Evidence map›Paper›PMID 31428800›Full record

ArticleCancer immunology, immunotherapy : CII2019

A VEGFR2-MICA bispecific antibody activates tumor-infiltrating lymphocytes and exhibits potent anti-tumor efficacy in mice.

Yao Xu, Xinrong Zhang, Yong Wang, Mingzhu Pan, Min Wang, Juan Zhang

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Controversial role of γδ T cells in colorectal cancer.American journal of cancer research · 2024
    Review
  4. Article
  5. Article
  6. 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

6 authors at 1 institution in 1 country.

Yao XuAntibody Engineering Laboratory, State Key Laboratory of Natural Medicines, School of Life Science and Technology, China Pharmaceutical University, 154#, Tong Jia Xiang 24, Nanjing, 210009, People's Republic of China.
Xinrong ZhangAntibody Engineering Laboratory, State Key Laboratory of Natural Medicines, School of Life Science and Technology, China Pharmaceutical University, 154#, Tong Jia Xiang 24, Nanjing, 210009, People's Republic of China.
Yong WangSanhome-CPU Joint Laboratory, China Pharmaceutical University, Nanjing, 210009, People's Republic of China.
Mingzhu PanAntibody Engineering Laboratory, State Key Laboratory of Natural Medicines, School of Life Science and Technology, China Pharmaceutical University, 154#, Tong Jia Xiang 24, Nanjing, 210009, People's Republic of China.
Min WangAntibody Engineering Laboratory, State Key Laboratory of Natural Medicines, School of Life Science and Technology, China Pharmaceutical University, 154#, Tong Jia Xiang 24, Nanjing, 210009, People's Republic of China.
Juan ZhangAntibody Engineering Laboratory, State Key Laboratory of Natural Medicines, School of Life Science and Technology, China Pharmaceutical University, 154#, Tong Jia Xiang 24, Nanjing, 210009, People's Republic of China. zhangjuan@cpu.edu.cn.ORCID http://orcid.org/0000-0003-1067-7878
China Pharmaceutical University · CN

Funding

Double First-Class University project CPU2018GY14Double First-Class University project CPU2018PZQ12Jiangsu Province Qinglan Project 2014Natural Science Foundation of Jiangsu Province BK20161459
6 · The paper itself

Abstract

MHC class I-related chain A (MICA) is one of the major ligands for natural killer group 2 member D (NKG2D), which is an activating NK receptor. MICA is expressed on the surface of human epithelial tumor cells, and its shedding from tumor cells leads to immunosuppression. To activate immune response in the tumor microenvironment, we designed an anti-VEGFR2-MICA bispecific antibody (JZC01), consisting of MICA and an anti-VEGFR2 single chain antibody fragment (JZC00) and explored its potential anti-tumor activity. JZC01 targeted vascular endothelial growth factor receptor 2 (VEGFR2) and inhibited tumorigenesis by blocking the VEGFR2 signaling pathway. Additionally, JZC01 promoted NK and CD8

Indexed as

AnimalsAntibodies, BispecificApoptosisCarcinoma, Lewis LungCD8-Positive T-LymphocytesCytotoxicity, ImmunologicDisease Models, AnimalHistocompatibility Antigens Class IHumansImmune ToleranceImmunotherapyInterferon-gammaKiller Cells, NaturalLung NeoplasmsLymphocyte ActivationLymphocytes, Tumor-InfiltratingAntibodies, BispecificHistocompatibility Antigens Class IInterferon-gammaKDR protein, humanMHC class I-related chain AVascular Endothelial Growth Factor Receptor-2Bispecific antibodyCancer immunotherapyTumor-infiltrating lymphocyteVEGFR2

Identifiers

PMID31428800
PMCPMC11028065
OpenAlexW2969718051

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.