Evidence map›Paper›PMID 19004620›Full record

ArticleJournal of dermatological science2009

Inflammatory papillomatous hyperplasia and epidermal necrosis in a transgenic rat for HIV-1.

Filiberto Cedeno-Laurent, Joseph Bryant, Rita Fishelevich, Odell D Jones, April Deng, Maria L Eng, Anthony A Gaspari, J Roberto Trujillo

Open access · greenAbstract read
In one paragraph

Article in Journal of dermatological science, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. New insights into HIV-1-primary skin disorders.Journal of the International AIDS Society · 2011
    Review
  4. Article
  5. 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

8 authors at 2 institutions in 2 countries.

Filiberto Cedeno-LaurentDivision of Basic Science, Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD 21201, USA. fcedeno@fas.harvard.edu
Joseph Bryant
Rita Fishelevich
Odell D Jones
April Deng
Maria L Eng
Anthony A Gaspari
J Roberto Trujillo
University of Maryland, Baltimore · USInstitute of Human Virology · NG

Funding

Keratinocyte Costimulation and Th2-Cell Immune DeviationR01AR050029 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI GASPARI, ANTHONY A · 2005 to 2009
$1.6M
NIAMS NIH HHS R01 AR050029
6 · The paper itself

Abstract

backgroundSkin lesions commonly affect AIDS patients. The pathogenesis of certain dermatologic disorders primarily associated to HIV-1 is unclear, and better forms of therapy for these conditions need to be discovered. Transgenic animal models represent a novel approach for the study of these disorders and for the quest of more effective forms of treatment.

objectiveCharacterize this HIV-1 transgenic rat as a model to study skin diseases related to HIV/AIDS.

methodsA transgenic rat was developed, using an HIV-1 construct with deleted gag and pol genes. Morphological and genotypical evaluations were followed by cytokine profile characterization of the lesions.

resultsWe report the characterization of a colony of HIV-1 transgenic rats that developed skin lesions in a frequency of 22.5%. Cutaneous expression of functional HIV-1 transgenes correlated precisely with the severity of the phenotype. In early stages, rats manifested localized areas of xerosis and dispersed papulosquamous lesions. These hyperplastic manifestations were observed in conjunction with an increased epidermal expression of tat protein and a Th1/Th2 profile of cytokines. As the lesions progressed, they formed inflammatory plaques that subsequently ulcerated. Histologically, these lesions displayed a profound lymphocytic infiltrate, epidermal necrosis, and a marked increase of both Th1 and Th2 derived cytokines. Moreover, the presence of circulating IgG antibodies against HIV-1 gp120 was detected.

conclusionThis animal model as other HIV-1 transgenic mice described in the past, is not able to fully explain the myriad of skin findings that can occur in HIV-infected humans; however, it represents a potential animal model system for the study of immune-mediated inflammatory skin diseases.

Indexed as

AnimalsCytokinesDermatitisDisease Models, AnimalEpidermisErythema MultiformeGenotypeHIV-1HIV AntibodiesHIV Envelope Protein gp120HIV InfectionsHyperplasiaNecrosisPhenotypeRatsRats, TransgenicCytokinesgp120 protein, Human immunodeficiency virus 1HIV AntibodiesHIV Envelope Protein gp120RNA, Messengertat Gene Products, Human Immunodeficiency Virus

Identifiers

PMID19004620
PMCPMC3125122
OpenAlexW2030566439

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.