Evidence map›Paper›PMID 19786539›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

CD8+ cell depletion of SHIV89.6P-infected macaques induces CD4+ T cell proliferation that contributes to increased viral loads.

Yvonne M Mueller, Duc H Do, Jean D Boyer, Muhamuda Kader, Joseph J Mattapallil, Mark G Lewis, David B Weiner, Peter D Katsikis

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

22 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  4. Article
  5. CD8Nature communications · 2023
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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

8 authors at 4 institutions in 1 country.

Yvonne M MuellerDepartment of Microbiology and Immunology, and Center for Immunology and Vaccine Sciences, Drexel University College of Medicine, Philadelphia, PA 19129, USA.
Duc H Do
Jean D Boyer
Muhamuda Kader
Joseph J Mattapallil
Mark G Lewis
David B Weiner
Peter D Katsikis
Drexel University · USUniformed Services University of the Health Sciences · USUniversity of Pennsylvania · USBioqual · US

Funding

IN VITRO STIMULATION OF HIV SPECIFIC CD8+ T CELLSR01AI046719 · NIAID · UNIVERSITY OF LOUISVILLE · PI KATSIKIS, PETER D · 1999 to 2010
$2.8M
IL-15 treatment of SIV-infected non-human primatesR01AI062437 · NIAID · DREXEL UNIVERSITY · PI KATSIKIS, PETER D · 2005 to 2008
$2.1M
Mucosal Epithelium and Long-Term Anti-Retroviral TherapyR21DE018339 · NIDCR · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI MATTAPALLIL, JOSEPH JOHN · 2007 to 2008
$673k
In vitro stimulation of HIV specific CD8+ T cellsR56AI046719 · NIAID · DREXEL UNIVERSITY · PI KATSIKIS, PETER D · 2005 to 2005
$375k
CD4 T cells and anti-viral control in SIV infectionK22AI071812 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI MATTAPALLIL, JOSEPH JOHN · 2007 to 2008
$270k
NIAID NIH HHS K22 AI071812NIAID NIH HHS K22 AI07812NIAID NIH HHS R01 AI046719NIAID NIH HHS R01 AI062437NIAID NIH HHS R01 AI46719NIAID NIH HHS R01 AI62437NIAID NIH HHS R56 AI046719NIDCR NIH HHS R21 DE018339PHS HHS R01 A1-071886
6 · The paper itself

Abstract

Previous studies have shown that depletion of CD8(+) cells during acute and chronic simian immunodeficiency virus (SIV) infection leads to increased viral replication, morbidity, and mortality, which have been attributed to loss of CD8(+) T cell-mediated control of SIV. However, these studies did not exclude that CD8(+) cell depletion increased homeostatic proliferation of CD4(+) T cells, resulting in increased viral targets and, therefore, viral rebound. Chronically SHIV89.6P-infected cynomolgus macaques were CD8(+) cell-depleted, and the frequency, cell number, and phenotype of CD4(+) T cells and viral infection were examined using flow cytometry and quantitative real-time PCR. The frequency and number of Ki-67-expressing CD4(+) T cells were increased with CD8(+) cell depletion. This proliferation of CD4(+) T cells occurred even in animals with no rebound of viral loads. Most of the proliferating cells were effector memory CD4(+) T cells. Plasma simian HIV (SHIV) RNA copies positively correlated with proliferating CD4(+) T cells and SHIV DNA copies in Ki-67(+) CD4(+) T cells. Although this study does not exclude an important role for virus-specific CD8(+) T cells in SIV and SHIV infection, our data suggest that homeostatic proliferation is an important contributor to increases in plasma viremia that follow CD8(+) cell depletion.

Indexed as

Lymphocyte DepletionSimian Immunodeficiency VirusAnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesKi-67 AntigenMacaca fascicularisSimian Acquired Immunodeficiency SyndromeViral LoadKi-67 Antigen

Identifiers

PMID19786539
PMCPMC2757467
OpenAlexW2111866704

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.