Induction of anti-DNA antibodies by immunization with anti-DNA antibodies: mechanism and characterization

Author:

Satake F1,Watanabe N2,Miyasaka N3,Kanai Y4,Kubota T5

Affiliation:

1. School of Allied Health Sciences, Tokyo Medical and Dental University, Tokyo, Japan; Gunma University School of Health Science, Maebashi, Japan.

2. School of Allied Health Sciences, Tokyo Medical and Dental University, Tokyo, Japan

3. The First Department of Medicine, Tokyo Medical and Dental University, Tokyo, Japan

4. Institute of Medical Sciences, The University of Tokyo, Tokyo, Japan

5. Tokyo Medical and Dental University School of Allied Health Sciences, 1-5-45 Yushima, Bunkyo, Tokyo 113-8519, Japan. Tel/Fax: (/ 81) 3 5803 5369;

Abstract

Two well-characterized IgG monoclonal antibodies, reactive with double-stranded (ds) DNA and nucleosomes, were administered to normal BALB/c mice to examine the reproducibility and the biology of a previously reported model of anti-DNA antibody induction by immunization with antiDNA antibodies. The monoclonal antibodies were purified either with or without a high-salt wash to remove nucleosomal antigens bound to them during the cell culture. Both monoclonal antibodies, but not normal IgG, induced significant IgG anti-dsDNA antibody production from 1 week to 25 weeks after the last immunization. The antibodies produced in this manner possess different binding preferences to ds synthetic polynucleotides than the antibodies used for the immunization, and they did not react with nucleosomes. The monoclonal antibodies purified with the high-salt wash were more effective in anti-DNA antibody induction than those purified without the high-salt wash. Even when bound to these monoclonal antibodies, neither dsDNA, nucleosomes, or ds synthetic polynucleotides exert significant antigenicity. For example, anti-DNA antibodies produced by mice immunized with an immune complex formed by poly(dA-dT) and one of the monoclonal antibodies that has a high affinity to this polynucleotide did not show an increased affinity to poly(dA-dT). Together, these results suggest that anti-DNA antibody molecules or processed antibody peptides, and not DNA/nucleosomes carried by anti-DNA antibodies, play a role in this model of anti-DNA antibody production.

Publisher

SAGE Publications

Subject

Rheumatology

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