ANTIBODY MULTISPECIFICITY IN IMMUNOASSAY INTERFERENCE

被引:71
作者
LEVINSON, SS [1 ]
机构
[1] UNIV LOUISVILLE,DEPT PATHOL,LOUISVILLE,KY 40292
关键词
ANTIBODY DIVERSITY; POLYSPECIFIC ANTIBODIES; RHEUMATOID FACTOR; IDIOTOPES; CROSS-REACTIVE IDIOTOPES; INTERNAL-IMAGE IDIOTOPES; IMMUNOREGULATORY NETWORK; HETEROPHILE ANTIBODIES; IMMUNOASSAY; INTERFERENCE; SPECIFICITY;
D O I
10.1016/0009-9120(92)80048-L
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Recent findings indicate that many endogenous antibodies exhibit multispecificity. These antibodies exhibit a potential for interference with immunoassays. Antibodies that interfere with immunoassays have been called heterophile or heterophilic antibodies. The purpose of this review is: (1) to identify the nature of heterophile antibodies; (2) to delineate the processes that produce them; (3) to examine the mechanisms by which these antibodies cause interference; and (4) to explore how this information can be used to reduce immunoassay interference. In addition to producing specific antibodies, the process of antibody production gives rise to rudimentary antibodies that are polyspecific; e.g., the antigen-combining sits has an affinity for antigens of different chemical composition. This process also generates idiotypic antibodies containing cross-reactive idiotopes. These antibodies along with rheumatoid factors, which are themselves polyspecific and rich in cross-reactive idiotopes, are inherent parts of the process of antibody production, and exhibit multispecificity. Mechanisms by which these antibodies cause immunoassay interference are outlined. These properties of antibodies may have substantial consequence in directing future assays toward greater clinical predictive value.
引用
收藏
页码:77 / 87
页数:11
相关论文
共 89 条
[1]   EVIDENCE FOR A SUBSET OF RHEUMATOID FACTORS THAT CROSS-REACT WITH DNA-HISTONE AND HAVE A DISTINCT CROSS-IDIOTYPE [J].
AGNELLO, V ;
ARBETTER, A ;
IBANEZDEKASEP, G ;
POWELL, R ;
TAN, EM ;
JOSLIN, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 1980, 151 (06) :1514-1527
[2]   RAJI CELL ASSAY FOR IMMUNE-COMPLEXES - EVIDENCE FOR DETECTION OF RAJI-DIRECTED IMMUNOGLOBULIN-G ANTIBODY IN SERA FROM PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
ANDERSON, CL ;
STILLMAN, WS .
JOURNAL OF CLINICAL INVESTIGATION, 1980, 66 (02) :353-360
[3]   BINDING OF CYTOSKELETAL PROTEINS BY MONOCLONAL ANTI-DNA LUPUS AUTOANTIBODIES [J].
ANDRESCHWARTZ, J ;
DATTA, SK ;
SHOENFELD, Y ;
ISENBERG, DA ;
STOLLAR, BD ;
SCHWARTZ, RS .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1984, 31 (02) :261-271
[4]  
BOERMAN OC, 1990, CLIN CHEM, V36, P888
[5]  
BOSCATO LM, 1986, CLIN CHEM, V32, P1491
[6]  
BOSCATO LM, 1988, CLIN CHEM, V34, P27
[7]  
BOSE R, 1988, IMMUNOLOGY, V63, P579
[8]   GUINEA-PIGS WITH INHERITED DEFICIENCIES OF COMPLEMENT COMPONENTS C2 OR C-4 HAVE CHARACTERISTICS OF IMMUNE-COMPLEX DISEASE [J].
BOTTGER, EC ;
HOFFMANN, T ;
HADDING, U ;
BITTERSUERMANN, D .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 78 (03) :689-695
[9]   CURRENT CONCEPTS - IMMUNOLOGY - IDIOTYPES AND IDIOTYPIC NETWORKS [J].
BURDETTE, S ;
SCHWARTZ, RS .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (04) :219-224
[10]   RHEUMATOID-FACTOR AND IMMUNE NETWORKS [J].
CARSON, DA ;
CHEN, PP ;
FOX, RI ;
KIPPS, TJ ;
JIRIK, F ;
GOLDFIEN, RD ;
SILVERMAN, G ;
RADOUX, V ;
FONG, S .
ANNUAL REVIEW OF IMMUNOLOGY, 1987, 5 :109-126