Evidence map›Paper›PMID 21159873›Full record

ArticleJournal of virology2011

Newcastle disease virus expressing a dendritic cell-targeted HIV gag protein induces a potent gag-specific immune response in mice.

Jad Maamary, Frida Array, Qinshan Gao, Adolfo García-Sastre, Ralph M Steinman, Peter Palese, Godwin Nchinda

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

27 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Article
  3. Harnessing IgG Fc glycosylation for clinical benefit.Current opinion in immunology · 2022
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Recent advances of oncolytic virus in cancer therapy.Human vaccines & immunotherapeutics · 2020
    Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Reverse Genetics of Newcastle Disease Virus.Methods in molecular biology (Clifton, N.J.) · 2017
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Daedalic DNA vaccination against self antigens as a treatment for chronic kidney disease.International journal of clinical and experimental pathology · 2013
    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

7 authors at 2 institutions in 1 country.

Jad MaamaryDepartment of Microbiology, Mount Sinai School of Medicine, New York, NY 10029, USA. Jad.maamary@mssm.edu
Frida Array
Qinshan Gao
Adolfo García-Sastre
Ralph M Steinman
Peter Palese
Godwin Nchinda
Icahn School of Medicine at Mount Sinai · USRockefeller University · US

Funding

Viral Pathogenesis and TherapeuticsU54AI057158 · NIAID · WADSWORTH CENTER · PI LIPKIN, W. IAN · 2003 to 2014
$100.8M
NIAID NIH HHS U54 AI057158NIAID NIH HHS U54AI057158PHS HHS P0IAI08325
6 · The paper itself

Abstract

Viral vaccine vectors have emerged as an attractive strategy for the development of a human immunodeficiency virus (HIV) vaccine. Recombinant Newcastle disease virus (rNDV) stands out as a vaccine vector since it has a proven safety profile in humans, it is a potent inducer of both alpha interferon (IFN-α) and IFN-β) production, and it is a potent inducer of dendritic cell (DC) maturation. Our group has previously generated an rNDV vector expressing a codon-optimized HIV Gag protein and demonstrated its ability to induce a Gag-specific CD8(+) T cell response in mice. In this report we demonstrate that the Gag-specific immune response can be further enhanced by the targeting of the rNDV-encoded HIV Gag antigen to DCs. Targeting of the HIV Gag antigen was achieved by the addition of a single-chain Fv (scFv) antibody specific for the DC-restricted antigen uptake receptor DEC205 such that the DEC205 scFv-Gag molecule was encoded for expression as a fusion protein. The vaccination of mice with rNDV coding for the DC-targeted Gag antigen induced an enhanced Gag-specific CD8(+) T cell response and enhanced numbers of CD4(+) T cells and CD8(+) T cells in the spleen relative to vaccination with rNDV coding for a nontargeted Gag antigen. Importantly, mice vaccinated with the DEC205-targeted vaccine were better protected from challenge with a recombinant vaccinia virus expressing the HIV Gag protein. Here we demonstrate that the targeting of the HIV Gag antigen to DCs via the DEC205 receptor enhances the ability of an rNDV vector to induce a potent antigen-specific immune response.

Indexed as

Gene ExpressionAnimalsAntibodies, ViralCell LineDendritic CellsFemalegag Gene Products, Human Immunodeficiency VirusGenetic VectorsHIV-1HIV InfectionsHumansMiceMice, Inbred BALB CNewcastle disease virusViral VaccinesAntibodies, Viralgag Gene Products, Human Immunodeficiency VirusViral Vaccines

Identifiers

PMID21159873
PMCPMC3067785
OpenAlexW2106572026

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.