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Clinical and Vaccine Immunology, January 2006, p. 19-25, Vol. 13, No. 1
1071-412X/06/$08.00+0 doi:10.1128/CVI.13.1.19-25.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Dean T. Nardelli,1,2
K. H. Kevin Luk,1,3
Monica C. Remington,1,4
Steven M. Callister,5 and
Ronald F. Schell1,2,3,4*
Wisconsin State Laboratory of Hygiene,1 Departments of Comparative Biomedical Sciences,2 Bacteriology,3 Medical Microbiology and Immunology, University of Wisconsin, Madison, Wisconsin 53706,4 Microbiology Research Laboratory and Department of Infectious Diseases, Gundersen Lutheran Medical Center, La Crosse, Wisconsin 546015
Received 11 July 2005/ Returned for modification 7 September 2005/ Accepted 21 September 2005
Determination of the immunological mediators responsible for promoting the production of borreliacidal antibody may facilitate the development of an improved borreliosis vaccine for human and veterinary use. Previously, we developed an in vitro assay to determine if borreliacidal antibody production could be augmented by treatment with different cytokines. In this study, in vitro treatment of lymph node cells producing borreliacidal antibody with recombinant interleukin-6 (rIL-6) resulted in a fourfold enhancement of anti-OspA borreliacidal antibody. Moreover, rIL-6 enhanced Western immunoblot titers and increased the number of B lymphocytes. In contrast, treatment of anti-OspA borreliacidal antibody-producing cells with anti-IL-6 resulted in a fourfold reduction in borreliacidal activity. Treatment with anti-IL-6 also inhibited enhanced borreliacidal antibody production induced by anti-gamma interferon. These data suggest that IL-6 plays a significant role in the production of anti-OspA borreliacidal antibodies.
Present address: Medical Science Laboratories, 11020 West Plank Court, Wauwatosa, WI 53226.
| Antimicrob. Agents Chemother. | Clin. Microbiol. Rev. | Infect. Immun. |
|---|---|---|
| J. Clin. Microbiol. | J. Virol. | ALL ASM JOURNALS |