Evidence map›Paper›PMID 8971011›Full record

ArticleJournal of virology1996

Intracellular expression of single-chain variable fragments to inhibit early stages of the viral life cycle by targeting human immunodeficiency virus type 1 integrase.

P Levy-Mintz, L Duan, H Zhang, B Hu, G Dornadula, M Zhu, J Kulkosky, D Bizub-Bender, A M Skalka, R J Pomerantz

Erratum issuedOpen 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. An erratum has been issued. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.6field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 114 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Engineering T Cells to Functionally Cure HIV-1 Infection.Molecular therapy : the journal of the American Society of Gene Therapy · 2015
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. HIV-1 IN inhibitors: 2010 update and perspectives.Current topics in medicinal chemistry · 2009
    Review
  14. Article
  15. Intracellular antibodies for proteomics.Journal of immunological methods · 2004
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

P Levy-MintzDivision of Infectious Diseases, Department of Medicine, Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.
L Duan
H Zhang
B Hu
G Dornadula
M Zhu
J Kulkosky
D Bizub-Bender
A M Skalka
R J Pomerantz
Thomas Jefferson University · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
INTRACELLULAR ANTIBODIES AND HIV 1R01AI036552 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI POMERANTZ, ROGER J · 1994 to 1997
–
RNA TUMOR VIRUS--DNA INTEGRATION/GENE EXPRESSION CONTROLR35CA047486 · NCI · INSTITUTE FOR CANCER RESEARCH · PI SKALKA, ANNA MARIE · 1990 to 1996
–
NCI NIH HHS CA06927NCI NIH HHS CA47486NIAID NIH HHS AI36552
6 · The paper itself

Abstract

Integration of viral DNA into a chromosome of the infected host cell is required for efficient replication of a retroviral genome, and this reaction is mediated by the virus-encoded enzyme integrase (IN). As IN plays a pivotal role in establishing infection during the early stages of the retroviral life cycle, it is an attractive target for therapeutic intervention. However, the lack of effective antiviral drug therapy against this enzyme has led to the testing of other novel approaches towards its inhibition. In these studies, a panel of anti-human immunodeficiency virus type 1 (anti-HIV-1) IN hybridomas has been used in the construction of single-chain variable antibody fragments (SFvs). The monoclonal antibodies produced by these hybridomas, and derived SFvs, bind to different domains within IN. We now demonstrate that intracellular expression of SFvs which bind to IN catalytic and carboxy-terminal domains results in resistance to productive HIV-1 infection. This inhibition of HIV-1 replication is observed with SFvs localized in either the cytoplasmic or nuclear compartment of the cell. The expression of anti-IN SFvs in human T-lymphocytic cells and peripheral blood mononuclear cells appears to specifically neutralize IN activity prior to integration and, thus, has an effect on the integration process itself. These data support our previous studies with an anti-HIV-1 reverse transcriptase SFv and demonstrate further that intracellularly expressed SFvs can gain access to viral proteins of the HIV-1 preintegration complex. This panel of anti-HIV-1 IN SFvs also provides the tools with which to dissect the molecular mechanism(s) directly involved in integration within HIV-1-infected cells.

Indexed as

Amino Acid SequenceAnimalsAntibodies, MonoclonalCell NucleusCloning, MolecularCytoplasmEscherichia coliGene ExpressionHIV-1HIV AntibodiesHIV IntegraseHumansImmunoglobulin GImmunoglobulin Variable RegionLeukocytes, MononuclearLymphocytesAntibodies, MonoclonalHIV AntibodiesHIV IntegraseImmunoglobulin GImmunoglobulin Variable Region

Identifiers

PMID8971011
PMCPMC190979
OpenAlexW2162994634

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.