Evidence map›Paper›PMID 16617103›Full record

Trial reportProceedings of the National Academy of Sciences of the United States of America2006

A live, attenuated recombinant West Nile virus vaccine.

Thomas P Monath, Jian Liu, Niranjan Kanesa-Thasan, Gwendolyn A Myers, Richard Nichols, Alison Deary, Karen McCarthy, Casey Johnson, Thomas Ermak, Sunheang Shin and 6 more

Erratum issuedOpen access · greenAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Proceedings of the National Academy of Sciences of the United States of America, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 93 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed, 1 pooled it
24.1field-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.

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

93 citing papers in PubMed, 1 synthesis or guideline pooled it, 226 citations in OpenAlex.

  1. Pooled it
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  8. Review
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  14. Self-Replicating RNA Derived from the Genomes of Positive-Strand RNA Viruses.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
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33 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

16 authors at 4 institutions in 2 countries.

Thomas P MonathAcambis, 38 Sidney Street, Cambridge, MA 02139, USA. tom.monath@acambis.com
Jian Liu
Niranjan Kanesa-Thasan
Gwendolyn A Myers
Richard Nichols
Alison Deary
Karen McCarthy
Casey Johnson
Thomas Ermak
Sunheang Shin
Juan Arroyo
Farshad Guirakhoo
Jeffrey S Kennedy
Francis A Ennis
Sharone Green
Philip Bedford
University of Massachusetts Chan Medical School · USAbcam (United States) · USFulbourn Hospital · GBJohnson County Clin-Trials (United States) · US

Funding

Technologies for Human Cellular ImmunologyU19AI057319 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FINBERG, ROBERT WILLIAM · 2003 to 2013
$34.4M
HUMAN IMMUNE RESPONSES TO YELLOW FEVER VIRUSK08AI001729 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI GREEN, SHARONE · 2000 to 2004
$588k
US BASED COLLABORATION IN EMERGING VIRAL AND PRION DISEASES-266025490N01AI025490 · NIAID · HEALTH RESEARCH, INC. · 2003 to 2004
–
NIAID NIH HHS K08 AI001729NIAID NIH HHS K08 AI01729NIAID NIH HHS N01 AI025490NIAID NIH HHS U19 AI057319
6 · The paper itself

Abstract

West Nile (WN) virus is an important cause of febrile exanthem and encephalitis. Since it invaded the U.S. in 1999, >19,000 human cases have been reported. The threat of continued epidemics has spurred efforts to develop vaccines. ChimeriVax-WN02 is a live, attenuated recombinant vaccine constructed from an infectious clone of yellow fever (YF) 17D virus in which the premembrane and envelope genes of 17D have been replaced by the corresponding genes of WN virus. Preclinical tests in monkeys defined sites of vaccine virus replication in vivo. ChimeriVax-WN02 and YF 17D had similar biodistribution but different multiplication kinetics. Prominent sites of replication were skin and lymphoid tissues, generally sparing vital organs. Viruses were cleared from blood by day 7 and from tissues around day 14. In a clinical study, healthy adults were inoculated with 5.0 log(10) plaque-forming units (PFU) (n = 30) or 3.0 log10 PFU (n = 15) of ChimeriVax-WN02, commercial YF vaccine (YF-VAX, n = 5), or placebo (n = 30). The incidence of adverse events in subjects receiving the vaccine was similar to that in the placebo group. Transient viremia was detected in 42 of 45 (93%) of ChimeriVax-WN02 subjects, and four of five (80%) of YF-VAX subjects. All subjects developed neutralizing antibodies to WN or YF, respectively, and the majority developed specific T cell responses. ChimeriVax-WN02 rapidly elicits strong immune responses after a single dose, and is a promising candidate warranting further evaluation for prevention of WN disease.

Indexed as

AdolescentAdultAnimalsDouble-Blind MethodFemaleHumansMacaca fascicularisMaleMolecular Sequence DataNeutralization TestsSafetyT-LymphocytesVaccines, AttenuatedVaccines, SyntheticViral VaccinesVirus ReplicationVaccines, AttenuatedVaccines, SyntheticViral Vaccines

Identifiers

PMID16617103
PMCPMC1436023
OpenAlexW2106056357

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.