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. 1989 Apr;134(4):761–785.

Immunophenotypic and antigen receptor gene rearrangement analysis in T cell neoplasia.

D M Knowles 1
PMCID: PMC1879785  PMID: 2495724

Abstract

The author reviews the immunophenotypic profiles displayed by the major clinicopathologic categories of T cell neoplasia, the immunophenotypic criteria useful in the immunodiagnosis of T cell neoplasia, and the contributions made by antigen receptor gene rearrangement analysis to the understanding of T cell neoplasia. Neoplasms belonging to distinct clinicopathologic categories of T cell neoplasia often exhibit characteristic immunophenotypic profiles. Approximately 80% of lymphoblastic lymphomas and 20% of acute lymphoblastic leukemias express phenotypes consistent with prethymic and intrathymic stages of T cell differentiation, including intranuclear terminal deoxynucleotidyl transferase. Cutaneous T cell lymphomas of mycosis fungoides type usually express pan-T cell antigens CD2, CD5, and CD3, often lack the pan-T cell antigen CD7, and usually express the mature, peripheral helper subset phenotype, CD4+ CD8-. Cutaneous T cell lymphomas of nonmycosis fungoides type and peripheral T cell lymphomas often lack one or more pan-T cell antigens and, in addition, occasionally express the anomalous CD4+ CD8+ or CD4- CD8- phenotypes. T gamma-lymphoproliferative disease is divisable into two broad categories: those cases that are CD3 antigen positive and exhibit clonal T cell receptor beta chain (TCR-beta) gene rearrangements and those cases that are CD3 antigen negative and exhibit the TCR-beta gene germline configuration. Human T cell lymphotropic virus-I (HTLV-I) associated Japanese, Carribean, and sporadic adult T cell leukemia/lymphomas usually express pan-T cell antigens, the CD4+ CD8- phenotype, and various T cell-associated activation antigens, including the interleukin-2 receptor (CD25). Immunophenotypic criteria useful in the immunodiagnosis of T cell neoplasia include, in increasing order of utility, T cell predominance, T cell subset antigen restriction, anomalous T cell subset antigen expression, and deletion of one or more pan-T cell antigens. Only in exceptional circumstances do normal, non-neoplastic T cell populations express the CD4- CD8- or the CD4+ CD8+ phenotype and/or lack one or more pan-T cell antigens. T cell receptor beta chain gene rearrangement analysis represents an accurate, objective, and sensitive molecular genetic marker of T cell lineage and clonality that allows discrimination among non-T cell, polyclonal T cell and monoclonal T cell populations. Non-T cells exhibit the TCR-beta gene germline configuration.(ABSTRACT TRUNCATED AT 400 WORDS)

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  1. Aisenberg A. C., Krontiris T. G., Mak T. W., Wilkes B. M. Rearrangement of the gene for the beta chain of the T-cell receptor in T-cell chronic lymphocytic leukemia and related disorders. N Engl J Med. 1985 Aug 29;313(9):529–533. doi: 10.1056/NEJM198508293130901. [DOI] [PubMed] [Google Scholar]
  2. Aisenberg A. C., Wilkes B. M. Unusual human lymphoma phenotype defined by monoclonal antibody. J Exp Med. 1980 Oct 1;152(4):1126–1131. doi: 10.1084/jem.152.4.1126. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Anderson K. C., Bates M. P., Slaughenhoupt B. L., Pinkus G. S., Schlossman S. F., Nadler L. M. Expression of human B cell-associated antigens on leukemias and lymphomas: a model of human B cell differentiation. Blood. 1984 Jun;63(6):1424–1433. [PubMed] [Google Scholar]
  4. Arnold A., Cossman J., Bakhshi A., Jaffe E. S., Waldmann T. A., Korsmeyer S. J. Immunoglobulin-gene rearrangements as unique clonal markers in human lymphoid neoplasms. N Engl J Med. 1983 Dec 29;309(26):1593–1599. doi: 10.1056/NEJM198312293092601. [DOI] [PubMed] [Google Scholar]
  5. Asou N., Matsuoka M., Hattori T., Kawano F., Maeda S., Shimada K., Takatsuki K. T cell gamma gene rearrangements in hematologic neoplasms. Blood. 1987 Mar;69(3):968–970. [PubMed] [Google Scholar]
  6. Balus L., Bassetti F., Gentili G. Granulomatous slack skin. Arch Dermatol. 1985 Feb;121(2):250–252. [PubMed] [Google Scholar]
  7. Band H., Hochstenbach F., McLean J., Hata S., Krangel M. S., Brenner M. B. Immunochemical proof that a novel rearranging gene encodes the T cell receptor delta subunit. Science. 1987 Oct 30;238(4827):682–684. doi: 10.1126/science.3672118. [DOI] [PubMed] [Google Scholar]
  8. Bank I., DePinho R. A., Brenner M. B., Cassimeris J., Alt F. W., Chess L. A functional T3 molecule associated with a novel heterodimer on the surface of immature human thymocytes. Nature. 1986 Jul 10;322(6075):179–181. doi: 10.1038/322179a0. [DOI] [PubMed] [Google Scholar]
  9. Barth R. K., Kim B. S., Lan N. C., Hunkapiller T., Sobieck N., Winoto A., Gershenfeld H., Okada C., Hansburg D., Weissman I. L. The murine T-cell receptor uses a limited repertoire of expressed V beta gene segments. Nature. 1985 Aug 8;316(6028):517–523. doi: 10.1038/316517a0. [DOI] [PubMed] [Google Scholar]
  10. Berliner N., Duby A. D., Linch D. C., Murre C., Quertermous T., Knott L. J., Azin T., Newland A. C., Lewis D. L., Galvin M. C. T cell receptor gene rearrangements define a monoclonal T cell proliferation in patients with T cell lymphocytosis and cytopenia. Blood. 1986 Apr;67(4):914–918. [PubMed] [Google Scholar]
  11. Bernard A., Boumsell L., Reinherz E. L., Nadler L. M., Ritz J., Coppin H., Richard Y., Valensi F., Dausset J., Flandrin G. Cell surface characterization of malignant T cells from lymphoblastic lymphoma using monoclonal antibodies: evidence for phenotypic differences between malignant T cells from patients with acute lymphoblastic leukemia and lymphoblastic lymphoma. Blood. 1981 Jun;57(6):1105–1110. [PubMed] [Google Scholar]
  12. Bertness V., Kirsch I., Hollis G., Johnson B., Bunn P. A., Jr T-cell receptor gene rearrangements as clinical markers of human T-cell lymphomas. N Engl J Med. 1985 Aug 29;313(9):534–538. doi: 10.1056/NEJM198508293130902. [DOI] [PubMed] [Google Scholar]
  13. Bier E., Hashimoto Y., Greene M. I., Maxam A. M. Active T-cell receptor genes have intron deoxyribonuclease hypersensitive sites. Science. 1985 Aug 9;229(4713):528–534. doi: 10.1126/science.3927483. [DOI] [PubMed] [Google Scholar]
  14. Borowitz M. J., Reichert T. A., Brynes R. K., Cousar J. B., Whitcomb C. C., Collins R. D., Crissman J. D., Byrne G. E., Jr The phenotypic diversity of peripheral T-cell lymphomas: the Southeastern Cancer Study Group experience. Hum Pathol. 1986 Jun;17(6):567–574. doi: 10.1016/s0046-8177(86)80128-9. [DOI] [PubMed] [Google Scholar]
  15. Borst J., van Dongen J. J., Bolhuis R. L., Peters P. J., Hafler D. A., de Vries E., van de Griend R. J. Distinct molecular forms of human T cell receptor gamma/delta detected on viable T cells by a monoclonal antibody. J Exp Med. 1988 May 1;167(5):1625–1644. doi: 10.1084/jem.167.5.1625. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Borst J., van de Griend R. J., van Oostveen J. W., Ang S. L., Melief C. J., Seidman J. G., Bolhuis R. L. A T-cell receptor gamma/CD3 complex found on cloned functional lymphocytes. Nature. 1987 Feb 19;325(6106):683–688. doi: 10.1038/325683a0. [DOI] [PubMed] [Google Scholar]
  17. Brenner M. B., McLean J., Dialynas D. P., Strominger J. L., Smith J. A., Owen F. L., Seidman J. G., Ip S., Rosen F., Krangel M. S. Identification of a putative second T-cell receptor. Nature. 1986 Jul 10;322(6075):145–149. doi: 10.1038/322145a0. [DOI] [PubMed] [Google Scholar]
  18. Brenner M. B., McLean J., Scheft H., Riberdy J., Ang S. L., Seidman J. G., Devlin P., Krangel M. S. Two forms of the T-cell receptor gamma protein found on peripheral blood cytotoxic T lymphocytes. Nature. 1987 Feb 19;325(6106):689–694. doi: 10.1038/325689a0. [DOI] [PubMed] [Google Scholar]
  19. Brenner M. B., McLean J., Scheft H., Warnke R. A., Jones N., Strominger J. L. Characterization and expression of the human alpha beta T cell receptor by using a framework monoclonal antibody. J Immunol. 1987 Mar 1;138(5):1502–1509. [PubMed] [Google Scholar]
  20. Brouet J. C., Sasportes M., Flandrin G., Preud'Homme J. L., Seligmann M. Chronic lymphocytic leukaemia of T-cell origin. Immunological and clinical evaluation in eleven patients. Lancet. 1975 Nov 8;2(7941):890–893. doi: 10.1016/s0140-6736(75)92127-3. [DOI] [PubMed] [Google Scholar]
  21. Bunn P. A., Jr, Schechter G. P., Jaffe E., Blayney D., Young R. C., Matthews M. J., Blattner W., Broder S., Robert-Guroff M., Gallo R. C. Clinical course of retrovirus-associated adult T-cell lymphoma in the United States. N Engl J Med. 1983 Aug 4;309(5):257–264. doi: 10.1056/NEJM198308043090501. [DOI] [PubMed] [Google Scholar]
  22. Burke J. S., Butler J. J. Malignant lymphoma with a high content of epitheloid histiocytes (Lennert's lymphoma). Am J Clin Pathol. 1976 Jul;66(1):1–9. doi: 10.1093/ajcp/66.1.1. [DOI] [PubMed] [Google Scholar]
  23. Burke J. S., Warnke R. A., Connors J. M., Beckstead J. H. Diffuse malignant lymphoma with cerebriform nuclei: A B-cell lymphoma studied with monoclonal antibodies. Am J Clin Pathol. 1985 Jun;83(6):753–759. doi: 10.1093/ajcp/83.6.753. [DOI] [PubMed] [Google Scholar]
  24. Casey T. T., Posey D. H., McCurley T. L. OKT4 epitope deficiency in significant proportions of the black population. A cause for underestimation of helper/suppressor lymphocyte ratios. Arch Pathol Lab Med. 1986 Aug;110(8):702–704. [PubMed] [Google Scholar]
  25. Catovsky D., Greaves M. F., Rose M., Galton D. A., Goolden A. W., McCluskey D. R., White J. M., Lampert I., Bourikas G., Ireland R. Adult T-cell lymphoma-leukaemia in Blacks from the West Indies. Lancet. 1982 Mar 20;1(8273):639–643. doi: 10.1016/s0140-6736(82)92200-0. [DOI] [PubMed] [Google Scholar]
  26. Catovsky D., Wechsler A., Matutes E., Gomez R., Bourikas G., Cherchi M., Pepys E. O., Pepys M. B., Kitani T., Hoffbrand A. V. The membrane phenotype of T-prolymphocytic leukaemia. Scand J Haematol. 1982 Nov;29(5):398–404. doi: 10.1111/j.1600-0609.1982.tb00614.x. [DOI] [PubMed] [Google Scholar]
  27. Chan J. K., Ng C. S., Lau W. H., Lo S. T. Most nasal/nasopharyngeal lymphomas are peripheral T-cell neoplasms. Am J Surg Pathol. 1987 Jun;11(6):418–429. doi: 10.1097/00000478-198706000-00002. [DOI] [PubMed] [Google Scholar]
  28. Chan W. C., Dahl C., Waldmann T., Link S., Mawle A., Nicholson J., Bach F. H., Bongiovanni K., McCue P. A., Winton E. F. Large granular lymphocyte proliferation: an analysis of T-cell receptor gene arrangement and expression and the effect of in vitro culture with inducing agents. Blood. 1988 Jan;71(1):52–58. [PubMed] [Google Scholar]
  29. Chen Z., Le Paslier D., Dausset J., Degos L., Flandrin G., Cohen D., Sigaux F. Human T cell gamma genes are frequently rearranged in B-lineage acute lymphoblastic leukemias but not in chronic B cell proliferations. J Exp Med. 1987 Apr 1;165(4):1000–1015. doi: 10.1084/jem.165.4.1000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Cheng G. Y., Minden M. D., Toyonaga B., Mak T. W., McCulloch E. A. T cell receptor and immunoglobulin gene rearrangements in acute myeloblastic leukemia. J Exp Med. 1986 Feb 1;163(2):414–424. doi: 10.1084/jem.163.2.414. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Chessells J. M., Hardisty R. M., Rapson N. T., Greaves M. F. Acute lymphoblastic leukaemia in children: Classification and prognosis. Lancet. 1977 Dec 24;2(8052-8053):1307–1309. doi: 10.1016/s0140-6736(77)90361-0. [DOI] [PubMed] [Google Scholar]
  32. Chien Y. H., Gascoigne N. R., Kavaler J., Lee N. E., Davis M. M. Somatic recombination in a murine T-cell receptor gene. Nature. 1984 May 24;309(5966):322–326. doi: 10.1038/309322a0. [DOI] [PubMed] [Google Scholar]
  33. Chien Y. H., Iwashima M., Kaplan K. B., Elliott J. F., Davis M. M. A new T-cell receptor gene located within the alpha locus and expressed early in T-cell differentiation. 1987 Jun 25-Jul 1Nature. 327(6124):677–682. doi: 10.1038/327677a0. [DOI] [PubMed] [Google Scholar]
  34. Clark D. M., Boylston A. W., Hall P. A., Carrel S. Antibodies to T cell antigen receptor beta chain families detect monoclonal T cell proliferation. Lancet. 1986 Oct 11;2(8511):835–837. doi: 10.1016/s0140-6736(86)92870-9. [DOI] [PubMed] [Google Scholar]
  35. Cleary M. L., Chao J., Warnke R., Sklar J. Immunoglobulin gene rearrangement as a diagnostic criterion of B-cell lymphoma. Proc Natl Acad Sci U S A. 1984 Jan;81(2):593–597. doi: 10.1073/pnas.81.2.593. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Colby T. V., Carrington C. B. Pulmonary lymphomas simulating lymphomatoid granulomatosis. Am J Surg Pathol. 1982 Jan;6(1):19–32. doi: 10.1097/00000478-198201000-00002. [DOI] [PubMed] [Google Scholar]
  37. Cossman J., Chused T. M., Fisher R. I., Magrath I., Bollum F., Jaffe E. S. Diversity of immunological phenotypes of lymphoblastic lymphoma. Cancer Res. 1983 Sep;43(9):4486–4490. [PubMed] [Google Scholar]
  38. Cossman J., Uppenkamp M., Sundeen J., Coupland R., Raffeld M. Molecular genetics and the diagnosis of lymphoma. Arch Pathol Lab Med. 1988 Feb;112(2):117–127. [PubMed] [Google Scholar]
  39. Croce C. M., Nowell P. C. Molecular basis of human B cell neoplasia. Blood. 1985 Jan;65(1):1–7. [PubMed] [Google Scholar]
  40. Deneau D. G., Wood G. S., Beckstead J., Hoppe R. T., Price N. Woringer-Kolopp disease (pagetoid reticulosis). Four cases with histopathologic, ultrastructural, and immunohistologic observations. Arch Dermatol. 1984 Aug;120(8):1045–1051. doi: 10.1001/archderm.120.8.1045. [DOI] [PubMed] [Google Scholar]
  41. Epstein A. L., Marder R. J., Winter J. N., Fox R. I. Two new monoclonal antibodies (LN-1, LN-2) reactive in B5 formalin-fixed, paraffin-embedded tissues with follicular center and mantle zone human B lymphocytes and derived tumors. J Immunol. 1984 Aug;133(2):1028–1036. [PubMed] [Google Scholar]
  42. Fairris G. M., Kirkham N., Goodwin P. G., Leppard B. J., White J. E. Erythrodermic follicular mucinosis. Clin Exp Dermatol. 1987 Jan;12(1):50–52. doi: 10.1111/j.1365-2230.1987.tb01857.x. [DOI] [PubMed] [Google Scholar]
  43. Flug F., Pelicci P. G., Bonetti F., Knowles D. M., 2nd, Dalla-Favera R. T-cell receptor gene rearrangements as markers of lineage and clonality in T-cell neoplasms. Proc Natl Acad Sci U S A. 1985 May;82(10):3460–3464. doi: 10.1073/pnas.82.10.3460. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Flynn K. J., Dehner L. P., Gajl-Peczalska K. J., Dahl M. V., Ramsay N., Wang N. Regressing atypical histiocytosis: a cutaneous proliferation of atypical neoplastic histiocytes with unexpectedly indolent biologic behavior. Cancer. 1982 Mar 1;49(5):959–970. doi: 10.1002/1097-0142(19820301)49:5<959::aid-cncr2820490521>3.0.co;2-j. [DOI] [PubMed] [Google Scholar]
  45. Foa R., Pelicci P. G., Migone N., Lauria F., Pizzolo G., Flug F., Knowles D. M., 2nd, Dalla-Favera R. Analysis of T-cell receptor beta chain (T beta) gene rearrangements demonstrates the monoclonal nature of T-cell chronic lymphoproliferative disorders. Blood. 1986 Jan;67(1):247–250. [PubMed] [Google Scholar]
  46. Foon K. A., Todd R. F., 3rd Immunologic classification of leukemia and lymphoma. Blood. 1986 Jul;68(1):1–31. [PubMed] [Google Scholar]
  47. Foroni L., Matutes E., Foldi J., Morilla R., Rabbitts T., Luzzatto L., Catovsky D. T-cell leukemias with rearrangement of the gamma but not beta T-cell receptor genes. Blood. 1988 Feb;71(2):356–362. [PubMed] [Google Scholar]
  48. Franchino C., Reich C., Distenfeld A., Ubriaco A., Knowles D. M. A clinicopathologically distinctive primary splenic histiocytic neoplasm. Demonstration of its histiocyte derivation by immunophenotypic and molecular genetic analysis. Am J Surg Pathol. 1988 May;12(5):398–404. [PubMed] [Google Scholar]
  49. Galton D. A., Goldman J. M., Wiltshaw E., Catovsky D., Henry K., Goldenberg G. J. Prolymphocytic leukaemia. Br J Haematol. 1974 May;27(1):7–23. doi: 10.1111/j.1365-2141.1974.tb06769.x. [DOI] [PubMed] [Google Scholar]
  50. Goding J. W., Burns G. F. Monoclonal antibody OKT-9 recognizes the receptor for transferrin on human acute lymphocytic leukemia cells. J Immunol. 1981 Sep;127(3):1256–1258. [PubMed] [Google Scholar]
  51. González-Sarmiento R., LeBien T. W., Bradley J. G., Greenberg J. M., Seidman J. G., Ang S., Kersey J. H. Acute leukemia expressing the gamma gene product of the putative second T cell receptor. J Clin Invest. 1987 Apr;79(4):1281–1284. doi: 10.1172/JCI112949. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Greenberg J. M., Kersey J. H. Terminal deoxynucleotidyl transferase expression can precede T cell receptor beta chain and gamma chain rearrangement in T cell acute lymphoblastic leukemia. Blood. 1987 Jan;69(1):356–360. [PubMed] [Google Scholar]
  53. Greenberg J. M., Quertermous T., Seidman J. G., Kersey J. H. Human T cell gamma-chain gene rearrangements in acute lymphoid and nonlymphoid leukemia: comparison with the T cell receptor beta-chain gene. J Immunol. 1986 Sep 15;137(6):2043–2049. [PubMed] [Google Scholar]
  54. Greer J. P., York J. C., Cousar J. B., Mitchell R. T., Flexner J. M., Collins R. D., Stein R. S. Peripheral T-cell lymphoma: a clinicopathologic study of 42 cases. J Clin Oncol. 1984 Jul;2(7):788–798. doi: 10.1200/JCO.1984.2.7.788. [DOI] [PubMed] [Google Scholar]
  55. Grogan T. M., Fielder K., Rangel C., Jolley C. J., Wirt D. P., Hicks M. J., Miller T. P., Brooks R., Greenberg B., Jones S. Peripheral T-cell lymphoma: aggressive disease with heterogeneous immunotypes. Am J Clin Pathol. 1985 Mar;83(3):279–288. doi: 10.1093/ajcp/83.3.279. [DOI] [PubMed] [Google Scholar]
  56. Grogan T. M., Richter L. C., Payne C. M., Rangel C. S. Signet-ring cell lymphoma of T-cell origin. An immunocytochemical and ultrastructural study relating giant vacuole formation to cytoplasmic sequestration of surface membrane. Am J Surg Pathol. 1985 Sep;9(9):684–692. [PubMed] [Google Scholar]
  57. Ha-Kawa K., Hara J., Keiko Y., Muraguchi A., Kawamura N., Ishihara S., Doi S., Yabuuchi H. Kappa-chain gene rearrangement in an apparent T-lineage lymphoma. J Clin Invest. 1986 Dec;78(6):1439–1442. doi: 10.1172/JCI112733. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Ha K., Minden M., Hozumi N., Gelfand E. W. Single allelic C mu gene rearrangements in patients with T cell and undifferentiated leukemia. Leuk Res. 1986;10(1):1–8. doi: 10.1016/0145-2126(86)90098-6. [DOI] [PubMed] [Google Scholar]
  59. Hattori T., Uchiyama T., Toibana T., Takatsuki K., Uchino H. Surface phenotype of Japanese adult T-cell leukemia cells characterized by monoclonal antibodies. Blood. 1981 Sep;58(3):645–647. [PubMed] [Google Scholar]
  60. Haynes B. F., Mann D. L., Hemler M. E., Schroer J. A., Shelhamer J. H., Eisenbarth G. S., Strominger J. L., Thomas C. A., Mostowski H. S., Fauci A. S. Characterization of a monoclonal antibody that defines an immunoregulatory T cell subset for immunoglobulin synthesis in humans. Proc Natl Acad Sci U S A. 1980 May;77(5):2914–2918. doi: 10.1073/pnas.77.5.2914. [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Headington J. T., Roth M. S., Ginsburg D., Lichter A. S., Hyder D., Schnitzer B. T-cell receptor gene rearrangement in regressing atypical histiocytosis. Arch Dermatol. 1987 Sep;123(9):1183–1187. [PubMed] [Google Scholar]
  62. Hedrick S. M., Nielsen E. A., Kavaler J., Cohen D. I., Davis M. M. Sequence relationships between putative T-cell receptor polypeptides and immunoglobulins. Nature. 1984 Mar 8;308(5955):153–158. doi: 10.1038/308153a0. [DOI] [PubMed] [Google Scholar]
  63. Hempstead R. W., Ackerman A. B. Follicular mucinosis. A reaction pattern in follicular epithelium. Am J Dermatopathol. 1985 Jun;7(3):245–257. [PubMed] [Google Scholar]
  64. Horning S. J., Weiss L. M., Crabtree G. S., Warnke R. A. Clinical and phenotypic diversity of T cell lymphomas. Blood. 1986 Jun;67(6):1578–1582. [PubMed] [Google Scholar]
  65. Hsu S. M., Jaffe E. S. Leu M1 and peanut agglutinin stain the neoplastic cells of Hodgkin's disease. Am J Clin Pathol. 1984 Jul;82(1):29–32. doi: 10.1093/ajcp/82.1.29. [DOI] [PubMed] [Google Scholar]
  66. Isaacson P. G., O'Connor N. T., Spencer J., Bevan D. H., Connolly C. E., Kirkham N., Pollock D. J., Wainscoat J. S., Stein H., Mason D. Y. Malignant histiocytosis of the intestine: a T-cell lymphoma. Lancet. 1985 Sep 28;2(8457):688–691. doi: 10.1016/s0140-6736(85)92930-7. [DOI] [PubMed] [Google Scholar]
  67. Isaacson P., Jones D. B., Sworn M. J., Wright D. H. Malignant histiocytosis of the intestine: report of three cases with immunological and cytochemical analysis. J Clin Pathol. 1982 May;35(5):510–516. doi: 10.1136/jcp.35.5.510. [DOI] [PMC free article] [PubMed] [Google Scholar]
  68. Isobe M., Erikson J., Emanuel B. S., Nowell P. C., Croce C. M. Location of gene for beta subunit of human T-cell receptor at band 7q35, a region prone to rearrangements in T cells. Science. 1985 May 3;228(4699):580–582. doi: 10.1126/science.3983641. [DOI] [PubMed] [Google Scholar]
  69. Jaffe E. S., Blattner W. A., Blayney D. W., Bunn P. A., Jr, Cossman J., Robert-Guroff M., Gallo R. C. The pathologic spectrum of adult T-cell leukemia/lymphoma in the United States. Human T-cell leukemia/lymphoma virus-associated lymphoid malignancies. Am J Surg Pathol. 1984 Apr;8(4):263–275. doi: 10.1097/00000478-198404000-00003. [DOI] [PubMed] [Google Scholar]
  70. Jaffe E. S., Strauchen J. A., Berard C. W. Predictability of immunologic phenotype by morphologic criteria in diffuse aggressive non-Hodgkin's lymphomas. Am J Clin Pathol. 1982 Jan;77(1):46–49. doi: 10.1093/ajcp/77.1.46. [DOI] [PubMed] [Google Scholar]
  71. Janossy G., Tidman N., Selby W. S., Thomas J. A., Granger S., Kung P. C., Goldstein G. Human T lymphocytes of inducer and suppressor type occupy different microenvironments. Nature. 1980 Nov 6;288(5786):81–84. doi: 10.1038/288081a0. [DOI] [PubMed] [Google Scholar]
  72. Jones C., Morse H. G., Kao F. T., Carbone A., Palmer E. Human T-cell receptor alpha-chain genes: location on chromosome 14. Science. 1985 Apr 5;228(4695):83–85. doi: 10.1126/science.3919444. [DOI] [PubMed] [Google Scholar]
  73. Kadin M. E., Kamoun M. Nonendemic adult T-cell leukemia/lymphoma. Hum Pathol. 1982 Aug;13(8):691–693. doi: 10.1016/s0046-8177(82)80290-6. [DOI] [PubMed] [Google Scholar]
  74. Kadin M. E., Vonderheid E. C., Sako D., Clayton L. K., Olbricht S. Clonal composition of T cells in lymphomatoid papulosis. Am J Pathol. 1987 Jan;126(1):13–17. [PMC free article] [PubMed] [Google Scholar]
  75. Kadin M., Nasu K., Sako D., Said J., Vonderheid E. Lymphomatoid papulosis. A cutaneous proliferation of activated helper T cells expressing Hodgkin's disease-associated antigens. Am J Pathol. 1985 May;119(2):315–325. [PMC free article] [PubMed] [Google Scholar]
  76. Kalyanaraman V. S., Sarngadharan M. G., Robert-Guroff M., Miyoshi I., Golde D., Gallo R. C. A new subtype of human T-cell leukemia virus (HTLV-II) associated with a T-cell variant of hairy cell leukemia. Science. 1982 Nov 5;218(4572):571–573. doi: 10.1126/science.6981847. [DOI] [PubMed] [Google Scholar]
  77. Knowles D. M., 2nd, Dodson L., Burke J. S., Wang J. M., Bonetti F., Pelicci P. G., Flug F., Dalla-Favera R., Wang C. Y. SIg-E- ("null-cell") non-Hodgkin's lymphomas. Multiparametric determination of their B- or T-cell lineage. Am J Pathol. 1985 Sep;120(3):356–370. [PMC free article] [PubMed] [Google Scholar]
  78. Knowles D. M., 2nd, Halper J. P. Human T-cell malignancies: Correlative clinical, histopathologic, immunologic, and cytochemical analysis of 23 cases. Am J Pathol. 1982 Feb;106(2):187–203. [PMC free article] [PubMed] [Google Scholar]
  79. Knowles D. M., 2nd, Halper J. P., Jakobiec F. A. T-lymphocyte subpopulations in B-cell-derived non-Hodgkin's lymphomas and Hodgkin's disease. Cancer. 1984 Aug 15;54(4):644–651. doi: 10.1002/1097-0142(1984)54:4<644::aid-cncr2820540410>3.0.co;2-a. [DOI] [PubMed] [Google Scholar]
  80. Knowles D. M., 2nd, Halper J. P., Jakobiec F. A. The immunologic characterization of 40 extranodal lymphoid infiltrates: usefulness in distinguishing between benign pseudolymphoma and malignant lymphoma. Cancer. 1982 Jun 1;49(11):2321–2335. doi: 10.1002/1097-0142(19820601)49:11<2321::aid-cncr2820491120>3.0.co;2-c. [DOI] [PubMed] [Google Scholar]
  81. Knowles D. M., 2nd, Jakobiec F. A., Halper J. P. Immunologic characterization of ocular adnexal lymphoid neoplasms. Am J Ophthalmol. 1979 May;87(5):603–619. doi: 10.1016/0002-9394(79)90291-5. [DOI] [PubMed] [Google Scholar]
  82. Knowles D. M., 2nd, Jakobiec F. A. Identification of T lymphocytes in ocular adnexal neoplasms by hybridoma monoclonal antibodies. Am J Ophthalmol. 1983 Feb;95(2):233–242. doi: 10.1016/0002-9394(83)90019-3. [DOI] [PubMed] [Google Scholar]
  83. Knowles D. M., 2nd, Neri A., Pelicci P. G., Burke J. S., Wu A., Winberg C. D., Sheibani K., Dalla-Favera R. Immunoglobulin and T-cell receptor beta-chain gene rearrangement analysis of Hodgkin's disease: implications for lineage determination and differential diagnosis. Proc Natl Acad Sci U S A. 1986 Oct;83(20):7942–7946. doi: 10.1073/pnas.83.20.7942. [DOI] [PMC free article] [PubMed] [Google Scholar]
  84. Knowles D. M., 2nd, Pelicci P. G., Dalla-Favera R. Immunoglobulin and T cell receptor beta chain gene DNA probes in the diagnosis and classification of human lymphoid neoplasia. Mol Cell Probes. 1987 Mar;1(1):15–31. doi: 10.1016/0890-8508(87)90004-1. [DOI] [PubMed] [Google Scholar]
  85. Knowles D. M., 2nd, Pelicci P. G., Dalla-Favera R. T-cell receptor beta chain gene rearrangements: genetic markers of T-cell lineage and clonality. Hum Pathol. 1986 Jun;17(6):546–551. doi: 10.1016/s0046-8177(86)80125-3. [DOI] [PubMed] [Google Scholar]
  86. Knowles D. M., 2nd The human T-cell leukemias: clinical, cytomorphologic, immunophenotypic, and genotypic characteristics. Hum Pathol. 1986 Jan;17(1):14–33. doi: 10.1016/s0046-8177(86)80151-4. [DOI] [PubMed] [Google Scholar]
  87. Korsmeyer S. J., Arnold A., Bakhshi A., Ravetch J. V., Siebenlist U., Hieter P. A., Sharrow S. O., LeBien T. W., Kersey J. H., Poplack D. G. Immunoglobulin gene rearrangement and cell surface antigen expression in acute lymphocytic leukemias of T cell and B cell precursor origins. J Clin Invest. 1983 Feb;71(2):301–313. doi: 10.1172/JCI110770. [DOI] [PMC free article] [PubMed] [Google Scholar]
  88. Korsmeyer S. J., Waldmann T. A. Immunoglobulin genes: rearrangement and translocation in human lymphoid malignancy. J Clin Immunol. 1984 Jan;4(1):1–11. doi: 10.1007/BF00915280. [DOI] [PubMed] [Google Scholar]
  89. Kung P. C., Long J. C., McCaffrey R. P., Ratliff R. L., Harrison T. A., Baltimore D. Terminal deoxynucleotidyl transferase in the diagnosis of leukemia and malignant lymphoma. Am J Med. 1978 May;64(5):788–794. doi: 10.1016/0002-9343(78)90518-1. [DOI] [PubMed] [Google Scholar]
  90. Kung P., Goldstein G., Reinherz E. L., Schlossman S. F. Monoclonal antibodies defining distinctive human T cell surface antigens. Science. 1979 Oct 19;206(4416):347–349. doi: 10.1126/science.314668. [DOI] [PubMed] [Google Scholar]
  91. Köhler G., Milstein C. Continuous cultures of fused cells secreting antibody of predefined specificity. Nature. 1975 Aug 7;256(5517):495–497. doi: 10.1038/256495a0. [DOI] [PubMed] [Google Scholar]
  92. Lanier L. L., Cwirla S., Federspiel N., Phillips J. H. Human natural killer cells isolated from peripheral blood do not rearrange T cell antigen receptor beta chain genes. J Exp Med. 1986 Jan 1;163(1):209–214. doi: 10.1084/jem.163.1.209. [DOI] [PMC free article] [PubMed] [Google Scholar]
  93. Lanier L. L., Cwirla S., Phillips J. H. Genomic organization of T cell gamma genes in human peripheral blood natural killer cells. J Immunol. 1986 Dec 1;137(11):3375–3377. [PubMed] [Google Scholar]
  94. Lanier L. L., Federspiel N. A., Ruitenberg J. J., Phillips J. H., Allison J. P., Littman D., Weiss A. The T cell antigen receptor complex expressed on normal peripheral blood CD4-, CD8- T lymphocytes. A CD3-associated disulfide-linked gamma chain heterodimer. J Exp Med. 1987 Apr 1;165(4):1076–1094. doi: 10.1084/jem.165.4.1076. [DOI] [PMC free article] [PubMed] [Google Scholar]
  95. Lanier L. L., Ruitenberg J. J., Phillips J. H. Human CD3+ T lymphocytes that express neither CD4 nor CD8 antigens. J Exp Med. 1986 Jul 1;164(1):339–344. doi: 10.1084/jem.164.1.339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  96. LeBoit P. E., Abel E. A., Cleary M. L., Hoppe R. T., Williams M. L., Wood G. S., Parslow T. G. Clonal rearrangement of the T cell receptor beta gene in the circulating lymphocytes of erythrodermic follicular mucinosis. Blood. 1988 May;71(5):1329–1333. [PubMed] [Google Scholar]
  97. LeBoit P. E., Beckstead J. H., Bond B., Epstein W. L., Frieden I. J., Parslow T. G. Granulomatous slack skin: clonal rearrangement of the T-cell receptor beta gene is evidence for the lymphoproliferative nature of a cutaneous elastolytic disorder. J Invest Dermatol. 1987 Aug;89(2):183–186. doi: 10.1111/1523-1747.ep12470557. [DOI] [PubMed] [Google Scholar]
  98. LeFranc M. P., Forster A., Baer R., Stinson M. A., Rabbitts T. H. Diversity and rearrangement of the human T cell rearranging gamma genes: nine germ-line variable genes belonging to two subgroups. Cell. 1986 Apr 25;45(2):237–246. doi: 10.1016/0092-8674(86)90388-0. [DOI] [PubMed] [Google Scholar]
  99. Lefranc M. P., Forster A., Rabbitts T. H. Genetic polymorphism and exon changes of the constant regions of the human T-cell rearranging gene gamma. Proc Natl Acad Sci U S A. 1986 Dec;83(24):9596–9600. doi: 10.1073/pnas.83.24.9596. [DOI] [PMC free article] [PubMed] [Google Scholar]
  100. Lefranc M. P., Rabbitts T. H. Two tandemly organized human genes encoding the T-cell gamma constant-region sequences show multiple rearrangement in different T-cell types. Nature. 1985 Aug 1;316(6027):464–466. doi: 10.1038/316464a0. [DOI] [PubMed] [Google Scholar]
  101. Leong A. S., Dale B. M., Liew S. H., Sage R. E., Forbes I. J. Node-based T cell lymphoma. The clinical, immunological and morphological spectrum. Pathology. 1981 Jan;13(1):79–95. doi: 10.3109/00313028109086832. [DOI] [PubMed] [Google Scholar]
  102. Levy R., Warnke R., Dorfman R. F., Haimovich J. The monoclonality of human B-cell lymphomas. J Exp Med. 1977 Apr 1;145(4):1014–1028. doi: 10.1084/jem.145.4.1014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  103. Linder J., Ye Y. L., Harrington D. S., Armitage J. O., Weisenburger D. D. Monoclonal antibodies marking T lymphocytes in paraffin-embedded tissue. Am J Pathol. 1987 Apr;127(1):1–8. [PMC free article] [PubMed] [Google Scholar]
  104. Link M. P., Stewart S. J., Warnke R. A., Levy R. Discordance between surface and cytoplasmic expression of the Leu-4 (T3) antigen in thymocytes and in blast cells from childhood T lymphoblastic malignancies. J Clin Invest. 1985 Jul;76(1):248–253. doi: 10.1172/JCI111954. [DOI] [PMC free article] [PubMed] [Google Scholar]
  105. Link M., Warnke R., Finlay J., Amylon M., Miller R., Dilley J., Levy R. A single monoclonal antibody identifies T-cell lineage of childhood lymphoid malignancies. Blood. 1983 Oct;62(4):722–728. [PubMed] [Google Scholar]
  106. Lipford E. H., Jr, Margolick J. B., Longo D. L., Fauci A. S., Jaffe E. S. Angiocentric immunoproliferative lesions: a clinicopathologic spectrum of post-thymic T-cell proliferations. Blood. 1988 Nov;72(5):1674–1681. [PubMed] [Google Scholar]
  107. Littman D. R., Newton M., Crommie D., Ang S. L., Seidman J. G., Gettner S. N., Weiss A. Characterization of an expressed CD3-associated Ti gamma-chain reveals C gamma domain polymorphism. Nature. 1987 Mar 5;326(6108):85–88. doi: 10.1038/326085a0. [DOI] [PubMed] [Google Scholar]
  108. Loh E. Y., Lanier L. L., Turck C. W., Littman D. R., Davis M. M., Chien Y. H., Weiss A. Identification and sequence of a fourth human T cell antigen receptor chain. Nature. 1987 Dec 10;330(6148):569–572. doi: 10.1038/330569a0. [DOI] [PubMed] [Google Scholar]
  109. Macaulay W. L. Lymphomatoid papulosis. A continuing self-healing eruption, clinically benign--histologically malignant. Arch Dermatol. 1968 Jan;97(1):23–30. doi: 10.1001/archderm.97.1.23. [DOI] [PubMed] [Google Scholar]
  110. Manzari V., Gismondi A., Barillari G., Morrone S., Modesti A., Albonici L., De Marchis L., Fazio V., Gradilone A., Zani M. HTLV-V: a new human retrovirus isolated in a Tac-negative T cell lymphoma/leukemia. Science. 1987 Dec 11;238(4833):1581–1583. doi: 10.1126/science.2825353. [DOI] [PubMed] [Google Scholar]
  111. Marcos M. R., Gaspar M. L., de la Hera A., Toribio M. L., Márquez C., Millán I., Martínez-A C. Selective expansion of a CD3+CD4-CD8- subpopulation in clinical groups associated with human immunodeficiency virus infection. Scand J Immunol. 1987 Apr;25(4):321–333. doi: 10.1111/j.1365-3083.1987.tb02197.x. [DOI] [PubMed] [Google Scholar]
  112. Marks S. M., Baltimore D., McCaffrey R. Terminal transferase as a predictor of initial responsiveness to vincristine and prednisone in blastic chronic myelogenous leukemia: a co-operative study. N Engl J Med. 1978 Apr 13;298(15):812–814. doi: 10.1056/NEJM197804132981503. [DOI] [PubMed] [Google Scholar]
  113. McKenna R. W., Parkin J., Kersey J. H., Gajl-Peczalska K. J., Peterson L., Brunning R. D. Chronic lymphoproliferative disorder with unusual clinical, morphologic, ultrastructural and membrane surface marker characteristics. Am J Med. 1977 Apr;62(4):588–596. doi: 10.1016/0002-9343(77)90422-3. [DOI] [PubMed] [Google Scholar]
  114. Meuer S. C., Acuto O., Hercend T., Schlossman S. F., Reinherz E. L. The human T-cell receptor. Annu Rev Immunol. 1984;2:23–50. doi: 10.1146/annurev.iy.02.040184.000323. [DOI] [PubMed] [Google Scholar]
  115. Miedema F., Terpstra F. G., Smit J. W., Daenen S., Gerrits W., Hegde U., Matutes E., Catovsky D., Greaves M. F., Melief C. J. Functional properties of neoplastic T cells in adult T cell lymphoma/leukemia patients from the Caribbean. Blood. 1984 Feb;63(2):477–481. [PubMed] [Google Scholar]
  116. Murphy G. F., Bhan A. K., Sato S., Harrist T. J., Mihm M. C., Jr Characterization of Langerhans cells by the use of monoclonal antibodies. Lab Invest. 1981 Nov;45(5):465–468. [PubMed] [Google Scholar]
  117. Murphy G. F., Bhan A. K., Sato S., Mihm M. C., Jr, Harrist T. J. A new immunologic marker for human Langerhans cells. N Engl J Med. 1981 Mar 26;304(13):791–792. doi: 10.1056/NEJM198103263041320. [DOI] [PubMed] [Google Scholar]
  118. Murphy S., Jaffe E. S. Terminal transferase activity and lymphoblastic neoplasms. N Engl J Med. 1984 Nov 22;311(21):1373–1375. doi: 10.1056/NEJM198411223112110. [DOI] [PubMed] [Google Scholar]
  119. Müller-Hermelink H. K., Stein H., Steinmann G., Lennert K. Malignant lymphoma of plasmacytoid T-cells. Morphologic and immunologic studies characterizing a special type of T-cell. Am J Surg Pathol. 1983 Dec;7(8):849–862. [PubMed] [Google Scholar]
  120. Nadler L. M., Korsmeyer S. J., Anderson K. C., Boyd A. W., Slaughenhoupt B., Park E., Jensen J., Coral F., Mayer R. J., Sallan S. E. B cell origin of non-T cell acute lymphoblastic leukemia. A model for discrete stages of neoplastic and normal pre-B cell differentiation. J Clin Invest. 1984 Aug;74(2):332–340. doi: 10.1172/JCI111428. [DOI] [PMC free article] [PubMed] [Google Scholar]
  121. Nathwani B. N., Diamond L. W., Winberg C. D., Kim H., Bearman R. M., Glick J. H., Jones S. E., Gams R. A., Nissen N. I., Rappaport H. Lymphoblastic lymphoma: a clinicopathologic study of 95 patients. Cancer. 1981 Dec 1;48(11):2347–2357. doi: 10.1002/1097-0142(19811201)48:11<2347::aid-cncr2820481102>3.0.co;2-x. [DOI] [PubMed] [Google Scholar]
  122. Ng C. S., Chan J. K., Lo S. T. Expression of natural killer cell markers in non-Hodgkin's lymphomas. Hum Pathol. 1987 Dec;18(12):1257–1262. doi: 10.1016/s0046-8177(87)80410-0. [DOI] [PubMed] [Google Scholar]
  123. O'Connor N. T., Wainscoat J. S., Weatherall D. J., Gatter K. C., Feller A. C., Isaacson P., Jones D., Lennert K., Pallesen G., Ramsey A. Rearrangement of the T-cell-receptor beta-chain gene in the diagnosis of lymphoproliferative disorders. Lancet. 1985 Jun 8;1(8441):1295–1297. doi: 10.1016/s0140-6736(85)92791-6. [DOI] [PubMed] [Google Scholar]
  124. Pelicci P. G., Allavena P., Subar M., Rambaldi A., Pirelli A., Di Bello M., Barbui T., Knowles D. M., 2nd, Dalla-Favera R., Mantovani A. T cell receptor (alpha, beta, gamma) gene rearrangements and expression in normal and leukemic large granular lymphocytes/natural killer cells. Blood. 1987 Nov;70(5):1500–1508. [PubMed] [Google Scholar]
  125. Pelicci P. G., Knowles D. M., 2nd, Dalla Favera R. Lymphoid tumors displaying rearrangements of both immunoglobulin and T cell receptor genes. J Exp Med. 1985 Sep 1;162(3):1015–1024. doi: 10.1084/jem.162.3.1015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  126. Pelicci P. G., Subar M., Weiss A., Dalla-Favera R., Littman D. R. Molecular diversity of the human T-gamma constant region genes. Science. 1987 Aug 28;237(4818):1051–1055. doi: 10.1126/science.3112943. [DOI] [PubMed] [Google Scholar]
  127. Phyliky R. L., Li C. Y., Yam L. T. T-cell chronic lymphocytic leukemia with morphologic and immunologic characteristics of cytotoxic/suppressor phenotype. Mayo Clin Proc. 1983 Nov;58(11):709–720. [PubMed] [Google Scholar]
  128. Picker L. J., Brenner M. B., Michie S., Warnke R. A. Expression of T cell receptor delta chains in benign and malignant T lineage lymphoproliferations. Am J Pathol. 1988 Sep;132(3):401–405. [PMC free article] [PubMed] [Google Scholar]
  129. Picker L. J., Brenner M. B., Weiss L. M., Smith S. D., Warnke R. A. Discordant expression of CD3 and T-cell receptor beta-chain antigens in T-lineage lymphomas. Am J Pathol. 1987 Dec;129(3):434–440. [PMC free article] [PubMed] [Google Scholar]
  130. Picker L. J., Weiss L. M., Medeiros L. J., Wood G. S., Warnke R. A. Immunophenotypic criteria for the diagnosis of non-Hodgkin's lymphoma. Am J Pathol. 1987 Jul;128(1):181–201. [PMC free article] [PubMed] [Google Scholar]
  131. Pinkus G. S., Said J. W., Hargreaves H. Malignant lymphoma, T-cell type. A distinct morphologic variant with large multilobated nuclei, with a report of four cases. Am J Clin Pathol. 1979 Oct;72(4):540–550. doi: 10.1093/ajcp/72.4.540. [DOI] [PubMed] [Google Scholar]
  132. Pinkus G. S., Thomas P., Said J. W. Leu-M1--a marker for Reed-Sternberg cells in Hodgkin's disease. An immunoperoxidase study of paraffin-embedded tissues. Am J Pathol. 1985 May;119(2):244–252. [PMC free article] [PubMed] [Google Scholar]
  133. Pittaluga S., Raffeld M., Lipford E. H., Cossman J. 3A1 (CD7) expression precedes T beta gene rearrangements in precursor T (lymphoblastic) neoplasms. Blood. 1986 Jul;68(1):134–139. [PubMed] [Google Scholar]
  134. Poppema S., Hollema H., Visser L., Vos H. Monoclonal antibodies (MT1, MT2, MB1, MB2, MB3) reactive with leukocyte subsets in paraffin-embedded tissue sections. Am J Pathol. 1987 Jun;127(3):418–429. [PMC free article] [PubMed] [Google Scholar]
  135. Quertermous T., Murre C., Dialynas D., Duby A. D., Strominger J. L., Waldman T. A., Seidman J. G. Human T-cell gamma chain genes: organization, diversity, and rearrangement. Science. 1986 Jan 17;231(4735):252–255. doi: 10.1126/science.3079918. [DOI] [PubMed] [Google Scholar]
  136. Rambaldi A., Pelicci P. G., Allavena P., Knowles D. M., 2nd, Rossini S., Bassan R., Barbui T., Dalla-Favera R., Mantovani A. T cell receptor beta chain gene rearrangements in lymphoproliferative disorders of large granular lymphocytes/natural killer cells. J Exp Med. 1985 Dec 1;162(6):2156–2162. doi: 10.1084/jem.162.6.2156. [DOI] [PMC free article] [PubMed] [Google Scholar]
  137. Raulet D. H., Garman R. D., Saito H., Tonegawa S. Developmental regulation of T-cell receptor gene expression. Nature. 1985 Mar 7;314(6006):103–107. doi: 10.1038/314103a0. [DOI] [PubMed] [Google Scholar]
  138. Reinherz E. L., Kung P. C., Goldstein G., Levey R. H., Schlossman S. F. Discrete stages of human intrathymic differentiation: analysis of normal thymocytes and leukemic lymphoblasts of T-cell lineage. Proc Natl Acad Sci U S A. 1980 Mar;77(3):1588–1592. doi: 10.1073/pnas.77.3.1588. [DOI] [PMC free article] [PubMed] [Google Scholar]
  139. Reinherz E. L., Schlossman S. F. Current concepts in immunology: Regulation of the immune response--inducer and suppressor T-lymphocyte subsets in human beings. N Engl J Med. 1980 Aug 14;303(7):370–373. doi: 10.1056/NEJM198008143030704. [DOI] [PubMed] [Google Scholar]
  140. Reinherz E. L., Schlossman S. F. The differentiation and function of human T lymphocytes. Cell. 1980 Apr;19(4):821–827. doi: 10.1016/0092-8674(80)90072-0. [DOI] [PubMed] [Google Scholar]
  141. Reynolds C. W., Foon K. A. T gamma-lymphoproliferative disease and related disorders in humans and experimental animals: a review of the clinical, cellular, and functional characteristics. Blood. 1984 Dec;64(6):1146–1158. [PubMed] [Google Scholar]
  142. Ritz J., Nadler L. M., Bhan A. K., Notis-McConarty J., Pesando J. M., Schlossman S. F. Expression of common acute lymphoblastic leukemia antigen (CALLA) by lymphomas of B-cell and T-cell lineage. Blood. 1981 Sep;58(3):648–652. [PubMed] [Google Scholar]
  143. Rivers J. K., Norris P. G., Greaves M. W., Smith N. P. Follicular mucinosis in association with Sézary syndrome. Clin Exp Dermatol. 1987 May;12(3):207–210. doi: 10.1111/j.1365-2230.1987.tb01898.x. [DOI] [PubMed] [Google Scholar]
  144. Roper M., Crist W. M., Metzgar R., Ragab A. H., Smith S., Starling K., Pullen J., Leventhal B., Bartolucci A. A., Cooper M. D. Monoclonal antibody characterization of surface antigens in childhood T-cell lymphoid malignancies. Blood. 1983 May;61(5):830–837. [PubMed] [Google Scholar]
  145. Saito H., Kranz D. M., Takagaki Y., Hayday A. C., Eisen H. N., Tonegawa S. A third rearranged and expressed gene in a clone of cytotoxic T lymphocytes. Nature. 1984 Nov 1;312(5989):36–40. doi: 10.1038/312036a0. [DOI] [PubMed] [Google Scholar]
  146. Sanchez N. P., Pittelkow M. R., Muller S. A., Banks P. M., Winkelmann R. K. The clinicopathologic spectrum of lymphomatoid papulosis: study of 31 cases. J Am Acad Dermatol. 1983 Jan;8(1):81–94. doi: 10.1016/s0190-9622(83)70011-3. [DOI] [PubMed] [Google Scholar]
  147. Seidman J. G., Leder P. The arrangement and rearrangement of antibody genes. Nature. 1978 Dec 21;276(5690):790–795. doi: 10.1038/276790a0. [DOI] [PubMed] [Google Scholar]
  148. Seremetis S. V., Pelicci P. G., Tabilio A., Ubriaco A., Grignani F., Cuttner J., Winchester R. J., Knowles D. M., 2nd, Dalla-Favera R. High frequency of clonal immunoglobulin or T cell receptor gene rearrangements in acute myelogenous leukemia expressing terminal deoxyribonucleotidyltransferase. J Exp Med. 1987 Jun 1;165(6):1703–1712. doi: 10.1084/jem.165.6.1703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  149. Sheibani K., Winberg C. D., van de Velde S., Blayney D. W., Rappaport H. Distribution of lymphocytes with interleukin-2 receptors (TAC antigens) in reactive lymphoproliferative processes, Hodgkin's disease, and non-Hodgkin's lymphomas. An immunohistologic study of 300 cases. Am J Pathol. 1987 Apr;127(1):27–37. [PMC free article] [PubMed] [Google Scholar]
  150. Sheibani K., Wu A., Ben-Ezra J., Stroup R., Rappaport H., Winberg C. Rearrangement of kappa-chain and T-cell receptor beta-chain genes in malignant lymphomas of "T-cell" phenotype. Am J Pathol. 1987 Nov;129(2):201–207. [PMC free article] [PubMed] [Google Scholar]
  151. Siu G., Clark S. P., Yoshikai Y., Malissen M., Yanagi Y., Strauss E., Mak T. W., Hood L. The human T cell antigen receptor is encoded by variable, diversity, and joining gene segments that rearrange to generate a complete V gene. Cell. 1984 Jun;37(2):393–401. doi: 10.1016/0092-8674(84)90369-6. [DOI] [PubMed] [Google Scholar]
  152. Snodgrass H. R., Dembić Z., Steinmetz M., von Boehmer H. Expression of T-cell antigen receptor genes during fetal development in the thymus. Nature. 1985 May 16;315(6016):232–233. doi: 10.1038/315232a0. [DOI] [PubMed] [Google Scholar]
  153. Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
  154. Spits H., Borst J., Tax W., Capel P. J., Terhorst C., de Vries J. E. Characteristics of a monoclonal antibody (WT-31) that recognizes a common epitope on the human T cell receptor for antigen. J Immunol. 1985 Sep;135(3):1922–1928. [PubMed] [Google Scholar]
  155. Stein H., Mason D. Y., Gerdes J., O'Connor N., Wainscoat J., Pallesen G., Gatter K., Falini B., Delsol G., Lemke H. The expression of the Hodgkin's disease associated antigen Ki-1 in reactive and neoplastic lymphoid tissue: evidence that Reed-Sternberg cells and histiocytic malignancies are derived from activated lymphoid cells. Blood. 1985 Oct;66(4):848–858. [PubMed] [Google Scholar]
  156. Strickler J. G., Weiss L. M., Copenhaver C. M., Bindl J., McDaid R., Buck D., Warnke R. Monoclonal antibodies reactive in routinely processed tissue sections of malignant lymphoma, with emphasis on T-cell lymphomas. Hum Pathol. 1987 Aug;18(8):808–814. doi: 10.1016/s0046-8177(87)80055-2. [DOI] [PubMed] [Google Scholar]
  157. Subar M., Giuseppe Pelicci P., Neri A., Allavena P., Littman D. R., Knowles D. M., 2nd, Dalla-Favera R. Patterns of T cell receptor gamma gene rearrangement and expression in B and T lymphoid malignancies. Leukemia. 1988 Jan;2(1):19–26. [PubMed] [Google Scholar]
  158. T-lymphoma associated with HTLV-I outside the Caribbean and Japan. Lancet. 1985 Aug 10;2(8450):337–338. [PubMed] [Google Scholar]
  159. T-lymphoma associated with HTLV-I outside the Caribbean and Japan. Lancet. 1985 Aug 10;2(8450):337–338. [PubMed] [Google Scholar]
  160. Talle M. A., Allegar N., Makowski M., Golstein G. Distinct classes of human T-cell activation antigens. Cell Immunol. 1984 Apr 1;84(2):285–298. doi: 10.1016/0008-8749(84)90100-x. [DOI] [PubMed] [Google Scholar]
  161. Tawa A., Benedict S. H., Hara J., Hozumi N., Gelfand E. W. Rearrangement of the T cell receptor gamma-chain gene in childhood acute lymphoblastic leukemia. Blood. 1987 Dec;70(6):1933–1939. [PubMed] [Google Scholar]
  162. Tawa A., Hozumi N., Minden M., Mak T. W., Gelfand E. W. Rearrangement of the T-cell receptor beta-chain gene in non-T-cell, non-B-cell acute lymphoblastic leukemia of childhood. N Engl J Med. 1985 Oct 24;313(17):1033–1037. doi: 10.1056/NEJM198510243131701. [DOI] [PubMed] [Google Scholar]
  163. Tonegawa S. Somatic generation of antibody diversity. Nature. 1983 Apr 14;302(5909):575–581. doi: 10.1038/302575a0. [DOI] [PubMed] [Google Scholar]
  164. Turner R. R., Wood G. S., Beckstead J. H., Colby T. V., Horning S. J., Warnke R. A. Histiocytic malignancies. Morphologic, immunologic, and enzymatic heterogeneity. Am J Surg Pathol. 1984 Jul;8(7):485–500. [PubMed] [Google Scholar]
  165. Uchiyama T., Yodoi J., Sagawa K., Takatsuki K., Uchino H. Adult T-cell leukemia: clinical and hematologic features of 16 cases. Blood. 1977 Sep;50(3):481–492. [PubMed] [Google Scholar]
  166. Uppenkamp M., Pittaluga S., Lipford E. H., Cossman J. Limited diversity and selection of rearranged gamma genes in polyclonal T cells. J Immunol. 1987 Mar 1;138(5):1618–1620. [PubMed] [Google Scholar]
  167. Vodinelich L., Tax W., Bai Y., Pegram S., Capel P., Greaves M. F. A monoclonal antibody (WT1) for detecting leukemias of T-cell precursors (T-ALL). Blood. 1983 Nov;62(5):1108–1113. [PubMed] [Google Scholar]
  168. Waldmann T. A., Davis M. M., Bongiovanni K. F., Korsmeyer S. J. Rearrangements of genes for the antigen receptor on T cells as markers of lineage and clonality in human lymphoid neoplasms. N Engl J Med. 1985 Sep 26;313(13):776–783. doi: 10.1056/NEJM198509263131303. [DOI] [PubMed] [Google Scholar]
  169. Waldmann T. A., Greene W. C., Sarin P. S., Saxinger C., Blayney D. W., Blattner W. A., Goldman C. K., Bongiovanni K., Sharrow S., Depper J. M. Functional and phenotypic comparison of human T cell leukemia/lymphoma virus positive adult T cell leukemia with human T cell leukemia/lymphoma virus negative Sézary leukemia, and their distinction using anti-Tac. Monoclonal antibody identifying the human receptor for T cell growth factor. J Clin Invest. 1984 Jun;73(6):1711–1718. doi: 10.1172/JCI111379. [DOI] [PMC free article] [PubMed] [Google Scholar]
  170. Waldmann T. A. The arrangement of immunoglobulin and T cell receptor genes in human lymphoproliferative disorders. Adv Immunol. 1987;40:247–321. doi: 10.1016/s0065-2776(08)60241-2. [DOI] [PubMed] [Google Scholar]
  171. Waldron J. A., Leech J. H., Glick A. D., Flexner J. M., Collins R. D. Malignant lymphoma of peripheral T-lymphocyte origin: immunologic, pathologic, and clinical features in six patients. Cancer. 1977 Oct;40(4):1604–1617. doi: 10.1002/1097-0142(197710)40:4<1604::aid-cncr2820400433>3.0.co;2-h. [DOI] [PubMed] [Google Scholar]
  172. Watanabe S., Sato Y., Shimoyama M., Minato K., Shimosato Y. Immunoblastic lymphadenopathy, angioimmunoblastic lymphadenopathy, and IBL-like T-cell lymphoma. A spectrum of T-cell neoplasia. Cancer. 1986 Nov 15;58(10):2224–2232. doi: 10.1002/1097-0142(19861115)58:10<2224::aid-cncr2820581011>3.0.co;2-3. [DOI] [PubMed] [Google Scholar]
  173. Weiss A., Imboden J., Hardy K., Manger B., Terhorst C., Stobo J. The role of the T3/antigen receptor complex in T-cell activation. Annu Rev Immunol. 1986;4:593–619. doi: 10.1146/annurev.iy.04.040186.003113. [DOI] [PubMed] [Google Scholar]
  174. Weiss L. M., Bindl J. M., Picozzi V. J., Link M. P., Warnke R. A. Lymphoblastic lymphoma: an immunophenotype study of 26 cases with comparison to T cell acute lymphoblastic leukemia. Blood. 1986 Feb;67(2):474–478. [PubMed] [Google Scholar]
  175. Weiss L. M., Crabtree G. S., Rouse R. V., Warnke R. A. Morphologic and immunologic characterization of 50 peripheral T-cell lymphomas. Am J Pathol. 1985 Feb;118(2):316–324. [PMC free article] [PubMed] [Google Scholar]
  176. Weiss L. M., Hu E., Wood G. S., Moulds C., Cleary M. L., Warnke R., Sklar J. Clonal rearrangements of T-cell receptor genes in mycosis fungoides and dermatopathic lymphadenopathy. N Engl J Med. 1985 Aug 29;313(9):539–544. doi: 10.1056/NEJM198508293130903. [DOI] [PubMed] [Google Scholar]
  177. Weiss L. M., Picker L. J., Grogan T. M., Warnke R. A., Sklar J. Absence of clonal beta and gamma T-cell receptor gene rearrangements in a subset of peripheral T-cell lymphomas. Am J Pathol. 1988 Mar;130(3):436–442. [PMC free article] [PubMed] [Google Scholar]
  178. Weiss L. M., Trela M. J., Cleary M. L., Turner R. R., Warnke R. A., Sklar J. Frequent immunoglobulin and T-cell receptor gene rearrangements in "histiocytic" neoplasms. Am J Pathol. 1985 Dec;121(3):369–373. [PMC free article] [PubMed] [Google Scholar]
  179. Weiss L. M., Wood G. S., Ellisen L. W., Reynolds T. C., Sklar J. Clonal T-cell populations in pityriasis lichenoides et varioliformis acuta (Mucha-Habermann disease). Am J Pathol. 1987 Mar;126(3):417–421. [PMC free article] [PubMed] [Google Scholar]
  180. Weiss L. M., Wood G. S., Trela M., Warnke R. A., Sklar J. Clonal T-cell populations in lymphomatoid papulosis. Evidence of a lymphoproliferative origin for a clinically benign disease. N Engl J Med. 1986 Aug 21;315(8):475–479. doi: 10.1056/NEJM198608213150802. [DOI] [PubMed] [Google Scholar]
  181. Weiss R. L., Kjeldsberg C. R., Colby T. V., Marty J. Multilobated B cell lymphomas. A study of 7 cases. Hematol Oncol. 1985 Apr-Jun;3(2):79–86. doi: 10.1002/hon.2900030202. [DOI] [PubMed] [Google Scholar]
  182. Wieczorek R., Buck D., Bindl J., Knowles D. M. Monoclonal antibody Leu-22 (L60) permits the demonstration of some neoplastic T cells in routinely fixed and paraffin-embedded tissue sections. Hum Pathol. 1988 Dec;19(12):1434–1443. doi: 10.1016/s0046-8177(88)80236-3. [DOI] [PubMed] [Google Scholar]
  183. Wieczorek R., Burke J. S., Knowles D. M., 2nd Leu-M1 antigen expression in T-cell neoplasia. Am J Pathol. 1985 Dec;121(3):374–380. [PMC free article] [PubMed] [Google Scholar]
  184. Wieczorek R., Suhrland M., Ramsay D., Reed M. L., Knowles D. M., 2nd Leu-M1 antigen expression in advanced (tumor) stage mycosis fungoides. Am J Clin Pathol. 1986 Jul;86(1):25–32. doi: 10.1093/ajcp/86.1.25. [DOI] [PubMed] [Google Scholar]
  185. Willemze R., Meyer C. J., Van Vloten W. A., Scheffer E. The clinical and histological spectrum of lymphomatoid papulosis. Br J Dermatol. 1982 Aug;107(2):131–144. doi: 10.1111/j.1365-2133.1982.tb00331.x. [DOI] [PubMed] [Google Scholar]
  186. Wong-Staal F., Gallo R. C. The family of human T-lymphotropic leukemia viruses: HTLV-I as the cause of adult T cell leukemia and HTLV-III as the cause of acquired immunodeficiency syndrome. Blood. 1985 Feb;65(2):253–263. [PubMed] [Google Scholar]
  187. Wood G. S., Burke J. S., Horning S., Doggett R. S., Levy R., Warnke R. A. The immunologic and clinicopathologic heterogeneity of cutaneous lymphomas other than mycosis fungoides. Blood. 1983 Aug;62(2):464–472. [PubMed] [Google Scholar]
  188. Wood G. S., Strickler J. G., Deneau D. G., Egbert B., Warnke R. A. Lymphomatoid papulosis expresses immunophenotypes associated with T cell lymphoma but not inflammation. J Am Acad Dermatol. 1986 Sep;15(3):444–458. doi: 10.1016/s0190-9622(86)70193-x. [DOI] [PubMed] [Google Scholar]
  189. Wood G. S., Weiss L. M., Hu C. H., Abel E. A., Hoppe R. T., Warnke R. A., Sklar J. T-cell antigen deficiencies and clonal rearrangements of T-cell receptor genes in pagetoid reticulosis (Woringer-Kolopp disease). N Engl J Med. 1988 Jan 21;318(3):164–167. doi: 10.1056/NEJM198801213180307. [DOI] [PubMed] [Google Scholar]
  190. Yanagi Y., Yoshikai Y., Leggett K., Clark S. P., Aleksander I., Mak T. W. A human T cell-specific cDNA clone encodes a protein having extensive homology to immunoglobulin chains. Nature. 1984 Mar 8;308(5955):145–149. doi: 10.1038/308145a0. [DOI] [PubMed] [Google Scholar]
  191. Yancopoulos G. D., Blackwell T. K., Suh H., Hood L., Alt F. W. Introduced T cell receptor variable region gene segments recombine in pre-B cells: evidence that B and T cells use a common recombinase. Cell. 1986 Jan 31;44(2):251–259. doi: 10.1016/0092-8674(86)90759-2. [DOI] [PubMed] [Google Scholar]
  192. Yoshikai Y., Clark S. P., Taylor S., Sohn U., Wilson B. I., Minden M. D., Mak T. W. Organization and sequences of the variable, joining and constant region genes of the human T-cell receptor alpha-chain. 1985 Aug 29-Sep 4Nature. 316(6031):837–840. doi: 10.1038/316837a0. [DOI] [PubMed] [Google Scholar]
  193. Yoshikai Y., Kimura N., Toyonaga B., Mak T. W. Sequences and repertoire of human T cell receptor alpha chain variable region genes in mature T lymphocytes. J Exp Med. 1986 Jul 1;164(1):90–103. doi: 10.1084/jem.164.1.90. [DOI] [PMC free article] [PubMed] [Google Scholar]
  194. van Dongen J. J., Hooijkaas H., Comans-Bitter M., Hählen K., de Klein A., van Zanen G. E., van't Veer M. B., Abels J., Benner R. Human bone marrow cells positive for terminal deoxynucleotidyl transferase (TdT), HLA-DR, and a T cell marker may represent prothymocytes. J Immunol. 1985 Nov;135(5):3144–3150. [PubMed] [Google Scholar]
  195. van Dongen J. J., Quertermous T., Bartram C. R., Gold D. P., Wolvers-Tettero I. L., Comans-Bitter W. M., Hooijkaas H., Adriaansen H. J., de Klein A., Raghavachar A. T cell receptor-CD3 complex during early T cell differentiation. Analysis of immature T cell acute lymphoblastic leukemias (T-ALL) at DNA, RNA, and cell membrane level. J Immunol. 1987 Feb 15;138(4):1260–1269. [PubMed] [Google Scholar]

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