Evidence map›Paper›PMID 8892897›Full record

ArticleJournal of virology1996

Intracellular expression of human immunodeficiency virus type 1 (HIV-1) protease variants inhibits replication of wild-type and protease inhibitor-resistant HIV-1 strains in human T-cell lines.

U Junker, S Escaich, I Plavec, J Baker, F McPhee, J R Rose, C S Craik, E Böhnlein

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-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

6 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Novel macromolecular inhibitors of human immunodeficiency virus-1 protease.Protein engineering, design & selection : PEDS · 2008
    Article
  3. Article
  4. Article
  5. Article
  6. 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 1 institution in 1 country.

U JunkerProgenesys Program at Systemix, Palo Alto, California 94304, USA.
S Escaich
I Plavec
J Baker
F McPhee
J R Rose
C S Craik
E Böhnlein
Genesys (United States) · US

Funding

SYNTHESIS, ENZYMOLOGY, AND DRUG DESIGNP01GM039552 · NIGMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI CRAIK, CHARLES SCOTT · 1987 to 1996
–
NIGMS NIH HHS GM 07175NIGMS NIH HHS GM39552
6 · The paper itself

Abstract

The enzymatic activity of the human immunodeficiency type 1 (HIV-1) protease (PR) is crucial to render HIV-1 virions mature and infectious. Hence, genetic intervention strategies based on trans-dominant (td) variants of the HIV-1 PR might be an alternative to current pharmacological and gene therapy regimens for AIDS. CD4-positive human CEM-SS T-cell lines were generated which constitutively expressed HIV-1 td PR variants. HIV-1 infection experiments demonstrated severely reduced HIV-1 replication in these td PR CEM-SS cell lines compared with control T cells expressing wild-type PR. Furthermore, replication of an HIV-1 isolate bearing a PR inhibitor-resistant PR was blocked, showing that genetic intervention strategies based on td PRs can be effective against HIV-1 isolates containing PR inhibitor-resistant mutants.

Indexed as

Genetic VariationVirus ReplicationCD4-Positive T-LymphocytesCell LineDrug Resistance, MicrobialGene ExpressionHIV-1HIV ProteaseHumansMethylurea CompoundsPlasmidsProtease InhibitorsPyridinesValineAbbott 77003HIV ProteaseMethylurea CompoundsProtease InhibitorsPyridinesValine

Identifiers

PMID8892897
PMCPMC190846
OpenAlexW2107807329

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.