STUDIES ON THE ADJUVANT ACTIVITY OF NONIONIC SURFACTANT VESICLES - ADJUVANT-DRIVEN IGG2A PRODUCTION INDEPENDENT OF MHC CONTROL

被引:17
作者
BREWER, JM
ALEXANDER, J
机构
[1] Department of Immunology, The Todd Centre, University of Strathclyde, Glasgow, G4 ONR
关键词
ADJUVANT; T-HELPER CELL TYPES 1 AND 2; ANTIBODIES; IGG2A; IGG1; MAJOR HISTOCOMPATABILITY COMPLEX;
D O I
10.1016/0264-410X(94)90265-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The ability, of non-ionic surfactant vesicles (NISV) to stimulate humoral responses to bovine serum albumin (BSA) in H-2b, H-2d and H-2k congenic mice on the Balb genetic background was compared with that of Freund's complete adjuvant (FCA). After two subcutaneous inoculations of BSA formulated in each adjuvant, the NISV preparation was found to stimulate significantly higher total antibody production than FCA in mice carrying the H-2b haplotype at all time points measured after secondary inoculation (2, 5 and 10 weeks) and in Balb/c mice (H-2d) at two weeks after inoculation. Both adjuvants were found to overcome the apparent non-responsiveness of Balb/B mice (H-2b) to BSA alone. Analysis of the IgG subclass responses to BSA revealed a pattern of IgG1 but not IgG2a production similar to that for whole immunoglobulin. IgG1 responses invariably differed significantly, not only between adjuvant formulations bur also between different H-2 haplotypes receiving the same inoculation. On the other hand, IgG2a responses did not differ significantly between H-2 haplotypes in animals given the same adjuvant preparations, although they did differ significantly in mice given BSA alone. Therefore, these results suggest that adjuvants cannot only circumvent antigen-specific nonresponsiveness or low responsiveness, but also can induce antibody isotype switching independent of major histocompatibility complex controls.
引用
收藏
页码:613 / 619
页数:7
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