Evidence map›Paper›PMID 15731219›Full record

ArticleJournal of virology2005

Signature for long-term vaccine-mediated control of a Simian and human immunodeficiency virus 89.6P challenge: stable low-breadth and low-frequency T-cell response capable of coproducing gamma interferon and interleukin-2.

Shanmugalakshmi Sadagopal, Rama Rao Amara, David C Montefiori, Linda S Wyatt, Silvija I Staprans, Natalia L Kozyr, Harold M McClure, Bernard Moss, Harriet L Robinson

Abstract read
In one paragraph

Article in Journal of virology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Article
  6. HIV-1 sub-type C chimaeric VLPs boost cellular immune responses in mice.Journal of immune based therapies and vaccines · 2010
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. DNA vaccines for HIV: challenges and opportunities.Springer seminars in immunopathology · 2006
    Review
  17. Review
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.

Shanmugalakshmi SadagopalYerkes National Primate Research Center of Emory University, 954 Gatewood Dr., Atlanta, GA 30329, USA.
Rama Rao Amara
David C Montefiori
Linda S Wyatt
Silvija I Staprans
Natalia L Kozyr
Harold M McClure
Bernard Moss
Harriet L Robinson

Funding

YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI ALTMAN, JOHN DAVID · 1985 to 2011
$114.0M
Recombinant Virus VaccinesZIAAI000416 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MOSS, BERNARD · 2009 to 2025
$17.3M
PROTEIN IMMUNOGENSP01AI043045 · NIAID · EMORY UNIVERSITY · PI ROBINSON, HARRIET L · 1998 to 2003
$5.6M
Recombinant Vaccines for Prevention of AIDS and Other DiseasesZ01AI000416 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI MOSS, BERNARD · 1985 to 2008
$3.3M
CORE--VIROLOGY FACILITYP30DA012121 · NIDA · EMORY UNIVERSITY · PI COMPANS, RICHARD W · 1998 to 2001
$1.8M
NCRR NIH HHS P51 RR000165NIAID NIH HHS P01 AI043045NIAID NIH HHS P01-AI43045NIDA NIH HHS P30 DA12121
6 · The paper itself

Abstract

In 2001, we reported 20 weeks of control of challenge with the virulent 89.6P chimera of simian and human immunodeficiency viruses (SHIV-89.6P) by a Gag-Pol-Env vaccine consisting of DNA priming and modified vaccinia virus Ankara boosting. Here we report that 22 out of 23 of these animals successfully controlled their viremia until their time of euthanasia at 200 weeks postchallenge. At euthanasia, all animals had low to undetectable viral loads and normal CD4 counts. During the long period of viral control, gamma interferon (IFN-gamma)-producing antiviral T cells were present at unexpectedly low breadths and frequencies. Most animals recognized two CD8 and one CD4 epitope and had frequencies of IFN-gamma-responding T cells from 0.01 to 0.3% of total CD8 or CD4 T cells. T-cell responses were remarkably stable over time and, unlike responses in most immunodeficiency virus infections, maintained good functional characteristics, as evidenced by coproduction of IFN-gamma and interleukin-2. Overall, high titers of binding and neutralizing antibody persisted throughout the postchallenge period. Encouragingly, long-term control was effective in macaques of diverse histocompatibility types.

Indexed as

AIDS VaccinesAnimalsCD4 Lymphocyte CountDisease Models, AnimalEpitopesGene Products, envGene Products, gagGene Products, polHIVInterferon-gammaInterleukin-2MacacaRNA, ViralSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusT-LymphocytesAIDS VaccinesEpitopesGene Products, envGene Products, gagGene Products, polInterferon-gammaInterleukin-2RNA, ViralVaccines, DNA

Identifiers

PMID15731219
PMCPMC1075739

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.