Evidence map›Paper›PMID 27737952›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2017

Persistent, Albeit Reduced, Chronic Inflammation in Persons Starting Antiretroviral Therapy in Acute HIV Infection.

Irini Sereti, Shelly J Krebs, Nittaya Phanuphak, James L Fletcher, Bonnie Slike, Suteeraporn Pinyakorn, Robert J O'Connell, Adam Rupert, Nicolas Chomont, Victor Valcour and 7 more

Open access · greenAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 171 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
171citing papers in PubMed, 1 pooled it
25.9field-weighted citation impact, top 1% 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

171 citing papers in PubMed, 1 synthesis or guideline pooled it, 258 citations in OpenAlex.

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  8. Lower Pretreatment Gut Integrity Is Independently Associated With Fat Gain on Antiretroviral Therapy.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2019
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111 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 9 institutions in 3 countries.

Irini SeretiLaboratory of Immunoregulation.
Shelly J KrebsThe Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda.
Nittaya PhanuphakSEARCH, Thai Red Cross AIDS Research Center.
James L FletcherSEARCH, Thai Red Cross AIDS Research Center.
Bonnie SlikeThe Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda.
Suteeraporn PinyakornThe Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda.
Robert J O'ConnellThe Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda.
Adam RupertAIDS Monitoring Laboratory, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, Maryland.
Nicolas ChomontCentre de Recherche du CHUM and Department of Microbiology, Infectiology and Immunology, Université de Montréal, Quebec, Canada.
Victor ValcourDepartment of Neurology, University of California San Francisco Memory and Aging Center, Sandler Neurosciences Center.
Jerome H KimThe Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda.
Merlin L RobbThe Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda.
Nelson L MichaelThe Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda.
Daniel C DouekVaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health.
Jintanat AnanworanichThe Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda.
Netanya S UtayDepartment of Internal Medicine, Division of Infectious Diseases, University of Texas Medical Branch at Galveston neutay@utmb.edu.
RV254/SEARCH 010, RV304/SEARCH 013 and SEARCH 011 protocol teams
Walter Reed Army Institute of Research · USThai Red Cross Society · THArmed Forces Research Institute of Medical Science · THCentre Hospitalier de l’Université de Montréal · CAHenry M. Jackson Foundation · USLeidos (United States) · USNational Institute of Allergy and Infectious Diseases · USThe University of Texas Medical Branch at Galveston · USUniversity of California, San Francisco · US

Funding

Immunopathogenic Mechanisms of Human Immunodeficiency Virus (HIV) DiseaseZIAAI001121 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI SERETI, IRINI · 2010 to 2025
$27.2M
Peripheral Reservoir of HIV DNA in Monocytes Pivotal to Cognition in HIVR01NS061696 · NINDS · UNIVERSITY OF HAWAII AT MANOA · PI VALCOUR, VICTOR · 2008 to 2012
$3.2M
Long-Term CNS Consequences of Treatment During Acute InfectionR01MH095613 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SPUDICH, SERENA S, VALCOUR, VICTOR · 2011 to 2015
$3.1M
NIMH NIH HHS R01 MH095613NINDS NIH HHS R01 NS061696
6 · The paper itself

Abstract

backgroundSerious non-AIDS events cause substantial disease and death despite human immunodeficiency virus (HIV) suppression with antiretroviral therapy (ART). Biomarkers of inflammation, coagulation cascade activation, and fibrosis predict these end-organ events. We aimed to determine whether ART initiation during acute HIV infection would attenuate changes in these biomarker levels.

methodsPlasma samples were obtained from participants starting ART during acute or chronic HIV infection and from HIV-uninfected participants from Bangkok, Thailand. Biomarkers of inflammation (C-reactive protein [CRP], interleukin 6, soluble interleukin 6 receptor [sIL-6R], soluble gp130, tumor necrosis factor [TNF]), enterocyte turnover (intestinal fatty acid binding protein [I-FABP]), lipopolysaccharide-induced monocyte activation (soluble CD14 [sCD14]), coagulation cascade activation [D-dimer], and fibrosis (hyaluronic acid [HA]) were measured at baseline and through 96 weeks of ART.

resultsCRP, TNF, sIL-6R, I-FABP, sCD14, D-dimer, and HA levels were elevated in acute HIV infection. Early ART was associated with increased I-FABP levels but normalization of TNF, sIL-6R, and D-dimer levels. CRP, sCD14, and HA levels decreased during ART but remained elevated compared with HIV-uninfected participants. Higher sCD14, CRP, and D-dimer levels were associated with higher peripheral blood mononuclear cell and gut integrated HIV DNA levels. Decreases in sCD14 and CRP levels were correlated with increases in CD4 T-cell counts.

conclusionsART initiated in early acute HIV infection was associated with normalization of the coagulation cascade and several systemic inflammatory biomarkers, but the acute-phase response, enterocyte turnover, monocyte activation, and fibrosis biomarkers remained elevated. Additional interventions to attenuate inflammation may be needed to optimize clinical outcomes in persons with HIV infection.

Indexed as

AdultAntiretroviral Therapy, Highly ActiveBiomarkersBlood CoagulationCD4 Lymphocyte CountFemaleFibrosisGastrointestinal MicrobiomeHIV InfectionsHumansInflammationInflammation MediatorsIntestinal MucosaMalePermeabilityViral LoadBiomarkersInflammation Mediatorsacute HIV infectionantiretroviral therapyinflammationmonocyte activationsIL-6R

Identifiers

PMID27737952
PMCPMC5215214
OpenAlexW2531567355

What OpenQuestion holds

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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.