CD56+ CD7+ stem cell leukemia/lymphoma with D2-Jδ1 rearrangement

Internal Medicine

Volumn 38, Issue 7, 1999, Pages 547-555

  Yoshida, Tetsuya ^a   Kimura, Nobuhiro ^a   Sawada, Hitoshi ^b   Suematsu, Eiichi ^c   Nagano, Mitsuyuki ^a   Akiyoshi, Tomi ^a   Motomura, Seiji ^c   Kikuchi, Masahiro ^a   Nishimura, Junji ^d   Tamura, Kazuo ^a  

^a FUKUOKA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b KOKURA MEMORIAL HOSPITAL   (Japan)

^c Fukuoka Teishin Hospital   (Japan)

^d KYUSHU UNIVERSITY   (Japan)

Author keywords

NK like T cells; NK related stem cell leukemia; NKT cell; Prothymocyte; T specific recombination

Indexed keywords

CD56 ANTIGEN; CD7 ANTIGEN; PRIMER DNA;

ACUTE DISEASE; ADULT; ARTICLE; B LYMPHOCYTE; CANCER STEM CELL; CYTOGENETICS; GENE REARRANGEMENT; GENETICS; GENOTYPE; HUMAN; IMMUNOLOGY; IMMUNOPHENOTYPING; LEUKEMIA; LYMPHOMA; MALE; METABOLISM; MIDDLE AGED; NATURAL KILLER CELL; NUCLEOTIDE SEQUENCE; PATHOLOGY; T LYMPHOCYTE;

ACUTE DISEASE; ADULT; ANTIGENS, CD56; ANTIGENS, CD7; B-LYMPHOCYTES; BASE SEQUENCE; CYTOGENETICS; DNA PRIMERS; GENE REARRANGEMENT, B-LYMPHOCYTE, HEAVY CHAIN; GENE REARRANGEMENT, BETA-CHAIN T-CELL ANTIGEN RECEPTOR; GENE REARRANGEMENT, DELTA-CHAIN T-CELL ANTIGEN RECEPTOR; GENE REARRANGEMENT, GAMMA-CHAIN T-CELL ANTIGEN RECEPTOR; GENOTYPE; HUMANS; IMMUNOPHENOTYPING; KILLER CELLS, NATURAL; LEUKEMIA; LYMPHOMA; MALE; MIDDLE AGED; T-LYMPHOCYTES; TUMOR STEM CELLS;

EID: 0033162796     PISSN: 09182918     EISSN: None     Source Type: Journal    
DOI: 10.2169/internalmedicine.38.547     Document Type: Article

References (45)

1. Ortaldo JR, Winkler-Pickett RT, Yagita H, Young HA. Comparative studies of CD3-and CD3+CD56+ cells: Examination of morphology, functions, T cell receptor rearrangement, and poreforming protein expression. Cell Immunol 136: 486-495, 1991.
2. Robertson MJ, Ritz J. Biology and clinical relevance of human natural killer cells. Blood 76: 2421-2438, 1990.
3. Lanier LL, Le AM, Civin CI, Loken MR, Phillips JH. The relationship of CD16 (Leu-11) and Leu-19 (NKH-1) antigen expression on human peripheral blood NK cells and cytotoxic T lymphocytes. J Immunol 136: 4480-4486, 1986.
4. Schmidt RE, Murray C, Daley JF, Schlossman SF, Ritz J. A subset of natural killer cells in peripheral blood displays a mature T cell phenotype. J Exp Med 164: 351-356, 1986.
5. Cerf-Bensussan N, Schneeberger EE, Bhan AK. Immunohistologic and immunoelectron microscopic characterization of the mucosal lymphocytes of human small intestine by the use of monoclonal antibodies. J Immunol 130: 2615-2622, 1983.
6. Deusch K, Pfeffer K, Reich K, et al. Phenotypic and functional characterization of human TCRγδ+ intestinal intraepithelial lymphocytes, in Current Topics in Microbiology and Immunology, vol 173. Pfeffer K, Heeg K, Wagner H, Riethmuller G, Eds. springer-Verlag Corp., New York, 1991: 279-283.
7. Van Tol EA, Verspaget HW, Pena AS, Kraemer CV, Lamers CB. The CD56 adhesion molecule is the major determinant for detecting non-major histocompatibility complex-restricted cytotoxic mononuclear cells from the intestinal lamina propria. Eur J Immunol 22: 23-29, 1992.
8. Abo T. Extrathymic pathways of T-cell differentiation: A primitive and fundamental immune system. Microbiol Immunol 37: 247-258, 1993.
9. Loughran TP Jr. Clonal disease of large granular lymphocytes. Blood 82: 1-14, 1993.
10. Imamura N, Kusunoki Y, Kawa-Ha K, et al. Aggresive natural killer cell leukaemia/lymphoma: Report of four cases and review of the literature. Possible existence of a new clinical entity originating from the third lineage of lymphoid cells. Br J Haematol 75: 49-59, 1990.
11. Macon WR, Williams ME, Greer JP, et al. Natural killer-like T-cell lymphomas: aggressive lymphomas of T-large granular lymphocytes. Blood 87: 1474-1483, 1996.
12. Scott AA, Head DR, Kopecky KJ, et al. HLA-DR-, CD33+, CD56+, CD16-myeloid/natural killer cell acute leukemia: A previously unrecognized form of acute leukemia potentially misdiagnosed as French-American-British acute myeloid leukemia-M3. Blood 84: 244-255, 1994.
13. Suzuki R, Yamamoto K, Seto M, et al. CD7+ and CD56+ myeloid/natural killer cell precursor acute leukemia: A distinct hematolymphoid disease entity. Blood 90: 2417-2428, 1997.
14. Kimura N, Akiyoshi T, Uchida T, et al. High prevalence of T-cell receptor Doδ2(Dδ)Jδ rearrangement in CD7-positive early T cell acute lymphoblastic leukemia. Leukemia 10: 650-657, 1996.
15. Akiyoshi TT, Kimura N, Uike N, et al. Genotypic and cytogenetic study of acute myelocytic leukemia and chronic myelocytic leukemia in blast crisis: specific δ rearrangement pattern does not involve Jδ gene locus. Leuk Res 15: 683-691, 1991.
16. Biondi A, Francia di Celle P, Rossi V, et al. High prevalence of T-cell receptor Vδ2-(D)-Dδ3 or Dδ1/2-Dδ3 rearrangements in B-precursor acute lymphoblastic leukemias. Blood 75: 1834-1840, 1990.
17. Breit TM, Wolvers-Tettero IL, Beishuizen A, Verhoeven MA, Van Wering ER, van Dongen JJ. Southern blot patterns, frequencies, and junctional diversity of T-cell receptor-δ gene rearrangements in acute lymphoblastic leukemia. Blood 82: 3063-3074, 1993.
18. Lauzurica P, Krangel M. Enhancer-dependent and -independent steps in the rearrangement of a human T cell receptor δ transgene. J Exp Med 179: 43-55, 1994.
19. Nagano M, Kimura N, Akiyoshi T, et al. T-stem cell leukemia/lymphoma with both myeloid lineage conversion and T-specific δ recombination. Leuk Res 21: 763-773, 1997.
20. Schmidt CA, Przybylski G, Tietze A, Oettle H, Siegert W, Ludwig WD. Acute myeloid and T-cell acute lymphoblastic leukaemia with aberrant antigen expression exhibit similar TCRδ gene rearrangements. Br J Haematol 92: 929-936, 1996.
21. ISCN. An international system for human cytogenetic nomenclature. Mitelman F, Ed. Basel, Karger, 1995.
22. Bennett JM, Catovsky D, Daniel MT, et al, and French-American-Brotish (FAB) co-operative group. Proposals for the classification of the acute leukaemias. Br J Haematol 33: 451-458, 1976.
23. Ravetch JV, Siebenlist U, Korsmeyer S, Waldmann T, Leder P. Structure of the human immunoglobulin μ locus: Characterization of embryonic and rearranged J and D genes. Cell 27: 583-591, 1981.
24. Kimura N, Toyonaga B, Yoshikai Y, Du RP, Mak TW. Sequences and repertoire of the human T cell receptor α and β chain variable region genes in thymocytes. Eur J Immunol 17: 375-383, 1987.
25. Lefranc MP, Rabbitts TH. Two tandemly organized human genes encoding the T-cell γ constant-region sequences show multiple rearrangement in different T-cell types. Nature 316: 464-466, 1985.
26. Takihara Y, Champagne E, Griesser H, et al. Sequence and organization of the human T cell δ chain gene. Eur J Immunol 18: 283-287, 1988.
27. Takihara Y, Tkachuk D, Michalopoulos E, et al. Sequence and organization of the diversity, joining, and constant region genes of the human T-cell δ-chainlocus. Proc Natl Acad Sci USA 85: 6097-6101, 1988.
28. Kimura N, Takihara Y, Akiyoshi T, et al. Rearrangement of T-cell receptor δ chain gene as a marker of lineage and clonality in T-cell lymphoproliferative disorders. Cancer Res 49: 4488-4492, 1989.
29. Ziemin-van der Poel S, McCabe NR, Gill HJ, et al. Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias. Proc Natl Acad Sci USA 88: 10735-10739, 1991.
30. Pui CH, Raimondi SC, Head DR, et al. Characterization of childhood acute leukemia with multiple myeloid and lymphoid markers at diagnosis and at relapse. Blood 78: 1327-1337, 1991.
31. Sanchez MJ, Muench MO, Roncarolo MG, Lanier LL, Phillips JH. Identification of a common T/natural killer cell progenitor in human fetal thymus. J Exp Med 180: 569-576, 1994.
32. Jaffe ES. Classification of natural killer (NK) cell and NK-like T-cell malignancies. Blood 87: 1207-1210, 1996.
33. Emile JF, Boulland ML, Haioun C, et al. CD5-CD56+ T-cell receptor silent peripheral T-cell lymphomas are natural killer cell lymphomas. Blood 87: 1466-1473, 1996.
34. van Dongen JJ, Comans-Bitter WM, Wolvers-Tettero IL, Borst J, Development of human T lymphocytes and their thymus-dependency. Thymus 16: 207-234, 1990.
35. Haynes BF, Denning SM, Singer KH, Kurtzberg J. Ontogeny of T-cell precursors: a model for the initial stages of human T-cell development. Immunol Today 10: 87-91, 1989.
36. Palacios R, Pelkonen J. Prethymic and intrathymic mouse T-cell progenitors: Growth requirements and analysis of the expression of genes encoding TCR/T3 components and other T-cell-specific molecules. Immunol Rev 104: 5-27, 1988.
37. Griffih JD, Ritz J, Nadler LM, Schlossman SF. Expression of myeloid differentiation antigens on normal and malignant myeloid cells. J Clin Invest 68: 932-941, 1981.
38. Andrews RG, Takahashi M, Segal GM, Powell JS, Bernstein ID, Singer JW. The L4F3 antigen is expressed by unipotent and multipotent colony forming cells but not by their precursors. Blood 68: 1030-1035, 1986.
39. Galy A, Travis M, Cen D, Chen B. Human T, B, natural killer, and dendric cells arise from a common bone marrow progenitor cell subset. Immunity 3: 459-473, 1995.
40. Kondo M, Weissman IL, Akashi K. Identification of clonogenic common lymphoid progenitors in mouse bone marrow. Cell 91: 661-672, 1997.
41. Wu L, Antica M, Johnson GR, Scollay R, Shortman K. Developmental potential of the earliest precursor cells from the adult mouse thymus. J Exp Med 174: 1617-1627, 1991.
42. Matsuzaki Y, Gyotoku J, Ogawa M, et al. Characterization of c-kit positive intrathymic stem cells that are restricted to lymphoid differentiation. J Exp Med 178: 1283-1292, 1993.
43. SumidaT, Sakamoto A, Murata H, et al. Selective reduction of T cells bearing invariant Vaα24JαQ antigen receptor in patients with systemic sclerosis. J Exp Med 182: 1163-1168, 1995.
44. Vicari AP, Zlotnik A. Mouse NK1.1+ T cells: a new family of T cells, Immunology Today 17: 71-76, 1996.
45. Kimura N, Yoshida T, Nagano M, Tamura K. Importance of TCRδ chain gene analysis on CD7+ and CD56+ myeloid/natural killer cell precursor acute leukemia. Blood 91: 2622-2624, 1998.