MOLECULAR CHARACTERIZATION OF ANTI-DNA ANTIBODIES INDUCED IN NORMAL MICE BY IMMUNIZATION WITH BACTERIAL-DNA - DIFFERENCES FROM SPONTANEOUS ANTI-DNA IN THE CONTENT AND LOCATION OF V(H) CDR3 ARGININES

Citation
Gs. Gilkeson et al., MOLECULAR CHARACTERIZATION OF ANTI-DNA ANTIBODIES INDUCED IN NORMAL MICE BY IMMUNIZATION WITH BACTERIAL-DNA - DIFFERENCES FROM SPONTANEOUS ANTI-DNA IN THE CONTENT AND LOCATION OF V(H) CDR3 ARGININES, The Journal of immunology, 151(3), 1993, pp. 1353-1364
Citations number
53
Categorie Soggetti
Immunology
Journal title
The Journal of immunology
ISSN journal
00221767 → ACNP
Volume
151
Issue
3
Year of publication
1993
Pages
1353 - 1364
Database
ISI
SICI code
0022-1767(1993)151:3<1353:MCOAAI>2.0.ZU;2-B
Abstract
Immunization of normal mice with bacterial DNA induces a significant a nti-DNA response that includes antibodies resembling some lupus anti-D NA in their binding properties, although lacking specificity for mamma lian dsDNA. To determine the structure of these induced antibodies and their relationship to anti-DNA from lupus mice, we have characterized the clonality and selected V-region sequences of a panel of 20 anti-D NA antibodies from 3 BALB/c mice immunized with ssDNA from Escherichia coli. Southern blot analysis of H and L chain rearrangements indicate d that two of the animals expressed pairs of clonally related antibodi es. Amino acid sequences of 10 of the induced antibodies demonstrated predominant utilization of J558 family V(H) genes and J(H)4 in associa tion with various D(H), Jkappa and Vkappa genes. Among the V(H) CDR3 o f these 10 antibodies, 4 displayed arginine residues as a result of N region additions. None of these antibodies, however, had more than one arginine residue in V(H) CDR3 nor arginines at positions 100 or 100a, characteristic features of lupus antibodies to dsDNA. These results s uggest that normal mice immunized with bacterial DNA display certain f acets of DNA Ag drive, although lacking the mechanisms for the product ion of antibodies to mammalian dsDNA.