Retroviruses in Human T-Cell Malignancies

References

• Martin M A, Bryan T, Rasheed S, et al. Identification and cloning of endogenous retroviral sequences present in human DNA. Proc Natl Acad Sci (USA) 1981; 78: 4892–4896
   PubMed Web of Science ®Google Scholar
• Bonner T A, O'Connel C O, Cohen M. Cloned endogenous retroviral sequences from human DNA. Proc Natl Acad Sci (USA) 1982; 80: 4709–4713
   Google Scholar
• Callahan R, Drohan W, Tronick S, et al. Detection and cloning of human DNA sequences related to the mouse mammary tumor virus genome. Proc Natl Acad Sci (USA) 1982; 79: 5503–5507
   PubMed Web of Science ®Google Scholar
• Bishop J M. Retroviruses. Ann Rev Biochem 1978; 47: 35–88
   PubMed Web of Science ®Google Scholar
• Duesberg P H. Transforming genes of retroviruses. Cold Spring Harbor Symp Quant Biol 1979; 44: 13–30
   Google Scholar
• Wong-Staal F, Gallo R C. The transforming genes of primate and other retroviruses and their human homologs. Viral Oncology, G Klein. Raven Press, New York 1982; 153–177
   Google Scholar
• Hayward W S, Neel B G, Astrin S M. Induction of lymphoid leukosis by avian leukosis virus: Activation of a cellular “one” gene by promoter insertion. Nature (London) 1981; 290: 475–480
   PubMed Web of Science ®Google Scholar
• Neel B G, Hayward W S, Robinson H L, et al. Avian leukosis virus-induced tumors have common proviral integration sites and synthesize discrete new RNAs: Oncogenesis by promotor insertion. Cell 1981; 23: 323–334
   PubMed Web of Science ®Google Scholar
• Jarrett W, Martin Crighton B. W, et al. Leukemia in the cat. Transmission experiments with leukaemia (lymphosarcoma). Nature (London) 1964; 202: 566–567
   PubMed Web of Science ®Google Scholar
• Hardy W D, McClelland A J, Zuckerman E E, . Immunology and epidemiology of feline leukemia virus nonproducer lymphomas. Viruses in Naturally Occurring Cancers, M Essex, G Todaro, H zur Hausen, et al. Cold Spring Harbor Press, New York 1980; Vol 7: 677–699
   Google Scholar
• Rokjo J L, Hoover E A, Quackenbush S L, et al. Reactivation of latent leukemia virus infection. Nature (London) 1982; 298: 385–388
   PubMed Web of Science ®Google Scholar
• Burny A, Bruck C, Chantrenne H, . Bovine leukemia virus: Molecular biology and epidemiology. Viral Oncology, G Klein, et al. Raven Press, New York 1980; 231–289
   Google Scholar
• Gilden R W, Long C W, Hanson M, et al. Characteristics of the major internal protein and RNA dependent DNA polymerase of bovine leukemia virus. J Gen Virol 1975; 29: 305–314
   PubMed Web of Science ®Google Scholar
• Morgan D A, Ruscetti F W, Gallo R C. Selective in vitro growth of T-lymphocytes from normal human bone marrow. Science 1976; 193: 1007–1008
   PubMed Web of Science ®Google Scholar
• Sarin P S, Gallo R C. Human T-cell growth factor. CRC Crit Rev Immunol 1984; 4: 279–305
   Google Scholar
• Poiesz B J, Ruscetti F W, Gazdar A F, et al. Detection and isolation of type C retrovirus particles from fresh and cultured lymphocytes of a patient with cutaneous T-cell lymphoma. Proc Natl Acad Sci (USA) 1980; 77: 7415–7419
   PubMed Web of Science ®Google Scholar
• Poiesz B J, Ruscetti F W, Reitz M S, et al. Isolation of a new type-C retrovirus (HTLV) in primary uncultured cells of a patient with Sezary T-cell leukemia. Nature (London) 1981; 294: 268–271
   PubMed Web of Science ®Google Scholar
• Takatsuki K, Uchiyama T, Ueshima Y, et al. Adult T-cell leukemia: further clinical observations and cytogenetic and functional studies of leukemic cells. Jpn J Clin Oncol 1979; 9: 317–324
   Web of Science ®Google Scholar
• Uchiyama T, Yodoi J, Sagawa K, et al. Adult T-cell leukemia: Clinical and hematologic features of 16 cases. Blood 1977; 50: 481–492
   PubMed Web of Science ®Google Scholar
• Catovsky D, Greaves M S, Rose M, et al. Adult T-cell lymphomaleukaemia in blacks from the West Indies. Lancet 1982; 2(#8273)639–642
   Google Scholar
• Rho H M, Poiesz B, Ruscetti F W, et al. Characterization of the reverse transcriptase from a new retrovirus (HTLV) produced by a human cutaneous T-cell lymphoma cell line. Virology 1981; 112: 355–360
   PubMed Web of Science ®Google Scholar
• Sarin P S, Gallo R C. Human T-cell leukemia-lymphoma virus (HTLV). Progress in Hematology, E B Brown. Grune and Stratton, New York 1983; Vol XIII: 149–161
   Google Scholar
• Reitz M S, Poiesz B J, Ruscetti F W, et al. Characterization and distribution of nucleic acid sequences of a novel type C retrovirus isolated from neoplastic human T lymphocytes. Proc Natl Acad Sci (USA) 1981; 78: 1887–1891
   PubMed Web of Science ®Google Scholar
• Kalyanaraman V S, Sarngadharan M G, Poiesz B J, et al. Immunological properties of a type C retrovirus isolated from cultured human T-rymphoma cells and comparison to other mammalian retroviruses. J Virol 1981; 38: 906–915
   PubMed Web of Science ®Google Scholar
• Robert-Guroff M, Ruscetti F W, Posner L E, et al. Detection of the human T-cell lymphoma virus p19 in cells of some patients with cutaneous T-cell lymphoma and leukemia using a monoclonal antibody. J Exp Med 1981; 154: 1957–1964
   PubMed Web of Science ®Google Scholar
• Popovic M, Sarin P S, Robert-Guroff M, et al. Isolation and transmission of human retrovirus (human T-cell leukemia virus). Science 1983; 219: 856–859
   PubMed Web of Science ®Google Scholar
• Miyoshi I, Kubonishi I, Yoshimoto S, et al. Type C virus particles in a cord T-cell line derived by co-cultivating normal human cord leukocytes and human leukemic T-cells. Nature (London) 1981; 294: 770–771
   PubMed Web of Science ®Google Scholar
• Yoshida M, Miyoshi I, Hinuma Y. Isolation and characterization of retrovirus from cell lines of human adult T-cell leukemia and its implication in the disease. Proc Natl Acad Sci (USA) 1982; 79: 2031–2035
   PubMed Web of Science ®Google Scholar
• Haynes B F, Miller S E, Palker T J, et al. Identification of human T-cell leukemia virus in a Japanese patient with adult cell leukemia and cutaneous lymphomatous vasculities. Proc Natl Acad Sci (USA) 1983; 80: 2054–2058
   PubMed Web of Science ®Google Scholar
• Vyth-Drees F A, de Vries J E. Human T-cell leukemia virus in lymphocytes from a T-cell leukaemia patient originating from Surinam. Lancet 1983; 2: 993
   Web of Science ®Google Scholar
• Sarin P S, Aoki T, Shibata A, et al. High incidence of human type-C retrovirus (HTLV) in family members of a HTLV-positive Japanese T-cell leukemia patient. Proc Natl Acad Sci (USA) 1983; 80: 2370–2374
   PubMed Web of Science ®Google Scholar
• Kalyanaraman V S, Sarngadharan M G, Robert-Guroff M, et al. A new subtype of human T-cell leukemia virus (HTLV-II) associated with a T-cell variant of hairy cell leukemia. Science 1982; 218: 571–573
   PubMed Web of Science ®Google Scholar
• Popovic M, Kalyanaraman V S, Sarngadharan M G, et al. The virus of Japanese adult T-cell leukemia is a member of the human T-cell leukemia virus group. Nature (London) 1982; 300: 63–66
   PubMed Web of Science ®Google Scholar
• Reitz M S, Jr, Popovic M, Haynes B F, et al. Relatedness by nucleic acid hybridization of new isolates of human T-cell leukemia-lymphoma virus (HTLV) and demonstration of provirus in uncultured leukemic blood cells. Virology 1983; 126: 688–692
   PubMed Web of Science ®Google Scholar
• Wong-Staal F, Hahn B, Manzari V, et al. A survey of human leukaemias for sequences of a human retrovirus, HTLV. Nature (London) 1983; 302: 626–628
   PubMed Web of Science ®Google Scholar
• Golde D W, Quan S, Cline M J. Human T-lymphocyte cell line producing colony stimulating factor. Blood 1978; 52: 1068–1072
   PubMed Web of Science ®Google Scholar
• Seiki M, Hattori S, Yoshida M. Human adult T-cell leukemia virus: molecular cloning of the provirus DNA and the unique terminal structure. Proc Natl Acad Sci (USA) 1982; 79: 6899–6902
   PubMed Web of Science ®Google Scholar
• Seiki M, Hattori S, Hirayama Y, et al. Human adult T-cell leukemia virus: complete nucleotide sequence of the provirus genome integrated in leukemia cell DNA. Proc Natl Acad Sci (USA) 1983; 80: 3618–3622
   PubMed Web of Science ®Google Scholar
• Manzari V, Wong-Staal F, Franchini G, et al. Human T-cell leukemia-lymphoma virus (HTLV): cloning of an integrated defective provirus and flanking cellular sequences. Proc Natl Acad Sci (USA) 1983; 80: 1574–1578
   PubMed Web of Science ®Google Scholar
• Schupbach J, Kalyanaraman V S, Sarngadharan M G, et al. Antibodies against three purified proteins of the human type C retrovirus, human T-cell leukemia-lymphoma virus, in adult T-cell leukemia-lymphoma patients and healthy blacks from the Caribbean. Cancer Res 1983; 43: 886–891
   PubMed Web of Science ®Google Scholar
• Oroszlan S, Sarngadharan M G, Copeland T D, et al. Primary structure analysis of the major internal protein p24 of human type C T-cell leukemia virus. Proc Natl Acad Sci (USA) 1982; 79: 1291–1294
   PubMed Web of Science ®Google Scholar
• Copeland T D, Oroszlan S, Kalyanaraman V S, et al. Complete amino acid sequence of human T-cell leukemia virus structural protein p15. FEBS 1983; 162: 390–395
   PubMed Web of Science ®Google Scholar
• Robert-Guroff M, Schupbach J, Blayney D W, . Sero-epidemiologic studies on HTLV-I. Human T-Cell Leukemia Viruses, R C Gallo, M Essex, L Gross, et al. Cold Spring Harbor Press, New York 1984; 285–295
   Google Scholar
• Blattner W A, Kalyanaraman V S, Robert-Guroff M, et al. The human type-C retrovirus, HTLV, in Blacks from the Caribbean region, and relationship to adult T-cell leukemia/lymphoma. Int J Cancer 1982; 30: 257–264
   PubMed Web of Science ®Google Scholar
• Gallo R C, Kalyanaraman V S, Sarngadharan M G, et al. Association of the human type C retrovirus with a subset of adult T-cell cancers. Cancer Res 1983; 43: 3892–3899
   PubMed Web of Science ®Google Scholar
• Robert-Guroff M, Nakao Y, Notake K, et al. Natural antibodies to human retrovirus HTLV in a cluster of Japanese patients with adult T cell leukemia. Science 1982; 215: 975–978
   PubMed Web of Science ®Google Scholar
• Taguchi H, Fujishita M, Miyoshi I, et al. HTLV antibody positivity and incidence of adult T-cell leukemia in Kochi prefecture, Japan. Lancet 1983; 2: 1029
   PubMed Web of Science ®Google Scholar
• Hinuma Y, Komoda H, Chosa T, et al. Antibodies to adult T-cell leukemia-virus-associated antigen (ATLA) in sera from patients with ATL and controls in Japan: a nation-wide seroepidemiologic study. Int J Cancer 1982; 29: 631–635
   PubMed Web of Science ®Google Scholar
• Robert-Guroff M, Kalyanaraman V S, Blattner W A, et al. Evidence for human T cell lymphoma-leukemia virus infection of family members of human T cell lymphoma-leukemia virus positive T cell leukemia-lymphoma patients. J Exp Med 1983; 157: 248–258
   PubMed Web of Science ®Google Scholar
• Miyoshi I, Yoshimoto Fujishita S. M, et al. Natural adult T-cell leukemia virus infection in Japanese monkeys. Lancet 1982; 2: 658–659
   PubMed Web of Science ®Google Scholar
• Popovic M, Lange-Wantzin G, Sarin P S, et al. Transformation of human umbilical cord blood T cells by human T cell leukemia/lymphoma virus. Proc Natl Acad Sci (USA) 1983; 80: 5402–5406
   PubMed Web of Science ®Google Scholar
• Markham P D, Salahuddin S Z, Kalyanaraman V S, et al. Infection and transformation of fresh human umbilical cord blood cells by multiple sources of human T-cell leukemia-lymphoma virus (HTLV). Int J Cancer 1983; 31: 413–420
   PubMed Web of Science ®Google Scholar
• Salahuddin S Z, Markham P D, Wong-Staal F, et al. Restricted expression of human T-cell leukemia-lymphoma virus (HTLV) in transformed human umbilical cord blood lymphocytes. Virology 1983; 129: 51–64
   PubMed Web of Science ®Google Scholar
• Ruscetti F W, Robert-Guroff M, Ceccherini-Nelli L, et al. Persistent in vitro infection by human T-cell leukemia-lymphoma virus (HTLV) of normal human T-lymphocytes from blood relatives of patients with HTLV-associated mature T-cell neoplasms. Int J Cancer 1983; 31: 171–183
   PubMed Web of Science ®Google Scholar
• Popovic M, Kalyanaraman V S, Mann D, . Infection and tranformation of T-cells by human T-cell leukemia/lymphoma virus of subgroups I and II. Human T-Cell Leukemia Viruses, R C Gallo, M Essex, L Gross, et al. Cold Spring Harbor Press, New York, in press
   Google Scholar
• Markham P D, Salahuddin S, Macchi B, Robert-Guroff M, Gallo R C. Transformation of different phenotypic types of human bone marrow T-lymphocytes of HTLV-I. Int J Cancer 1984; 33: 13–17
   PubMed Web of Science ®Google Scholar
• Gallo R C, Mann D, Broder S, et al. Human T-cell leukemia-lymphoma virus (HTLV) is in T- but not B-lymphocytes from a patient with cutaneous T-cell lymphoma. Proc Natl Acad Sci (USA) 1982; 79: 4680–4683
   Google Scholar
• Gallo R C, Popovic M, Lange-Wantzin G, . Stem cells, leukemia viruses, and leukemia of man. Haemopoietic Stem Cells, S A Killmann, E P Cronkite, C N Muller-Berat, et al. Copenhagen, Munksgaard 1983; 155–170
   Google Scholar
• Gallo R C, Wong-Staal F, Sarin P S. Cellular one genes, T-cell leukemia-lymphoma virus, and leukemias and lymphomas of man. Leukaemia Today—Mechanisms of Viral Leukaemogenesis, J V Dacie, J M Goldman, J O Jarrett. Churchill Livingstone, London 1984; 11–34
   Google Scholar
• Mann D L, Popovic M, Murray C, et al. Cell surface antigen expression in newborn cord blood lymphocytes infected with HTLV. J Immunol 1983; 131: 2021–2024
   PubMed Web of Science ®Google Scholar
• Mann D L, Popovic M, Sarin P S, et al. Cell lines producing human T-cell lymphoma virus show altered HLA expression. Nature (London) 1983; 305: 58–60
   PubMed Web of Science ®Google Scholar
• Yamamoto N, Matsumoto T, Koyanagi T, et al. Unique cell lines harboring both Epstein-Barr virus and adult T-cell leukemia virus established from leukemia patients. Nature (London) 1982; 249: 367–369
   Google Scholar
• Miyoshi I, Taguchi H, Fujishita M, et al. Transformation of monkey lymphocytes with adult T-cell leukemia virus. Lancet 1982; 1: 1016
   PubMed Web of Science ®Google Scholar
• Miyoshi I, Yoshimoto S, Taguchi H, et al. Transformation of rabbit lymphocytes with T-cell leukemia virus. GANN 1983; 74: 1–4
   PubMedGoogle Scholar
• Salahuddin S, Markham P D, Lindner S G, et al. Lymphokine production by cultured human T cells transformed by human T cell leukemia-lymphoma virus-I. Science 1984; 223: 703–707
   PubMed Web of Science ®Google Scholar
• Clark S C, Arya S K, Wong-Staal F, et al. Human T cell growth factor: Partial amino acid sequence, cDNA cloning, and organization and expression in normal and leukemic cells. Proc Natl Acad Sci (USA) 1984; 81: 2543–2547
   PubMed Web of Science ®Google Scholar
• Westin E H, Wong-Staal F, Gelmann E P, et al. Expression of cellular homologues of retroviral one genes in human hematopoietic cells. Proc Natl Acad Sci (USA) 1982; 79: 2490–2494
   PubMed Web of Science ®Google Scholar
• Doolittle R F, Humkapillar M W, Hood L E, et al. Simian sarcoma virus one gene, vsis, is derived from the gene (or genes) encoding a platelet-derived growth factor. Science 1983; 221: 275–277
   PubMed Web of Science ®Google Scholar
• Waterfield M D, Scrace G T, Whittle N, et al. Platelet derived growth factor is structurally related to the putative transforming protein p24 of simian sarcoma virus. Nature (London) 1983; 304: 35–39
   PubMed Web of Science ®Google Scholar
• Sarin P S, Gallo R C. Role of viruses in the etiology of acquired immune deficiency syndrome. AIDS, A Basic Guide for Clinicians, P Ebbesen, R Biggar, M Melbye. Copenhagen, C Munksgaard 1984; 173–183
   Google Scholar
• Gallo R C, Sarin P S, Gelmann E P, et al. Isolation of human T-cell leukemia virus in acquired immune deficiency syndrome (AIDS). Science 1983; 220: 865–867
   PubMed Web of Science ®Google Scholar
• Gallo R C, Salahuddin S Z, Popovic M, et al. Frequent detection and isolation of a human T-lymphotropic retrovirus, HTLV-III, from patients with AIDS and at risk for AIDS. Science 1984; 224: 500–503
   PubMed Web of Science ®Google Scholar
• Popovic M, Sarngadharan M G, Read E, et al. Detection, isolation, and continuous production of cytopathic human T-lymphotropic retroviruses (HTLV-III) from patients with AIDS and pre-AIDS. Science 1984; 224: 497–500
   PubMed Web of Science ®Google Scholar
• Barre-Sinoussi F., Chermann J C, Rey F, et al. Isolation of a T-lymphotropic retrovirus from a patient at risk for AIDS. Science 1983; 220: 868–871
   PubMed Web of Science ®Google Scholar
• Sarngadharan M G, Popovic M, Bruch L, et al. Antibodies reactive with a human T-lymphotropic retrovirus (HTLV-III) in the sera of patients with acquired immune deficiency syndrome. Science 1984; 224: 506–508
   PubMed Web of Science ®Google Scholar
• Schupbach J, Popovic M, Gilden R V, et al. Serologic analysis of a new subgroup of human T-lymphotropic retrovirus (HTLV-III) associated with AIDS. Science 1984; 24: 503–508
   Google Scholar
• Essex M, McLane M F, Lee T H, et al. Antibodies to cell membrane antigens associated with human T-cell leukemia virus in patients with AIDS. Science 1983; 220: 859–862
   PubMed Web of Science ®Google Scholar
• Essex M, McLane M, Lee T H, . Distribution of antibodies to HTLV-MA in patients with AIDS and related control groups. Human T-Cell Leukemia Viruses, R C Gallo, M Essex, L Gross, et al. Cold Spring Harbor Press, New York, in press
   Google Scholar
• Gelmann E P, Popovic M, Blayney D, et al. Proviral DNA of a retrovirus, human T-cell leukemia/lymphoma virus in two patients with AIDS. Science 1983; 220: 862–865
   PubMed Web of Science ®Google Scholar