Limited replication of yellow fever 17DD and 17D-Dengue recombinant viruses in rhesus monkeys

Dendritic cells (DCs) are targets for dengue virus (DENV) and yellow fever virus (YF) replication and are the first cell population to interact with these viruses during a

In our efforts to develop a live attenuated dengue vaccine based on chimeric yellow fever 17D vi- ruses (Caufour et al. 2007) and in the unavailability of wild type dengue viruses

A recombinant yellow fever (YF) 17D virus expressing the reporter green fluorescent protein (GFP) with the stem-anchor (SA) region of E protein fused to its carboxy terminus was

Multiple sequence alignment of NS3 from MGTV and representative of tick-borne encephalitis virus (TBEV), mosquito- borne [dengue virus type 2 (DENV-2) and yellow fever

This study aimed to estimate and compare the se- roconversion rates and antibody titres against YF 30 or more days after vaccination with substrains 17DD and WHO 17D-213/77

In this study the kinetics of humoral and cellular immune responses in first-time vaccinees and re-vaccinees with the yellow fever 17DD vaccine virus was analyzed.. Flow

The real-time RT-PCR was able to detect the virus genome in 15 of 17 serum samples from cattle and horses obtained during an outbreak of Alagoas virus.. Unfortunately, the VSV

peak viremia of our 17D-D2 chimera was lower than that observed for ChimeriVax- D2 virus inoculated into the CNS of rhesus monkeys in a similar test but using a mixture of all