Evidence map›Paper›PMID 20001854›Full record

ArticleThe Journal of infectious diseases2010

Immunologic and virologic events in early HIV infection predict subsequent rate of progression.

Anuradha Ganesan, Pratip K Chattopadhyay, Tess M Brodie, Jing Qin, Wenjuan Gu, John R Mascola, Nelson L Michael, Dean A Follmann, Mario Roederer, Infectious Disease Clinical Research Program HIV Working Group

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

47 citing papers in PubMed, 85 citations in OpenAlex.

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  9. Malignancy and viral infections in Sub-Saharan Africa: A review.Frontiers in virology (Lausanne, Switzerland) · 2023
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  13. Naive CD4+ T Cells Harbor a Large Inducible Reservoir of Latent, Replication-competent Human Immunodeficiency Virus Type 1.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2019
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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.

Anuradha GanesanNational Naval Medical Center, Infectious Disease Clinical Research Program, Uniformed Services University, Bethesda, Maryland 20892, USA.
Pratip K Chattopadhyay
Tess M Brodie
Jing Qin
Wenjuan Gu
John R Mascola
Nelson L Michael
Dean A Follmann
Mario Roederer
Infectious Disease Clinical Research Program HIV Working Group
National Institute of Allergy and Infectious Diseases · USMilitary University · RUScience Applications International Corporation (United States) · USWalter Reed National Military Medical Center · US

Funding

Functional And Phenotypic Characterization Of T Cells In ManZIAAI005021 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI ROEDERER, MARIO · 2009 to 2022
$14.4M
CCR NIH HHS HHSN261200800001CIntramural NIH HHS Z99 AI999999Intramural NIH HHS ZIA AI005021NCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

backgroundVariability in human immunodeficiency virus (HIV) disease progression cannot be fully predicted by CD4(+) T cell counts or viral load (VL). Because central memory T (T(CM)) cells play a critical role in the pathogenesis of simian immunodeficiency virus disease, we hypothesized that quantifying these cells in early HIV infection could provide prognostic information.

methodsWe measured expression of CD45RO, chemokine (C-C motif) receptor (CCR) 5, CCR7, CD27, and CD28 to enumerate naive and memory subsets in samples from recently infected individuals. We also quantified proliferation, CD127 expression, and cell-associated VL. Disease progression was compared across subgroups defined by these measurements, using Kaplan-Meier survival curves and multivariate Cox proportional hazards regression.

resultsFour hundred sixty-six subjects contributed 101 events. The proportion or absolute count of T(CM) cells did not correlate with disease progression, defined as the time to AIDS or death. However, significant associations were observed for proliferation within CD4(+) or CD8(+) T cells, loss of naive or CD127(+) memory CD8(+) T cells, and CD4(+) T cell-associated VL.

conclusionsOur results demonstrate that the extent of the immunopathogenesis established early in HIV infection predicts the course of future disease. Because antiretroviral drug treatment reverses such defects in part, our study provides mechanistic clues to why early use of antiretrovirals may prove beneficial.

Indexed as

Immunologic MemoryAcquired Immunodeficiency SyndromeAdolescentAdultAnti-Retroviral AgentsCD28 AntigensDisease ProgressionDrug Administration ScheduleFemaleHIV InfectionsHumansKaplan-Meier EstimateLeukocyte Common AntigensMaleMiddle AgedProportional Hazards ModelsAnti-Retroviral AgentsCCR7 protein, humanCD28 AntigensLeukocyte Common AntigensReceptors, CCR5Receptors, CCR7Tumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID20001854
PMCPMC2939466
OpenAlexW2156364173

What OpenQuestion holds

Textmetadata
LicenceTDM
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.