Evidence map›Paper›PMID 27799218›Full record

ArticleAntimicrobial agents and chemotherapy2017

TLR7 Agonist GS-9620 Is a Potent Inhibitor of Acute HIV-1 Infection in Human Peripheral Blood Mononuclear Cells.

Rujuta A Bam, Derek Hansen, Alivelu Irrinki, Andrew Mulato, Gregg S Jones, Joseph Hesselgesser, Christian R Frey, Tomas Cihlar, Stephen R Yant

Open access · hybridAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

36 citing papers in PubMed, 58 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Short-Course Toll-Like Receptor 9 Agonist Treatment Impacts Innate Immunity and Plasma Viremia in Individuals With Human Immunodeficiency Virus Infection.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2017
    Trial
  4. Article
  5. Article
  6. Article
  7. Synthesis and Optimization of 1-Substituted Imidazo[4,5-ACS medicinal chemistry letters · 2023
    Article
  8. Article
  9. Article
  10. Review
  11. Self-assembling peptides as immunomodulatory biomaterials.Frontiers in bioengineering and biotechnology · 2023
    Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
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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

9 authors at 1 institution in 1 country.

Rujuta A BamDepartment of Biology, Gilead Sciences, Inc., Foster City, California, USA.
Derek HansenDepartment of Biology, Gilead Sciences, Inc., Foster City, California, USA.
Alivelu IrrinkiDepartment of Biology, Gilead Sciences, Inc., Foster City, California, USA.
Andrew MulatoDepartment of Biology, Gilead Sciences, Inc., Foster City, California, USA.
Gregg S JonesDepartment of Biology, Gilead Sciences, Inc., Foster City, California, USA.
Joseph HesselgesserDepartment of Biology, Gilead Sciences, Inc., Foster City, California, USA.
Christian R FreyDepartment of Biology, Gilead Sciences, Inc., Foster City, California, USA.
Tomas CihlarDepartment of Biology, Gilead Sciences, Inc., Foster City, California, USA.
Stephen R YantDepartment of Biology, Gilead Sciences, Inc., Foster City, California, USA stephen.yant@gilead.com.
Gilead Sciences (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GS-9620 is a potent and selective oral Toll-like receptor 7 (TLR7) agonist that directly activates plasmacytoid dendritic cells (pDCs). GS-9620 suppressed hepatitis B virus (HBV) in animal models of chronic infection and transiently activated HIV expression ex vivo in latently infected peripheral blood mononuclear cells (PBMCs) from virally suppressed patients. Currently, GS-9620 is under clinical evaluation for treating chronic HBV infection and for reducing latent reservoirs in virally suppressed HIV-infected patients. Here, we investigated the in vitro anti-HIV-1 activity of GS-9620. GS-9620 potently inhibited viral replication in PBMCs, particularly when it was added 24 to 48 h prior to HIV infection (50% effective concentration = 27 nM). Depletion of pDCs but not other immune cell subsets from PBMC cultures suppressed GS-9620 antiviral activity. Although GS-9620 was inactive against HIV in purified CD4

Indexed as

AntibodiesAntiviral AgentsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesHIV-1HIV InfectionsHumansInterferon-alphaInterferonsInterleukin-6Leukocytes, MononuclearMacrophagesPteridinesToll-Like Receptor 7Virus ReplicationAntibodiesAntiviral AgentsInterferon-alphaInterferonsInterleukin-6PteridinesToll-Like Receptor 7vesatolimodantiviral agentsGS-9620human immunodeficiency virusinterferonsTLR7

Identifiers

PMID27799218
PMCPMC5192112
OpenAlexW2545020953

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.