TY - JOUR
T1 - Immunoglobulin VH genes in thymic MALT lymphoma are biased toward a restricted repertoire and are frequently unmutated
AU - Yoshida, Megumi
AU - Okabe, Mitsukuni
AU - Eimoto, Tadaaki
AU - Shimizu, Shinichiro
AU - Ueda-Otsuka, Kayo
AU - Okamoto, Masataka
AU - Ishii, Genichiro
AU - Ueda, Ryuzo
AU - Chan, John K.C.
AU - Nakamura, Shigeo
AU - Inagaki, Hiroshi
PY - 2006/2
Y1 - 2006/2
N2 - Thymic MALT lymphoma shows certain distinctive features among MALT lymphomas, such as expression of IgA isotype, consistent lack of API2-MALT1 gene fusion, and very strong association with autoimmune disease, especially Sjogren's syndrome. To help clarify the nature of the clonal lymphoid infiltrates, we analysed the usage and somatic hypermutation of the Ig heavy chain variable region (VH) genes in nine different cases. The VH rearrangement was potentially functional in all cases and was restricted to the VH3 family. VH usage was biased toward VH3-30 (five cases) and VH3-23 (three cases) segments, which have both been frequently expressed by autoimmune B cells. Somatic hypermutation was absent in five cases. Fewer than the expected replacement mutations were found in the framework regions in two cases, indicating a negative antigen selection pressure. Ongoing mutation was absent in all cases. D segment usage was varied, whereas JH segment usage was restricted to JH4. The observed patterns of VH usage and mutations suggested that specific antigens may play a pathologically relevant role in the genesis or progression of thymic MALT lymphoma.
AB - Thymic MALT lymphoma shows certain distinctive features among MALT lymphomas, such as expression of IgA isotype, consistent lack of API2-MALT1 gene fusion, and very strong association with autoimmune disease, especially Sjogren's syndrome. To help clarify the nature of the clonal lymphoid infiltrates, we analysed the usage and somatic hypermutation of the Ig heavy chain variable region (VH) genes in nine different cases. The VH rearrangement was potentially functional in all cases and was restricted to the VH3 family. VH usage was biased toward VH3-30 (five cases) and VH3-23 (three cases) segments, which have both been frequently expressed by autoimmune B cells. Somatic hypermutation was absent in five cases. Fewer than the expected replacement mutations were found in the framework regions in two cases, indicating a negative antigen selection pressure. Ongoing mutation was absent in all cases. D segment usage was varied, whereas JH segment usage was restricted to JH4. The observed patterns of VH usage and mutations suggested that specific antigens may play a pathologically relevant role in the genesis or progression of thymic MALT lymphoma.
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U2 - 10.1002/path.1889
DO - 10.1002/path.1889
M3 - Article
C2 - 16353132
AN - SCOPUS:32244444669
VL - 208
SP - 415
EP - 422
JO - Investigative and Cell Pathology
JF - Investigative and Cell Pathology
SN - 0022-3417
IS - 3
ER -