Novel Human Monoclonal Antibody Combination Effectively Neutralizing Natural Rabies Virus Variants and Individual In Vitro Escape Mutants.

Bibliographic Details
Title: Novel Human Monoclonal Antibody Combination Effectively Neutralizing Natural Rabies Virus Variants and Individual In Vitro Escape Mutants.
Authors: Bakker, Alexander B. H.1, Marissen, Wilfred E.1, Kramer, R. Arjen1, Rice, Amy B.2, Weldon, William C.3, Niezgoda, Michael3, Hanlon, Cathleen A.3, Thijsse, Sandra1, Backus, Harold H. J.1, De Kruif, John1, Dietzschold, Bernhard2, Rupprecht, Charles E.3, Goudsmit, Jaap1 j.goudsmit@crucell.com
Source: Journal of Virology. Jul2005, Vol. 79 Issue 14, p27-27. 1p.
Subject Terms: *RABIES, *MONOCLONAL antibodies, *IMMUNOGLOBULINS, *GLYCOPROTEINS, *EPITOPES
Abstract: The need to replace rabies immune globulin (RIG) as an essential component of rabies postexposure prophylaxis is widely acknowledged. We set out to discover a unique combination of human monoclonal antibodies (MAbs) able to replace RIG. Stringent criteria concerning neutralizing potency, affinity, breadth of neutralization, and coverage of natural rabies virus (RV) isolates and in vitro escape mutants were set for each individual antibody, and the complementarities of the two MAbs were defined at the onset. First, we identified and characterized one human MAb (CR57) with high in vitro and in vivo neutralizing potency and a broad neutralization spectrum. The linear antibody binding site was mapped on the RV glycoprotein as antigenic site I by characterizing CR57 escape mutants. Secondly, we selected using phage display a complementing antibody (CR4098) that recognized a distinct, nonoverlapping epitope (antigenic site III), showed similar neutralizing potency and breadth as CR57, and neutralized CR57 escape mutants. Reciprocally, CR57 neutralized RV variants escaping CR4098. Analysis of glycoprotein sequences of natural RV isolates revealed that the majority of strains contain both intact epitopes, and the few remaining strains contain at least one of the two. In vitro exposure of RV to the combination of CR57 and CR4098 yielded no escape mutants. In conclusion, a novel combination of human MAbs was discovered suitable to replace RIG. [ABSTRACT FROM AUTHOR]
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Database: Academic Search Complete
More Details
ISSN:0022538X
DOI:10.1128/JVI.79.14.9062-9068.2005
Published in:Journal of Virology
Language:English