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. 1997 Dec;71(12):9124–9133. doi: 10.1128/jvi.71.12.9124-9133.1997

The superantigen-homologous viral immediate-early gene ie14/vsag in herpesvirus saimiri-transformed human T cells.

A Knappe 1, C Hiller 1, M Thurau 1, S Wittmann 1, H Hofmann 1, B Fleckenstein 1, H Fickenscher 1
PMCID: PMC230213  PMID: 9371569

Abstract

Herpesvirus saimiri C488 transforms human T lymphocytes to stable growth in culture. The growth-transformed human T cells harbor the viral genome in a nonintegrated episomal form without production of virus particles. In these cells, virus gene expression was previously found to be confined to the transforming genes stpC and tip. In order to analyze virus gene expression in more detail, we applied a subtractive hybridization technique and compared stimulated virus-transformed cells with uninfected parental T cells of the same donor. A number of known T-cell activation genes were isolated. Viral stpC/tip cDNAs were enriched after subtraction. In addition, the viral immediate-early, superantigen-homologous gene ie14/vsag was represented by numerous cDNA clones that comprised the entire spliced transcript. Whereas a weak basal expression of ie14/vsag was detected by reverse transcription-PCR only, the phorbol ester-induced transcripts were readily shown by Northern blotting. ie14/vsag, which before had been classified as a major immediate-early gene of herpesvirus saimiri, is localized within a highly conserved region with extensive homologies to the cellular genome. Mutant viruses without the ie14/vsag gene are replication competent and fully capable of transforming human and marmoset T cells. Since ie14/vsag is transiently expressed after stimulation, it may increase T-cell proliferation in an activation-dependent and superantigen-like but apparently Vbeta-independent way.

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Selected References

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  1. Ahuja S. K., Murphy P. M. Molecular piracy of mammalian interleukin-8 receptor type B by herpesvirus saimiri. J Biol Chem. 1993 Oct 5;268(28):20691–20694. [PubMed] [Google Scholar]
  2. Albrecht J. C., Fleckenstein B. New member of the multigene family of complement control proteins in herpesvirus saimiri. J Virol. 1992 Jun;66(6):3937–3940. doi: 10.1128/jvi.66.6.3937-3940.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Albrecht J. C., Nicholas J., Biller D., Cameron K. R., Biesinger B., Newman C., Wittmann S., Craxton M. A., Coleman H., Fleckenstein B. Primary structure of the herpesvirus saimiri genome. J Virol. 1992 Aug;66(8):5047–5058. doi: 10.1128/jvi.66.8.5047-5058.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Albrecht J. C., Nicholas J., Cameron K. R., Newman C., Fleckenstein B., Honess R. W. Herpesvirus saimiri has a gene specifying a homologue of the cellular membrane glycoprotein CD59. Virology. 1992 Sep;190(1):527–530. doi: 10.1016/0042-6822(92)91247-r. [DOI] [PubMed] [Google Scholar]
  5. Biesinger B., Müller-Fleckenstein I., Simmer B., Lang G., Wittmann S., Platzer E., Desrosiers R. C., Fleckenstein B. Stable growth transformation of human T lymphocytes by herpesvirus saimiri. Proc Natl Acad Sci U S A. 1992 Apr 1;89(7):3116–3119. doi: 10.1073/pnas.89.7.3116. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Biesinger B., Trimble J. J., Desrosiers R. C., Fleckenstein B. The divergence between two oncogenic Herpesvirus saimiri strains in a genomic region related to the transforming phenotype. Virology. 1990 Jun;176(2):505–514. doi: 10.1016/0042-6822(90)90020-r. [DOI] [PubMed] [Google Scholar]
  7. Biesinger B., Tsygankov A. Y., Fickenscher H., Emmrich F., Fleckenstein B., Bolen J. B., Bröker B. M. The product of the Herpesvirus saimiri open reading frame 1 (tip) interacts with T cell-specific kinase p56lck in transformed cells. J Biol Chem. 1995 Mar 3;270(9):4729–4734. doi: 10.1074/jbc.270.9.4729. [DOI] [PubMed] [Google Scholar]
  8. Bodemer W., Niller H. H., Nitsche N., Scholz B., Fleckenstein B. Organization of the thymidylate synthase gene of herpesvirus saimiri. J Virol. 1986 Oct;60(1):114–123. doi: 10.1128/jvi.60.1.114-123.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Bröker B. M., Tsygankov A. Y., Müller-Fleckenstein I., Guse A. H., Chitaev N. A., Biesinger B., Fleckenstein B., Emmrich F. Immortalization of human T cell clones by Herpesvirus saimiri. Signal transduction analysis reveals functional CD3, CD4, and IL-2 receptors. J Immunol. 1993 Aug 1;151(3):1184–1192. [PubMed] [Google Scholar]
  10. Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem. 1987 Apr;162(1):156–159. doi: 10.1006/abio.1987.9999. [DOI] [PubMed] [Google Scholar]
  11. De Carli M., Berthold S., Fickenscher H., Fleckenstein I. M., D'Elios M. M., Gao Q., Biagiotti R., Giudizi M. G., Kalden J. R., Fleckenstein B. Immortalization with herpesvirus saimiri modulates the cytokine secretion profile of established Th1 and Th2 human T cell clones. J Immunol. 1993 Nov 1;151(9):5022–5030. [PubMed] [Google Scholar]
  12. Desrosiers R. C., Bakker A., Kamine J., Falk L. A., Hunt R. D., King N. W. A region of the Herpesvirus saimiri genome required for oncogenicity. Science. 1985 Apr 12;228(4696):184–187. doi: 10.1126/science.2983431. [DOI] [PubMed] [Google Scholar]
  13. Desrosiers R. C., Burghoff R. L., Bakker A., Kamine J. Construction of replication-competent Herpesvirus saimiri deletion mutants. J Virol. 1984 Feb;49(2):343–348. doi: 10.1128/jvi.49.2.343-348.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Desrosiers R. C., Falk L. A. Herpesvirus saimiri strain variability. J Virol. 1982 Jul;43(1):352–356. doi: 10.1128/jvi.43.1.352-356.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Desrosiers R. C., Silva D. P., Waldron L. M., Letvin N. L. Nononcogenic deletion mutants of herpesvirus saimiri are defective for in vitro immortalization. J Virol. 1986 Feb;57(2):701–705. doi: 10.1128/jvi.57.2.701-705.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Duboise S. M., Guo J., Desrosiers R. C., Jung J. U. Use of virion DNA as a cloning vector for the construction of mutant and recombinant herpesviruses. Proc Natl Acad Sci U S A. 1996 Oct 15;93(21):11389–11394. doi: 10.1073/pnas.93.21.11389. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Feinberg A. P., Vogelstein B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem. 1983 Jul 1;132(1):6–13. doi: 10.1016/0003-2697(83)90418-9. [DOI] [PubMed] [Google Scholar]
  18. Fickenscher H., Biesinger B., Knappe A., Wittmann S., Fleckenstein B. Regulation of the herpesvirus saimiri oncogene stpC, similar to that of T-cell activation genes, in growth-transformed human T lymphocytes. J Virol. 1996 Sep;70(9):6012–6019. doi: 10.1128/jvi.70.9.6012-6019.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Fickenscher H., Bökel C., Knappe A., Biesinger B., Meinl E., Fleischer B., Fleckenstein B., Bröker B. M. Functional phenotype of transformed human alphabeta and gammadelta T cells determined by different subgroup C strains of herpesvirus Saimiri. J Virol. 1997 Mar;71(3):2252–2263. doi: 10.1128/jvi.71.3.2252-2263.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Fodor W. L., Rollins S. A., Bianco-Caron S., Rother R. P., Guilmette E. R., Burton W. V., Albrecht J. C., Fleckenstein B., Squinto S. P. The complement control protein homolog of herpesvirus saimiri regulates serum complement by inhibiting C3 convertase activity. J Virol. 1995 Jun;69(6):3889–3892. doi: 10.1128/jvi.69.6.3889-3892.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Fossiez F., Djossou O., Chomarat P., Flores-Romo L., Ait-Yahia S., Maat C., Pin J. J., Garrone P., Garcia E., Saeland S. T cell interleukin-17 induces stromal cells to produce proinflammatory and hematopoietic cytokines. J Exp Med. 1996 Jun 1;183(6):2593–2603. doi: 10.1084/jem.183.6.2593. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Geck P., Whitaker S. A., Medveczky M. M., Medveczky P. G. Expression of collagenlike sequences by a tumor virus, herpesvirus saimiri. J Virol. 1990 Jul;64(7):3509–3515. doi: 10.1128/jvi.64.7.3509-3515.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Irving S. G., June C. H., Zipfel P. F., Siebenlist U., Kelly K. Mitogen-induced genes are subject to multiple pathways of regulation in the initial stages of T-cell activation. Mol Cell Biol. 1989 Mar;9(3):1034–1040. doi: 10.1128/mcb.9.3.1034. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Jung J. U., Desrosiers R. C. Association of the viral oncoprotein STP-C488 with cellular ras. Mol Cell Biol. 1995 Dec;15(12):6506–6512. doi: 10.1128/mcb.15.12.6506. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Jung J. U., Desrosiers R. C. Distinct functional domains of STP-C488 of herpesvirus saimiri. Virology. 1994 Nov 1;204(2):751–758. doi: 10.1006/viro.1994.1590. [DOI] [PubMed] [Google Scholar]
  26. Jung J. U., Desrosiers R. C. Herpesvirus saimiri oncogene STP-C488 encodes a phosphoprotein. J Virol. 1992 Mar;66(3):1777–1780. doi: 10.1128/jvi.66.3.1777-1780.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Jung J. U., Desrosiers R. C. Identification and characterization of the herpesvirus saimiri oncoprotein STP-C488. J Virol. 1991 Dec;65(12):6953–6960. doi: 10.1128/jvi.65.12.6953-6960.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Jung J. U., Lang S. M., Friedrich U., Jun T., Roberts T. M., Desrosiers R. C., Biesinger B. Identification of Lck-binding elements in tip of herpesvirus saimiri. J Biol Chem. 1995 Sep 1;270(35):20660–20667. doi: 10.1074/jbc.270.35.20660. [DOI] [PubMed] [Google Scholar]
  29. Jung J. U., Lang S. M., Jun T., Roberts T. M., Veillette A., Desrosiers R. C. Downregulation of Lck-mediated signal transduction by tip of herpesvirus saimiri. J Virol. 1995 Dec;69(12):7814–7822. doi: 10.1128/jvi.69.12.7814-7822.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Jung J. U., Stäger M., Desrosiers R. C. Virus-encoded cyclin. Mol Cell Biol. 1994 Nov;14(11):7235–7244. doi: 10.1128/mcb.14.11.7235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Jung J. U., Trimble J. J., King N. W., Biesinger B., Fleckenstein B. W., Desrosiers R. C. Identification of transforming genes of subgroup A and C strains of Herpesvirus saimiri. Proc Natl Acad Sci U S A. 1991 Aug 15;88(16):7051–7055. doi: 10.1073/pnas.88.16.7051. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Klein J. L., Fickenscher H., Holliday J. E., Biesinger B., Fleckenstein B. Herpesvirus saimiri immortalized gamma delta T cell line activated by IL-12. J Immunol. 1996 Apr 15;156(8):2754–2760. [PubMed] [Google Scholar]
  33. Koomey J. M., Mulder C., Burghoff R. L., Fleckenstein B., Desrosiers R. C. Deletion of DNA sequence in a nononcogenic variant of Herpesvirus saimiri. J Virol. 1984 May;50(2):662–665. doi: 10.1128/jvi.50.2.662-665.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Lund T., Medveczky M. M., Geck P., Medveczky P. G. A herpesvirus saimiri protein required for interleukin-2 independence is associated with membranes of transformed T cells. J Virol. 1995 Jul;69(7):4495–4499. doi: 10.1128/jvi.69.7.4495-4499.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Lund T., Medveczky M. M., Medveczky P. G. Herpesvirus saimiri Tip-484 membrane protein markedly increases p56lck activity in T cells. J Virol. 1997 Jan;71(1):378–382. doi: 10.1128/jvi.71.1.378-382.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Lund T., Medveczky M. M., Neame P. J., Medveczky P. G. A herpesvirus saimiri membrane protein required for interleukin-2 independence forms a stable complex with p56lck. J Virol. 1996 Jan;70(1):600–606. doi: 10.1128/jvi.70.1.600-606.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Medveczky M. M., Geck P., Sullivan J. L., Serbousek D., Djeu J. Y., Medveczky P. G. IL-2 independent growth and cytotoxicity of herpesvirus saimiri-infected human CD8 cells and involvement of two open reading frame sequences of the virus. Virology. 1993 Oct;196(2):402–412. doi: 10.1006/viro.1993.1495. [DOI] [PubMed] [Google Scholar]
  38. Medveczky M. M., Geck P., Vassallo R., Medveczky P. G. Expression of the collagen-like putative oncoprotein of Herpesvirus saimiri in transformed T cells. Virus Genes. 1993 Dec;7(4):349–365. doi: 10.1007/BF01703391. [DOI] [PubMed] [Google Scholar]
  39. Medveczky M. M., Szomolanyi E., Hesselton R., DeGrand D., Geck P., Medveczky P. G. Herpesvirus saimiri strains from three DNA subgroups have different oncogenic potentials in New Zealand white rabbits. J Virol. 1989 Sep;63(9):3601–3611. doi: 10.1128/jvi.63.9.3601-3611.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Medveczky P., Szomolanyi E., Desrosiers R. C., Mulder C. Classification of herpesvirus saimiri into three groups based on extreme variation in a DNA region required for oncogenicity. J Virol. 1984 Dec;52(3):938–944. doi: 10.1128/jvi.52.3.938-944.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Meinl E., Hohlfeld R., Wekerle H., Fleckenstein B. Immortalization of human T cells by Herpesvirus saimiri. Immunol Today. 1995 Feb;16(2):55–58. doi: 10.1016/0167-5699(95)80087-5. [DOI] [PubMed] [Google Scholar]
  42. Mittrücker H. W., Müller-Fleckenstein I., Fleckenstein B., Fleischer B. CD2-mediated autocrine growth of herpes virus saimiri-transformed human T lymphocytes. J Exp Med. 1992 Sep 1;176(3):909–913. doi: 10.1084/jem.176.3.909. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Mittrücker H. W., Müller-Fleckenstein I., Fleckenstein B., Fleischer B. Herpes virus saimiri-transformed human T lymphocytes: normal functional phenotype and preserved T cell receptor signalling. Int Immunol. 1993 Aug;5(8):985–990. doi: 10.1093/intimm/5.8.985. [DOI] [PubMed] [Google Scholar]
  44. Murphy C., Kretschmer C., Biesinger B., Beckers J., Jung J., Desrosiers R. C., Müller-Hermelink H. K., Fleckenstein B. W., Rüther U. Epithelial tumours induced by a herpesvirus oncogene in transgenic mice. Oncogene. 1994 Jan;9(1):221–226. [PubMed] [Google Scholar]
  45. Murthy S. C., Trimble J. J., Desrosiers R. C. Deletion mutants of herpesvirus saimiri define an open reading frame necessary for transformation. J Virol. 1989 Aug;63(8):3307–3314. doi: 10.1128/jvi.63.8.3307-3314.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Nava V. E., Cheng E. H., Veliuona M., Zou S., Clem R. J., Mayer M. L., Hardwick J. M. Herpesvirus saimiri encodes a functional homolog of the human bcl-2 oncogene. J Virol. 1997 May;71(5):4118–4122. doi: 10.1128/jvi.71.5.4118-4122.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Neipel F., Albrecht J. C., Ensser A., Huang Y. Q., Li J. J., Friedman-Kien A. E., Fleckenstein B. Human herpesvirus 8 encodes a homolog of interleukin-6. J Virol. 1997 Jan;71(1):839–842. doi: 10.1128/jvi.71.1.839-842.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Neipel F., Albrecht J. C., Fleckenstein B. Cell-homologous genes in the Kaposi's sarcoma-associated rhadinovirus human herpesvirus 8: determinants of its pathogenicity? J Virol. 1997 Jun;71(6):4187–4192. doi: 10.1128/jvi.71.6.4187-4192.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Neubauer R. H., Wallen W. C., Rabin H. Stimulation of Herpesvirus saimiri expression in the absence of evidence for type C virus activation in a marmoset lymphoid cell line. J Virol. 1974 Oct;14(4):745–750. doi: 10.1128/jvi.14.4.745-750.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Nicholas J., Smith E. P., Coles L., Honess R. Gene expression in cells infected with gammaherpesvirus saimiri: properties of transcripts from two immediate-early genes. Virology. 1990 Nov;179(1):189–200. doi: 10.1016/0042-6822(90)90288-3. [DOI] [PubMed] [Google Scholar]
  51. Pacheco-Castro A., Márquez C., Toribio M. L., Ramiro A. R., Trigueros C., Regueiro J. R. Herpesvirus saimiri immortalization of alpha beta and gamma delta human T-lineage cells derived from CD34+ intrathymic precursors in vitro. Int Immunol. 1996 Nov;8(11):1797–1805. doi: 10.1093/intimm/8.11.1797. [DOI] [PubMed] [Google Scholar]
  52. Rother R. P., Rollins S. A., Fodor W. L., Albrecht J. C., Setter E., Fleckenstein B., Squinto S. P. Inhibition of complement-mediated cytolysis by the terminal complement inhibitor of herpesvirus saimiri. J Virol. 1994 Feb;68(2):730–737. doi: 10.1128/jvi.68.2.730-737.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Rouvier E., Luciani M. F., Mattéi M. G., Denizot F., Golstein P. CTLA-8, cloned from an activated T cell, bearing AU-rich messenger RNA instability sequences, and homologous to a herpesvirus saimiri gene. J Immunol. 1993 Jun 15;150(12):5445–5456. [PubMed] [Google Scholar]
  54. Russo J. J., Bohenzky R. A., Chien M. C., Chen J., Yan M., Maddalena D., Parry J. P., Peruzzi D., Edelman I. S., Chang Y. Nucleotide sequence of the Kaposi sarcoma-associated herpesvirus (HHV8). Proc Natl Acad Sci U S A. 1996 Dec 10;93(25):14862–14867. doi: 10.1073/pnas.93.25.14862. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Schirm S., Müller I., Desrosiers R. C., Fleckenstein B. Herpesvirus saimiri DNA in a lymphoid cell line established by in vitro transformation. J Virol. 1984 Mar;49(3):938–946. doi: 10.1128/jvi.49.3.938-946.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Schneider U., Schwenk H. U., Bornkamm G. Characterization of EBV-genome negative "null" and "T" cell lines derived from children with acute lymphoblastic leukemia and leukemic transformed non-Hodgkin lymphoma. Int J Cancer. 1977 May 15;19(5):621–626. doi: 10.1002/ijc.2910190505. [DOI] [PubMed] [Google Scholar]
  57. Smith C. A. A novel viral homologue of Bcl-2 and Ced-9. Trends Cell Biol. 1995 Sep;5(9):344–344. doi: 10.1016/s0962-8924(00)89061-3. [DOI] [PubMed] [Google Scholar]
  58. Szomolanyi E., Medveczky P., Mulder C. In vitro immortalization of marmoset cells with three subgroups of herpesvirus saimiri. J Virol. 1987 Nov;61(11):3485–3490. doi: 10.1128/jvi.61.11.3485-3490.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Thome M., Schneider P., Hofmann K., Fickenscher H., Meinl E., Neipel F., Mattmann C., Burns K., Bodmer J. L., Schröter M. Viral FLICE-inhibitory proteins (FLIPs) prevent apoptosis induced by death receptors. Nature. 1997 Apr 3;386(6624):517–521. doi: 10.1038/386517a0. [DOI] [PubMed] [Google Scholar]
  60. Trimble J. J., Murthy S. C., Bakker A., Grassmann R., Desrosiers R. C. A gene for dihydrofolate reductase in a herpesvirus. Science. 1988 Mar 4;239(4844):1145–1147. doi: 10.1126/science.2830673. [DOI] [PubMed] [Google Scholar]
  61. Troidl B., Simmer B., Fickenscher H., Müller-Fleckenstein I., Emmrich F., Fleckenstein B., Gebhart E. Karyotypic characterization of human T-cell lines immortalized by Herpesvirus saimiri. Int J Cancer. 1994 Feb 1;56(3):433–438. doi: 10.1002/ijc.2910560325. [DOI] [PubMed] [Google Scholar]
  62. Weber F., Meinl E., Drexler K., Czlonkowska A., Huber S., Fickenscher H., Müller-Fleckenstein I., Fleckenstein B., Wekerle H., Hohlfeld R. Transformation of human T-cell clones by Herpesvirus saimiri: intact antigen recognition by autonomously growing myelin basic protein-specific T cells. Proc Natl Acad Sci U S A. 1993 Dec 1;90(23):11049–11053. doi: 10.1073/pnas.90.23.11049. [DOI] [PMC free article] [PubMed] [Google Scholar]
  63. Wiese N., Tsygankov A. Y., Klauenberg U., Bolen J. B., Fleischer B., Bröker B. M. Selective activation of T cell kinase p56lck by Herpesvirus saimiri protein tip. J Biol Chem. 1996 Jan 12;271(2):847–852. doi: 10.1074/jbc.271.2.847. [DOI] [PubMed] [Google Scholar]
  64. Yao Z., Fanslow W. C., Seldin M. F., Rousseau A. M., Painter S. L., Comeau M. R., Cohen J. I., Spriggs M. K. Herpesvirus Saimiri encodes a new cytokine, IL-17, which binds to a novel cytokine receptor. Immunity. 1995 Dec;3(6):811–821. doi: 10.1016/1074-7613(95)90070-5. [DOI] [PubMed] [Google Scholar]
  65. Yao Z., Maraskovsky E., Spriggs M. K., Cohen J. I., Armitage R. J., Alderson M. R. Herpesvirus saimiri open reading frame 14, a protein encoded by T lymphotropic herpesvirus, binds to MHC class II molecules and stimulates T cell proliferation. J Immunol. 1996 May 1;156(9):3260–3266. [PubMed] [Google Scholar]
  66. Yao Z., Painter S. L., Fanslow W. C., Ulrich D., Macduff B. M., Spriggs M. K., Armitage R. J. Human IL-17: a novel cytokine derived from T cells. J Immunol. 1995 Dec 15;155(12):5483–5486. [PubMed] [Google Scholar]
  67. Yasukawa M., Inoue Y., Kimura N., Fujita S. Immortalization of human T cells expressing T-cell receptor gamma delta by herpesvirus saimiri. J Virol. 1995 Dec;69(12):8114–8117. doi: 10.1128/jvi.69.12.8114-8117.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  68. Zhong W., Wang H., Herndier B., Ganem D. Restricted expression of Kaposi sarcoma-associated herpesvirus (human herpesvirus 8) genes in Kaposi sarcoma. Proc Natl Acad Sci U S A. 1996 Jun 25;93(13):6641–6646. doi: 10.1073/pnas.93.13.6641. [DOI] [PMC free article] [PubMed] [Google Scholar]
  69. Zipfel P. F., Irving S. G., Kelly K., Siebenlist U. Complexity of the primary genetic response to mitogenic activation of human T cells. Mol Cell Biol. 1989 Mar;9(3):1041–1048. doi: 10.1128/mcb.9.3.1041. [DOI] [PMC free article] [PubMed] [Google Scholar]
  70. zur Hausen H., O'Neill F. J., Freese U. K., Hecker E. Persisting oncogenic herpesvirus induced by the tumour promotor TPA. Nature. 1978 Mar 23;272(5651):373–375. doi: 10.1038/272373a0. [DOI] [PubMed] [Google Scholar]

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