Recombinant measles viruses efficiently entering cells through targeted receptors.

Abstract:

:We sought proof of principle that one of the safest human vaccines, measles virus Edmonston B (MV-Edm), can be genetically modified to allow entry via cell surface molecules other than its receptor CD46. Hybrid proteins consisting of the epidermal growth factor (EGF) or the insulin-like growth factor 1 (IGF1) linked to the extracellular (carboxyl) terminus of the MV-Edm attachment protein hemagglutinin (H) were produced. The standard H protein gene was replaced by one coding for H/EGF or H/IGF1 in cDNA copies of the MV genome. Recombinant viruses were rescued and replicated to titers approaching those of the parental strain. MV displaying EGF or IGF1 efficiently entered CD46-negative rodent cells expressing the human EGF or the IGF1 receptor, respectively, and the EGF virus caused extensive syncytium formation and cell death. Taking advantage of a factor Xa protease recognition site engineered in the hybrid H proteins, the displayed domain was cleaved off from virus particles, and specific entry in rodent cells was abrogated. These studies prove that MV can be engineered to selectively eliminate cells expressing a targeted receptor and provide insights into the mechanism of MV entry.

journal_name

J Virol

journal_title

Journal of virology

authors

Schneider U,Bullough F,Vongpunsawad S,Russell SJ,Cattaneo R

doi

10.1128/jvi.74.21.9928-9936.2000

subject

Has Abstract

pub_date

2000-11-01 00:00:00

pages

9928-36

issue

21

eissn

0022-538X

issn

1098-5514

journal_volume

74

pub_type

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