Complement-fixing islet cell antibodies in type-1 diabetes can trigger the assembly of the terminal complement complex on human islet cells and are potentially cytotoxic

被引:19
作者
Radillo, O
Nocera, A
Leprini, A
Barocci, S
Mollnes, TE
Pocecco, M
Pausa, M
Valente, U
Betterle, C
Tedesco, F
机构
[1] IST INFANZIA, PEDIAT CLIN, BURLO GAROFOLO, TRIESTE, ITALY
[2] IST INFANZIA, CLIN OSTETR & GINECOL, BURLO GAROFOLO, TRIESTE, ITALY
[3] OSPED SAN MARTINO GENOVA, SERV IMMUNOL, GENOA, ITALY
[4] UNIV GENOA, IST ANAT UMANA, GENOA, ITALY
[5] NORDLAND CENT HOSP, DEPT IMMUNOL & TRANSFUS MED, BODO, NORWAY
[6] OSPED SAN MARTINO GENOVA, DIV CHIRURG TRAPIANTI, GENOA, ITALY
[7] UNIV PADUA, IST SEMEIOT MED, PADUA, ITALY
[8] UNIV TRIESTE, IST PATOL GEN, TRIESTE, ITALY
来源
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY | 1996年 / 79卷 / 03期
关键词
D O I
10.1006/clin.1996.0071
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Forty-one sera of patients with IDDM (insulin-dependent diabetes mellitus) containing complement fixing islet cell antibodies were analyzed for their ability to activate TCC (terminal complement complex). Eighteen sera were found to promote deposition of TCC on human islets of pancreatic cryostat sections with a nonhomogeneous pattern of distribution corresponding to that of insulin. Activation of TCC by IDDM serum and binding of this complex to islet cells was confirmed using purified islets. Flow cytometric analysis of islet cell treated with a TCC+ IDDM serum showed IgG binding to the cell surface. The same serum had a cytotoxic effect on islet cells in the presence of human C. These results obtained with a homologous system of C activation by IDDM sera suggest that TCC may contribute, at least in part, to the pancreatic beta cell damage. (C) 1996 Academic Press, Inc.
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页码:217 / 223
页数:7
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