Abstract:
:Monoclonal gammopathies (MG) are monoclonal proliferative disorders of B cells at the differentiation stage of Ig production. They can be detected in the serum, either as transient or as persistent homogenous immunoglobulin (H-Ig) components. The exact phenotype, localization, and cell lineage origin of the precursor cells of MG are unknown, but may be crucial for both the correct diagnosis and for timely efficient treatment of the malignant forms. We used for the first time transgenic (Tg) mice (Sp6; mu/kappa) to study the origin of MG. In the mu, kappa Tg mice a small proportion of B cells can still produce endogenous IgM. These cells are of B-1 cell origin. The MG in Tg mice showed a later onset and a lower frequency than those in littermate control mice, mainly due to a four times lower frequency of benign monoclonal gammopathy. The 10% of B-1 cells that were able to produce endogenous Ig led to the development of MG in a frequency that was half the number of MG found in normal littermates. None of the MG in Tg mice produced an Ig of the Tg origin and therefore it can be concluded that they originated from B-1 cells.
journal_name
Eur J Immunoljournal_title
European journal of immunologyauthors
van Arkel C,Hopstaken CM,Zurcher C,Bos NA,Kroese FG,Savelkoul HF,Benner R,Radl Jdoi
10.1002/eji.1830270943subject
Has Abstractpub_date
1997-09-01 00:00:00pages
2436-40issue
9eissn
0014-2980issn
1521-4141journal_volume
27pub_type
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