Abstract
Until recently, T cells were believed not to be involved in chronic myeloid leukemia. We describe an example of CML in T lymphoblastic crisis with massive generalized lymphadenopathy in which the blasts were CD2(+), CD5(+), and CD7(+), variably CD1(+) and CD3(+), and both responded to and could be induced to produce the T cell growth factor, interleukin-2. Additionally, the blasts were shown to contain the CML-related tyrosine kinase P210bcr-abl rather than the smaller kinase associated with Ph1(+) ALL. Finally, the participation of the T lymphoid lineage in the CML clone was proven by the presence of the same BCR rearrangement in blasts as in granulocytes, suggesting the existence of a bone marrow progenitor common to the T cell and myeloid lineages.
Publication types
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Antigens, CD / analysis
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Blast Crisis / genetics
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Blast Crisis / metabolism
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Blast Crisis / pathology
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Bone Marrow / immunology
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Bone Marrow / metabolism
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Bone Marrow / pathology*
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Fusion Proteins, bcr-abl / metabolism
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Gene Rearrangement, gamma-Chain T-Cell Antigen Receptor
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Hematopoietic Stem Cells / immunology
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Hematopoietic Stem Cells / metabolism
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Hematopoietic Stem Cells / pathology*
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Humans
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Interleukin-2 / biosynthesis
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Interleukin-2 / pharmacology
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / genetics
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / metabolism
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / pathology*
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Male
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Neoplastic Stem Cells / immunology
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Neoplastic Stem Cells / metabolism
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Neoplastic Stem Cells / pathology*
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Oncogenes
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Protein-Tyrosine Kinases / metabolism
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T-Lymphocytes / immunology
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T-Lymphocytes / metabolism
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T-Lymphocytes / pathology*
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Tumor Cells, Cultured / metabolism
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Tumor Cells, Cultured / pathology
Substances
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Antigens, CD
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Interleukin-2
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Protein-Tyrosine Kinases
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Fusion Proteins, bcr-abl