COMPARISON BETWEEN THE MHC-RESTRICTED ANTIBODY REPERTOIRE TO ASCARIS ANTIGENS IN ADJUVANT-ASSISTED IMMUNIZATION OR INFECTION

被引:19
作者
CHRISTIE, JF [1 ]
FRASER, EM [1 ]
KENNEDY, MW [1 ]
机构
[1] UNIV GLASGOW,WELLCOME LABS EXPTL PARASITOL,GLASGOW G61 1QH,SCOTLAND
基金
英国惠康基金;
关键词
ASCARIS-SUUM; NEMATODE; ANTIBODY REPERTOIRE; ES ANTIGENS; SOMATIC ANTIGENS; ALLERGEN; MAJOR HISTOCOMPATIBILITY COMPLEX; ADJUVANT;
D O I
10.1111/j.1365-3024.1992.tb00006.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Genetic restrictions to the immune repertoire will be an important consideration in the development of anti-nematode vaccines. It has already been established that the major histocompatibility complex (MHC) limits responsiveness to nematode antigens in infection, but little is known of whether this also applies under other routes of sensitization, such as with adjuvants. The specificity of the antibody response was, therefore, compared in infection and adjuvant-assisted immunization using secreted and somatic antigens of Ascaris suum as a model system in mice and rats. The findings were, first, that the lack of responsiveness to certain antigens in infection was not circumvented by Freund's adjuvant-based immunization, despite the fact that the latter generally elicited higher levels of response. Secondly, that adjuvant-assisted immunization could elicit responses to parasite products which were not detectable in the context of infection. Conversely, some specificities were detectable in infection but absent under adjuvant immunization. Finally, immunization with a defined parasite allergen (ABA-1) in Freund's adjuvant did not provoke an IgE response which would be anticipated if the molecule were to have an intrinsic allergenic property. These results are likely to be of general importance to the application of subunit or recombinant vaccines against nematodiases and to the hypersensitivity reactions which vaccination might engender or recall.
引用
收藏
页码:59 / 73
页数:15
相关论文
共 32 条
[1]  
ALMOND NM, 1986, TROP MED PARASITOL, V37, P381
[2]   A HYPOTHETICAL MODEL OF THE FOREIGN ANTIGEN-BINDING SITE OF CLASS-II HISTOCOMPATIBILITY MOLECULES [J].
BROWN, JH ;
JARDETZKY, T ;
SAPER, MA ;
SAMRAOUI, B ;
BJORKMAN, PJ ;
WILEY, DC .
NATURE, 1988, 332 (6167) :845-850
[3]  
CHRISTIE JF, 1990, IMMUNOLOGY, V69, P596
[4]   IMPROVED IMMUNOGENICITY OF A PEPTIDE EPITOPE AFTER FUSION TO HEPATITIS-B CORE PROTEIN [J].
CLARKE, BE ;
NEWTON, SE ;
CARROLL, AR ;
FRANCIS, MJ ;
APPLEYARD, G ;
SYRED, AD ;
HIGHFIELD, PE ;
ROWLANDS, DJ ;
BROWN, F .
NATURE, 1987, 330 (6146) :381-384
[5]  
ELSE KJ, 1991, IMMUNOLOGY, V72, P508
[6]   GENETICALLY-DETERMINED INFLUENCES ON THE ABILITY OF POOR RESPONDER MICE TO RESPOND TO IMMUNIZATION AGAINST TRICHURIS-MURIS [J].
ELSE, KJ ;
WAKELIN, D .
PARASITOLOGY, 1990, 100 :479-489
[7]   MHC-RESTRICTED ANTIBODY-RESPONSES TO TRICHURIS-MURIS EXCRETORY SECRETORY (E/S) ANTIGEN [J].
ELSE, KJ ;
WAKELIN, D ;
WASSOM, DL ;
HAUDA, KM .
PARASITE IMMUNOLOGY, 1990, 12 (05) :509-527
[8]  
GAJEWSKI TF, 1991, J IMMUNOL, V146, P1750
[9]   DIFFERENT T-HELPER CELL SUBSETS ELICITED IN MICE UTILIZING 2 DIFFERENT ADJUVANT VEHICLES - THE ROLE OF ENDOGENOUS INTERLEUKIN-1 IN PROLIFERATIVE RESPONSES [J].
GRUN, JL ;
MAURER, PH .
CELLULAR IMMUNOLOGY, 1989, 121 (01) :134-145
[10]   THE ANTIBODY RECOGNITION PROFILES OF HUMANS NATURALLY INFECTED WITH ASCARIS-LUMBRICOIDES [J].
HASWELLELKINS, MR ;
KENNEDY, MW ;
MAIZELS, RM ;
ELKINS, DB ;
ANDERSON, RM .
PARASITE IMMUNOLOGY, 1989, 11 (06) :615-627