Evidence map›Paper›PMID 16977404›Full record

ReviewSpringer seminars in immunopathology2006

Recombinant vesicular stomatitis virus as an HIV-1 vaccine vector.

David K Clarke, David Cooper, Michael A Egan, R Michael Hendry, Christopher L Parks, Stephen A Udem

Open access · bronzeAbstract readReview
In one paragraph

Review in Springer seminars in immunopathology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 7% 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 72 citations in OpenAlex.

  1. Pooled it
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  14. Viral Vectors in Gene Therapy.Diseases (Basel, Switzerland) · 2018
    Review
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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

6 authors at 3 institutions in 2 countries.

David K ClarkeDepartment of Vaccines Discovery Research, Wyeth Research, Wyeth, Pearl River, NY 10965, USA.
David Cooper
Michael A Egan
R Michael Hendry
Christopher L Parks
Stephen A Udem
Women's Health Research Institute · CAPearl River Community College · USInternational AIDS Vaccine Initiative · US

Funding

HIV Vaccine Design and Development Teams-26625458N01AI025458 · NIAID · WYETH PHARMACEUTICALS INC. · 2003 to 2005
–
NIAID NIH HHS N01-AI-25458
6 · The paper itself

Abstract

Recombinant vesicular stomatitis virus (rVSV) is currently under evaluation as a human immunodeficiency virus (HIV)-1 vaccine vector. The most compelling reasons to develop rVSV as a vaccine vector include a very low seroprevalence in humans, the ability to infect and robustly express foreign antigens in a broad range of cells, and vigorous growth in continuous cell lines used for vaccine manufacture. Numerous preclinical studies with rVSV vectors expressing antigens from a variety of human pathogens have demonstrated the versatility, flexibility, and potential efficacy of the rVSV vaccine platform. When administered to nonhuman primates (NHPs), rVSV vectors expressing HIV-1 Gag and Env elicited robust HIV-1-specific cellular and humoral immune responses, and animals immunized with rVSV vectors expressing simian immunodeficiency virus (SIV) Gag and HIV Env were protected from AIDS after challenge with a pathogenic SIV/HIV recombinant. However, results from an exploratory neurovirulence study in NHPs indicated that these prototypic rVSV vectors might not be adequately attenuated for widespread use in human populations. To address this safety concern, a variety of different attenuation strategies, designed to produce a range of further attenuated rVSV vectors, are currently under investigation. Additional modifications of further attenuated rVSV vectors to upregulate expression of HIV-1 antigens and coexpress molecular adjuvants are also being developed in an effort to balance immunogenicity and attenuation.

Indexed as

AIDS VaccinesGenetic VectorsAdjuvants, ImmunologicAnimalsAntiretroviral Therapy, Highly ActiveGene Products, envGene Products, gagHIV-1HIV AntigensHIV InfectionsHumansImmunologic FactorsSimian Acquired Immunodeficiency SyndromeVaccines, SyntheticVesicular stomatitis Indiana virusAdjuvants, ImmunologicAIDS VaccinesGene Products, envGene Products, gagHIV AntigensImmunologic FactorsVaccines, Synthetic

Identifiers

PMID16977404
PMCPMC7079905
OpenAlexW2090738896

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.