Evidence map›Paper›PMID 31677920›Full record

ReviewTrends in pharmacological sciences2019

The B7x Immune Checkpoint Pathway: From Discovery to Clinical Trial.

Peter John, Yao Wei, Weifeng Liu, Meirong Du, Fangxia Guan, Xingxing Zang

Open access · greenAbstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

45 citing papers in PubMed, 71 citations in OpenAlex.

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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

6 authors at 3 institutions in 2 countries.

Peter JohnDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, New York, NY 10461, USA.
Yao WeiDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, New York, NY 10461, USA.
Weifeng LiuDepartment of Biochemistry, Albert Einstein College of Medicine, New York, NY 10461, USA.
Meirong DuHospital of Obstetrics and Gynecology, Fudan University Shanghai Medical College, Shanghai 200011, China.
Fangxia GuanSchool of Life Sciences, Zhengzhou University, Zhengzhou 450001, Henan, China.
Xingxing ZangDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, New York, NY 10461, USA; Department of Medicine, Albert Einstein College of Medicine, New York, NY 10461, USA; Department of Urology, Albert Einstein College of Medicine, New York, NY 10461, USA. Electronic address: xingxing.zang@einstein.yu.edu.
Albert Einstein College of Medicine · USShanghai Medical College of Fudan University · CNZhengzhou University · CN

Funding

Tumor-expressed immune checkpoint B7x-mediated resistance to anti-CTLA-4 therapy.R01CA175495 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI ZANG, XINGXING · 2014 to 2025
$5.1M
Mechanisms and Therapies of B7x and B7-H3 in T1DR01DK100525 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI ZANG, XINGXING · 2015 to 2019
$1.9M
B7x in Cancer: Mechanisms and TherapiesF30CA224931 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI JOHN, PETER · 2018 to 2021
$201k
NCI NIH HHS F30 CA224931NCI NIH HHS R01 CA175495NIDDK NIH HHS R01 DK100525
6 · The paper itself

Abstract

B7x (B7 homolog x, also known as B7-H4, B7S1, and VTCN1) was discovered by ourselves and others in 2003 as the seventh member of the B7 family. It is an inhibitory immune checkpoint of great significance to human disease. Tissue-expressed B7x minimizes autoimmune and inflammatory responses. It is overexpressed in a broad spectrum of human cancers, where it suppresses antitumor immunity. Further, B7x and PD-L1 tend to have mutually exclusive expression in cancer cells. Therapeutics targeting B7x are effective in animal models of cancers and autoimmune disorders, and early-phase clinical trials are underway to determine the efficacy and safety of targeting B7x in human diseases. It took 15 years moving from the discovery of B7x to clinical trials. Further studies will be necessary to identify its receptors, reveal its physiological functions in organs, and combine therapies targeting B7x with other treatments.

Indexed as

AnimalsAntineoplastic Agents, ImmunologicalArthritis, RheumatoidClinical Trials, Phase I as TopicHumansImmune ToleranceModels, MolecularMolecular Targeted TherapyNeoplasmsRandomized Controlled Trials as TopicSignal TransductionTranslational Research, BiomedicalV-Set Domain-Containing T-Cell Activation Inhibitor 1Antineoplastic Agents, ImmunologicalV-Set Domain-Containing T-Cell Activation Inhibitor 1VTCN1 protein, humanVtcn1 protein, mouseautoimmunityB7xcancerimmune checkpointimmunotherapyinflammation

Identifiers

PMID31677920
PMCPMC6907741
OpenAlexW2983436315

What OpenQuestion holds

Textmetadata
LicenceTDM
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.