INTERNATIONAL COLLABORATION COMPARING NEUTRALIZATION AND BINDING ASSAYS FOR MONOCLONAL-ANTIBODIES TO SIMIAN IMMUNODEFICIENCY VIRUS

被引:11
作者
DSOUZA, MP
KENT, KA
THIRIART, C
COLLIGNON, C
MILMAN, G
机构
[1] NATL INST BIOL STAND & CONTROLS,POTTERS BAR EN6 3QG,HERTS,ENGLAND
[2] SMITHKLINE BEECHAM BIOL SA,B-1330 RIXENSART,BELGIUM
关键词
D O I
10.1089/aid.1993.9.415
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Thirteen laboratories characterized a coded panel of 10 MAbs to SIV(mac)251 envelope protein in a collaboration organized by the National Institute of Allergy and Infectious Diseases (NIAID). The MAbs were examined against SIV isolates in neutralization and radioimmune precipitation, immunoblot, enzyme-linked immunosorbent, and radioimmune assays. Although laboratories employed diverse neutralization assays that varied in sensitivity there was agreement on the relative ability of the MAbs to neutralize SIV(mac)251. Additionally, even though the quantity of any single MAb required to neutralize SIV(mac)7251 varied between laboratories, there was agreement on the rank-order strength for the rive neutralizing MAbs. Based on the data from this study, the MAbs were classified according to their neutralization potential as high efficiency (MAb concentration, <5 mug/ml), low efficiency (MAb concentration, 5-100 mug/ml), or nonneutralizing (MAb concentration, >100 mug/ml). The MAbs could be assigned to four serological groups based on ability to cross-neutralize and bind different SIV isolates. The distinction between groups I, II, and III were based on the limited neutralization data obtained with the sooty mangabey isolate.
引用
收藏
页码:415 / 422
页数:8
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