Evidence map›Paper›PMID 21502083›Full record

Trial reportThe Journal of infectious diseases2011

Valganciclovir reduces T cell activation in HIV-infected individuals with incomplete CD4+ T cell recovery on antiretroviral therapy.

Peter W Hunt, Jeffrey N Martin, Elizabeth Sinclair, Lorrie Epling, Juli Teague, Mark A Jacobson, Russell P Tracy, Lawrence Corey, Steven G Deeks

2 registry-linked trialsOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 210 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
210citing papers in PubMed, 3 pooled it
19.4field-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.

NCT00264290 phase4completednot on this map

Valganciclovir to Reduce T Cell Activation in HIV Infection

TypeinterventionalSponsorUniversity of California, San FranciscoRan2006 to 2008Enrolled30ConditionsHIV Infections, Cytomegalovirus InfectionsArmsValganciclovir, Placebo
NCT06626555 phase2not yet recruitingnot on this mapstarted 2024, after this paper: background citation

Pilot, Randomized, Open-Label, Non-Active Comparator Controlled Clinical Trial to Evaluate the Effects of Letermovir Prophylaxis on T-cell Immune Activation in Participants With Treated HIV-1 Infection

TypeinterventionalSponsorUniversity College, LondonRan2024 to 2026Enrolled36ConditionsHIVArmsLetermovir
3 · Its place in the literature

Who cites it

210 citing papers in PubMed, 3 syntheses or guidelines pooled it, 343 citations in OpenAlex.

  1. Pooled it
  2. Adjunct Therapy for CD4Frontiers in immunology · 2021
    Pooled it
  3. Pooled it
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  5. Randomized Trial of Ruxolitinib in Antiretroviral-Treated Adults With Human Immunodeficiency Virus.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
    Trial
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  9. Effects of Fish Oil on HIV-Related Inflammation and Markers of Immunosenescence: A Randomized Clinical Trial.Journal of alternative and complementary medicine (New York, N.Y.) · 2018
    Trial
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150 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 1 country.

Peter W HuntDepartment of Medicine, University of California, San Francisco, USA. phunt@php.ucsf.edu
Jeffrey N Martin
Elizabeth Sinclair
Lorrie Epling
Juli Teague
Mark A Jacobson
Russell P Tracy
Lawrence Corey
Steven G Deeks
University of California, San Francisco · USUniversity of Vermont · USUniversity of Washington · US

Funding

UCSF CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTEUL1RR024131 · NCRR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JOHNSTON, S. CLAIBORNE · 2006 to 2011
$111.2M
Virology CoreP30AI027763 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI STEVEN Grant DEEKS · 1988 to 2026
$93.6M
Ujima Mentoring ProgramP30MH062246 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Sheri Ann Lippman · 2001 to 2026
$57.4M
UCSF-GIVI CENTER FOR AIDS RESEARCHP30MH059037 · NIMH · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI VOLBERDING, PAUL A · 1998 to 2001
$4.9M
The Determinants of T Cell Activation in HIV InfectionK23AI065244 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HUNT, PETER W · 2005 to 2009
$716k
Treatment Intensification for Drug-Resistant HIVR21AI055273 · NIAID · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI DEEKS, STEVEN GRANT · 2003 to 2004
$454k
NCRR NIH HHS UL1 RR024131NIAID NIH HHS AI055273NIAID NIH HHS AI065244NIAID NIH HHS K23 AI065244NIAID NIH HHS P30 AI027763NIAID NIH HHS P30 AI27763NIAID NIH HHS R21 AI055273NIMH NIH HHS P30 MH059037NIMH NIH HHS P30 MH062246NIMH NIH HHS P30 MH59037NIMH NIH HHS P30 MH62246
6 · The paper itself

Abstract

backgroundElevated immune activation persists during treated human immunodeficiency virus (HIV) infection and is associated with blunted CD4 recovery and premature mortality, but its causes remain incompletely characterized. We hypothesized that asymptomatic cytomegalovirus (CMV) replication might contribute to immune activation in this setting.

methodsThirty antiretroviral therapy-treated HIV-infected CMV-seropositive participants with CD4 counts <350 cells/mm(3) were randomized to receive valganciclovir 900 mg daily or placebo for 8 weeks, followed by an additional 4-week observation period. The primary outcome was the week 8 change in percentage of activated (CD38(+) HLA-DR(+)) CD8(+) T cells.

resultsFourteen participants were randomized to valganciclovir and 16 to placebo. Most participants (21 [70%] of 30) had plasma HIV RNA levels <75 copies/mL. The median CD4 count was 190 (IQR: 134-232) cells/mm(3), and 12 (40%) of 30 had detectable CMV DNA in saliva, plasma, or semen at baseline. CMV DNA continued to be detectable at weeks 4-12 in 7 (44%) of 16 placebo-treated participants, but in none of the valganciclovir-treated participants (P = .007). Valganciclovir-treated participants had significantly greater reductions in CD8 activation at weeks 8 (P = .03) and 12 (P = .02) than did placebo-treated participants. These trends were significant even among those with undetectable plasma HIV RNA levels.

conclusionsCMV (and/or other herpesvirus) replication is a significant cause of immune activation in HIV-infected individuals with incomplete antiretroviral therapy-mediated CD4(+) T cell recovery. CLINICAL TRIALS REGISTRATION: NCT00264290.

Indexed as

Anti-HIV AgentsCD4-Positive T-LymphocytesCytomegalovirusCytomegalovirus InfectionsDNA, ViralGanciclovirHIV InfectionsHumansLymphocyte ActivationSalivaSemenValganciclovirVirus ReplicationAnti-HIV AgentsDNA, ViralGanciclovirValganciclovir

Identifiers

PMID21502083
PMCPMC3080892
OpenAlexW2159360702

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.