Functional analysis of the classical, alternative, and MBL pathways of the complement system:: standardization and validation of a simple ELISA

被引:232
作者
Seelen, MA
Roos, A
Wieslander, J
Mollnes, TE
Sjöholm, AG
Wurzner, R
Loos, M
Tedesco, F
Sim, RB
Garred, P
Alexopoulos, E
Turner, MW
Daha, MR
机构
[1] Leiden Univ, Med Ctr, Dept Nephrol, NL-2333 ZA Leiden, Netherlands
[2] Wieslab IDEON, Lund, Sweden
[3] Univ Hosp Oslo, Inst Immunol, Rikshosp, Oslo, Norway
[4] Lund Univ, Inst Lab Med, Sect Microbiol Immunol & Glycobiol, Lund, Sweden
[5] Innsbruck Med Univ, Dept Hyg Microbiol & Social Med, Innsbruck, Austria
[6] Johannes Gutenberg Univ Mainz, Inst Med Microbiol & Hyg, D-6500 Mainz, Germany
[7] Univ Trieste, Dept Physiol & Pathol, Trieste, Italy
[8] Univ Oxford, Med Res Council Immunochem Unit, Dept Biochem, Oxford, England
[9] Univ Copenhagen Hosp, Tissue Typing Lab 7631, Dept Clin Immunol, Rigshosp, DK-2100 Copenhagen, Denmark
[10] Hippokrateion Hosp, Dept Nephrol, Thessaloniki, Greece
[11] Inst Child Hlth, Immunobiol Unit, London, England
关键词
systemic lupus erythematosus; MBL pathways; ELISA;
D O I
10.1016/j.jim.2004.11.016
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Primary defence against invading microorganisms depends on a functional innate immune system and the complement system plays a major role in such immunity. Deficiencies in one of the components of the complement system can cause severe and recurrent infections, systemic diseases, such as systemic lupus erythematosus (SLE) and renal disease. Screening for complement deficiencies in the classical or alternative complement pathways has mainly been performed by haemolytic assays. Here. we describe a simple ELISA-based format for the evaluation of three pathways of complement activation. The assays are based on specific coatings for each pathway in combination with specific buffer systems. We have standardized these assays and defined cut off values to detect complement deficiencies at the different levels of the complement system. The results demonstrate the value of these ELISA-based procedures for the functional assessment of complement deficiencies in clinical practice. The assay is now available commercially in kit form. (C) 2004 Published by Elsevier B.V.
引用
收藏
页码:187 / 198
页数:12
相关论文
共 29 条
[1]   Mechanisms of phagocytosis in macrophages [J].
Aderem, A ;
Underhill, DM .
ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 :593-623
[2]   C1-inhibitor deficiency and angioedema [J].
Carugati, A ;
Pappalardo, E ;
Zingale, LC ;
Cicardi, M .
MOLECULAR IMMUNOLOGY, 2001, 38 (2-3) :161-173
[3]  
DAHA MR, 1979, J IMMUNOL, V122, P801
[4]   MANNOSE-BINDING PROTEIN GENE POLYMORPHISM IN SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
DAVIES, EJ ;
SNOWDEN, N ;
HILLARBY, MC ;
CARTHY, D ;
GRENNAN, DM ;
THOMSON, W ;
OLLIER, WER .
ARTHRITIS AND RHEUMATISM, 1995, 38 (01) :110-114
[5]   Impact of mannose-binding lectin on susceptibility to infectious diseases [J].
Eisen, DP ;
Minchinton, RM .
CLINICAL INFECTIOUS DISEASES, 2003, 37 (11) :1496-1505
[6]   NEW PROCEDURE FOR THE DETECTION OF COMPLEMENT DEFICIENCY BY ELISA - ANALYSIS OF ACTIVATION PATHWAYS AND CIRCUMVENTION OF RHEUMATOID-FACTOR INFLUENCE [J].
FREDRIKSON, GN ;
TRUEDSSON, L ;
SJOHOLM, AG .
JOURNAL OF IMMUNOLOGICAL METHODS, 1993, 166 (02) :263-270
[7]   Association of mannose-binding lectin polymorphisms with sepsis and fatal outcome, in patients with systemic inflammatory response syndrome [J].
Garred, P ;
Strom, JJ ;
Quist, L ;
Taaning, E ;
Madsen, HO .
JOURNAL OF INFECTIOUS DISEASES, 2003, 188 (09) :1394-1403
[8]   Mannose-binding lectin deficiency - revisited [J].
Garred, P ;
Larsen, F ;
Madsen, HO ;
Koch, C .
MOLECULAR IMMUNOLOGY, 2003, 40 (2-4) :73-84
[9]  
Garred P, 2000, J RHEUMATOL, V27, P26
[10]  
IKEDA K, 1987, J BIOL CHEM, V262, P7451