Evidence map›Paper›PMID 22138406›Full record

ArticleImmunology letters2012

Soluble B7-H1: differences in production between dendritic cells and T cells.

Xavier Frigola, Brant A Inman, Christopher J Krco, Xin Liu, Susan M Harrington, Peggy A Bulur, Allan B Dietz, Haidong Dong, Eugene D Kwon

Abstract readLetter
In one paragraph

Article in Immunology letters, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed, 4 pooled it
0.7field-weighted citation impact, top 28% 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

93 citing papers in PubMed, 4 syntheses or guidelines pooled it, 139 citations in OpenAlex.

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33 more citing papers are in PubMed but not listed here.

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

9 authors at 2 institutions in 1 country.

Xavier Frigola
Brant A Inman
Christopher J Krco
Xin Liu
Susan M Harrington
Peggy A Bulur
Allan B Dietz
Haidong Dong
Eugene D Kwon
Mayo Clinic · USDuke Medical Center · US

Funding

Clinical Impact of B7-H Immune Cell Coregulators in Renal Cell CarcinomaR01CA134345 · NCI · MAYO CLINIC ROCHESTER · PI DONG, HAIDONG, KWON, EUGENE D. · 2009 to 2014
$1.5M
NCI NIH HHS R01 CA134345
6 · The paper itself

Abstract

Tumor cells aberrantly express several T cell inhibitory molecules including members of the B7-H co-regulatory family. Presumably tumor-expressed B7-H1 and B7-H3 confer resistance to elimination by the immune system. In addition, elevated levels of soluble B7-H1 (sB7-H1) has been identified in the sera of cancer patients, including renal carcinoma patients and is associated with increased cancer related death. Here we report that sB7-H1 is produced and released by activated mature dendritic cells (mDC). Immature DC, macrophages, monocytes, or T cells are refractory to releasing sB7-H1. Exposure of CD4+ and CD8+ T cells to mDC-derived sB7-H1 molecules induced apoptosis. These data suggest that the immunobiology of B7-H1 is perhaps more complex than previously thought. sB7-H1 molecules may represent an unanticipated contributing factor to immune homeostasis. That both immune and tumor cells can be sources of sB7-H1 suggests that optimization of co-regulatory blockade immunotherapy for solid malignancies of necessity will require impact of targeting tumor and immune-derived B7-H1 molecules.

Indexed as

ApoptosisB7-H1 AntigenCarcinoma, Renal CellDendritic CellsHomeostasisHumansKidney NeoplasmsLymphocyte ActivationSolubilityT-LymphocytesB7-H1 Antigen

Identifiers

PMID22138406
PMCPMC3901160
OpenAlexW2088763423

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.