
The molecular basis for the immunogenicity of Cryptococcus neoformans mannoproteins
Author(s) -
Levitz Stuart M.,
Specht Charles A.
Publication year - 2006
Publication title -
fems yeast research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.991
H-Index - 92
eISSN - 1567-1364
pISSN - 1567-1356
DOI - 10.1111/j.1567-1364.2006.00071.x
Subject(s) - biology , cryptococcus neoformans , mannose , immunogenicity , serine , antigen , threonine , microbiology and biotechnology , biochemistry , immunology , phosphorylation
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.