Evidence map›Paper›PMID 21422177›Full record

ArticleInfection and immunity2011

CD4+ T cells mediate the protective effect of the recombinant Asp f3-based anti-aspergillosis vaccine.

Diana Diaz-Arevalo, Karine Bagramyan, Teresa B Hong, James I Ito, Markus Kalkum

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Roles of theJournal of fungi (Basel, Switzerland) · 2025
    Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. TheMicrobiology spectrum · 2022
    Article
  8. Depletion of CD8Transboundary and emerging diseases · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Advances in Fungal Peptide Vaccines.Journal of fungi (Basel, Switzerland) · 2020
    Review
  14. Linear Epitopes ofFrontiers in immunology · 2017
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. BioResearch open access · 2016
    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 3 institutions in 1 country.

Diana Diaz-ArevaloCity of Hope, Beckman Research Institute, Department of Immunology, 1500 East Duarte Road, Duarte, CA 91010-3000, USA.
Karine Bagramyan
Teresa B Hong
James I Ito
Markus Kalkum
Beckman Research InstituteCity of Hope · USOffice of Infectious Diseases · US

Funding

Signal-amplifying biomarkers for the diagnosis of invasive fungal infections.R21AI075230 · NIAID · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI KALKUM, MARKUS · 2007 to 2008
$456k
NIAID NIH HHS AI075230-01NIAID NIH HHS R21 AI075230
6 · The paper itself

Abstract

The mortality and morbidity caused by invasive aspergillosis present a major obstacle to the successful treatment of blood cancers with hematopoietic cell transplants. Patients who receive hematopoietic cell transplants are usually immunosuppressed for extended periods, and infection with the ubiquitous mold Aspergillus fumigatus is responsible for most cases of aspergillosis. Previously, we demonstrated that vaccination with recombinant forms of the A. fumigatus protein Asp f3 protected cortisone acetate-immunosuppressed mice from experimentally induced pulmonary aspergillosis. Here, we investigated the vaccine's protective mechanism and evaluated in particular the roles of antibodies and T cells. After vaccination, Asp f3-specific preinfection IgG titers did not significantly differ between surviving and nonsurviving mice, and passive transfer of anti-Asp f3 antibodies did not protect immunosuppressed recipients from aspergillosis. We experimentally confirmed Asp f3's predicted peroxisomal localization in A. fumigatus hyphae. We found that fungal Asp f3 is inaccessible to antibodies, unless both cell walls and membranes have been permeabilized. Antibody-induced depletion of CD4+ T cells reduced the survival of recombinant Asp f3 (rAsp f3)-vaccinated mice to nonimmune levels, and transplantation of purified CD4+ T cells from rAsp f3-vaccinated mice into nonimmunized recipients transferred antifungal protection. In addition, residues 60 to 79 and 75 to 94 of Asp f3 contain epitopes that induce proliferation of T cells from vaccinated survivors. Vaccine-primed CD4+ T cells are not expected to clear the fungal pathogen directly; however, they may locally activate immunosuppressed phagocytes that elicit the antifungal effect.

Indexed as

AllergensAnimalsAntibodies, FungalAntigens, PlantAspergillosisAspergillus fumigatusCD4-Positive T-LymphocytesFemaleFungal VaccinesLymphocyte ActivationMiceRabbitsVaccines, SyntheticAllergensAntibodies, FungalAntigens, PlantAsp f 3 allergenFungal VaccinesVaccines, Synthetic

Identifiers

PMID21422177
PMCPMC3125823
OpenAlexW2129795013

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.