Evidence map›Paper›PMID 22028796›Full record

ArticlePloS one2011

Active and passive immunization with rHyr1p-N protects mice against hematogenously disseminated candidiasis.

Guanpingsheng Luo, Ashraf S Ibrahim, Samuel W French, John E Edwards, Yue Fu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

39 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Promising immunotherapeutic targets for treating candidiasis.Frontiers in cellular and infection microbiology · 2024
    Review
  11. Review
  12. Article
  13. Review
  14. bioRxiv : the preprint server for biology · 2023
    Article
  15. Article
  16. Review
  17. Antibodies targetingFrontiers in immunology · 2022
    Article
  18. Vaccines against candidiasis: Status, challenges and emerging opportunity.Frontiers in cellular and infection microbiology · 2022
    Review
  19. 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 1 country.

Guanpingsheng LuoDivision of Infectious Diseases, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California, United States of America.
Ashraf S Ibrahim
Samuel W French
John E Edwards
Yue Fu
UCLA Medical Center · USHarbor–UCLA Medical Center · US

Funding

Novel Toxins and Receptors in Mucormycosis Pathogenesis and TreatmentR01AI063503 · NIAID · LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER · PI IBRAHIM, ASHRAF S. · 2006 to 2025
$7.3M
Vaccine Strategies for Disseminated CandidiasisR01AI063382 · NIAID · LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER · PI EDWARDS, JOHN E · 2006 to 2017
$3.0M
CANDIDA ADHERENCE &PENETRATION--VASCULAR ENDOTHELIUMR01AI019990 · NIAID · LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER · PI EDWARDS, JOHN E · 1986 to 2009
$2.5M
An Ftr1 vaccine to abrogate mucormycosisR21AI082414 · NIAID · LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER · PI IBRAHIM, ASHRAF S. · 2010 to 2011
$386k
Functional Screening for Candida Virulence GPI-proteinsR21AI066010 · NIAID · LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER · PI FU, YUE · 2007 to 2008
$378k
Bcr1p as a candida neutrophil resistance regulatorR03AI083251 · NIAID · LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER · PI FU, YUE · 2009 to 2010
$141k
NIAID NIH HHS AI063382NIAID NIH HHS R01 AI019990NIAID NIH HHS R01 AI063382NIAID NIH HHS R01 AI063503NIAID NIH HHS R01 AI19990NIAID NIH HHS R03 AI083251NIAID NIH HHS R21 AI066010NIAID NIH HHS R21 AI082414
6 · The paper itself

Abstract

We previously reported that Candida albicans cell surface protein Hyr1 encodes a phagocyte killing resistance factor and active vaccination with a recombinant N-terminus of Hyr1 protein (rHyr1p-N), significantly protects immunocompetent mice from disseminated candidiasis. Here we report the marked efficacy of rHyr1p-N vaccine on improving the survival and reducing the fungal burden of disseminated candidiasis in both immunocompetent and immunocompromised mice using the FDA-approved adjuvant, alum. Importantly, we also show that pooled rabbit anti-Hyr1p polyclonal antibodies raised against 8 different peptide regions of rHyr1p-N protected mice in a hematogenously disseminated candidiasis model, raising the possibility of developing a successful passive immunotherapy strategy to treat this disease. Our data suggest that the rabbit anti-Hyr1p antibodies directly neutralized the Hyr1p virulence function, rather than enhanced opsonophagocytosis for subsequent killing by neutrophil in vitro. Finally, the rHyr1p-N vaccine was protective against non-albicans Candida spp. These preclinical data demonstrate that rHyr1p-N is likely to be a novel target for developing both active and passive immunization strategies against Candida infections.

Indexed as

Adjuvants, ImmunologicAlum CompoundsAmino Acid SequenceAnimalsAntibodies, FungalCandida albicansCandidiasisCross ReactionsFemaleFungal ProteinsFungal VaccinesImmunization, PassiveImmunocompetenceImmunocompromised HostMiceMice, Inbred BALB CAdjuvants, ImmunologicAlum Compoundsaluminum sulfateAntibodies, FungalFungal ProteinsFungal VaccinesHYR1 protein, Candida albicansPeptide FragmentsRecombinant Proteins

Identifiers

PMID22028796
PMCPMC3189951
OpenAlexW2076492225

What OpenQuestion holds

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LicenceCC BY
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.