T Cell Receptor Vβ Repertoires of Angioimmunoblastic Lymphadenopathy-like T Cell Lymphoma

References

• Shimoyama M., Minato K., Saito H., Takenaka T., Watanabe S., Nagatani T., Naruto M. Immunoblastic lymphadenopathy (IBL)-like T-cell lymphoma. Jpn. J. Clin. Oncol. 1979; 9(Suppl.)347–356
   Google Scholar
• Frizzera G., Moran E. M., Rappaport H. Angio-immunoblastic lymphadenopathy with dysproteinemia. Lancet 1974; 1: 1070–1073
   PubMed Web of Science ®Google Scholar
• Lukes R. J., Tindle B. H. Immunoblastic lymphadenopathy: A hyperimmune entity resembling Hodgkin's disease. N. Engl. J. Med. 1975; 292: 1–8
   PubMed Web of Science ®Google Scholar
• Fisher R. I., Jaffe E. S., Braylan R. C., Anderson J. C., Tan H. K. Immunoblastic lymphadenopathy: Evolution into a malignant lymphoma with plasmacytoid features. Am. J. Med. 1976; 61: 553–559
   PubMed Web of Science ®Google Scholar
• Nathwani B. N., Rappaport H., Moran E. M., Pangalis G. A., Kim H. Malignant lymphoma arising in angioimmunoblastic lymphadenopathy. Cancer 1978; 41: 578–606
   PubMed Web of Science ®Google Scholar
• Lukes R. J., Tindle B. H. Immunoblastic lymphadenopathy: A prelymphomatous state of immunoblastic sarcoma. Cancer Res. 1978; 64: 241–246
   Google Scholar
• Weiss L. M., Strickler J. G., Dorfman R. F., Horning S. J., Wamke R. A., Sklar J. Clonal T cell populations in the angioimmunoblastic lymphadenopathy and angioimmunoblastic lymphadenopathy-like lymphoma. Am. J. Pathol. 1986; 122: 392–397
   PubMed Web of Science ®Google Scholar
• Griesser H., Feller A., Lennert K., Minden M., Mak T. W. Rearrangement of the B chain of the T cell antigen receptor and immunoglobulin genes in lymphoproliferative disorders. J. Clin. Invest. 1986; 78: 1179–1184
   PubMed Web of Science ®Google Scholar
• Bahler D. W., Berry G., Oksenberg J., Wamke R. A., Levy R. Diversity of T-cell antigen receptor variable genes used by mycosis fungoides cells. Am. J. Pathol. 1992; 140: 1–8
   PubMed Web of Science ®Google Scholar
• Jack A. S., Boylston A. W., Carrel S., Grigor I. Cutaneous T-cell lymphoma cells employ a restricted change of T-cell antigen receptor variable region genes. Am. J. Pathol. 1990; 136: 17–21
   PubMed Web of Science ®Google Scholar
• Poppema S., Hepperle B. Restricted V gene usage in T-cell lymphomas as detected by anti-T-cell receptor variable region reagents. Am. J. Pathol. 1991; 138: 1479–1484
   PubMed Web of Science ®Google Scholar
• Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J. Mol. Biol., 98: 503–517
   PubMed Web of Science ®Google Scholar
• Yanagi Y., Yoshikai Y., Leggett K., Clark S., Alexander I., Mak T. W. A human T cell-specific cDNA clone encodes a protein having extensive homology to immunoglobulin chains. Nature 1984; 308: 145–149
   PubMed Web of Science ®Google Scholar
• Yoshikai Y., Anatoniou D., Clark S. P., Yanagi Y., Sangster R., Elsen P. V., Terhorst C., Mak T. W. Sequence and expression of transcripts of the human T-cell receptor β-chain genes. Nature 1984; 312: 521–524
   PubMed Web of Science ®Google Scholar
• Leiden J. M., Strominger J. L. Generation of diversity of the B chain of the human T-lymphocyte receptor for antigen. Proc. Natl. Acad. Sci. USA 1986; 83: 4456–4460
   PubMed Web of Science ®Google Scholar
• Bahler D. W., Berry G., Oksenberg J., Wamke R. A., Levy R. Diversity of T-cell antigen receptor variable genes used by mycosis fungoides cells. Am. J. Pathol. 1992; 140: 1–8
   PubMed Web of Science ®Google Scholar
• Arnold A., Cossman J., Bakhshi A., Jaffe E. S., Waldmann E. A., Korsmeyer S. J. Immunoglobulin-gene rearrangements as unique clonal markers in human lymphoid neoplasms. N. Engl. J. Med. 1983; 309: 1593–1599
   PubMed Web of Science ®Google Scholar
• Cleary M. L., Chao J., Wamke R., Sklar J. Im-monoglobulin gene rearrangement as a diagnostic criterion of B cell lymphoma. Proc. Natl. Acad. Sci. USA 1984; 81: 593–597
   PubMed Web of Science ®Google Scholar
• Minden M. D., Toyonaga B., Ha K., Yanagi Y., Chin B., Gelfand E., Mak T. W. Somatic rearrangement of T-cell antigen receptor gene in human T-cell malignancies. Proc. Natl. Acad. Sci. USA 1985; 82: 1224–1227
   PubMed Web of Science ®Google Scholar
• Weiss L. M., Jaffe E. S., Liu X. F., Chen Y. Y., Shibata D., Medeiros L. J. Detection and localization of Epstein-Barr viral genomes in angioimmunoblastic lymphadenopathy and angioimmunoblastic lymphadenopathy-like lymphoma. Blood 1992; 79: 1789–1795
   PubMed Web of Science ®Google Scholar
• Anagnostopoulos I., Hummel M., Finn T., Tiemann M., Korbjuhn P., Dimmler C., Gatter K., Dallenbach F., Parwaresch M. R., Stein H. Heterogeneous Epstein-Barr virus infection patterns in peripheral T-cell lymphoma of angioimmunoblastic lymphadenopathy type. Blood 1992; 80: 1804–1812
   PubMed Web of Science ®Google Scholar
• Yu A. M., Song R. L., Yu Z., Chen Y. P., Wang F. Z., Na L. X., Xie G. L., Yang M. J. Detection of human cytomegalovirus antigen and DNA in lymph nodes and peripheral blood mononuclear cells of patients with angioimmunoblastic lymphadenopathy with dysproteinemia. Arch. Pathol. Lab. Med. 1992; 116: 490–494
   PubMed Web of Science ®Google Scholar
• Wucherpfennig K. W., Ota K., Endo N., Seidman J. G., Rosenzweig A., Weiner H. L., Hafler D. A. Shared human T-cell receptor Vβ usage to immunodominant regions of myelin basic protein. Science 1990; 248: 1016–1019
   PubMed Web of Science ®Google Scholar
• Sumida T., Yonaha F., Maeda T., Tanabe E., Koike T., Tomioka H., Yoshida S. T cell receptor repertoire of infiltrating T cells in lips of Sjogren's syndrome patients. J. Clin. Invest. 1992; 89: 681–685
   PubMed Web of Science ®Google Scholar
• Choi Y., Kotzin B., Herron L., Callahan J., Marrack P., Kappler J. Interaction of Staphylococcus aureus toxin “superantigens” with human T cells. Proc. Natl. Acad. Sci. USA 1989; 86: 8941–8945
   PubMed Web of Science ®Google Scholar
• Frankel W. N., Rudy C., Cotfin J. M. Linkage of Mis genes to endogeneous mammary tumor viruses of inbred mice. Nature 1991; 349: 526–528
   PubMed Web of Science ®Google Scholar