HIV-1 gp120 glycosylation is cell type-specific and influences reactivity with HIV-1-specific antibodies

被引:0
作者
Raska, M. [1 ,2 ]
Elliott, M. C. [2 ]
Hall, S. [2 ]
Czernekova, L. [1 ]
Zachova, K. [1 ]
Moldoveanu, Z. [2 ]
Brown, R. [2 ]
Mestecky, J. [2 ,3 ]
Novak, J. [2 ]
机构
[1] Palacky Univ, Dept Immunol, Olomouc, Czech Republic
[2] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL USA
[3] Charles Univ Prague, Inst Microbiol & Immunol, Prague, Czech Republic
来源
CENTENNIAL RETROVIRUS MEETING | 2010年
关键词
VACCINE;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
N-glycans of HIV-1 gp120 are thought to affect folding and shield the virus from reactivity with antibodies (Abs). We analyzed glycosylation patterns of gp120 produced in five different human and animal cell lines. Gp120 produced by human embryonic kidney and T cells contained mostly high-mannose glycans, whereas gp120 from human rhabdomyosarcoma and hepatocellular carcinoma and Chinese-hamster ovary cells displayed higher proportion of complex glycans. This differential glycosylation affected reactivities with V3-loop-specific monoclonal Abs (mAbs), as well as with Abs from sera of HIV-1-infected patients. Our results underscore the importance of selection of the cells producing recombinant glycoprotein(s) for immunization, as well as the target tissue for DNA vaccination.
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页码:55 / 59
页数:5
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