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Journal of Clinical Microbiology, November 1998, p. 3198-3204, Vol. 36, No. 11
Departments of
Neuropharmacology,1
Immunology,3 and
Molecular
Biology,4 The Scripps Research Institute, La
Jolla, California, and
Sezione di Microbiologia e Virologia,
Dipartimento di Scienze Chirurgiche e Trapianti d'Organo
Università di Cagliari, Cagliari, Italy2
Received 3 June 1998/Returned for modification 13 August
1998/Accepted 20 August 1998
We report the characterization of a type-common human recombinant
monoclonal antibody previously isolated by antigen selection from a
phage-displayed combinatorial antibody library established from a
herpes simplex virus (HSV)-seropositive individual. Competition with
well-characterized murine monoclonal antibodies and immunodetection of
gD truncations revealed that this antibody recognizes the group Ib
antigenic site of glycoprotein D, a highly conserved and protective type-common determinant. To our knowledge, this is the first human group Ib monoclonal antibody ever described. The antibody also displayed first-order neutralization kinetics and a high neutralization rate constant, was capable of completely inhibiting syncytium formation
by a fusogenic strain of HSV type 1, and efficiently neutralized
low-passage clinical isolates of both HSV serotypes. Taken together
with our earlier observations of the in vivo antiviral activities of
this human recombinant antibody in animal models of HSV infection, the
present results support the high therapeutic potential of this
antibody.
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Characterization of a Type-Common Human Recombinant
Monoclonal Antibody to Herpes Simplex Virus with High
Therapeutic Potential
*
Corresponding author. Mailing address: Department of
Neuropharmacology, The Scripps Research Institute, CVN 12, 10550 N. Torrey Pines Rd., La Jolla, CA 92037. Phone: (619) 784-7180. Fax: (619) 784-7393. E-mail: psanna{at}Sage.scripps.edu.
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