Evidence map›Paper›PMID 19109567›Full record

ArticleBlood2009

B7-H4-deficient mice display augmented neutrophil-mediated innate immunity.

Gefeng Zhu, Mathew M Augustine, Takeshi Azuma, Liqun Luo, Sheng Yao, Sudarshan Anand, A Cecilia Rietz, Jiaqiang Huang, Haiying Xu, Andrew S Flies and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 79 citations in OpenAlex.

  1. Pooled it
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  18. Tumor Regression and Delayed Onset Toxicity Following B7-H4 CAR T Cell Therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2016
    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

15 authors at 4 institutions in 1 country.

Gefeng ZhuDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.
Mathew M Augustine
Takeshi Azuma
Liqun Luo
Sheng Yao
Sudarshan Anand
A Cecilia Rietz
Jiaqiang Huang
Haiying Xu
Andrew S Flies
Sarah J Flies
Koji Tamada
Marco Colonna
Jan M A van Deursen
Lieping Chen
Johns Hopkins University · USJohns Hopkins Medicine · USMayo Clinic in Arizona · USWashington University in St. Louis · US

Funding

PANCREAS CANCER MESOTHELIN ANIMAL MODELU19CA113341 · NCI · JOHNS HOPKINS UNIVERSITY · PI PARDOLL, DREW M. · 2005 to 2009
$5.7M
MOLECULAR MECHANISMS OF TUMOR-INDUCED TOLERANCER01CA097085 · NCI · YALE UNIVERSITY · PI CHEN, LIEPING · 2002 to 2011
$3.5M
Therapeutic Manipulation of the B7-like MoleculesR01CA098731 · NCI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI CHEN, LIEPING · 2003 to 2007
$1.7M
NCI NIH HHS CA113341NCI NIH HHS CA97085NCI NIH HHS CA98731NCI NIH HHS R01 CA097085NCI NIH HHS R01 CA098731NCI NIH HHS U19 CA113341
6 · The paper itself

Abstract

B7-H4 is an immunoglobulin superfamily molecule and shown to be inhibitory for T-cell responses. To explore physiologic roles of B7-H4, we created B7-H4-deficient (KO) mice by genetic targeting. B7-H4KO mice are healthy and their T- and B-cell responses to polyclonal antigens are in normal range. However, B7-H4KO mice are more resistant to infection by Listeria monocytogenes than their littermates. Within 3 days after infection, bacterial colonies in livers and spleens are significantly lower than the controls, suggesting a role of B7-H4 in enhancing innate immunity. Further studies demonstrate that neutrophils increase in peripheral organs of B7-H4KO mice more so than their littermates but their bactericidal functions remain unchanged. Augmented innate resistance is completely dependent on neutrophils, even in the absence of adaptive immunity. In vitro B7-H4 inhibits the growth of bone marrow-derived neutrophil progenitors, suggesting an inhibitory function of B7-H4 in neutrophil expansion. Our results identify B7-H4 as a negative regulator of the neutrophil response to infection and provide a new target for manipulation of innate immunity.

Indexed as

AnimalsB7-1 AntigenB-LymphocytesBone Marrow CellsCD11b AntigenFemaleHematopoietic Stem CellsListeriosisMaleMiceMice, Inbred StrainsMice, KnockoutNeutrophilsPhagocytosisReceptors, ChemokineRespiratory BurstB7-1 AntigenCD11b AntigenGr-1 protein, mouseReceptors, ChemokineV-Set Domain-Containing T-Cell Activation Inhibitor 1Vtcn1 protein, mouse

Identifiers

PMID19109567
PMCPMC2647680
OpenAlexW2103137174

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.