Evidence map›Paper›PMID 28680905›Full record

ArticleOpen forum infectious diseases2017

High Cellular Monocyte Activation in People Living With Human Immunodeficiency Virus on Combination Antiretroviral Therapy and Lifestyle-Matched Controls Is Associated With Greater Inflammation in Cerebrospinal Fluid.

Thijs Booiman, Ferdinand W Wit, Irma Maurer, Davide De Francesco, Caroline A Sabin, Agnes M Harskamp, Maria Prins, Paolo Garagnani, Chiara Pirazzini, Claudio Franceschi and 6 more

Open access · goldAbstract read
In one paragraph

Article in Open forum infectious diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

23 citing papers in PubMed, 32 citations in OpenAlex.

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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

16 authors at 10 institutions in 5 countries.

Thijs BooimanDepartment of Experimental Immunology and.
Ferdinand W WitDepartment of Global Health and Division of Infectious Disease, Academic Medical Center, University of Amsterdam, Netherlands.
Irma MaurerDepartment of Experimental Immunology and.
Davide De FrancescoDepartment of Infection and Population Health, University College London, United Kingdom.
Caroline A SabinDepartment of Infection and Population Health, University College London, United Kingdom.
Agnes M HarskampDepartment of Experimental Immunology and.
Maria PrinsPublic Health Service, Amsterdam, Netherlands.
Paolo GaragnaniDepartment of Experimental, Diagnostic and Specialty Medicine, Alma Mater Studiorum Universita di Bologna, Italy.
Chiara PirazziniIstituto di Ricovero e Cura a Carattere Scientifico, Institute of Neurological Sciences of Bologna, Bellaria Hospital, Italy.
Claudio FranceschiDepartment of Experimental, Diagnostic and Specialty Medicine, Alma Mater Studiorum Universita di Bologna, Italy.
Dietmar FuchsDivision of Biological Chemistry, Biocenter Innsbruck Medical University Center for Chemistry and Biomedicine, Austria.
Magnus GisslénInstitute of Biomedicine, Department of Infectious Diseases, the Sahlgrenska Academy at the University of Gothenburg, Sweden.
Alan WinstonImperial College of Science, Technology and Medicine, London, United Kingdom.
Peter ReissDepartment of Global Health and Division of Infectious Disease, Academic Medical Center, University of Amsterdam, Netherlands.
Neeltje A KootstraDepartment of Experimental Immunology and.
Comorbidity in Relation to AIDS (COBRA) Collaboration
Amsterdam Institute for Global Health and Development · NLUniversity of Bologna · ITUniversity College London · GBImperial College London · GBUniversity of Gothenburg · SEGGD Amsterdam · NLInnsbruck Medical University · ATInstitute of Neurological Sciences · ITAcademic Medical Center · NLStichting HIV Monitoring · NL

Funding

Department of Health NIHR-RP-011-048
6 · The paper itself

Abstract

backgroundIncreased monocyte activation and intestinal damage have been shown to be predictive for the increased morbidity and mortality observed in treated people living with human immunodeficiency virus (PLHIV).

methodsA cross-sectional analysis of cellular and soluble markers of monocyte activation, coagulation, intestinal damage, and inflammation in plasma and cerebrospinal fluid (CSF) of PLHIV with suppressed plasma viremia on combination antiretroviral therapy and age and demographically comparable HIV-negative individuals participating in the Comorbidity in Relation to AIDS (COBRA) cohort and, where appropriate, age-matched blood bank donors (BBD).

resultsPeople living with HIV, HIV-negative individuals, and BBD had comparable percentages of classical, intermediate, and nonclassical monocytes. Expression of CD163, CD32, CD64, HLA-DR, CD38, CD40, CD86, CD91, CD11c, and CX3CR1 on monocytes did not differ between PLHIV and HIV-negative individuals, but it differed significantly from BBD. Principal component analysis revealed that 57.5% of PLHIV and 62.5% of HIV-negative individuals had a high monocyte activation profile compared with 2.9% of BBD. Cellular monocyte activation in the COBRA cohort was strongly associated with soluble markers of monocyte activation and inflammation in the CSF.

conclusionsPeople living with HIV and HIV-negative COBRA participants had high levels of cellular monocyte activation compared with age-matched BBD. High monocyte activation was predictive for inflammation in the CSF.

Indexed as

CSFHIVimmune activationinflammationmonocyte.

Identifiers

PMID28680905
PMCPMC5494939
OpenAlexW2619202492

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Registered trials

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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.