Evidence map›Paper›PMID 9621031›Full record

ArticleJournal of virology1998

Rabbit cells expressing human CD4 and human CCR5 are highly permissive for human immunodeficiency virus type 1 infection.

R F Speck, M L Penn, J Wimmer, U Esser, B F Hague, T J Kindt, R E Atchison, M A Goldsmith

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. The wide utility of rabbits as models of human diseases.Experimental & molecular medicine · 2018
    Review
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  18. HIV type-1 infection of the cotton rat (Sigmodon fulviventer and S. hispidus).Proceedings of the National Academy of Sciences of the United States of America · 1998
    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 4 institutions in 2 countries.

R F SpeckGladstone Institute of Virology and Immunology, University of California, San Francisco, California 94141-9100, USA.
M L Penn
J Wimmer
U Esser
B F Hague
T J Kindt
R E Atchison
M A Goldsmith
Institute of Virology of the Slovak Academy of Sciences · SKNational Institute of Allergy and Infectious Diseases · USNational Institutes of Health · USUniversity of California, San Francisco · US

Funding

NEF GENE OF HIV1R01AI028240 · NIAID · J. DAVID GLADSTONE INSTITUTES · PI GREENE, WARNER C · 1989 to 1999
–
TRANSGENIC RABBITS--A NOVEL ANIMAL MODEL FOR HIV DISEASER21AI042654 · NIAID · J. DAVID GLADSTONE INSTITUTES · PI GOLDSMITH, MARK A · 1997 to 1999
–
NIAID NIH HHS AI28240-09S1NIAID NIH HHS AI42654-01
6 · The paper itself

Abstract

To evaluate the feasibility of using transgenic rabbits expressing CCR5 and CD4 as a small-animal model of human immunodeficiency virus type 1 (HIV) disease, we examined whether the expression of the human chemokine receptor (CCR5) and human CD4 would render a rabbit cell line (SIRC) permissive to HIV replication. Histologically, SIRC cells expressing CD4 and CCR5 formed multinucleated cells (syncytia) upon exposure to BaL, a macrophagetropic strain of HIV that uses CCR5 for cell entry. Intracellular viral capsid p24 staining showed abundant viral gene expression in BaL-infected SIRC cells expressing CD4 and CCR5. In contrast, neither SIRC cells expressing CD4 alone nor murine 3T3 cells expressing CCR5 and CD4 exhibited significant expression of p24. These stably transfected rabbit cells were also highly permissive for the production of virions upon infection by two other CCR5-dependent strains (JR-CSF and YU-2) but not by a CXCR4-dependent strain (NL4-3). The functional integrity of these virions was demonstrated by the successful infection of human peripheral blood mononuclear cells (PBMC) with viral stocks prepared from these transfected rabbit cells. Furthermore, primary rabbit PBMC were found to be permissive for production of infectious virions after circumventing the cellular entry step. These results suggest that a transgenic rabbit model for the study of HIV disease may be feasible.

Indexed as

AnimalsCD4 AntigensElectroporationGene Products, nefGene Products, revGene Products, tatGenes, ViralHeLa CellsHIV-1HumansMicenef Gene Products, Human Immunodeficiency VirusRabbitsReceptors, CCR5rev Gene Products, Human Immunodeficiency Virustat Gene Products, Human Immunodeficiency VirusCD4 AntigensGene Products, nefGene Products, revGene Products, tatnef Gene Products, Human Immunodeficiency VirusReceptors, CCR5rev Gene Products, Human Immunodeficiency Virustat Gene Products, Human Immunodeficiency Virus

Identifiers

PMID9621031
PMCPMC110246
OpenAlexW2105214575

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.