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[Gamma-1 heavy chain disease with the demonstration of Bence-Jones proteins].

作者信息

Hauke G, Krawinkel U, Schiltz E, Metz B, Hollmann A, Peter H H

机构信息

Abteilung für Rheumatologie und Klinische Immunologie, Universität Freiburg.

出版信息

Immun Infekt. 1991 Jun;19(3):89-90.

PMID:1916871
Abstract

We describe a 61-year-old patient suffering from gamma-1-heavy-chain disease (gamma 1-HCD) associated with Bence-Jones-lambda proteinemia and proteinuria. The analysis of the patients gamma 1-HCD protein (WIN) shows a deletion of the complete Fd fragment. The N-terminal seven amino-acid residue does not resemble any of the known immunoglobulin-heavy-chain variable regions. Unexpectedly, in PBL-DNA and in DNA from EBV-immortalized cells we found in addition to the expected predominantly rearranged Ig-lambda-light-chain gene a predominant rearrangement of an Ig-kappa gene. These findings show that the gamma-1-heavy-chain disease of the patient involves a defective regulation of Ig-light-chain-gene activation as well.

摘要

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