Evidence map›Paper›PMID 20048044›Full record

ArticleInfection and immunity2010

Cryptococcus neoformans variants generated by phenotypic switching differ in virulence through effects on macrophage activation.

A Guerrero, N Jain, X Wang, B C Fries

Abstract read
In one paragraph

Article in Infection and immunity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Similar evolutionary trajectories in an environmentalProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  4. Article
  5. Review
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  13. Article
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  16. Review
  17. Article
  18. Paradoxical roles of alveolar macrophages in the host response to Cryptococcus neoformans.Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy · 2012
    Review
  19. Regulatory circuitry governing fungal development, drug resistance, and disease.Microbiology and molecular biology reviews : MMBR · 2011
    Review
  20. Review
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

4 authors at 1 institution in 1 country.

A GuerreroDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
N Jain
X Wang
B C Fries
Albert Einstein College of Medicine · US

Funding

response to phenotypic switch variants to C. neoformansR01AI059681 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI FRIES, BETTINA · 2004 to 2014
$3.6M
NIAID NIH HHS R01 AI059681NIAID NIH HHS R01 AI059681-05
6 · The paper itself

Abstract

Macrophages have a central role in the pathogenesis of cryptococcosis since they are an important line of defense, serve as a site for fungal replication, and also can contribute to tissue damage. The objective of this study was to investigate the interaction of macrophages with cells from smooth-colony variants (SM) and mucoid-colony variants (MC) arising from phenotypic switching of Cryptococcus neoformans. Alveolar macrophages (AMs) isolated from SM- and MC-infected mice exhibited differences in gene and surface expression of PD-L1, PD-L2, and major histocompatibility class II (MHC-II). PD-L1 and PD-L2 are the ligands for PD1 and are differentially regulated in Th1- and Th2-type cells. In addition, macrophage activation in SM- and MC-infected mice was characterized as alternatively activated. Flow cytometric and cytokine analysis demonstrated that MC infection was associated with the emergence of Th17 cells and higher levels of interleukin-17 (IL-17) in lung tissue, which were reduced by AM depletion. In conclusion, our results indicate that macrophages play a significant role in maintaining damage-promoting inflammation in the lung during MC infection, which ultimately results in death.

Indexed as

Macrophage ActivationAnimalsB7-1 AntigenB7-H1 AntigenCryptococcus neoformansGene Expression ProfilingHistocompatibility Antigens Class IIMacrophages, AlveolarMembrane GlycoproteinsMiceMice, Inbred BALB CMice, Inbred C57BLPeptidesPhenotypeProgrammed Cell Death 1 Ligand 2 ProteinVirulenceB7-1 AntigenB7-H1 AntigenCd274 protein, mouseHistocompatibility Antigens Class IIMembrane GlycoproteinsPdcd1lg2 protein, mousePeptidesProgrammed Cell Death 1 Ligand 2 Protein

Identifiers

PMID20048044
PMCPMC2825907
OpenAlexW2152394793

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.