Evidence map›Paper›PMID 25404522›Full record

ArticleThe Journal of infectious diseases2015

HIV Type 1 Disease Progression to AIDS and Death in a Rural Ugandan Cohort Is Primarily Dependent on Viral Load Despite Variable Subtype and T-Cell Immune Activation Levels.

Michael A Eller, Marc S Opollo, Michelle Liu, Andrew D Redd, Leigh Anne Eller, Cissy Kityo, Joshua Kayiwa, Oliver Laeyendecker, Maria J Wawer, Mark Milazzo and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-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

13 citing papers in PubMed, 27 citations in OpenAlex.

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  10. CD4 Cell Count: Declining Value for Antiretroviral Therapy Eligibility.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2016
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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

19 authors at 9 institutions in 3 countries.

Michael A EllerUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring Henry M. Jackson Foundation for the Advancement of Military Medicine.
Marc S OpolloMakerere University Walter Reed Project.
Michelle LiuUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring Henry M. Jackson Foundation for the Advancement of Military Medicine.
Andrew D ReddLaboratory of Immunoregulation, National Institute of Allergy and Infectious Disease, National Institutes of Health, Bethesda.
Leigh Anne EllerUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring Henry M. Jackson Foundation for the Advancement of Military Medicine.
Cissy KityoJoint Clinical Research Center.
Joshua KayiwaJoint Clinical Research Center.
Oliver LaeyendeckerLaboratory of Immunoregulation, National Institute of Allergy and Infectious Disease, National Institutes of Health, Bethesda School of Medicine.
Maria J WawerBloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland.
Mark MilazzoUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring Henry M. Jackson Foundation for the Advancement of Military Medicine.
Noah KiwanukaSchool of Public Health Rakai Health Sciences Program, Uganda Virus Research Institute, Entebbe.
Ronald H GrayBloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland.
David SerwaddaSchool of Public Health Rakai Health Sciences Program, Uganda Virus Research Institute, Entebbe.
Nelson K SewankamboFaculty of Medicine, Makerere University College of Health Sciences, Kampala Rakai Health Sciences Program, Uganda Virus Research Institute, Entebbe.
Thomas C QuinnLaboratory of Immunoregulation, National Institute of Allergy and Infectious Disease, National Institutes of Health, Bethesda School of Medicine.
Nelson L MichaelUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring.
Fred Wabwire-MangenMakerere University Walter Reed Project School of Public Health.
Johan K SandbergCenter for Infectious Medicine, Department of Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden.
Merlin L RobbUS Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring Henry M. Jackson Foundation for the Advancement of Military Medicine.
Henry M. Jackson Foundation · USJohns Hopkins University · USMakerere University Walter Reed Project · UGNational Institute of Allergy and Infectious Diseases · USUganda Virus Research Institute · UGWalter Reed Army Institute of Research · USIndiana University School of MedicineKarolinska University Hospital · SEMakerere University · UG

Funding

International Center for Excellence in Research (ICER) in Uganda: Impact of ARVsZIAAI001040 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI REYNOLDS, STEVEN · 2009 to 2025
$23.5M
International Studies of the Acquired Immune Deficiency Syndrome (AIDS)ZIAAI000361 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI REDD, ANDREW · 2009 to 2025
$15.8M
Intramural NIH HHS
6 · The paper itself

Abstract

backgroundUntreated human immunodeficiency virus type 1 (HIV) infection is associated with persistent immune activation, which is an independent driver of disease progression in European and United States cohorts. In Uganda, HIV-1 subtypes A and D and recombinant AD viruses predominate and exhibit differential rates of disease progression.

methodsHIV-1 seroconverters (n = 156) from rural Uganda were evaluated to assess the effects of T-cell activation, viral load, and viral subtype on disease progression during clinical follow-up.

resultsThe frequency of activated T cells was increased in HIV-1-infected Ugandans, compared with community matched uninfected individuals, but did not differ significantly between viral subtypes. Higher HIV-1 load, subtype D, older age, and high T-cell activation levels were associated with faster disease progression to AIDS or death. In a multivariate Cox regression analysis, HIV-1 load was the strongest predictor of progression, with subtype also contributing. T-cell activation did not emerge an independent predictor of disease progression from this particular cohort.

conclusionsThese findings suggest that the independent contribution of T-cell activation on morbidity and mortality observed in European and North American cohorts may not be directly translated to the HIV epidemic in East Africa. In this setting, HIV-1 load appears to be the primary determinant of disease progression.

Indexed as

Disease ProgressionViral LoadAdolescentAdultFemaleGenotypeHIV-1HIV InfectionsHumansLymphocyte ActivationMaleRural PopulationSurvival AnalysisT-LymphocytesUgandaYoung AdultAIDSHIV-1immune activationPD-1subtype Dviral load

Identifiers

PMID25404522
PMCPMC4425824
OpenAlexW2144284788

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.