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Development of a humanized monoclonal antibody with therapeutic potential against West Nile virus
被引:411
作者:
Oliphant, T
Engle, M
Nybakken, GE
Doane, C
Johnson, S
Huang, L
Gorlatov, S
Mehlhop, E
Marri, A
Chung, KM
Ebel, GD
Kramer, LD
Fremont, DH
Diamond, MS
机构:
[1] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[4] MacroGenics, Rockville, MD 20850 USA
[5] New York State Dept Hlth, Wadsworth Ctr, Slingerlands, NY 12159 USA
关键词:
D O I:
10.1038/nm1240
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Neutralization of West Nile virus (WNV) in vivo correlates with the development of an antibody response against the viral envelope ( E) protein. Using random mutagenesis and yeast surface display, we defined individual contact residues of 14 newly generated monoclonal antibodies against domain III of the WNV E protein. Monoclonal antibodies that strongly neutralized WNV localized to a surface patch on the lateral face of domain III. Convalescent antibodies from individuals who had recovered from WNV infection also detected this epitope. One monoclonal antibody, E16, neutralized 10 different strains in vitro, and showed therapeutic efficacy in mice, even when administered as a single dose 5 d after infection. A humanized version of E16 was generated that retained antigen specificity, avidity and neutralizing activity. In postexposure therapeutic trials in mice, a single dose of humanized E16 protected mice against WNV-induced mortality, and may therefore be a viable treatment option against WNV infection in humans.
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页码:522 / 530
页数:9
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