Evidence map›Paper›PMID 12857905›Full record

ArticleJournal of virology2003

Improved protection of rhesus macaques against intrarectal simian immunodeficiency virus SIV(mac251) challenge by a replication-competent Ad5hr-SIVenv/rev and Ad5hr-SIVgag recombinant priming/gp120 boosting regimen.

Jun Zhao, Joel Pinczewski, Victor R Gómez-Román, David Venzon, V S Kalyanaraman, Phillip D Markham, Kristine Aldrich, Matthew Moake, David C Montefiori, Yuanmei Lou and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

18 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Adenoviruses as vaccine vectors.Molecular therapy : the journal of the American Society of Gene Therapy · 2004
    Review
  17. Article
  18. 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

12 authors at 3 institutions in 1 country.

Jun ZhaoBasic Research Laboratory, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Joel Pinczewski
Victor R Gómez-Román
David Venzon
V S Kalyanaraman
Phillip D Markham
Kristine Aldrich
Matthew Moake
David C Montefiori
Yuanmei Lou
George N Pavlakis
Marjorie Robert-Guroff
National Cancer Institute · USBioScience Laboratories (United States) · USDuke Medical Center · US

Funding

HUMORAL AND CELLULAR IMMUNE RESPONSES TO HUMAN AND NONHUMAN PRIMATE RETROVIRUSESZ01BC005536 · NCI · BASIC SCIENCES · PI ROBERT-GUROFF, MARJORIE · 1996 to 2007
$4.1M
Pathogenic mech. of HIV, viral reservoirs /sanctuariesZ01BC010397 · BC · BASIC SCIENCES · PI PAVLAKIS, GEORGE N. · 2000 to 2005
–
NIAID NIH HHS N01 AI015430NIAID NIH HHS N01-AI15430
6 · The paper itself

Abstract

In this study we investigated the ability of a replication-competent Ad5hr-SIVenv/rev and Ad5hr-SIVgag recombinant priming/gp120 boosting regimen to induce protective immunity in rhesus macaques against pathogenic simian immunodeficiency virus(mac251). Immunization of macaques by two sequential administrations of the same recombinants by the same route resulted in boosting and persistence of SIV-specific cellular immune responses for 42 weeks past the initial immunization. Anti-SIV gp120 immunoglobulin G (IgG) and IgA antibodies were induced in secretory fluids, and all macaques exhibited serum neutralizing antibody activity. After intrarectal SIV(mac251) challenge, all of the macaques became infected. However, relative protection, as assessed by statistically significant lower SIV viral loads in plasma at both acute infection and set point, was observed in 8 out of 12 immunized non-Mamu-A(*)01 animals. Elevated mean cellular immune responses to Gag and Env, neutralizing antibody activity, and IgG and IgA binding antibody levels were observed in the eight protected macaques. Statistically significant correlations with protective outcome were observed for cellular immune responses to SIV Env and Gag and for SIV gp120-specific IgG antibodies in nasal and vaginal fluids. Two macaques that exhibited the greatest and most persistent viremia control also exhibited strong CD8(+) T-cell antiviral activity. The results suggest that a spectrum of immune responses may be necessary for adequate control of viral replication and disease progression and highlight a potential role for nonneutralizing antibodies at mucosal sites.

Indexed as

AdenoviridaeAdministration, RectalAnimalsAntibodies, ViralFemaleGene Products, envGene Products, gagGene Products, revImmunity, MucosalImmunizationImmunization, SecondaryMacaca mulattaMembrane GlycoproteinsRecombination, GeneticRNA, ViralSAIDS VaccinesAntibodies, ViralGene Products, envGene Products, gagGene Products, revgp120 protein, Simian immunodeficiency virusMembrane GlycoproteinsRNA, ViralSAIDS VaccinesVaccines, SyntheticViral Envelope ProteinsViral Proteins

Identifiers

PMID12857905
PMCPMC165263
OpenAlexW2129793752

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.