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Hodgkin's Disease: Immunoglobulin Heavy and Light Chain Gene Rearrangements Revealed in Single Hodgkin/Reed-Sternberg Cells

Overview
Journal Mol Pathol
Specialty Molecular Biology
Date 1999 Aug 10
PMID 10439838
Citations 3
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Abstract

Aim: To corroborate and investigate the nature of Hodgkin/Reed-Sternberg cells (H/R-S) of various subtypes of Hodgkin's disease.

Method: Single H/R-S cells were micro-picked from frozen sections of tissues affected by Hodgkin's disease. The DNA from these cells was amplified by the polymerase chain reaction (PCR) with immunoglobulin heavy chain (IgH) gene FRIIIa/JH primers and light chain gene family specific primers.

Results: Fifty two of 135 isolated cells gave specific reaction products (36%). IgH and V kappa 4 gene rearrangements were found repeatedly in many H/R-S cells from one case of lymphocyte predominant Hodgkin's disease. Repeated V kappa 4 and individual IgH/V kappa 4,2 rearrangements were seen in one case, and individual IgH and V lambda 3/V kappa 4 rearrangements were seen in another case of nodular sclerosis-type Hodgkin's disease. Repeated IgH/V lambda 3 and individual V lambda 2,4 rearrangements, repeated V kappa 4 and individual IgH/V kappa 3 rearrangements, and repeated IgH and individual V kappa 3/V kappa 4 rearrangement were detected, respectively, in three cases of mixed cellularity-type Hodgkin's disease. Repeated and individual IgH rearrangements were found in another two cases of mixed cellularity-type Hodgkin's disease.

Conclusion: The H/R-S cells isolated from lymphocyte predominant Hodgkin's disease had IgH and V kappa 4 gene rearrangements, which supports the conclusion that this disease results from a proliferation of neoplastic B cells. The IgH and kappa and/or lambda gene rearrangements seen in H/R-S cells isolated from classic Hodgkin's disease (mixed cellularity-type and nodular sclerosis-type) support the theory that these cells derive from B lineage cells at various stages of differentiation. To our knowledge, this is first time that lambda gene rearrangements have been detected in H/R-S cells.

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References
1.
Graninger W, Goldman P, Morton C, OBrien S, Korsmeyer S . The kappa-deleting element. Germline and rearranged, duplicated and dispersed forms. J Exp Med. 1988; 167(2):488-501. PMC: 2188845. DOI: 10.1084/jem.167.2.488. View

2.
Ohno T, Stribley J, Wu G, Hinrichs S, Weisenburger D, Chan W . Clonality in nodular lymphocyte-predominant Hodgkin's disease. N Engl J Med. 1997; 337(7):459-65. DOI: 10.1056/NEJM199708143370704. View

3.
Deane M, Norton J . Immunoglobulin heavy chain variable region family usage is independent of tumor cell phenotype in human B lineage leukemias. Eur J Immunol. 1990; 20(10):2209-17. DOI: 10.1002/eji.1830201009. View

4.
Ruprai A, Pringle J, Angel C, Kind C, LAUDER I . Localization of immunoglobulin light chain mRNA expression in Hodgkin's disease by in situ hybridization. J Pathol. 1991; 164(1):37-40. DOI: 10.1002/path.1711640107. View

5.
Zukerberg L, Collins A, Ferry J, Harris N . Coexpression of CD15 and CD20 by Reed-Sternberg cells in Hodgkin's disease. Am J Pathol. 1991; 139(3):475-83. PMC: 1886227. View