Rare occurrence of IgVH gene translocations and restricted IgVH gene repertoire in ocular MALT-type lymphoma

FISH studies on 37 ocular MALT-type lymphomas yielded chromosomal translocations affecting MAL andT1 BCL10 in 1 case each, no evidence for a break in the FOXP1 locus, and trisomy 3 in 14 out of 34 cases (41%). Three out of 8 cases analyzed used the highly mutated VH3-23 gene and showed ongoing somatic hypermutations.

[1]  D. de Jong,et al.  Chlamydia psittaci is variably associated with ocular adnexal MALT lymphoma in different geographical regions , 2006, The Journal of pathology.

[2]  A. Rosenwald,et al.  Genetic rearrangement of FOXP1 is predominantly detected in a subset of diffuse large B-cell lymphomas with extranodal presentation , 2006, Leukemia.

[3]  Shigeo Nakamura,et al.  Immunoglobulin VH genes in thymic MALT lymphoma are biased toward a restricted repertoire and are frequently unmutated , 2006, The Journal of pathology.

[4]  H. Stein,et al.  Molecular analysis of immunoglobulin genes in primary intraocular lymphoma. , 2005, Investigative ophthalmology & visual science.

[5]  E. Jaffe Pathology and Genetics: Tumours of Haematopoietic and Lymphoid Tissues , 2003 .

[6]  D. Hossfeld E.S. Jaffe, N.L. Harris, H. Stein, J.W. Vardiman (eds). World Health Organization Classification of Tumours: Pathology and Genetics of Tumours of Haematopoietic and Lymphoid Tissues , 2002 .

[7]  E. Berg,et al.  World Health Organization Classification of Tumours , 2002 .

[8]  N. Nakamura,et al.  Immunoglobulin heavy chain gene analysis of ocular adnexal extranodal marginal zone B-cell lymphoma. , 2001, Investigative ophthalmology & visual science.

[9]  T. Yoshino,et al.  Clinical, Histopathological, and Immunogenetic Analysis of Ocular Adnexal Lymphoproliferative Disorders: Characterization of MALT Lymphoma and Reactive Lymphoid Hyperplasia , 2001, Modern Pathology.

[10]  G. Gaedicke,et al.  The B cell superantigen-like interaction of intravenous immunoglobin (IVIG) with Fab fragments of V(H) 3-23 and 3-30/3-30.5 germline gene origin cloned from a patient with Kawasaki disease is enhanced after IVIG therapy. , 2001, Clinical immunology.

[11]  X. Mariette,et al.  Structural analysis of human antibodies to proteinase 3 from patients with Wegener granulomatosis. , 1997, Journal of immunology.