Evidence map›Paper›PMID 28069805›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

Different Lymphocyte Populations Direct Dichotomous Eosinophil or Neutrophil Responses to Pulmonary Cryptococcus Infection.

Darin L Wiesner, Kyle D Smith, Sakeen W Kashem, Paul R Bohjanen, Kirsten Nielsen

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 40 citations in OpenAlex.

  1. Trial
  2. Article
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  6. Article
  7. Inbred Mouse Models inJournal of fungi (Basel, Switzerland) · 2024
    Review
  8. Article
  9. Review
  10. Article
  11. Immunity to fungi in the lung.Seminars in immunology · 2023
    Review
  12. Article
  13. Adaptive immunology ofFrontiers in immunology · 2023
    Review
  14. Article
  15. Article
  16. Use of Clinical Isolates to Establish Criteria for a Mouse Model of LatentFrontiers in cellular and infection microbiology · 2021
    Article
  17. Article
  18. Article
  19. Animal Models ofFrontiers in immunology · 2020
    Review
  20. Article
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

5 authors at 2 institutions in 2 countries.

Darin L WiesnerDepartment of Microbiology and Immunology, University of Minnesota, Minneapolis, MN 55455.
Kyle D SmithDepartment of Microbiology and Immunology, University of Minnesota, Minneapolis, MN 55455.
Sakeen W KashemCenter for Immunology, University of Minnesota, Minneapolis, MN 55455; and.
Paul R BohjanenDepartment of Microbiology and Immunology, University of Minnesota, Minneapolis, MN 55455.
Kirsten NielsenDepartment of Microbiology and Immunology, University of Minnesota, Minneapolis, MN 55455; knielsen@umn.edu.
University of Minnesota · USInstitute of Infection and Immunity · CA

Funding

University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR000114 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$35.0M
IMMUNOLOGY TRAINING PROGRAMT32AI007313 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Carla Rothlin · 1989 to 2026
$5.7M
Pheromones and Titan Cell Production in Cryptococcus neoformansR01AI080275 · NIAID · UNIVERSITY OF MINNESOTA · PI NIELSEN, KIRSTEN · 2011 to 2015
$1.8M
Outcomes of Cryptococcal Meningitis in UgandaK24AI096925 · NIAID · UNIVERSITY OF MINNESOTA · PI BOHJANEN, PAUL R · 2011 to 2015
$1.0M
Control of cryptococcal infection through manipulation of the host immune response.R21AI122352 · NIAID · UNIVERSITY OF MINNESOTA · PI NIELSEN, KIRSTEN · 2016 to 2017
$419k
NCATS NIH HHS UL1 TR000114NIAID NIH HHS K24 AI096925NIAID NIH HHS R01 AI080275NIAID NIH HHS R21 AI122352NIAID NIH HHS T32 AI007313
6 · The paper itself

Abstract

Many pulmonary infections elicit lymphocyte responses that lead to an accumulation of granulocytes in the lungs. A variety of lymphocytes are capable of directing eosinophils or neutrophils to the lungs, but the contribution of each subset remains enigmatic. In this study, we used a murine model to examine lymphocyte subsets that ultimately drive the eosinophil or neutrophil response to infection with the fungal pathogen Cryptococcus neoformans. We show that granulocytes are produced in the bone marrow, released into the blood stream, and accumulate in the lungs under the instruction of lung parenchymal lymphocytes. The eosinophils that populated the lungs of wild-type animals were highly dependent on Th cells or IL-5. Surprisingly, infected mice with Th cell impairment experienced a compensatory neutrophil response that required IL-17A. This unexpected swing in the response prompted us to investigate the ability of different lymphocyte subsets to produce this dichotomous eosinophilia or neutrophilia. We used mice with lymphocyte deficiencies to determine which of the remaining IL-5- or IL-17A-producing lymphocyte subsets dominated the neutrophil or eosinophil response. Finally, skewing the response toward neutrophil-inducing lymphocytes correlated with accelerated disease. Our data collectively demonstrate that the predominance of a lymphocyte subset determines the functional consequences of an immune response to pulmonary fungal infection that can ultimately affect disease.

Indexed as

AnimalsBone Marrow CellsCryptococcosisCryptococcus neoformansDisease Models, AnimalEosinophiliaEosinophilsInterleukin-17Interleukin-5LungLung Diseases, FungalLymphocyte SubsetsMiceNeutrophilsInterleukin-17Interleukin-5

Identifiers

PMID28069805
PMCPMC5296217
OpenAlexW2575644119

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.