Evidence map›Paper›PMID 18000037›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Protection against simian/human immunodeficiency virus (SHIV) 89.6P in macaques after coimmunization with SHIV antigen and IL-15 plasmid.

Jean D Boyer, Tara M Robinson, Michele A Kutzler, Gordon Vansant, David A Hokey, Sanjeev Kumar, Rose Parkinson, Ling Wu, Maninder K Sidhu, George N Pavlakis and 8 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

57 citing papers in PubMed, 87 citations in OpenAlex.

  1. Trial
  2. Review
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  5. Review
  6. Therapeutic Vaccines for the Treatment of HIV.Translational research : the journal of laboratory and clinical medicine · 2020
    Review
  7. Article
  8. Article
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  11. Review
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  18. Article
  19. The current state of tuberculosis vaccines.Human vaccines & immunotherapeutics · 2013
    Review
  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

18 authors at 6 institutions in 1 country.

Jean D BoyerDepartment of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, 422 Curie Boulevard, Philadelphia, PA 19104, USA.
Tara M Robinson
Michele A Kutzler
Gordon Vansant
David A Hokey
Sanjeev Kumar
Rose Parkinson
Ling Wu
Maninder K Sidhu
George N Pavlakis
Barbara K Felber
Charles Brown
Peter Silvera
Mark G Lewis
Joseph Monforte
Thomas A Waldmann
John Eldridge
David B Weiner
University of Pennsylvania · USNational Cancer Institute · USGenomatica (United States) · USBioqual · USNational Institute of Allergy and Infectious Diseases · USSouthern Research Institute · US

Funding

Pathophysiology of Primary Effusion LymphomaK08AI050010 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI WHELAN, JOHN PATRICK · 2002 to 2006
$601k
Intramural NIH HHSNIAID NIH HHS N01 AI050010NIAID NIH HHS N01-AI-50010PHS HHS P01-A1-071739PHS HHS R01-A1-071186
6 · The paper itself

Abstract

The cell-mediated immune profile induced by a recombinant DNA vaccine was assessed in the simian/HIV (SHIV) and macaque model. The vaccine strategy included coimmunization of a DNA-based vaccine alone or in combination with an optimized plasmid encoding macaque IL-15 (pmacIL-15). We observed strong induction of vaccine-specific IFN-gamma-producing CD8(+) and CD4(+) effector T cells in the vaccination groups. Animals were subsequently challenged with 89.6p. The vaccine groups were protected from ongoing infection, and the IL-15 covaccinated group showed a more rapidly controlled infection than the group treated with DNA vaccine alone. Lymphocytes isolated from the group covaccinated with pmacIL-15 had higher cellular proliferative responses than lymphocytes isolated from the macaques that received SHIV DNA alone. Vaccine antigen activation of lymphocytes was also studied for a series of immunological molecules. Although mRNA for IFN-gamma was up-regulated after antigen stimulation, the inflammatory molecules IL-8 and MMP-9 were down-regulated. These observed immune profiles are potentially reflective of the ability of the different groups to control SHIV replication. This study demonstrates that an optimized IL-15 immune adjuvant delivered with a DNA vaccine can impact the cellular immune profile in nonhuman primates and lead to enhanced suppression of viral replication.

Indexed as

ImmunizationAnimalsCell ProliferationGene Expression RegulationGene Products, gagHumansInterferon-gammaInterleukin-15Lymph NodesMacacaPlasmidsRetroviridae ProteinsSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusT-LymphocytesVirus ReplicationGene Products, gagInterferon-gammaInterleukin-15Retroviridae Proteins

Identifiers

PMID18000037
PMCPMC2141831
OpenAlexW1984511743

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.