The molecular basis for the immunogenicity of Cryptococcus neoformans mannoproteins

被引:116
作者
Levitz, Stuart M.
Specht, Charles A.
机构
[1] Boston Med Ctr, Dept Med, Boston, MA USA
[2] Boston Univ, Sch Med, Boston, MA 02118 USA
关键词
glycosylation; mannose receptor; glycosylphosphatidylinositol anchor; vaccine; cryptococcosis;
D O I
10.1111/j.1567-1364.2006.00071.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
T-cell-mediated immunity is necessary for effective host defenses against infections caused by Cryptococcus neoformans. Clinical and experimental studies have identified a heterogeneous family of mannoproteins as critical cryptococcal antigens responsible for stimulating T-cell responses. The archetypal mannoprotein has a signal sequence, a functional domain, a serine/threonine-rich region and a site for attachment of a glycosylphosphatidylinositol anchor. Extensive O-mannosylation, which occurs at the serine/threonine region, facilitates recognition by mannose receptors on antigen-presenting cells, particularly dendritic cells. This results in efficient antigen uptake, processing and presentation to T cells. Inhibition of mannose receptors or deglycosylation of mannoproteins profoundly inhibits T-cell responses, demonstrating the crucial contribution of mannosylation to immunogenicity.
引用
收藏
页码:513 / 524
页数:12
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