Evidence map›Paper›PMID 29677122›Full record

ReviewViruses2018

Applications of the FIV Model to Study HIV Pathogenesis.

Craig Miller, Zaid Abdo, Aaron Ericsson, John Elder, Sue VandeWoude

Open access · goldAbstract readReview
In one paragraph

Review in Viruses, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
1.9field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 31 citations in OpenAlex.

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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 4 institutions in 1 country.

Craig MillerDepartment of Veterinary Pathobiology, Oklahoma State University, Stillwater, OK 74078, USA. craig.miller@okstate.edu.ORCID 0000-0002-3638-5665
Zaid AbdoDepartment of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, CO 80523, USA. Zaid.Abdo@colostate.edu.
Aaron EricssonDepartment of Veterinary Pathobiology, University of Missouri, Columbia, MO 65201, USA. EricssonA@missouri.edu.
John ElderDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA 92037, USA. jelder@scripps.edu.
Sue VandeWoudeDepartment of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, CO 80523, USA. Sue.Vandewoude@colostate.edu.
Colorado State University · USOklahoma State University · USScripps Research Institute · USUniversity of Missouri · US

Funding

Biomedical Research Training for VeterinariansT32OD010437 · OD · COLORADO STATE UNIVERSITY · PI Gregg A Dean, KELLY S SANTANGELO · 2012 to 2026
$6.2M
MOLECULAR CHARACTERIZATION OF FIVR01AI025825 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI ELDER, JOHN H · 1987 to 2015
$6.0M
Impact of gut microbiota and segmented filamentous bacteria on colitis-associated colorectal cancerK01OD019924 · OD · UNIVERSITY OF MISSOURI-COLUMBIA · PI ERICSSON, AARON · 2016 to 2020
$573k
FIV as a model to study pathogenesis and treatment of HIV-induced oral disease in childrenF32DE026679 · NIDCR · COLORADO STATE UNIVERSITY · PI MILLER, CRAIG ANDREW · 2016 to 2017
$105k
NIAID NIH HHS R01 AI025825NIDCR NIH HHS F32 DE026679NIH HHS K01 OD019924NIH HHS T32 OD010437
6 · The paper itself

Abstract

Feline immunodeficiency virus (FIV) is a naturally-occurring retrovirus that infects domestic and non-domestic feline species, producing progressive immune depletion that results in an acquired immunodeficiency syndrome (AIDS). Much has been learned about FIV since it was first described in 1987, particularly in regard to its application as a model to study the closely related lentivirus, human immunodeficiency virus (HIV). In particular, FIV and HIV share remarkable structure and sequence organization, utilize parallel modes of receptor-mediated entry, and result in a similar spectrum of immunodeficiency-related diseases due to analogous modes of immune dysfunction. This review summarizes current knowledge of FIV infection kinetics and the mechanisms of immune dysfunction in relation to opportunistic disease, specifically in regard to studying HIV pathogenesis. Furthermore, we present data that highlight changes in the oral microbiota and oral immune system during FIV infection, and outline the potential for the feline model of oral AIDS manifestations to elucidate pathogenic mechanisms of HIV-induced oral disease. Finally, we discuss advances in molecular biology, vaccine development, neurologic dysfunction, and the ability to apply pharmacologic interventions and sophisticated imaging technologies to study experimental and naturally occurring FIV, which provide an excellent, but often overlooked, resource for advancing therapies and the management of HIV/AIDS.

Indexed as

AnimalsCatsDisease Models, AnimalFeline Acquired Immunodeficiency SyndromeHIVHIV InfectionsHumansImmunodeficiency Virus, FelineViral VaccinesViral Vaccinesanimal modelsfeline immunodeficiency virusFIVHIVhuman immunodeficiency viruslentiviral pathogenesismolecular biologyopportunistic disease

Identifiers

PMID29677122
PMCPMC5923500
OpenAlexW2796906322

What OpenQuestion holds

Textmetadata
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.