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Development of a Cocktail of Recombinant‐Expressed Human Rabies Virus–Neutralizing Monoclonal Antibodies for Postexposure Prophylaxis of Rabies
Author(s) -
Mikhail Prosniak,
Milosz Faber,
Cathleen A. Hanlon,
Charles E. Rupprecht,
D. Craig Hooper,
Bernhard Dietzschold
Publication year - 2003
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/375247
Subject(s) - virology , rabies virus , rabies , monoclonal antibody , recombinant dna , neutralizing antibody , lyssavirus , duck embryo vaccine , antibody , virus , rhabdoviridae , biology , medicine , immunology , gene , biochemistry
To provide a cost-effective and safe replacement for human rabies immunoglobulin (HRIG), we used DNA recombinant technology to express 3 human rabies virus-neutralizing human monoclonal antibodies (huMAbs) in a rhabdovirus vector (RhV). Infection of either baby hamster kidney cells or CHO cells, with the resulting RhV-huMAb recombinant viruses, yielded high-level production (< or =40 micro g/mL/48 h) of RhV recombinant-expressed huMAbs (rhuMAbs) that differ in both isotype and epitope-recognition specificity. A cocktail of these rhuMAbs neutralizes several fixed and street wild-type rabies viruses (RVs). Mice and hamsters treated only once with this rhuMAb cocktail after infection with a lethal dose of RV were protected. In the mouse models, the postexposure prophylaxis (PEP) efficacy obtained with the rhuMAb cocktail was comparable to that obtained with HRIG, a finding strongly suggesting that rhuMAbs should be given serious consideration for use in future PEP of humans.

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