Evidence map›Paper›PMID 16611905›Full record

ArticleJournal of virology2006

Recombinant vesicular stomatitis virus vectors expressing herpes simplex virus type 2 gD elicit robust CD4+ Th1 immune responses and are protective in mouse and guinea pig models of vaginal challenge.

Robert J Natuk, David Cooper, Min Guo, Priscilla Calderon, Kevin J Wright, Farooq Nasar, Susan Witko, Diane Pawlyk, Margaret Lee, Joanne DeStefano and 9 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
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

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. HSV-2: in pursuit of a vaccine.The Journal of clinical investigation · 2011
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Recombinant vectors as influenza vaccines.Current topics in microbiology and immunology · 2009
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Recombinant vesicular stomatitis virus as an HIV-1 vaccine vector.Springer seminars in immunopathology · 2006
    Review
  19. 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

19 authors at 1 institution in 1 country.

Robert J NatukDepartment of Vaccines Discovery Research, Wyeth Research, 401 N. Middletown Rd., Pearl River, New York 10965, USA. natukr@wyeth.com
David Cooper
Min Guo
Priscilla Calderon
Kevin J Wright
Farooq Nasar
Susan Witko
Diane Pawlyk
Margaret Lee
Joanne DeStefano
Donna Tummolo
Aaron S Abramovitz
Seema Gangolli
Narender Kalyan
David K Clarke
R Michael Hendry
John H Eldridge
Stephen A Udem
Jacek Kowalski
Pearl River Community College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recombinant vesicular stomatitis virus (rVSV) vectors offer an attractive approach for the induction of robust cellular and humoral immune responses directed against human pathogen target antigens. We evaluated rVSV vectors expressing full-length glycoprotein D (gD) from herpes simplex virus type 2 (HSV-2) in mice and guinea pigs for immunogenicity and protective efficacy against genital challenge with wild-type HSV-2. Robust Th1-polarized anti-gD immune responses were demonstrated in the murine model as measured by induction of gD-specific cytotoxic T lymphocytes and increased gamma interferon expression. The isotype makeup of the serum anti-gD immunoglobulin G (IgG) response was consistent with the presence of a Th1-CD4+ anti-gD response, characterized by a high IgG2a/IgG1 IgG subclass ratio. Functional anti-HSV-2 neutralizing serum antibody responses were readily demonstrated in both guinea pigs and mice that had been immunized with rVSV-gD vaccines. Furthermore, guinea pigs and mice were prophylactically protected from genital challenge with high doses of wild-type HSV-2. In addition, guinea pigs were highly protected against the establishment of latent infection as evidenced by low or absent HSV-2 genome copies in dorsal root ganglia after virus challenge. In summary, rVSV-gD vectors were successfully used to elicit potent anti-gD Th1-like cellular and humoral immune responses that were protective against HSV-2 disease in guinea pigs and mice.

Indexed as

AnimalsAntibody FormationFemaleGenetic VectorsGlycoproteinsGuinea PigsHerpes Simplex Virus VaccinesHerpesvirus 2, HumanMiceModels, AnimalTh1 CellsVaginaVesicular stomatitis Indiana virusViral Envelope ProteinsGlycoproteinsHerpes Simplex Virus VaccinesViral Envelope Proteins

Identifiers

PMID16611905
PMCPMC1472036
OpenAlexW2113280299

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.