Evidence map›Paper›PMID 17221337›Full record

ReviewArchivum immunologiae et therapiae experimentalis

Eicosanoid regulation of pulmonary innate immunity post-hematopoietic stem cell transplantation.

Megan N Ballinger, Tracy R McMillan, Bethany B Moore

Abstract readReview
In one paragraph

Review in Archivum immunologiae et therapiae experimentalis. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Observational
  2. Review
  3. Review
  4. Prostaglandin EPharmacology & therapeutics · 2018
    Review
  5. Elevated prostaglandin EMucosal immunology · 2018
    Article
  6. Too much of a good thing: How modulating LTBSeminars in immunology · 2017
    Review
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  12. Review
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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

3 authors at 1 institution in 1 country.

Megan N BallingerUniversity of Michigan, Ann Arbor, MI, USA.
Tracy R McMillan
Bethany B Moore
University of Michigan–Ann Arbor · US

Funding

PULMONARY CELLULAR AND MOLECULAR BIOLOGY TRAININGT32HL007749 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Robert Pickett Dickson · 1993 to 2026
$19.9M
SCOR IN THE PATHOBIOLOGY OF FIBROTIC LUNG DISEASEP50HL056402 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SIMON, RICHARD H · 1997 to 2006
$13.3M
RESEARCH TRAINING IN EXPERIMENTAL IMMUNOPATHOLOGYT32AI007413 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Bethany B. Moore · 1993 to 2026
$9.8M
PGE2 Regulation of Host Defense post-BMTR01AI065543 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOORE, BETHANY B. · 2007 to 2011
$1.9M
PGE2 Regulation of Epithelial/Fibroblast InteractionsR01HL071586 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOORE, BETHANY B. · 2003 to 2006
$1.3M
NHLBI NIH HHS HL071586NHLBI NIH HHS P50 HL056402NHLBI NIH HHS P50HL56402NHLBI NIH HHS R01 HL071586NHLBI NIH HHS T32 HL007749NIAID NIH HHS R01 AI065543NIAID NIH HHS T32 AI007413
6 · The paper itself

Abstract

Hematopoietic stem cell transplantation (HSCT) is a therapeutic option for a number of malignant and inherited disorders. However, the efficacy of this therapy is limited by a number of serious infectious and noninfectious complications. Pulmonary infections represent a significant cause of morbidity and mortality post-HSCT and can occur both pre- and post-hematopoietic reconstitution. Susceptibility to Gram-negative bacterial infections despite full hematopoietic engraftment suggests that innate immunity remains impaired months to years post-HSCT. This review will describe the process and complications of HSCT and will summarize what is known about innate immune reconstitution post-HSCT. Data from the literature as well as our own laboratory will be presented to suggest that an eicosanoid imbalance characterized by over-production of prostaglandins and under-production of leukotrienes leads to impaired lung phagocyte function post-HSCT. Of therapeutic interest, strategies which limit production of prostaglandins can improve pulmonary host defense in animal HSCT models, which suggests that this may also be beneficial for human HSCT recipients.

Indexed as

Hematopoietic Stem Cell TransplantationImmunity, InnateAnimalsEicosanoidsHumansLungEicosanoids

Identifiers

PMID17221337
PMCPMC3313470
OpenAlexW2037054057

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.