Functional heterogeneity in the antibodies produced to Borrelia burgdorferi

Authors
Citation
Jl. Benach, Functional heterogeneity in the antibodies produced to Borrelia burgdorferi, WIEN KLIN W, 111(22-23), 1999, pp. 985-989
Citations number
63
Categorie Soggetti
General & Internal Medicine
Journal title
WIENER KLINISCHE WOCHENSCHRIFT
ISSN journal
00435325 → ACNP
Volume
111
Issue
22-23
Year of publication
1999
Pages
985 - 989
Database
ISI
SICI code
0043-5325(199912)111:22-23<985:FHITAP>2.0.ZU;2-N
Abstract
Antibodies to outer surface molecules of Borrelia burgdorferi (Osp) that ha ve a bactericidal action in the absence of complement have been described. These antibodies are primarily monoclonal to antigenic determinants in OspA and OspB. One of these, CB2, is an IgG1 monoclonal antibody that recognize s an epitope in the carboxy terminus of OspB. The specificity of CB2 is cri tically dependent on the presence of a lysine (Lys) residue in position 253 , not only for binding but also for killing the spirochete. This antibody h as been used successfully to select escape variants or mutants that are mis sing the Lys residue either by a mutation or by deletion as a result of pre mature stop codons. Other antibodies to OspA, OspB, and p39 have also been characterized with similar properties. Another important feature of CB2 is that its bactericidal action is not dependent on agglutination, since Fab f ragments of the whole immunoglobulin molecule can also kill in the absence of complement synergy. The killing action of CB2 is not inhibited by protea se inhibitors, and is dependent on the presence of calcium. Upon contact wi th Borrelia burgdorferi, CB2 causes lysis of the outer membrane and the for mation of a spheroplast. The bactericidal mechanism of this antibody is not known. The sequence of t he heavy and light chain variable regions of CB2 have striking homology to murine antibodies of the autoimmune repertoire, and some of these antibodie s have catalytic properties. In general, catalytic antibodies have enzymati c rates of acceleration that are significantly less than those of proteolyt ic enzymes. If CB2 were a catalytic antibody, its substrate specificity may be expected to be broader. CB2 does not cleave recombinant OspB, nor does it cleave other protein substrates. Its killing activity is not dependent o n proteolysis. Because the bactericidal action of CB2 involves the destruct ion of the outer membrane, it is possible that a phospholipase could be ass ociated with the mechanism. The mobility of spirochetal lipids is altered a fter incubation with CB2, and the bactericidal activity is reduced in the p resence of phospholipase inhibitors. These studies suggest that the bacteri cidal mechanism of CB2, and other similar antibodies, is novel.