Evidence map›Paper›PMID 18645523›Full record

ArticleJournal of acquired immune deficiency syndromes (1999)2008

In vitro characterization of multidrug-resistant HIV-1 isolates from a recently infected patient associated with dual tropism and rapid disease progression.

Hiroshi Mohri, Martin Markowitz

Abstract read
In one paragraph

Article in Journal of acquired immune deficiency syndromes (1999), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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  10. Clinical significance of HIV-1 coreceptor usage.Journal of translational medicine · 2011
    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

2 authors at 1 institution in 1 country.

Hiroshi MohriAaron Diamond AIDS Research Center, Rockefeller University, New York, NY 10016, USA.
Martin Markowitz
Aaron Diamond AIDS Research Center · US

Funding

WOUND HEALING IN INDIVIDUALS OF DIFFERENT AGE AND GENETIC BACKGROUNDM01RR000102 · NCRR · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 1985 to 2006
$32.8M
VIRAL AND IMMUNE CONSEQUENCES OF EARLY HIV1 THERAPYU01AI041534 · NIAID · AARON DIAMOND AIDS RESEARCH CENTER · PI MARKOWITZ, MARTIN H · 1997 to 2006
$10.1M
TRANSMISSION AND VIRAL DYMANICS OF DRUG RESISTANT HIV-1R01AI047033 · NIAID · AARON DIAMOND AIDS RESEARCH CENTER · PI MARKOWITZ, MARTIN H · 2000 to 2011
$6.0M
CORE--VIROLOGYP30AI042848 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HO, DAVID D · 1998 to 2002
$4.3M
NOVEL ASSAYS FOR MEASURING THE INHIBITION OF VIRUS ENTRYR44AI048990 · NIAID · MONOGRAM BIOSCIENCES, INC. · PI PETROPOULOS, CHRISTOS J · 2003 to 2005
$2.6M
NCRR NIH HHS M01 RR000102NCRR NIH HHS M01RR00102NIAID NIH HHS AI41534NIAID NIH HHS P30 AI042848NIAID NIH HHS P30-AI042848NIAID NIH HHS R01 AI047033NIAID NIH HHS R01-AI47033NIAID NIH HHS R44 AI048990NIAID NIH HHS R44-AI048990NIAID NIH HHS U01 AI041534
6 · The paper itself

Abstract

objectiveMultidrug-resistant (MDR) HIV-1 variants are thought to be less fit than wild-type virus. In 2005, we reported a case of transmitted MDR HIV-1 infection associated with dual tropism and rapid clinical progression. Here we report the in vitro characterization of the virus isolates.

methodsReplication characteristics of bulk and clonal isolates from this case (MDR-1) were examined and compared with these of a panel of transmitted MDR and wild-type (WT) viruses (MDR-2 approximately 4, WT-1, 2).

resultsInfectivity and frequency of infectious virion of propagated isolates were high in MDR-1 biological clones (mean titer, 3.5 x 10(5) TCID50/mL; mean frequency of infectious virion, 1/2444) and its bulk isolate (3.2 x 10(6) TCID50/mL; 1/301) as compared with the other biological clones (7.3 x 10(3) TCID50/mL; 1/21,320). Upslope (log10 p24/mL/d) of viral replication in peripheral blood mononuclear cell culture was much higher in MDR-1 clones (1.30 +/- 0.30: mean +/- SD) than those of MDR-2 approximately 4 (0.75 +/- 0.08) or WT-1, WT-2 clones (0.82 +/- 0.03). The bulk isolate and dual-tropic biological clones from MDR-1 depleted CD4+ T cells very rapidly in vitro compared with the other viruses tested.

conclusionsThese findings support the hypothesis that MDR HIV-1 can effectively evolve and compensate not only to retain high-level replication but also to exhibit virulence associated with rapid disease progression.

Indexed as

Drug Resistance, Multiple, ViralAnti-HIV AgentsCD4 Lymphocyte CountCD4-Positive T-LymphocytesCells, CulturedCytopathogenic Effect, ViralDisease ProgressionHIV-1HIV InfectionsHIV Protease InhibitorsHumansLeukocytes, MononuclearReverse Transcriptase InhibitorsViral LoadVirus ReplicationAnti-HIV AgentsHIV Protease InhibitorsReverse Transcriptase Inhibitors

Identifiers

PMID18645523
PMCPMC3725736
OpenAlexW2060181051

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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.