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Article
Nature Immunology  4, 343 - 349 (2003)
Published online: 10 March 2003; | doi:10.1038/ni911

Hypergammaglobulinemia and autoantibody induction mechanisms in viral infections

Lukas Hunziker1, 2, 3, Mike Recher1, 3, Andrew J. Macpherson1, Adrian Ciurea1, Stefan Freigang1, Hans Hengartner1 & Rolf M. Zinkernagel1

1  Institute for Experimental Immunology, University Hospital, Schmelzbergstrasse 12, CH-8091 Zurich, Switzerland.

2  University Hospital Basel, Internal Medicine A, Petersgraben 4, 4021 Basel, Switzerland.

3  These authors contributed equally to this work.

Correspondence should be addressed to Lukas Hunziker lhunziker@uhbs.ch or Mike Recher mike.recher@usz.ch
Polyclonal hypergammaglobulinemia is a characteristic of chronic inflammatory conditions, including persisting viral infections and autoimmune diseases. Here we have studied hypergammaglobulinemia in mice infected with lymphocytic choriomeningitis virus (LCMV), which induces nonspecific immunoglobulins as a result of switching natural IgM specificities to IgG. The process is dependent on help from CD4+ T cells that specifically recognize LCMV peptides presented by B cells on major histocompatibility complex class II molecules. Thus, hypergammaglobulinemia may arise when specific helper T cells recognize B cells that have processed viral antigens irrespective of the B cell receptor specificity. This nonspecific B cell activation may contribute to antibody-mediated autoimmunity.

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Nature Immunology
ISSN: 1529-2908
EISSN: 1529-2916
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