Evidence map›Paper›PMID 38858494›Full record

ArticleActa pharmacologica Sinica2024

T cell-redirecting antibody for treatment of solid tumors via targeting mesothelin.

Jun-Jun Liu, Zhi-di Pan, Ya-Li Yue, Shu-Sheng Wang, Jie Chen, Hua Jiang, Bao-Hong Zhang, Ming-Yuan Wu, Yun-Sheng Yuan, Yan-Lin Bian and 6 more

Abstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2024. 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
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  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

16 authors.

Jun-Jun Liu *Engineering Research Center of Cell and Therapeutic Antibody, Ministry of Education, School of Pharmacy, Shanghai Jiao Tong University, Shanghai, 200240, China.
Zhi-di Pan *Jecho Institute, Shanghai, 200240, China.
Ya-Li YueEngineering Research Center of Cell and Therapeutic Antibody, Ministry of Education, School of Pharmacy, Shanghai Jiao Tong University, Shanghai, 200240, China.
Shu-Sheng WangJecho Laboratories, Inc., Frederick, MD, 21704, USA.
Jie ChenJecho Institute, Shanghai, 200240, China.
Hua JiangJecho Laboratories, Inc., Frederick, MD, 21704, USA.
Bao-Hong ZhangEngineering Research Center of Cell and Therapeutic Antibody, Ministry of Education, School of Pharmacy, Shanghai Jiao Tong University, Shanghai, 200240, China.
Ming-Yuan WuEngineering Research Center of Cell and Therapeutic Antibody, Ministry of Education, School of Pharmacy, Shanghai Jiao Tong University, Shanghai, 200240, China.
Yun-Sheng YuanEngineering Research Center of Cell and Therapeutic Antibody, Ministry of Education, School of Pharmacy, Shanghai Jiao Tong University, Shanghai, 200240, China.
Yan-Lin BianEngineering Research Center of Cell and Therapeutic Antibody, Ministry of Education, School of Pharmacy, Shanghai Jiao Tong University, Shanghai, 200240, China.
Hai-Yang YinJecho Institute, Shanghai, 200240, China.
Lei WangEngineering Research Center of Cell and Therapeutic Antibody, Ministry of Education, School of Pharmacy, Shanghai Jiao Tong University, Shanghai, 200240, China.
Jun-Yan LiEngineering Research Center of Cell and Therapeutic Antibody, Ministry of Education, School of Pharmacy, Shanghai Jiao Tong University, Shanghai, 200240, China.
John GillyJecho Biopharmaceuticals Co., Ltd, Tianjin, 300450, China.
Yue-Qing XieJecho Institute, Shanghai, 200240, China. yueqingxie@jecholabs.com.
Jian-Wei ZhuEngineering Research Center of Cell and Therapeutic Antibody, Ministry of Education, School of Pharmacy, Shanghai Jiao Tong University, Shanghai, 200240, China. jianweiz@sjtu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T cell engaging bispecific antibodies (TCBs) have recently become significant in cancer treatment. In this study we developed MSLN490, a novel TCB designed to target mesothelin (MSLN), a glycosylphosphatidylinositol (GPI)-linked glycoprotein highly expressed in various cancers, and evaluated its efficacy against solid tumors. CDR walking and phage display techniques were used to improve affinity of the parental antibody M912, resulting in a pool of antibodies with different affinities to MSLN. From this pool, various bispecific antibodies (BsAbs) were assembled. Notably, MSLN490 with its IgG-[L]-scFv structure displayed remarkable anti-tumor activity against MSLN-expressing tumors (EC

Indexed as

GPI-Linked ProteinsMesothelinAnimalsAntibodies, BispecificAntineoplastic AgentsCell Line, TumorFemaleHT29 CellsHumansMiceMice, Inbred BALB CMice, NudeNeoplasmsPaclitaxelAntibodies, BispecificAntineoplastic AgentsGPI-Linked ProteinsMesothelinMSLN protein, humanMsln protein, mousePaclitaxelmesothelinMSLN490paclitaxelsolid tumorsT cell engaging bispecific antibodies

Identifiers

PMID38858494
PMCPMC11420237

What OpenQuestion holds

Textmetadata
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.