Evidence map›Paper›PMID 19843977›Full record

ReviewAntiviral chemistry & chemotherapy2009

Antiretroviral therapy in macrophages: implication for HIV eradication.

Christina Gavegnano, Raymond F Schinazi

Abstract readReview
In one paragraph

Review in Antiviral chemistry & chemotherapy, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

60 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Induction of a NaAutophagy · 2018
    Article
  17. Review
  18. Article
  19. Review
  20. 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

2 authors at 1 institution in 1 country.

Christina GavegnanoCenter for AIDS Research, Laboratory of Biochemical Pharmacology, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Raymond F Schinazi
Emory University · US

Funding

Virology and Molecular Biomarkers CoreP30AI050409 · NIAID · EMORY UNIVERSITY · PI Carlos del Rio · 2002 to 2026
$74.0M
Synthesis and Biotransformation of Anti-HIV ProdrugsR37AI025899 · NIAID · UNIVERSITY OF GEORGIA (UGA) · PI CHU, CHUNG K · 2001 to 2010
$4.4M
Rational Design of NRTI for Drug Resistant HIV-1R01AI071846 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MELLORS, JOHN W · 2007 to 2010
$2.9M
Primate Model Towards HIV Eradication StrategiesR01RR025996 · NCRR · UNIVERSITY OF CALIFORNIA AT DAVIS · PI NORTH, THOMAS W, SCHINAZI, RAYMOND FELIX · 2009 to 2011
$2.2M
NUCLEOSIDES WITH DUAL ANTI-HIV AND HBV ACTIVITYR37AI041980 · NIAID · EMORY UNIVERSITY · PI SCHINAZI, RAYMOND FELIX · 2000 to 2009
$2.1M
Primate Model Towards HIV Eradication StrategiesR01OD011094 · OD · EMORY UNIVERSITY · PI NORTH, THOMAS W, SCHINAZI, RAYMOND FELIX · 2012 to 2012
$706k
NCRR NIH HHS 1R01-RR0-25996NCRR NIH HHS R01 RR025996NCRR NIH HHS R01-RR-25996NIAID NIH HHS 2P30-AI-50409NIAID NIH HHS 5R01-AI-071846NIAID NIH HHS 5R37-AI-025899NIAID NIH HHS 5R37-AI-041980NIAID NIH HHS P30 AI050409NIAID NIH HHS R01 AI071846NIAID NIH HHS R37 AI025899NIAID NIH HHS R37 AI041980NIH HHS R01 OD011094
6 · The paper itself

Abstract

HIV type-1 (HIV-1) accounts for more than 25 million deaths and nearly 40 million people are infected worldwide. A significant obstacle in clearing virus from infected individuals is latently infected viral reservoirs. Latent HIV-1 can emerge with recrudescence as a productive infection later in disease progression and could provide a source for the emergence of resistant HIV-1. It is widely recognized that macrophages represent a latently infected viral reservoir and are a significant and critical HIV-1 target cell in vivo. Macrophages can be divided into multiple subsets of macrophage-like cells, all of which are susceptible to HIV-1 infection, including dendritic cells, Langerhans cells, alveolar macrophages, mucosal macrophages and microglial cells. Current antiretroviral therapy (ART) often displays differential antiviral activity in macrophages relative to CD4(+) T-lymphocytes. Significant work has been performed to establish antiviral activity of many clinically approved ART in macrophages; however, a direct link between antiviral activity and specific mechanisms responsible for these antiviral effects are incompletely understood. This review identifies many understudied areas of research, along with topics for further research in the field of HIV therapy and eradication. Discussion focuses upon the known cellular pharmacology and antiviral activity of antiretroviral agents in macrophages and its relationship to latency, chronic HIV-1 infection and therapeutic strategies to eradicate systemic HIV-1 infection.

Indexed as

Anti-Retroviral AgentsHIV InfectionsHumansMacrophagesMononuclear Phagocyte SystemAnti-Retroviral Agents

Identifiers

PMID19843977
PMCPMC2978531
OpenAlexW2082211638

What OpenQuestion holds

Textmetadata
LicenceTDM
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.