Skip to main content

Abstract

It has long been hypothesized that viruses play an important role in the etiology of some forms of insulin-dependent diabetes mellitus (IDDM). This hypothesis began to develop following the initial report of an association between community outbreaks of mumps and the occurrence of IDDM [38] and was supported by the discovery of a seasonal variation in the incidence of new cases of IDDM [27]. Subsequent studies have suggested correlations between rubella [21, 50, 73] cytomegalovirus [43], reovirus [109] and group B Coxsackie virus [28] infections and IDDM. Additionally, the description of B-cell death associated with insulitis, as eloquently described by Gepts [31] has been considered to be consistent with the pathogenesis of an ongoing viral infection.

This work was supported by research grants AM 17631, AM 27722, and AM 36175 from the National Institute of Arthritis, Diabetes, Digestive, and Kidney Diseases to EHL and by research grants ES 03456 and a Research Career Development Award ES 00150 from the National Institute of Environmental Health Sciences to GLW.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 84.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Ahmad N, Abraham AA (1982) Pancreatic isleitis with Coxsackie virus B5 infection. Human Pathol 13:661–662

    CAS  Google Scholar 

  2. Appel MC, Rossini AA, Williams RM, Like AA (1978) Viral studies in streptozotocin-induced pancreatic insulitis. Diabetologia 15: 327–336

    PubMed  CAS  Google Scholar 

  3. Barrett-Conner E (1985) Is insulin-dependent diabetes mellitus caused by Coxsackie B infection? A review of the epidemiologic evidence. Rev Infect Dis 7: 207–215

    Google Scholar 

  4. Blay RA, Bigley NJ, Giron DJ (1985) A murine model of insulin-dependent diabetes mellitus resulting from the cumulative effects of the nondiabetogenic strain of encephalomyocarditis virus and a single low dose of streptozotocin. Diabetes 31: 288–1292

    Google Scholar 

  5. Boucher DL, Notkins AL (1973) Virus-induced diabetes mellitus. I. Hyperglycemia and hypoinsulinemia in mice infected with encephalomyocarditis virus. J Exp Med 137:1226–1239

    PubMed  CAS  Google Scholar 

  6. Boucher DL, Hayashi Y, Rosenthal J, Notkins AL (1975) Virus induced diabetes. I. Influence of sex and strain of the host. J Infect Dis 131: 462–466

    PubMed  CAS  Google Scholar 

  7. Buschard K, Rygaard J, Lund E (1976) The inability of a diabetogenic virus to induce diabetes in athymic nude mice. Acta Pathol Microbiol Scand 84: 299–303

    CAS  Google Scholar 

  8. Clark EA, Windsor NT, Struge J, Stanton TH (1980) Mutations that influence natural killer cell-mediated cytotoxicity in rodents. In: Huberman RB (ed) Natural cell-mediated immunity against tumors. Academic, New York, pp 417–429

    Google Scholar 

  9. Chairez R, Yoon JW, Notkins AL (1978) Virus-induced diabetes mellitus. X. Attachment of encephalomyocarditis virus and permissiveness of cultured pancreatic beta cells to infection. Virol 85:606–611

    CAS  Google Scholar 

  10. Champsaur H, Dussaix E, Samolyk D, Fabre M, Bach C, Assan R (1980) Diabetes and Coxsackie B5 infection. Lancet 1: 251 (letter)

    PubMed  Google Scholar 

  11. Craighead JE (1966) Pathogenicity of the M and E variants of the encephalomyocarditis (EMC) virus. I. Myocardiotropic and neurotropic properties. Am J Pathol 48: 333–345

    PubMed  CAS  Google Scholar 

  12. Craighead JE, McLane MF (1968) Diabetes mellitus: induction in mice by encephalomyocarditis virus. Science 162: 913–914

    PubMed  CAS  Google Scholar 

  13. Craighead JE, Steinke J (1971) Diabetes mellitus-like syndrome in mice infected with encephalomyocarditis virus. Am J Pathol 63:119–134

    PubMed  CAS  Google Scholar 

  14. Craighead JE, Kanich RE, Kessler JB (1974) Lesions of the islets of Langerhans in encephalomyocarditis virus-infected mice with a diabetes mellitus-like disease. Am J Pathol 74: 287–294

    PubMed  CAS  Google Scholar 

  15. D’Andrea BJ, Wilson GL, Craighead JE (1981) Effect of genetic obesity in mice on the induction of diabetes by encephalomyocarditis virus. Diabetes 30: 451–454

    PubMed  Google Scholar 

  16. Defoe DC, Naji A, Plotkin SA, Barker CF (1980) Susceptibility to diabetogenic virus: host versus pancreatic factors. J Surg Res 28: 338–347

    Google Scholar 

  17. De Maeyer-Guignard JE, Dandoy F, Bailey DW, De Maeyer E (1986) Interferon structural genes do not participate in quantitative regulation of interferon production by If loci as shown in C57BL/6 mice that are congenic with BALB/c mice at the alpha interferon gene cluster. J Virol 58:743–747

    PubMed  Google Scholar 

  18. Eberhardt MS, Wagener DK, Orchard TJ, LaPorte RE, Cavender DE, Rabin BS, Atchison RW, Kuller LH, Drash AL, Becker DJ (1985) HLA heterogeneity of insulin-dependent diabetes mellitus at diagnosis. Diabetes 34: 1247–1252

    PubMed  CAS  Google Scholar 

  19. Eisenbarth GS (1986) Type I diabetes mellitus: a chronic autoimmune disease. N Engl J Med 314:1360–1368

    PubMed  CAS  Google Scholar 

  20. Elder JH (1984) On the role of recombinant retroviruses in murine leukemia. In: Notkins AL, Oldstone MBA (eds) Concepts in viral pathogenesis. Springer, Berlin Heidelberg New York, pp 86–93

    Google Scholar 

  21. Forrest JM, Menses MA, Burgess JA (1971) High frequency of diabetes mellitus in young adults with congenital rubella. Lancet 2: 332–334

    PubMed  CAS  Google Scholar 

  22. Friedman SB, Grota LJ, Glasgow LA (1972) Differential susceptibility of male and female mice to encephalomyocarditis virus. Effects of castration, adrenalectomy, and administration of sex hormones. Infect Immun 5: 637–644

    PubMed  CAS  Google Scholar 

  23. Fujinami RS, Oldstone MBA (1985) Amino acid homology between the encephalitogenic site of myelin basic protein and virus: mechanism for autoimmunity. Science 230: 1043–1045

    PubMed  CAS  Google Scholar 

  24. Fujino-Kurihara H, Fujita H, Hakura A, Nonaka K, Tarui S (1985) Morphological aspects on pancreatic islets of non-obese diabetic (NOD) mice. Virchows Arch 49: 107–120

    CAS  Google Scholar 

  25. Gaines KL, Kayes SG, Wilson GL (1987) Factors affecting the infection of the D variant of encephalomyocarditis virus in the B cells of C57BL/6J mice. Diabetologia 30: 419–425

    PubMed  CAS  Google Scholar 

  26. Gaines KL, Kayes SG, Wilson GL (1986) Altered pathogenesis in encephalomyocarditis virus (D variant)-infected diabetes-susceptible and -resistant strains of mice. Diabetologia 29: 313–320

    PubMed  CAS  Google Scholar 

  27. Gamble DR, Taylor KW (1969) Seasonal incidence of diabetes mellitus. Br Med J 3: 627–630

    PubMed  CAS  Google Scholar 

  28. Gamble DR, Kinsley ML, Fitzgerald MG, Bolton R, Taylor KW (1969) Viral antibodies in diabetes mellitus. Br Med J 3: 627–630

    PubMed  CAS  Google Scholar 

  29. Gardner MB, Henderson BE, Officer JE, Rongey RW, Parker JC, Oliver C, Estes JD, Huebner RJ (1973) A spontaneous lower motor neuron disease apparently caused by indigenous type-C RNA virus in wild mice. JNCI 51: 1243–1254

    PubMed  Google Scholar 

  30. Garzeiii C, Taub FE, Scharff JE, Prabhakar BS, Ginsberg-Fellner F, Notkins AL (1984) Epstein-Barr virus-transformed lymphocytes produce monoclonal antibodies that react with antigens in multiple organs. J Virol 52: 722–725

    Google Scholar 

  31. Gepts W (1965) Pathologic anatomy of the pancreas in juvenile diabetes mellitus. Diabetes 14: 619–633

    PubMed  CAS  Google Scholar 

  32. Gepts W (1984) The pathology of the pancreas in human diabetes. In: Andreani D, DiMario U, Federlin KF, Heding LG (eds) Immunology in diabetes. Kimpton, London, pp 21–34

    Google Scholar 

  33. Ginsberg-Fellner F, Witt ME, Yagihashi S, Dobersen MJ, Taub F, Fedun B, McEvoy RC, Roman SH, Davies TF, Cooper LZ, Rubinstein P, Notkins AL (1984) Congenital rubella as a model for type 1 (insulin dependent) diabetes mellitus: increased prevalence of islet cell surface antibodies. Diabetologia [Suppl] 27: 87–89

    Google Scholar 

  34. Giron DJ, Patterson RR (1982) Effect of steroid hormones on virus-induced diabetes mellitus. Infect Immun 37: 820–822

    PubMed  CAS  Google Scholar 

  35. Gould CL, Trombley ML, Bigley NJ, McMannama KG, Giron DJ (1984) Replication of diabetogenic and nondiabetogenic variants of encephalomyocarditis (EMC) virus in ICR Swiss mice. Proc Soc Exp Biol Med 175: 449–453

    PubMed  CAS  Google Scholar 

  36. Gould CL, McMannama KC, Bigley NJ, Giron DJ (1985 a) Exacerbation of the pathogenesis of the diabetogenic variant of encephalomyocarditis virus in mice by interferon. J Interferon Res 5: 33–37

    PubMed  Google Scholar 

  37. Gould CL, McMannama KG, Bigley NJ, Giron DJ (1985b) Virus-induced murine diabetes: enhancement by immunosuppression. Diabetes 34: 1217–1221

    PubMed  Google Scholar 

  38. Gunderson E (1927) Is diabetes of infectious origin? J Infect Dis 41:197–202

    Google Scholar 

  39. Harrison AK, Murphy FA (1975) Murine oncornavirus activation in the pancreas during infection with Venezuelan equine encephalitis virus. JNKI 55: 917–923

    CAS  Google Scholar 

  40. Hayashi K, Boucher DW, Notkins AL (1974) Virus-induced diabetes mellitus. II. Relationship between beta cell damage and hyperglycemia in mice infected with the encephalomyocarditis virus. Am J Pathol 75: 91–102

    PubMed  CAS  Google Scholar 

  41. Huang TTF, Calarco AG (1981) Evidence for the cell surface expression of intracisternal A particle associated antigens during early mouse development. Dev Biol 82: 338–392

    Google Scholar 

  42. Huber SA, Babu PG, Craighead JE (1985) Genetic influences on the immunologic pathogenesis of encephalomyocarditis (EMC) virus-induced diabetes mellitus. Diabetes 34:1186–90

    PubMed  CAS  Google Scholar 

  43. Hultquist G, Nosvall S, Sundstrom C (1973) Insulitis in cytomegalovirus infection in a newborn infant. Upsala J Med Sci 78: 139–144

    PubMed  CAS  Google Scholar 

  44. Irvine WJ, McCallum CJ, Gray RS, Campbell CJ, Duncan LJP, Farquhar JW, Vaughan H, Morris PJ (1977) Pancreatic islet-cell antibodies in diabetes mellitus correlated with the duration and type of diabetes, coexistent autoimmune disease and HLA type. Diabetes 26: 138–147

    PubMed  CAS  Google Scholar 

  45. Iwo K, Bellomo SC, Mukai N, Craighead JE (1983) Encephalomyocarditis virus-induced diabetes in mice: long-term changes in the structure and function of the islets of Langerhans. Diabetologia 25: 35–44

    Google Scholar 

  46. Izui S, Elder JH, McConahey PJ, Dixon FJ (1981) Identification of retroviral gp70 antibodies involved in circulating immune complexes in NZB x NZW mice. J Exp Med 153:1151–1160

    PubMed  CAS  Google Scholar 

  47. Jansen FK, Muntefering H, Schmidt WAK (1977) Virus-induced diabetes and the immune system. I. Suggestion that appearance of diabetes depends on immune reactions. Diabetologia 13: 545–549

    PubMed  CAS  Google Scholar 

  48. Jansen FK, Thurneyssen O, Munterfering H (1979) Virus-induced diabetes and the immune system. II. Evidence for an immune pathogenesis of the acute phase of diabetes. Biomedicine 31:1–2

    PubMed  CAS  Google Scholar 

  49. Johnson DA, Elder JH (1983) Antibody directed to determinants of a Moloney virus derived MCF gp70 recognizes a thymic differentiation antigen. J Exp Med 159: 1751–1756

    Google Scholar 

  50. Johnson GM, Tudor RB (1970) Diabetes mellitus and congenital rubella infection. Am J Dis Child 120: 453–455

    PubMed  Google Scholar 

  51. Leiter EH, Cunliffe-Beamer T (1977) Exocrine pancreatic insufficiency syndrome in CBA/J mice III. Pathological and genetic analysis. Gastroenterol 73: 260–266

    CAS  Google Scholar 

  52. Leiter EH, Malinoski F, Eppig JJ (1978) An epithelial cell line with chronic polyoma infection established from a spontaneous mouse pancreatic adenocarcinoma. Cancer Res 38: 969–977

    PubMed  CAS  Google Scholar 

  53. Leiter EH, Bedigian HG (1979) Intracisternal type A particles in genetically diabetic mice: identification in pancreas and induction in cultured B-cells. Diabetologia 17: 175–185

    PubMed  CAS  Google Scholar 

  54. Leiter EH, Kuff EL (1984) Intracisternal type A particles in murine pancreatic B cells: immunocytochemical demonstration of increased antigen (p73) in genetically diabetic mice. Am J Pathol 114:46–55

    PubMed  CAS  Google Scholar 

  55. Leiter EH (1985) Type C retrovirus production by pancreatic B-cells: association with accelerated pathogenesis in C3H-db/db (“diabetes”) mice. Am J Pathol 119: 22–32

    PubMed  CAS  Google Scholar 

  56. Leiter EH, Yoon J-W, Kuff EL (1985) Spontaneous autoantibody production against insulin and retrovirus distinguishes C57BL/KsJ from C57BL/6J mice. Diabetes 34 [Suppl 1]: 80A

    Google Scholar 

  57. Leiter EH, Fewell JW, Kuff EL (1986) Glucose induces intracisternal type A retroviral gene transcription and translation in pancreatic B-cells. J Exp Med 163: 87–100

    PubMed  CAS  Google Scholar 

  58. Leiter EH, Prochazka M (1987) Effect of immunodeficiency on diabetogenesis in genetically diabetic (db/db) mice. J Immunol 138: 3224–3229

    PubMed  CAS  Google Scholar 

  59. Like AA, Chick WL (1970) Studies in the diabetic mutant mouse. II. Electron microscopy of pancreatic islets. Diabetologia 6: 216–242

    PubMed  CAS  Google Scholar 

  60. Like AA, Rossini AA (1976) Streptozotocin-induced pancreatic insulitis: new model of diabetes mellitus. Science 193: 415–417

    PubMed  CAS  Google Scholar 

  61. Lutton CW, Gauntt CJ (1985) Ameliorating effect of IFN-B and anti-IFN-B on Coxsackie virus B3-induced myocarditis in mice. J Interferon Res 5:137–146

    PubMed  CAS  Google Scholar 

  62. Lyons MJ, Faust IM, Hemmes RB, Buskirk DR, Hirsch J, Zabriskie JB (1982) A virally induced obesity syndrome in mice. Science 216: 82–85

    PubMed  CAS  Google Scholar 

  63. Moore KW, Jardieu P, Mietz JA, Trounstine ML, Kuff EL, Ishizaka K, Martens CL (1986) Rodent IgE-binding factor genes are members of an endogenous retrovirus-like gene family. J Immunol 136: 4283–4290

    PubMed  CAS  Google Scholar 

  64. Monif GRG, Avery GB, Korones SB, Sever JL (1965) Post-mortem isolation of rubella virus from three children with rubella-syndrome defects. Lancet I: 723–725

    Google Scholar 

  65. Morrow PL, Freedman A, Craighead JE (1980) Testosterone effect on experimental diabetes mellitus in encephalomyocarditis (EMC) virus-infected mice. Diabetologia 18: 247–249

    PubMed  CAS  Google Scholar 

  66. Murnane TG, Craighead JE, Mondragon H, Shelokov A (1960) Fatal disease of swine due to encephalomyocarditis virus. Science 131: 498–499

    PubMed  CAS  Google Scholar 

  67. Nielsen DA, Welsh M, Casadaban MJ, Steiner DF (1985) Control of insulin gene expression in pancreatic B-cells and in an insulin-producing cell line, RIN-5F cells. I. Effects of glucose and cyclic AMP on the transcription of insulin mRNA. J Biol Chem 260:13585–13589

    PubMed  CAS  Google Scholar 

  68. Oldstone MBA, Southern P, Rodriquez M, Lampert P (1984) Virus persists in B-cells of islets of Langerhans and is associated with chemical manifestations of diabetes. Science 224: 1440–1443

    PubMed  CAS  Google Scholar 

  69. Onodera T, Toniolo A, Ray UR, Jenson AB, Knazek RA, Notkins AL (1981) Virus induced diabetes mellitus. XX. Polyendocrinopathy and autoimmunity. J Exp Med 153:1457–1473

    PubMed  CAS  Google Scholar 

  70. Onodera T, Ray UR, Melez KA, Suzuki H, Toniolo A, Notkins AL (1982) Virus induced diabetes mellitus: autoimmunity and polyendocrine disease prevented by immunosuppression. Nature 27: 66–68

    Google Scholar 

  71. Paavonen T, Anderson LC, Aldercreutz H (1981) Sex hormone regulation of in vitro immune response. J Exp Med 154:1935–1945

    PubMed  CAS  Google Scholar 

  72. Perrotti N, Grunberger G, Richert ND, Taylor SI (1986) Immunological similarity between the insulin receptor and the protein encoded by the src oncogene. Endocrinology 118: 2349–2354

    PubMed  CAS  Google Scholar 

  73. Plotkin SA, Kaye R (1970) Diabetes and congenital rubella. Pediatrics 46: 650–651

    PubMed  CAS  Google Scholar 

  74. Plotz PH (1983) Autoantibodies are anti-idiotype antibodies to antiviral antibodies. Lancet 11:824–826

    Google Scholar 

  75. Rabinowe SL, George KL, Laughlin R, Soeldner JS, Eisenbarth GS (1986) Congenital rubella: monoclonal antibody defined T cell abnormalities in young adults. Am J Med 81: 779–782

    PubMed  CAS  Google Scholar 

  76. Ray U, Aulakh G, McClintock PR, Yoon JW, Notkins JW (1983) Virus-induced diabetes: difference in the RNA finger prints of diabetogenic and nondiabetogenic variants of encephalomyocarditis virus. J Gen Virol 64: 947–950

    PubMed  CAS  Google Scholar 

  77. Rayfield EJ, Gorelkin L, Curnow RT, Jahrling PB (1976) Virus-induced pancreatic disease by Venezuelan encephalitis virus. Alterations in glucose tolerance and insulin resistance. Diabetes 25:623–631

    PubMed  CAS  Google Scholar 

  78. Rayfield EJ, Yoon J-W (1981) Role of viruses in diabetes. In: Cooperstein SJ, Watkins D (eds) The islets of Langerhans: biochemistry, physiology, and pathology. Academic, New York, pp 428–451

    Google Scholar 

  79. Rayfield EJ, Seto Y, Walsh S, McEvoy RC (1981) Virus-induced alterations in insulin release in hamster islets of Langerhans. J Clin Invest 68:1172–1181

    PubMed  CAS  Google Scholar 

  80. Rayfield EJ, Kelly KJ (1985) A direct mechanism by which rubella virus impairs insulin secretion. Diabetes 34 [Suppl 1]: 271A

    Google Scholar 

  81. Rayfield EJ, Kelly KJ (1986) Virus-induced alterations in cyclic adenosine monophosphate generation in hamster islets of Langerhans. J Clin Invest 77: 958–963

    PubMed  CAS  Google Scholar 

  82. Rayfield EJ, Kelly KJ, Yoon J-W (1986) Rubella virus-induced diabetes in the hamster. Diabetes 35:1278–1281

    PubMed  CAS  Google Scholar 

  83. Rodriguez M, Garrett RS, Raitt M, Lampert PW, Oldstone MBA (1985) Virus persists in B cells of islets of Langerhans and infection is associated with chemical manifestations of diabetes. Am J Pathol 121: 497–504

    PubMed  CAS  Google Scholar 

  84. Ross ME, Onodera T, Brown KS, Notkins AL (1976) Virus-induced diabetes mellitus. IV. Genetic and environmental factors influencing the development of diabetes after infection with the M variant of encephalomyocarditis virus. Diabetes 25:190–197

    PubMed  CAS  Google Scholar 

  85. Rossini AA, Appel MA, Williams RM, Like AA (1977) Genetic influence of the streptozotocin-induced insulitis and hyperglycemia. Diabetes 26: 916–920

    PubMed  CAS  Google Scholar 

  86. Rotter JI, Rimoin DL (1978) Heterogeneity in diabetes mellitus. Diabetes 27: 599–608

    PubMed  CAS  Google Scholar 

  87. Rubinstein P, Walker ME, Fedun B, Witt ME, Cooper LZ, Ginsberg-Fellner F (1982) The HLA system in congenital rubella patients with and without diabetes. Diabetes 31: 1088–1091

    PubMed  CAS  Google Scholar 

  88. Sass B, Vernon ML, Peters RL, Kelloff GJ (1978) Mammary tumors, hepatocellular carcinomas, and pancreatic islet changes in C3H-Avymice. JNCI 60: 611–621

    PubMed  CAS  Google Scholar 

  89. Sege K, Peterson PA (1980) Anti-idiotypic antibodies raised against anti-insulin antibodies cross-react with the insulin receptor. In: Irvine WJ (ed) Immunology of diabetes. Teviot, Edinburgh, pp 195–204

    Google Scholar 

  90. Serreze DV, Leiter EH, Kuff EL, Jardieu P, Ishizaka K (1988) Molecular mimicry between insulin and retroviral antigen p73: development of cross reactive autoantibodies in sera of NOD and C57BL/KsJ-db/db mice. Diabetes, in press

    Google Scholar 

  91. Southern P, Oldstone MBA (1986) Medical consequences of persistent viral infection. N Engl J Med 314: 359–367

    PubMed  CAS  Google Scholar 

  92. Srinivasappa J, Saegusa J, Prabhakar BS, Gentry MK, Buchmeier MJ, Wiktor TJ, Koprowski H, Oldstone MBA, Notkins AL (1986a) Molecular mimicry: frequency of reactivity of monoclonal antiviral antibodies with normal tissues. J Virol 57: 397–401

    PubMed  CAS  Google Scholar 

  93. Srinivasappa J, Asher DM, Pomeroy KY, Yoon J-W, Gajdusek DC, Notkins AL (1986b) Virus-induced diabetes mellitus: slow viruses. Symposium program. In: Jaworski MA, Mollnar GD, Rajotte RV, Singh B (eds) Elsevier Science, Amsterdam The Immunology of diabetes mellitus meeting. Edmonton, pp 33

    Google Scholar 

  94. Stewart WE (1979) The interferon system. Springer, Berlin Heidelberg New York, pp 199–200

    Google Scholar 

  95. Talal N (1976) Disordered immunologic regulation and autoimmunity. Transplant Rev 31: 240–263

    PubMed  CAS  Google Scholar 

  96. Teich N (1984) Taxonomy of retroviruses. In: Weiss R, Teich N, Varmus H, Coffin J (eds) RNA tumor viruses, vol 1, 2nd edn. Cold Spring Harbor Publications, Cold Spring Harbor, pp 25–207

    Google Scholar 

  97. Terres G, Morrison SL, Habicht GS (1968) A quantitative difference in the immune response between male and female mice. Proc Soc Exp Biol Med 127: 664–668

    PubMed  CAS  Google Scholar 

  98. Toniolo A, Onodera T, Yoon JW, Notkins JW (1980) Induction of diabetes by cumulative environmental insults from viruses and chemicals. Nature 288: 383–385

    PubMed  CAS  Google Scholar 

  99. Vialettes B, Baume D, Charpin C, De Maeyer-Guignard J, Vague P (1983) Assessment of viral and immune factors in EMC virus-induced diabetes. Effects of cyclosporin A and interferon. J Clin Lab Immunol 10: 35–40

    PubMed  CAS  Google Scholar 

  100. Weiss R, Teich N, Varmus H, Coffin J (eds) (1984) RNA tumor viruses. Molecular biology of tumor viruses, 2 vols, 2nd edn. Cold Spring Harbor Publications, Cold Spring Harbor, pp 1–1233

    Google Scholar 

  101. Wellmann KF, Amsterdam D, Brooks JE, Volk BW (1972) Fine structure of pancreatic islets of mice infected with the M variant of the encephalomyocarditis virus. Diabetologia 8: 349–357

    Google Scholar 

  102. Wellmann KF, Amsterdam D, Brooks JE, Volk BW (1975) Glucose tolerance and pancreatic ultrastructure in mice with long-term diabetes induced by EMC virus (M variant). Proc Soc Exp Biol Med 148: 261–262

    PubMed  CAS  Google Scholar 

  103. Welsh M, Nielsen DA, Mackrell AJ, Steiner DF (1985) Control of insulin gene expression in pancreatic B cells and in an insulin-producing cell line, RIN5F cells II. Regulation of insulin mRNA stability. J Biol Chem 260:13590–13594

    PubMed  CAS  Google Scholar 

  104. Wilson GL, D’Andrea BJ, Bellomo SC, Craighead JE (1980) Encephalomyocarditis virus infection of cultured murine pancreatic B cells. Nature 285:112–113

    PubMed  CAS  Google Scholar 

  105. Wilson GL, Bellomo SC, Craighead JE (1983) Effect of interferon on encephalomyocarditis virus infection of cultured mouse pancreatic B cells. Diabetologia 24: 38–41

    PubMed  CAS  Google Scholar 

  106. Yoon J-W, Notkins AL (1976) Virus-induced diabetes mellitus. VI. Genetically determined host differences in the replication of encephalomyocarditis virus in pancreatic B cells. J Exp Med 143:1170–1185

    PubMed  CAS  Google Scholar 

  107. Yoon J-W, Austin M, Onodera T, Notkins AL (1979) Virus-induced diabetes mellitus: isolation of a virus from the pancreas of a child with diabetic ketoacidosis. N Engl J Med 300: 1173–1179

    PubMed  CAS  Google Scholar 

  108. Yoon J-W, McClintock PR, Onodera T, Notkins AL (1980) Virus-induced diabetes mellitus. XVIII. Inhibition by a non-diabetogenic variant of encephalomyocarditis virus. J Exp Med 152:878–891

    PubMed  CAS  Google Scholar 

  109. Yoon J-W, Selvaggio S, Onodera T, Wheeler J, Jenson AB (1981) Infection of cultured human pancreatic B cells with reovirus type 3. Diabetologia 20: 462–467

    PubMed  CAS  Google Scholar 

  110. Yoon J-W, London WT, Curfman BL, Brown RL, Notkins AL (1985) Coxsackie B4 produces transient diabetes in nonhuman primates. Diabetes 35: 712–716

    Google Scholar 

  111. Yoon J-W, McClintock PR, Bachurski CJ, Longstreth JD, Notkins AL (1985) Virus-induced diabetes mellitus: no evidence for immune mechanisms in the destruction of beta cells by the D-variant of encephalomyocarditis virus. Diabetes 34: 922–925

    PubMed  CAS  Google Scholar 

  112. Yoon J-W, Ray UR (1986) Perspectives on the role of viruses in insulin-dependent diabetes. Diabetes Care 8: 39–44

    Google Scholar 

Download references

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1988 Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

Leiter, E.H., Wilson, G.L. (1988). Viral Interactions with Pancreatic B-Cells. In: Lefèbvre, P.J., Pipeleers, D.G. (eds) The Pathology of the Endocrine Pancreas in Diabetes. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-72691-0_6

Download citation

  • DOI: https://doi.org/10.1007/978-3-642-72691-0_6

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-72693-4

  • Online ISBN: 978-3-642-72691-0

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics