MHC class I- and class II-restricted processing and presentation of microencapsulated antigens

被引:93
作者
Men, Y
Audran, R
Thomasin, C
Eberl, G
Demotz, S
Merkle, HP
Gander, B
Corradin, G [1 ]
机构
[1] Univ Lausanne, Inst Biochem, CH-1066 Epalinges, Switzerland
[2] Swiss Fed Inst Technol, Dept Pharm, CH-8057 Zurich, Switzerland
关键词
D O I
10.1016/S0264-410X(98)00321-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Macrophages were found of having a strong capacity of phagocytosing small size microcapsules (MS) and presentating microencapsulated antigens to either CD4+ and CD8+ T cells, The class I-restricted presentation of microencapsulated tetanus toroid by macrophages requires an intracellular processing which might follow the phagosome-to-cytosol route to enter the classical MHC class I presentation pathway. In contrast, presentation of microencapsulated cytotoxic peptide PbCS252-260 to specific CD8+ T cells has been observed with different APC and is not blocked by cytochalasin D, suggesting that peptide released from MS may directly bind to MHC class I molecules on the cell surface. In the case of MHC class II-restricted T cells, prefixation or treatment of macrophages with chloroquine, brefeldin A and cycloheximide inhibits the presentation of microencapsulated and soluble tetanus toroid. These findings illustrate the capacity of microencapsulated antigens to enter different presentation pathways and should facilitate the development of subunit vaccines. (C) 1999 Elsevier Science Ltd. All rights reserved.
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收藏
页码:1047 / 1056
页数:10
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