Evidence map›Paper›PMID 10233914›Full record

ArticleJournal of virology1999

Redox and activation status of monocytes from human immunodeficiency virus-infected patients: relationship with viral load.

C Elbim, S Pillet, M H Prevost, A Preira, P M Girard, N Rogine, H Matusani, J Hakim, N Israel, M A Gougerot-Pocidalo

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

44 citing papers in PubMed, 118 citations in OpenAlex.

  1. Article
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  4. Single-cell analysis of CD14Frontiers in immunology · 2025
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  16. Redox-Modulating Agents in the Treatment of Viral Infections.International journal of molecular sciences · 2020
    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

10 authors at 4 institutions in 2 countries.

C ElbimINSERM U 479 and Service d'Immunologie et d'Hématologie, CHU Xavier Bichat, Paris, France.
S Pillet
M H Prevost
A Preira
P M Girard
N Rogine
H Matusani
J Hakim
N Israel
M A Gougerot-Pocidalo
Inserm · FRInstitut Pasteur · FRHôpital Rothschild · FRHôpital Xavier Arnozan · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monocytes are precursors of tissue macrophages, which are major targets of human immunodeficiency virus type 1 (HIV-1) infection. Although few blood monocytes are infected, their resulting activation could play a key role in the pathogenesis of HIV disease by modulating their transendothelial migration and inducing the production of reactive oxygen species (ROS). ROS participate in chronic inflammation, HIV replication, and the apoptosis of immune system cells seen in HIV-infected subjects. Published data on monocyte activation are controversial, possibly because most studies have involved monocytes isolated from their blood environment by various procedures that may alter cell responses. We therefore used flow cytometry to study, in whole blood, the activation and redox status of monocytes from HIV-infected patients at different stages of the disease. We studied the expression of adhesion molecules, actin polymerization, and cellular levels of H2O2, Bcl-2, and thioredoxin. Basal H2O2 production correlated with viral load and was further enhanced by bacterial N-formyl peptides and endotoxin. The enhanced H2O2 production by monocytes from asymptomatic untreated patients with CD4(+) cell counts above 500/microliter was associated with a decrease in the levels of Bcl-2 and thioredoxin. In contrast, in patients with AIDS, Bcl-2 levels returned to normal and thioredoxin levels were higher than in healthy controls. Restoration of these antioxidant and antiapoptotic molecules might explain, at least in part, why monocyte numbers remain relatively stable throughout the disease. Alterations of adhesion molecule expression and increased actin polymerization could play a role in transendothelial migration of these activated monocytes.

Indexed as

Drosophila ProteinsTranscription FactorsAdultDNA-Binding ProteinsFemaleHIV InfectionsHLA-DR AntigensHumansHydrogen PeroxideMacrophage-1 AntigenMaleMiddle AgedMonocytesOxidation-ReductionProto-Oncogene Proteins c-bcl-2Reactive Oxygen SpeciesDNA-Binding ProteinsDrosophila ProteinsHLA-DR AntigensHydrogen PeroxideMacrophage-1 AntigenProto-Oncogene Proteins c-bcl-2Reactive Oxygen SpeciesTranscription FactorsTrl protein, Drosophila

Identifiers

PMID10233914
PMCPMC112496
OpenAlexW2111732142

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.