Antineutrophil cytoplasmic antibodies and associated diseases: A review of the clinical and laboratory features

被引:172
作者
Savige, J [1 ]
Davies, D
Falk, RJ
Jennette, JC
Wiik, A
机构
[1] Univ Melbourne, Austin & Repatriat Med Ctr, Dept Med, Heidelberg, Vic 3084, Australia
[2] Liverpool Hosp, SW Area Pathol Serv, Liverpool, NSW, Australia
[3] Univ N Carolina, Dept Pathol, Chapel Hill, NC USA
[4] Univ N Carolina, Dept Lab Med, Chapel Hill, NC USA
[5] Univ N Carolina, Dept Med, Chapel Hill, NC USA
[6] Statens Serum Inst, Dept Autoimmunol, DK-2300 Copenhagen, Denmark
关键词
ANCA; crescentic glomerulonephritis; microscopic polyangiitis; pauciimmune segmental necrotizing glomerulonephritis; small vessel vasculitis; Wegener's granulomatosis;
D O I
10.1046/j.1523-1755.2000.057003846.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
There have been a number of recent advances in this held. First. the "International Consensus Statement on Testing and Reporting of Antineutrophil Cytoplasmic Antibodies (ANCA)" has been developed to optimize ANCA testing. It requires that all sera are tested by indirect immunofluorescent (IIF) examination of normal peripheral blood neutrophils and, where there is positive fluorescence, in enzyme-linked immunosorbent assays (ELISAs) for antibodies against both proteinase 3 (PR3) and myeloperoxidase (MPO). Testing will be further improved when international standards and common ELISA units are available. Second, new diagnostic criteria for the small vessel vasculitides that take into account ANCA-positivity and target antigen specificity as well as histologic features are currently being produced. Third, we understand that the complications associated with treatment of the ANCA-associated vasculitides are often more hazardous than the underlying disease. and regimens that use effective but less toxic agents are being evaluated. The factors associated with increased risk of relapse, however, remain incompletely understood. Finally. ANCA with specificities other than PR3 and MPO are present in many nonvasculitic autoimmune diseases. Their clinical significance is still largely unclear, and some of the target antigens are present in other cells as well as neutrophils and thus are not strictly "ANCA."
引用
收藏
页码:846 / 862
页数:17
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