Evidence map›Paper›PMID 19487479›Full record

ArticleInfection and immunity2009

A genetically engineered live attenuated vaccine of Coccidioides posadasii protects BALB/c mice against coccidioidomycosis.

Jianmin Xue, Xia Chen, Dale Selby, Chiung-Yu Hung, Jieh-Juen Yu, Garry T Cole

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

83 citing papers in PubMed, 103 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Drug Discovery and Repurposing forJournal of fungi (Basel, Switzerland) · 2025
    Review
  7. Article
  8. Early immune response toMicrobiology spectrum · 2025
    Article
  9. Article
  10. Article
  11. From soil to clinic: current advances in understandingMicrobiology and molecular biology reviews : MMBR · 2024
    Review
  12. Article
  13. Article
  14. The Host Response to Coccidioidomycosis.Journal of fungi (Basel, Switzerland) · 2024
    Review
  15. Article
  16. Host tracheal and intestinal microbiomes inhibitbioRxiv : the preprint server for biology · 2023
    Article
  17. Review
  18. Review
  19. Article
  20. Coccidioides Species: A Review of Basic Research: 2022.Journal of fungi (Basel, Switzerland) · 2022
    Review

23 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Jianmin XueDepartment of Biology and South Texas Center for Emerging Infectious Diseases, University of Texas, San Antonio, 78249, USA.
Xia Chen
Dale Selby
Chiung-Yu Hung
Jieh-Juen Yu
Garry T Cole
Texas Center for Infectious Disease · USWilford Hall Medical Center · US

Funding

A Recombinant Protein Vaccine Against CoccidioidomycosisR01AI071118 · NIAID · UNIVERSITY OF TEXAS SAN ANTONIO · PI COLE, GARRY THOMAS · 2008 to 2012
$1.8M
NIAID NIH HHS AI071118NIAID NIH HHS R01 AI071118
6 · The paper itself

Abstract

Coccidioidomycosis (also known as San Joaquin Valley fever) is an occupational disease. Workers exposed to outdoor dust which contains spores of the soil-inhabiting fungus have a significantly increased risk of respiratory infection. In addition, people with compromised T-cell immunity, the elderly, and certain racial groups, particularly African-Americans and Filipinos, who live in regions of endemicity in the southwestern United States have an elevated incidence of symptomatic infection caused by inhalation of spores of Coccidioides posadasii or Coccidioides immitis. Recurring epidemics and escalation of medical costs have helped to motivate production of a vaccine against valley fever. The major focus has been the development of a defined, T-cell-reactive, recombinant protein vaccine. However, none of the products described to date have provided full protection to coccidioidal disease-susceptible BALB/c mice. Here we describe the first genetically engineered, live, attenuated vaccine that protects both BALB/c and C57BL/6 mice against coccidioidomycosis. Two chitinase genes (CTS2 and CTS3) were disrupted to yield the attenuated strain, which was unable to endosporulate and was no longer infectious. Vaccinated survivors mounted an immune response characterized by production of both T-helper-1- and T-helper-2-type cytokines. Histology revealed well-formed granulomas and markedly diminished inflammation. Significantly fewer organisms were observed in the lungs of survivors than in those of nonvaccinated mice. Additional investigations are required to further define the nature of the live, attenuated vaccine-induced immunity against Coccidioides infection.

Indexed as

AnimalsChitinasesCoccidioidesCoccidioidomycosisColony Count, MicrobialCytokinesDNA, FungalFungal ProteinsFungal VaccinesGene Knockout TechniquesGene OrderHumansLungMiceMice, Inbred BALB CMice, Inbred C57BLChitinasesCytokinesDNA, FungalFungal ProteinsFungal VaccinesVaccines, Attenuated

Identifiers

PMID19487479
PMCPMC2715678
OpenAlexW2127573804

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.