Evidence map›Paper›PMID 12743287›Full record

ArticleJournal of virology2003

Comparative immunogenicity in rhesus monkeys of DNA plasmid, recombinant vaccinia virus, and replication-defective adenovirus vectors expressing a human immunodeficiency virus type 1 gag gene.

Danilo R Casimiro, Ling Chen, Tong-Ming Fu, Robert K Evans, Michael J Caulfield, Mary-Ellen Davies, Aimin Tang, Minchun Chen, Lingyi Huang, Virginia Harris and 29 more

2 registry-linked trialsOpen access · greenAbstract readComparative Study
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. It is linked to 2 registered trials, which are not on this map. Cited by 192 papers.

0numbers the graph read from it
0cells of the map it votes in
192citing papers in PubMed
10.6field-weighted citation impact, top 1% 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.

NCT00089531 phase1completednot on this mapstarted 2004, after this paper: background citation

A Phase I Clinical Trial to Evaluate the Safety and Immunogenicity of a 6-Plasmid Multiclade HIV-1 DNA Vaccine, VRC-HIVDNA016-00-VP, in Uninfected Adult Volunteers

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2004 to 2008Enrolled15ConditionsHIV InfectionsArmsVRC-HIVDNA016-00-VP
NCT00479999 phase1completednot on this mapstarted 2007, after this paper: background citation

VRC 012: A Phase I Clinical Trial of the Safety and Immunogenicity of an HIV-1 Adenoviral Vector Serotype 35 Vaccine: Dose Escalation as a Single Agent and Prime-Boost Schedules With an HIV-1 Adenoviral Vector Serotype 5 Vaccine in Uninfected Adults

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2007 to 2014Enrolled35ConditionsAIDS Vaccines, HIV Infections, HIV-1ArmsVRC-HIVADV027-00-VP, VRC-HIVADV038-00-VP
3 · Its place in the literature

Who cites it

192 citing papers in PubMed, 398 citations in OpenAlex.

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  11. Development of mRNA rabies vaccines.Human vaccines & immunotherapeutics · 2024
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132 more citing papers are in PubMed but not listed here.

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

39 authors at 2 institutions in 2 countries.

Danilo R CasimiroDepartment of Viral Vaccine Research, Merck and Company, West Point, Pennsylvania 19486, USA. danilo_casimiro@merck.com
Ling Chen
Tong-Ming Fu
Robert K Evans
Michael J Caulfield
Mary-Ellen Davies
Aimin Tang
Minchun Chen
Lingyi Huang
Virginia Harris
Daniel C Freed
Keith A Wilson
Sheri Dubey
De-Min Zhu
Denise Nawrocki
Henryk Mach
Robert Troutman
Lynne Isopi
Donna Williams
William Hurni
Zheng Xu
Jeffrey G Smith
Su Wang
Xu Liu
Liming Guan
Romnie Long
Wendy Trigona
Gwendolyn J Heidecker
Helen C Perry
Natasha Persaud
Timothy J Toner
Qin Su
Xiaoping Liang
Rima Youil
Michael Chastain
Andrew J Bett
David B Volkin
Emilio A Emini
John W Shiver
Institut de Recherche Vaccinale · FRUnited States Military Academy · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular immune responses, particularly those associated with CD3(+) CD8(+) cytotoxic T lymphocytes (CTL), play a primary role in controlling viral infection, including persistent infection with human immunodeficiency virus type 1 (HIV-1). Accordingly, recent HIV-1 vaccine research efforts have focused on establishing the optimal means of eliciting such antiviral CTL immune responses. We evaluated several DNA vaccine formulations, a modified vaccinia virus Ankara vector, and a replication-defective adenovirus serotype 5 (Ad5) vector, each expressing the same codon-optimized HIV-1 gag gene for immunogenicity in rhesus monkeys. The DNA vaccines were formulated with and without one of two chemical adjuvants (aluminum phosphate and CRL1005). The Ad5-gag vector was the most effective in eliciting anti-Gag CTL. The vaccine produced both CD4(+) and CD8(+) T-cell responses, with the latter consistently being the dominant component. To determine the effect of existing antiadenovirus immunity on Ad5-gag-induced immune responses, monkeys were exposed to adenovirus subtype 5 that did not encode antigen prior to immunization with Ad5-gag. The resulting anti-Gag T-cell responses were attenuated but not abolished. Regimens that involved priming with different DNA vaccine formulations followed by boosting with the adenovirus vector were also compared. Of the formulations tested, the DNA-CRL1005 vaccine primed T-cell responses most effectively and provided the best overall immune responses after boosting with Ad5-gag. These results are suggestive of an immunization strategy for humans that are centered on use of the adenovirus vector and in which existing adenovirus immunity may be overcome by combined immunization with adjuvanted DNA and adenovirus vector boosting.

Indexed as

Adenoviruses, HumanAdjuvants, ImmunologicAIDS VaccinesAnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesGenes, gagGenetic VectorsHIV-1HIV AntibodiesHIV InfectionsHumansImmunizationMacaca mulattaPlasmidsRecombination, GeneticAdjuvants, ImmunologicAIDS VaccinesHIV AntibodiesVaccines, DNA

Identifiers

PMID12743287
PMCPMC154996
OpenAlexW2148029978

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.