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• W2022280131 abstract "Objective Immunization with peptide fragments of autoantigens may lead to an immune response at both the T and B cell level that is directed not only at the immunogen, but also at the autoantigen from which the peptide came. In addition, a complex multicomponent particle may become the target of this expanded immune response. The purpose of this study was to determine the ability of several different peptides from 60-kd Ro to induce expansion of the immune response to the Ro/La RNP particle. Methods We immunized BALB/c mice with 3 different oligopeptides from human 60-kd Ro (or, SSA). Results Animals immunized with peptides either identical to or differing by only 1 amino acid developed autoimmunity to the entire Ro RNP particle. Animals immunized with a human peptide highly divergent from the corresponding mouse sequence developed an immune response to the immunogen only and showed little evidence of epitope spreading. Furthermore, these mice did not have antibodies that bound the poorly conserved mouse homolog peptide, and the antibody response to this peptide did not include IgG1. Conclusion These data indicate that B lymphocytes specific for the self-peptide that is homologous to the immunogen are a critical determinant for spreading of the immune response to other components of self." @default.
• W2022280131 created "2016-06-24" @default.
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• W2022280131 date "1999-05-01" @default.
• W2022280131 modified "2023-09-24" @default.
• W2022280131 title "Immunization of mice with human 60-kd Ro peptides results in epitope spreading if the peptides are highly homologous between human and mouse" @default.
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• W2022280131 doi "https://doi.org/10.1002/1529-0131(199905)42:5<1017::aid-anr22>3.0.co;2-7" @default.
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