Evidence map›Paper›PMID 25172497›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Protective actions of aspirin-triggered (17R) resolvin D1 and its analogue, 17R-hydroxy-19-para-fluorophenoxy-resolvin D1 methyl ester, in C5a-dependent IgG immune complex-induced inflammation and lung injury.

Huifang Tang, Yanlan Liu, Chunguang Yan, Nicos A Petasis, Charles N Serhan, Hongwei Gao

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
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  9. Article
  10. Roles of Resolvins in Chronic Inflammatory Response.International journal of molecular sciences · 2022
    Review
  11. Article
  12. Molecular Pharmacology of Inflammation Resolution in Atherosclerosis.International journal of molecular sciences · 2022
    Review
  13. The Role of Serum Resolvin D1 Levels in Determining the Presence and Prognosis of ST-Segment Elevation Myocardial Infarction.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2022
    Article
  14. 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

6 authors at 4 institutions in 2 countries.

Huifang TangDepartment of Anesthesiology, Perioperative, and Pain Medicine, Center for Experimental Therapeutics and Reperfusion Injury, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115; Zhejiang Respiratory Drugs Research Laboratory of the State Food and Drug Administration of China, School of Medicine, Zhejiang University, Hangzhou, Zhejiang 310058, China;
Yanlan LiuDepartment of Anesthesiology, Perioperative, and Pain Medicine, Center for Experimental Therapeutics and Reperfusion Injury, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115;
Chunguang YanDepartment of Anesthesiology, Perioperative, and Pain Medicine, Center for Experimental Therapeutics and Reperfusion Injury, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115;
Nicos A PetasisDepartment of Chemistry, University of Southern California, Los Angeles, CA 90089; and Loker Hydrocarbon Research Institute, University of Southern California, Los Angeles, CA 90089.
Charles N SerhanDepartment of Anesthesiology, Perioperative, and Pain Medicine, Center for Experimental Therapeutics and Reperfusion Injury, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115; hgao@zeus.bwh.harvard.edu cnserhan@zeus.bwh.harvard.edu.
Hongwei GaoDepartment of Anesthesiology, Perioperative, and Pain Medicine, Center for Experimental Therapeutics and Reperfusion Injury, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115; hgao@zeus.bwh.harvard.edu cnserhan@zeus.bwh.harvard.edu.
Harvard University · USBrigham and Women's Hospital · USNational Medical Products Administration · CNUniversity of Southern California · US

Funding

Resolution Mechanisms in Acute Inflammation: Resolution PharmacologyP01GM095467 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI SERHAN, CHARLES NICHOLAS · 2011 to 2020
$14.8M
STAT3 and its Acetylation in Acute Lung InjuryR01HL092905 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI GAO, HONGWEI · 2008 to 2012
$1.8M
NHLBI NIH HHS 3R01HL092905-02S1NHLBI NIH HHS 5R01HL092905NHLBI NIH HHS R01 HL092905NIGMS NIH HHS 5P01GM095467NIGMS NIH HHS P01 GM095467
6 · The paper itself

Abstract

Increasing evidence suggests that the novel anti-inflammatory and proresolving mediators such as the resolvins play an important role during inflammation. However, the functions of these lipid mediators in immune complex-induced lung injury remain unknown. In this study, we determined the role of aspirin-triggered resolvin D1 (AT-RvD1) and its metabolically stable analog, 17R-hydroxy-19-para-fluorophenoxy-resolvin D1 methyl ester (p-RvD1), in IgG immune complex-induced inflammatory responses in myeloid cells and injury in the lung. We show that lung vascular permeability in the AT-RvD1- or p-RvD1-treated mice was significantly reduced when compared with values in mice receiving control vesicle during the injury. Furthermore, i.v. administration of either AT-RvD1 or p-RvD1 caused significant decreases in the bronchoalveolar lavage fluid contents of neutrophils, inflammatory cytokines, and chemokines. Of interest, AT-RvD1 or p-RvD1 significantly reduced bronchoalveolar lavage fluid complement C5a level. By EMSA, we demonstrate that IgG immune complex-induced activation of NF-κB and C/EBPβ transcription factors in the lung was significantly inhibited by AT-RvD1 and p-RvD1. Moreover, AT-RvD1 dramatically mitigates IgG immune complex-induced NF-κB and C/EBP activity in alveolar macrophages. Also, secretion of TNF-α, IL-6, keratinocyte cell-derived chemokine, and MIP-1α from IgG immune complex-stimulated alveolar macrophages or neutrophils was significantly decreased by AT-RvD1. These results suggest a new approach to the blocking of immune complex-induced inflammation.

Indexed as

Acute Lung InjuryPneumoniaAnimalsAntigen-Antibody ComplexAnti-Inflammatory Agents, Non-SteroidalAspirinBronchoalveolar Lavage FluidCCAAT-Enhancer-Binding ProteinsCell LineChemokine CCL3Complement C5aCytokinesDocosahexaenoic AcidsImmunoglobulin GMacrophages, AlveolarMiceAntigen-Antibody ComplexAnti-Inflammatory Agents, Non-SteroidalAspirinCCAAT-Enhancer-Binding ProteinsCcl3 protein, mouseChemokine CCL3Complement C5aCytokinesDocosahexaenoic AcidsImmunoglobulin GNF-kappa Bresolvin D1

Identifiers

PMID25172497
PMCPMC4170233
OpenAlexW1540021305

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.