The immune response to bacterial dextrans. VI. No correlation between the frequency of cells expressing a major anti-dextran idiotype and the idiotype profiles of specific antibody responses
Autor: | Antonio Coutinho, D. Portnoi, I Lundkvist |
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Rok vydání: | 1989 |
Předmět: |
Idiotype
Immunogen Immunology Context (language use) Hemolytic Plaque Technique Epitope Epitopes Leukocyte Count Mice Immune system Immunoglobulin Idiotypes Antibody Specificity Animals B-Lymphocytes Mice Inbred BALB C biology Stem Cells Dextrans General Medicine Molecular biology Antibodies Bacterial Rats Inbred F344 Clone Cells Rats Mice Inbred C57BL biology.protein Antibody Clone (B-cell biology) |
Zdroj: | Scopus-Elsevier |
ISSN: | 0300-9475 |
Popis: | C57BL/6 mice respond to Dextran B512 (Dex) with a predominant idiotype (Id) (17-9) while no such Id-positive antibodies are identified in the specific antibody response of BALB/c mice. We used limiting dilution systems to determine the absolute frequencies of clonal B-cell precursors producing the 17-9 Id in these two mouse strains and analysed the correlation between Id-expression and antibody activity at the clonal level. The results show very similar frequencies of anti-Dex and Id-positive B cells in both strains, but C57BL/6 mice contained fourfold higher frequencies of Dex-specific clonal precursors which are Id-positive. This kind of clone, although not used in the specific response of BALB/c mice, constitute roughly 20% of their anti-Dex repertoire and they are readily induced in this strain. Thus, immunization of both strains with anti-idiotypic antibodies results in the production of Id-positive anti-Dex antibodies with serum titres that directly correlate with precursor frequencies. The results show, therefore, that the section of clonal repertoires utilized in a primary immune response varies with the immunogen, even if thymus-independent. These observations are discussed in the context of the genetic controls of anti-Dex antibody responses and on the general question of the utilization of available antibody repertoires in immune responses. |
Databáze: | OpenAIRE |
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