The serine protease granzyme M is preferentially expressed in NK-cell, γδ T-cell, and intestinal T-cell lymphomas:: evidence of origin from lymphocytes involved in innate immunity

被引:62
作者
Krenacs, L
Smyth, MJ
Bagdi, E
Krenacs, T
Kopper, L
Rudiger, T
Zettl, A
Muller-Hermelink, HK
Jaffe, ES
Raffeld, M [1 ]
机构
[1] NCI, Specialized Diagnost Unit, Pathol Lab, NIH, Bethesda, MD 20892 USA
[2] Bay Zoltan Fdn Appl Res, Lab Tumor Pathol & Mol Diagnost, Inst Biotechnol, Szeged, Hungary
[3] Peter MacCallum Canc Inst, Div Canc Immunol, E Melboune, Vic, Australia
[4] Semmelweis Univ, Inst Pathol & Expt Canc Res 1, H-1085 Budapest, Hungary
[5] Univ Wurzburg, Dept Pathol, D-97070 Wurzburg, Germany
[6] NCI, Hematopathol Sect, Pathol Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1182/blood-2002-09-2908
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Granzyme M (GM) is a novel serine protease whose expression is highly restricted to natural killer (NK) cells, CD3(+)CD56(+) T cells, and gammadelta T cells. Using a GM-specific monoclonal antibody, We analyzed the expression of GM in 214 mature T-cell and NK-cell lymphomas. GM was preferentially expressed in nasal NK/T-cell lymphomas (100%), gammadelta T-cell lymphomas (100%), and intestinal T-cell lymphomas (85%). In contrast, GM expression was present at low prevalence in mycosis fungoides/Sezary syndrome (3%) anaplastic large-cell lymphoma (6%), panniculitis-like T-cell lymphoma (11%), and angioimmunoblastic T-cell lymphoma (0%) cases. Peripheral T-cell lymphomas of unspecified subtype showed an intermediate frequency (37%) of GM expression, consistent with their heterogeneous origin. We conclude that GM expression is a distinctive feature of the nasal NK/T-cell, gammadelta T-cell, and intestinal T-cell lymphomas, and suggest that these tumors develop from lymphocytes involved in innate: immunity.(C) 2003 by The American Society of Hematology.
引用
收藏
页码:3590 / 3593
页数:4
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