Evidence map›Paper›PMID 19339948›Full record

ReviewCurrent opinion in HIV and AIDS2009

CCR5 monoclonal antibodies for HIV-1 therapy.

William C Olson, Jeffrey M Jacobson

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in HIV and AIDS, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

24 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Dual CCR5/CCR2 targeting: opportunities for the cure of complex disorders.Cellular and molecular life sciences : CMLS · 2019
    Review
  5. Current and Future Therapeutic Strategies for Lentiviral Eradication from Macrophage Reservoirs.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2019
    Review
  6. Review
  7. Development of Antibody Therapeutics against Flaviviruses.International journal of molecular sciences · 2017
    Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. HIV/AIDS: modified stem cells in the spotlight.Cellular and molecular life sciences : CMLS · 2014
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Pharmacological modulation of chemokine receptor function.British journal of pharmacology · 2012
    Review
  20. Natural anti-CCR5 antibodies in HIV-infection and -exposure.Journal of translational medicine · 2011
    Review
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 2 institutions in 1 country.

William C OlsonProgenics Pharmaceuticals Inc, Tarrytown, NY 10591, USA. olson@progenics.com
Jeffrey M Jacobson
Drexel University · USProgenics Pharmaceuticals (United States) · US

Funding

Viral Host And Combinational Influences on PRO 140U19AI066329 · NIAID · PROGENICS PHARMACEUTICALS, INC. · PI OLSON, WILLIAM C · 2005 to 2010
$10.6M
NIAID NIH HHS AI066329NIAID NIH HHS U19 AI066329
6 · The paper itself

Abstract

purpose of reviewTo summarize emerging clinical and preclinical data pertaining to the use of CCR5 monoclonal antibodies (mAbs) as therapies for HIV-1 infection. The epitope specificity of CCR5 mAbs is discussed in relation to its critical impact on antiviral activity and CCR5 antagonism. We compare and contrast mAbs and small-molecule CCR5 antagonists in terms of their binding and antiviral properties. Two CCR5 mAbs have entered clinical testing and have successfully completed proof-of-concept studies in HIV-infected individuals, providing initial information on the potential therapeutic utility of these agents. RECENT

findingsNew studies support the view that the most potent antiviral CCR5 mAbs recognize the second extracellular loop of CCR5 either exclusively or in combination with the amino terminus. Studies have revealed fundamental differences in how mAbs and small molecules bind CCR5 and inhibit HIV-1. CCR5 mAbs and small-molecule CCR5 antagonists have demonstrated consistent antiviral synergy and limited or no viral cross-resistance in independent studies. Single intravenous infusions of CCR5 mAbs significantly reduced HIV-1 RNA levels in infected individuals for 2-3 weeks without appreciable toxicity. SUMMARY: CCR5 mAbs have demonstrated broad and potent antiviral activity in vitro. Clinical studies have established CCR5 mAbs as potent antiretroviral agents with prolonged activity following a single dose. CCR5 mAbs represent both a distinct class of CCR5 inhibitor and a novel approach to HIV-1 therapy.

Indexed as

CCR5 Receptor AntagonistsAntibodies, MonoclonalAnti-HIV AgentsHIV InfectionsReceptors, CCR5Receptors, HIVTreatment OutcomeViral LoadAntibodies, MonoclonalAnti-HIV AgentsCCR5 Receptor AntagonistsReceptors, CCR5Receptors, HIV

Identifiers

PMID19339948
PMCPMC2760828
OpenAlexW2054587758

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.