3-positive tumor cell lines in vitro by improving T cell activation and proliferation. This bispecific antibody also demonstrated potent antitumor activity in humanized mice xenograft models. These results revealed that the novel anti-B7-H3 × anti-CD3 bispecific antibody has the potential to be employed in treatment of B7-H3-positive solid tumors.

Indexed as

B7-H3bispecific T cell engagerimmunotherapysolid tumor

Identifiers

PMID35207448
PMCPMC8879513
OpenAlexW4205551017

What OpenQuestion holds

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LicenceCC BY
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.