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Abstract

In mice with targeted disruption of the gene that encodes interleukin-6 (IL-6), greatly reduced numbers of immunoglobulin A (IgA)-producing cells were observed at mucosae and grossly deficient local antibody responses were recorded after mucosal challenge with either ovalbumin or vaccinia virus. The IgA response in the lungs was completely restored after intranasal infection with recombinant vaccinia viruses engineered to express IL-6. These findings demonstrate a critical role for IL-6 in vivo in the development of local IgA antibody responses and illustrate the effectiveness of vector-directed cytokine gene therapy.

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Published In

Science
Volume 264 | Issue 5158
22 April 1994

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Published in print: 22 April 1994

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Authors

Affiliations

Alistair J. Ramsay
The John Curtin School of Medical Research, Australian National University, Canberra 0200, Australia.
Alan J. Husband
Department of Veterinary Pathology, University of Sydney, Sydney NSW 2006, Australia.
lan A. Ramshaw
The John Curtin School of Medical Research, Australian National University, Canberra 0200, Australia.
Shisan Bao
Department of Veterinary Pathology, University of Sydney, Sydney NSW 2006, Australia.
Klaus I. Matthaei
The John Curtin School of Medical Research, Australian National University, Canberra 0200, Australia.
Georges Koehler
Max Planck Institute for Immunobiology, Stuebeweg 51, D-79108 Freiburg, Germany.
Manfred Kopf
Max Planck Institute for Immunobiology, Stuebeweg 51, D-79108 Freiburg, Germany.

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