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Research Paper

rDEN2/4Δ30(ME), a Live Attenuated Chimeric Dengue Serotype 2 Vaccine, is Safe and Highly Immunogenic in Healthy Dengue-Naïve Adults

Anna P. Durbin, Julie H. McArthur, Jennifer A. Marron, Joseph E. Blaney, Bhavin Thumar, Kimberli Wanionek and Brian R. Murphy

volume 2 | issue 6

november/december 2006
Pages: 255 - 260

This is an open-access article

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rDEN2/4Δ30(ME) is an attenuated chimeric dengue virus in which the prM and E structural proteins of the DEN4 candidate vaccine rDEN4∆30 have been replaced by those of the prototypic DEN2 NGC virus. rDEN2/4Δ30(ME) was evaluated at a dose of 1,000 PFU in 20 healthy dengue-naïve adult volunteers. Eight volunteers received placebo. Volunteers were monitored closely for adverse events and serum was collected for determination of the level and duration of viremia and neutralizing antibody response. The vaccine was well tolerated by all volunteers. The most common adverse events observed were a transient asymptomatic rash and mild neutropenia. All vaccinees seroconverted to DEN2 and maintained significant antibody titers throughout the six-month trial duration. Eleven vaccinees had vaccine virus recovered from the blood during the study. RNA derived from virus isolates obtained from viremic volunteers was sequenced for confirmation of retention of the ∆30 mutation in the 3´ UTR. The Δ30 mutation remained unchanged in each isolate, confirming the stability of the Δ30 mutation. Further evaluation of this vaccine in a tetravalent formulation is warranted.

Authors

Anna P. Durbin

Johns Hopkins Bloomberg School of Public Health; Baltimore MD, USA

Julie H. McArthur

Johns Hopkins Bloomberg School of Public Health; Baltimore MD, USA

Jennifer A. Marron

Johns Hopkins Bloomberg School of Public Health; Baltimore MD, USA

Joseph E. Blaney

National Institute of Allergy and Infectious Diseases, National Institutes of Health; Bethesda MD, USA

Bhavin Thumar

Johns Hopkins Bloomberg School of Public Health; Baltimore MD, USA

Kimberli Wanionek

Johns Hopkins Bloomberg School of Public Health; Baltimore MD, USA

Brian R. Murphy

National Institute of Allergy and Infectious Diseases, National Institutes of Health; Bethesda MD, USA


This is an open-access article

 Download PDF

If the document does not open, please right-click on the link (control-click on a Macintosh) and select the option to save the file to disk.