Abstract
Priming of adult responder mice with optimal immunogenic doses of dextran α,1–6 results in reduced antibody responses to secondary antigenic challenge. We have now quantified dextran-specific clonal precursors in the large and small B-lymphocyte compartments within several days or several months after priming with either dextran or antiidiotypic antibodies directed to a dominant idiotype of C57BL/6 mice which accounts for more than 50 % of the antibody response. The results show that 《secondary unresponsiveness》 correlates with idiotype-directed depletion of the appropriate specificities from the immunocompetent resting B-cell pool.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have