Evidence map›Paper›PMID 26076730›Full record

ArticleHuman gene therapy2015

Preclinical Assessment of Mutant Human TRIM5α as an Anti-HIV-1 Transgene.

Ulrike Jung, Kevin Urak, Maxime Veillette, Marie-Édith Nepveu-Traversy, Quang Toan Pham, Sophie Hamel, John J Rossi, Lionel Berthoux

Open access · greenAbstract read
In one paragraph

Article in Human gene therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Restriction of HIV-1 and other retroviruses by TRIM5.Nature reviews. Microbiology · 2019
    Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Stem cell-based therapies for HIV/AIDS.Advanced drug delivery reviews · 2016
    Review
  14. Review
  15. Review
  16. 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 3 institutions in 2 countries.

Ulrike Jung1 Division of Molecular & Cell Biology, Beckman Research Institute of the City of Hope , Duarte, California.
Kevin Urak1 Division of Molecular & Cell Biology, Beckman Research Institute of the City of Hope , Duarte, California.
Maxime Veillette2 Laboratory of Retrovirology, Department of Medical Biology, Université du Québec, Trois-Rivières, Canada.
Marie-Édith Nepveu-Traversy2 Laboratory of Retrovirology, Department of Medical Biology, Université du Québec, Trois-Rivières, Canada.
Quang Toan Pham2 Laboratory of Retrovirology, Department of Medical Biology, Université du Québec, Trois-Rivières, Canada.
Sophie Hamel2 Laboratory of Retrovirology, Department of Medical Biology, Université du Québec, Trois-Rivières, Canada.
John J Rossi1 Division of Molecular & Cell Biology, Beckman Research Institute of the City of Hope , Duarte, California.
Lionel Berthoux2 Laboratory of Retrovirology, Department of Medical Biology, Université du Québec, Trois-Rivières, Canada.
Université du Québec à Trois-Rivières · CABeckman Research InstituteCity of Hope · US

Funding

YEAST SYSTEM FOR DEVELOPING ANTI-HIV-1 RIBOZYMESR01AI029329 · NIAID · LOMA LINDA UNIVERSITY · PI ROSSI, JOHN JOSEPH · 1990 to 2018
$3.9M
Canadian Institutes of Health Research MOP-102712NIAID NIH HHS R01 AI029329PHS HHS 5R1A1042552
6 · The paper itself

Abstract

Current HIV-1 gene therapy approaches aim at stopping the viral life cycle at its earliest steps, such as entry or immediate postentry events. Among the most widely adopted strategies are CCR5 downregulation/knockout and the use of broadly neutralizing antibodies. However, the long-term efficacy and side effects are still unclear. TRIM5α is an interferon-stimulated restriction factor that can intercept incoming retroviruses within one hour of cytosolic entry and potently inhibit the infectivity of restriction-sensitive viruses. The human TRIM5α (TRIM5αhu) generally does not efficiently target HIV-1, but point mutations in its capsid-binding domain can confer anti-HIV-1 activity. Although the mechanisms by which TRIM5αhu mutants inhibit HIV-1 are relatively well understood, their characterization as potential transgenes for gene therapy is lacking. Additionally, previous reports of general immune activation by overexpression of TRIM5α have hindered its broad adoption as a potential transgene. Here we demonstrate the ability of the R332G-R335G TRIM5αhu mutant to efficiently restrict highly divergent HIV-1 strains, including Group O, as well as clinical isolates bearing cytotoxic T lymphocyte escape mutations. R332G-R335G TRIM5αhu efficiently protected human lymphocytes against HIV-1 infection, even when expressed at relatively low levels following lentiviral transduction. Most importantly, under these conditions Rhesus macaque TRIM5α (TRIM5αRh) and TRIM5αhu (wild-type or mutated) had no major effects on the NF-κB pathway. Transgenic TRIM5α did not modulate the kinetics of IκBα, JunB, and TNFAIP3 expression following TNF-α treatment. Finally, we show that human lymphocytes expressing R332G-R335G TRIM5αhu have clear survival advantages over unmodified parental cells in the presence of pathogenic, replication-competent HIV-1. These results support the relevance of R332G-R335G and other mutants of TRIM5αhu as candidate effectors for HIV-1 gene therapy.

Indexed as

Genetic TherapyAnimalsAntiviral Restriction FactorsCarrier ProteinsHIV-1HIV InfectionsHumansLentivirusLymphocytesMacaca mulattaMutant ProteinsMutationProtein BindingTransgenesTripartite Motif ProteinsUbiquitin-Protein LigasesAntiviral Restriction FactorsCarrier ProteinsMutant ProteinsTRIM5 protein, humanTripartite Motif ProteinsUbiquitin-Protein Ligases

Identifiers

PMID26076730
PMCPMC4630796
OpenAlexW1715606990

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.