IMMUNOGENICITY AND ANTIGENICITY OF SYNTHETIC PEPTIDES DERIVED FROM THE MITE ALLERGEN-DER-P-I

被引:24
作者
JEANNIN, P
DELNESTE, Y
BUISINE, E
LEMAO, J
DIDIERLAURENT, A
STEWART, GA
TARTAR, A
TONNEL, AB
PESTEL, J
机构
[1] INST PASTEUR, INSERM, CJF 90-06, BP 245, F-59019 LILLE, FRANCE
[2] INST PASTEUR, CNRS, URA 624, F-59019 LILLE, FRANCE
[3] INST PASTEUR, CNRS, URA 1309, F-59019 LILLE, FRANCE
[4] INST PASTEUR, F-75724 PARIS, FRANCE
[5] LAB STALLERGENES, F-94264 FRESNES, FRANCE
[6] PRINCESS MARGARET HOSP CHILDREN, WESTERN AUSTRALIAN RES INST CHILD HLTH, PERTH, WA 6008, AUSTRALIA
关键词
D O I
10.1016/0161-5890(93)90459-O
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As an immunogen must contain both B- and T-cell epitopes, small peptides are usually reported as non-immunogenic unless coupled to a protein carrier. In this study, the immunogenicity of the Der p I synthetic uncoupled peptides (p52-71, p89-104, p 117-133 and p 176-187) previously reported as B-cell epitopes, was evaluated. Different schedules of immunization were used. Results indicated that by using the Vaitukaikis' method three injections of the same peptide without protein carrier was sufficient to induce an specific anti-peptide IgG antibody response (evaluated by ELISA). Indeed, the 16-20 amino-acid long peptides p52-71, p 117-133 and p89-104 were revealed highly immunogenic in rabbits. Furthermore anti-peptide p52-71 and pl 17-133 antibodies were shown by Western-blotting or by neutralization assay to recognize the Der p I molecule either in denaturated or native form as well as Der f I (major allergen of Dermatophagoides farinae). Finally, taking into account the location of Der p I-derived peptides in the three-dimensional model of Der p I, the antigenicity and immunogenicity of peptides were discussed.
引用
收藏
页码:1511 / 1518
页数:8
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