Evidence map›Paper›PMID 18500928›Full record

ArticleThe Journal of infectious diseases2008

Caspofungin modulates inflammatory responses to Aspergillus fumigatus through stage-specific effects on fungal beta-glucan exposure.

T M Hohl, M Feldmesser, D S Perlin, E G Pamer

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
9.4field-weighted citation impact, top 1% 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

58 citing papers in PubMed, 116 citations in OpenAlex.

  1. Article
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  6. Targeting β-glucans, vital components of theFrontiers in immunology · 2023
    Review
  7. Article
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  11. Review
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  13. Review
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  15. Review
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  18. Article
  19. Echinocandin Resistance in Candida.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2015
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

T M HohlInfectious Diseases Service, Memorial Sloan-Kettering Cancer Center and Immunology Program, Sloan-Kettering Institute, New York 10021, USA. hohlt@mskcc.org
M Feldmesser
D S Perlin
E G Pamer
Memorial Sloan Kettering Cancer Center · USAlbert Einstein College of Medicine · USInternational Center for Public Health · US

Funding

CD4 T Cell Responses to M. Tuberculosis InfectionR01AI080619 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI GLICKMAN, MICHAEL S, PAMER, ERIC G. · 2009 to 2013
$2.3M
Characterization of Aspergillus fumigatus specific CD4 T cell responses.R01AI067359 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI PAMER, ERIC G. · 2006 to 2010
$2.2M
Monoclonal antibodies to inhibit Aspergillus germinationR01AI059663 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI FELDMESSER, MARTA L. · 2006 to 2010
$1.9M
Aspergillosis: Engineering Antibody for DiagnosisR21AI065745 · NIAID · ALBERT EINSTEIN COL OF MED YESHIVA UNIV · PI FELDMESSER, MARTA L. · 2005 to 2006
$449k
Monocyte-mediated Host Defense against Aspergillus fumigatusK08AI071998 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI HOHL, TOBIAS M · 2008 to 2010
$330k
NIAID NIH HHS R01 AI059663NIAID NIH HHS R01 AI067359NIAID NIH HHS R01 AI080619NIAID NIH HHS R01 AI67359NIAID NIH HHS R21 AI065745
6 · The paper itself

Abstract

Echinocandins target fungal beta-1,3 glucan synthesis and are used clinically to treat invasive aspergillosis. Although echinocandins do not completely inhibit in vitro growth of Aspergillus fumigatus, they do induce morphological changes in fungal hyphae. Because beta-1,3 glucans activate host antifungal pathways via the Dectin-1 receptor, we investigated the effect of echinocandins on inflammatory responses to A. fumigatus. Caspofungin- or micafungin-treated conidia and germlings induced less secretion of tumor necrosis factor (TNF) and CXCL2 by macrophages than did their untreated counterparts. Diminished secretion of TNF and CXCL2 correlated with diminished beta-glucan exposure on echinocandin-treated germ tubes. In contrast to treated conidia and germlings, echinocandin-treated hyphae stimulated increased release of TNF and CXCL2 by macrophages and demonstrated intense staining with a beta-glucan-specific antibody, particularly at hyphal tips. Our experiments demonstrate that echinocandin-induced morphological changes in A. fumigatus hyphae are accompanied by increased beta-glucan exposure, with consequent increases in Dectin-1-mediated inflammatory responses by macrophages.

Indexed as

Antifungal AgentsAspergillosisAspergillus fumigatusbeta-GlucansCandida albicansCaspofunginChemokine CXCL2EchinocandinsHumansInflammationLipopeptidesMicroscopy, ConfocalTumor Necrosis Factor-alphaAntifungal Agentsbeta-GlucansCaspofunginChemokine CXCL2EchinocandinsLipopeptidesTumor Necrosis Factor-alpha

Identifiers

PMID18500928
PMCPMC2587116
OpenAlexW2130778407

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.