Evidence map›Paper›PMID 21757617›Full record

ArticleBlood2011

IL-15 delays suppression and fails to promote immune reconstitution in virally suppressed chronically SIV-infected macaques.

Enrico Lugli, Yvonne M Mueller, Mark G Lewis, Francois Villinger, Peter D Katsikis, Mario Roederer

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

37 citing papers in PubMed, 48 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Two subsets of stem-like CD8Nature immunology · 2020
    Article
  10. Article
  11. Review
  12. CXCR3 Identifies Human Naive CD8Journal of immunology (Baltimore, Md. : 1950) · 2019
    Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. CD16Blood advances · 2018
    Article
  18. Progress in achieving long-term HIV remission.Current opinion in HIV and AIDS · 2018
    Review
  19. Article
  20. Article
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

6 authors at 5 institutions in 1 country.

Enrico LugliImmunoTechnology Section, Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Yvonne M Mueller
Mark G Lewis
Francois Villinger
Peter D Katsikis
Mario Roederer
Drexel University · USBioqual · USEmory National Primate Research CenterNational Institute of Allergy and Infectious Diseases · USNational Institutes of Health · US

Funding

RESOURCE FOR NONHUMAN PRIMATE IMMUNE REAGENTSR24RR016988 · NCRR · EMORY UNIVERSITY · PI VILLINGER, FRANCOIS J · 2002 to 2011
$3.6M
T Cell Dynamics In SIV-infected MacaquesZIAAI005019 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI ROEDERER, MARIO · 2009 to 2014
$3.5M
IN VITRO STIMULATION OF HIV SPECIFIC CD8+ T CELLSR01AI046719 · NIAID · UNIVERSITY OF LOUISVILLE · PI KATSIKIS, PETER D · 1999 to 2010
$2.8M
Phosphorothioate Oligonucleotides as Microbicides against HIV TransmissionR21AI082680 · NIAID · DREXEL UNIVERSITY · PI KATSIKIS, PETER D · 2010 to 2011
$414k
Intramural NIH HHSNCRR NIH HHS R24 RR016988NCRR NIH HHS R24RR016988NIAID NIH HHS R01 AI046719NIAID NIH HHS R21 AI082680
6 · The paper itself

Abstract

Human immunodeficiency virus (HIV) infection is characterized by a progressive loss of memory CD4(+) T cells in multiple tissues, especially at mucosal surfaces where most of these cells reside. Although antiretroviral therapy (ART) suppresses viral replication and promotes the recovery of peripheral CD4(+) T cells, HIV-infected patients fail to fully reconstitute the CD4(+) T-cell pool at mucosal sites. IL-15 has been shown to preferentially expand memory-phenotype T cells and promote their migration to nonlymphoid tissues. Here we examined IL-15 treatment in combination with highly active ART in chronically SIV-infected rhesus macaques and found that IL-15 delayed viral suppression and failed to enhance ART-induced total and antigen-specific CD4(+) T-cell reconstitution at mucosal and lymphoid sites. IL-15 was able to induce the transient proliferation of SIV-specific, CMV-specific, and total memory CD8(+) T cells, but not of SIV-specific or total CD4(+) T cells. Moreover, upon treatment interruption, macaques receiving combined IL-15+ART lost CD4(+) T cells faster than those receiving ART alone. These results suggest that the combination of IL-15 with highly active ART is not more efficient than ART alone in promoting CD4(+) T-cell recovery in HIV-infected individuals and may accelerate CD4+ T-cell loss after treatment interruption.

Indexed as

Adaptive ImmunityAdenineAnimalsAnti-Retroviral AgentsAntiretroviral Therapy, Highly ActiveCD4 Lymphocyte CountCD4-Positive T-LymphocytesDeoxycytidineDrug Evaluation, PreclinicalDrug Therapy, CombinationEmtricitabineImmunity, MucosalImmunologic FactorsImmunotherapyInterleukin-15Lymphocyte ActivationAdenineAnti-Retroviral AgentsDeoxycytidineEmtricitabineImmunologic FactorsInterleukin-15OrganophosphonatesPyrrolidinonesRaltegravir PotassiumTenofovir

Identifiers

PMID21757617
PMCPMC3167360
OpenAlexW2086608172

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.