EVALUATION OF MONOCLONAL-ANTIBODIES HAVING SPECIFICITY FOR HUMAN-IGG SUBCLASSES - RESULTS OF THE 2ND IUIS WHO COLLABORATIVE STUDY

被引:48
作者
JEFFERIS, R
REIMER, CB
SKVARIL, F
DELANGE, GG
GOODALL, DM
BENTLEY, TL
PHILLIPS, DJ
VLUG, A
HARADA, S
RADL, J
CLAASSEN, E
BOERSMA, JA
COOLEN, J
机构
[1] UNIV BERN,CH-3000 BERN,SWITZERLAND
[2] SHIONOGI INST MED SCI,OSAKA,JAPAN
[3] TNO,INST EXPTL GERONTOL,RIJSWIJK,NETHERLANDS
[4] TNO,MED BIOL LAB,RIJSWIJK,NETHERLANDS
[5] CTR DIS CONTROL,ATLANTA,GA 30333
[6] NETHERLANDS RED CROSS,BLOOD TRANSFUS SERV,CENT LAB,AMSTERDAM,NETHERLANDS
关键词
MONOCLONAL ANTIBODY; IGG SUBCLASSES; SPECIFICITY;
D O I
10.1016/0165-2478(92)90141-A
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Following the 1st IUIS/WHO Collaborative Study of monoclonal anti-IgG subclass antibodies, a panel of WHO Specificity Reference Reagents (SRR) was established [Jefferis, R., et al. (1985) Immunol. Lett., 10, 223]. At the time, the hope was expressed that further reagents particularly for IgG2, and other allotypic specificities would become available which could be applied in a wide range of assay protocols. The 2nd study reports the evaluation of nineteen anti-subclass and seven anti-allotype monoclonal antibodies. The anti-IgG1 antibody HP6187 was equivalent in performance to the SRR. Others, that were not of the mouse IgG1 isotype, may be useful for particular applications. The anti-IgG2 antibody HP6200 could be a valuable addition to the WHO SRR; it is specific for an epitope in the Fab region but does not have the light chain bias of HP6014. Antibodies of putative allotype specificity exhibited the claimed specificity when used within protocols similar to those employed by the originating laboratory. It appears to be inherent in the nature of the epitopes (allotopes) recognized that it will take several years before reagents applicable to a wide range of techniques will become available.
引用
收藏
页码:143 / 168
页数:26
相关论文
共 36 条
[1]   GAMMA GLOBULIN ANTIGENIC TYPES DEFINED BY HEAVY CHAIN DETERMINANTS [J].
BALLIEUX, RE ;
PUTNAM, FW ;
BERNIER, GM ;
TOMINAGA, K .
SCIENCE, 1964, 145 (362) :168-&
[2]  
Boersma W J, 1988, Adv Exp Med Biol, V237, P125
[3]  
BOERSMA WJA, 1989, PROTIDES B, V36, P161
[4]  
BOERSMA WJA, 1989, PROTIDES B, V36, P157
[5]  
BOERSMA WJA, 1991, LYMPHATIC TISSUES AND IN VIVO IMMUNE RESPONSES, P273
[6]   SEQUENTIAL DOUBLE IMMUNOCYTOCHEMICAL STAINING FOR INSITU IDENTIFICATION OF AN AUTO-ANTI-ALLOTYPE IMMUNE-RESPONSE IN ALLOTYPE-SUPPRESSED RABBITS [J].
CLAASSEN, E ;
ADLER, LT .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1988, 36 (12) :1455-1461
[7]   DOUBLE IMMUNOCYTOCHEMICAL STAINING FOR THE INSITU STUDY OF ALLOTYPE DISTRIBUTION DURING AN ANTI-TRINITROPHENYL IMMUNE-RESPONSE IN CHIMERIC RABBITS [J].
CLAASSEN, E ;
ADLER, LT ;
ADLER, FL .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1986, 34 (08) :989-994
[8]  
De Lange GG, 1988, ADV FORENSIC HAEMOGE, V2, P64
[9]  
DELANGE GG, 1989, PROTIDES B, V36, P49
[10]  
DELANGE GG, 1989, EXP CLIN IMMUNOGENET, V6, P18