Human cytomegalovirus (HCMV) is a widely circulating pathogen that causes severe disease in immunocompromised patients and infected fetuses. By immortalizing memory B cells from HCMV-immune donors, we isolated a panel of human monoclonal antibodies that neutralized at extremely low concentrations (90% inhibitory concentration [IC90] values ranging from 5 to 200 pM) HCMV infection of endothelial, epithelial, and myeloid cells. With the single exception of an antibody that bound to a conserved epitope in the UL128 gene product, all other antibodies bound to conformational epitopes that required expression of two or more proteins of the gH/gL/UL128-131A complex. Antibodies against gB, gH, or gM/gN were also isolated and, albeit less potent, were able to neutralize infection of both endothelial-epithelial cells and fibroblasts. This study describes unusually potent neutralizing antibodies against HCMV that might be used for passive immunotherapy and identifies, through the use of such antibodies, novel antigenic targets in HCMV for the design of immunogens capable of eliciting previously unknown neutralizing antibody responses. Copyright © 2010, American Society for Microbiology.

Macagno, A., Bernasconi, N., Vanzetta, F., Dander, E., Sarasini, A., Revello, M., et al. (2010). Isolation of human monoclonal antibodies that potently neutralize human cytomegalovirus infection by targeting different epitopes on the gH/gL/UL128-131A complex. JOURNAL OF VIROLOGY, 84(2), 1005-1013 [10.1128/JVI.01809-09].

Isolation of human monoclonal antibodies that potently neutralize human cytomegalovirus infection by targeting different epitopes on the gH/gL/UL128-131A complex

DANDER, ERICA;
2010

Abstract

Human cytomegalovirus (HCMV) is a widely circulating pathogen that causes severe disease in immunocompromised patients and infected fetuses. By immortalizing memory B cells from HCMV-immune donors, we isolated a panel of human monoclonal antibodies that neutralized at extremely low concentrations (90% inhibitory concentration [IC90] values ranging from 5 to 200 pM) HCMV infection of endothelial, epithelial, and myeloid cells. With the single exception of an antibody that bound to a conserved epitope in the UL128 gene product, all other antibodies bound to conformational epitopes that required expression of two or more proteins of the gH/gL/UL128-131A complex. Antibodies against gB, gH, or gM/gN were also isolated and, albeit less potent, were able to neutralize infection of both endothelial-epithelial cells and fibroblasts. This study describes unusually potent neutralizing antibodies against HCMV that might be used for passive immunotherapy and identifies, through the use of such antibodies, novel antigenic targets in HCMV for the design of immunogens capable of eliciting previously unknown neutralizing antibody responses. Copyright © 2010, American Society for Microbiology.
Articolo in rivista - Articolo scientifico
Membrane Glycoproteins; Cell Line; Viral Envelope Proteins; Epitopes; Cytomegalovirus; Cytomegalovirus Infections; Female; Neutralization Tests; Antibodies, Neutralizing; Animals; Humans; Antibodies, Viral; Pregnancy Complications, Infectious; Pregnancy; Mice; Molecular Sequence Data; Antibodies, Monoclonal; Amino Acid Sequence
English
2010
84
2
1005
1013
none
Macagno, A., Bernasconi, N., Vanzetta, F., Dander, E., Sarasini, A., Revello, M., et al. (2010). Isolation of human monoclonal antibodies that potently neutralize human cytomegalovirus infection by targeting different epitopes on the gH/gL/UL128-131A complex. JOURNAL OF VIROLOGY, 84(2), 1005-1013 [10.1128/JVI.01809-09].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/16313
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