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Journal of Clinical Pathology. Supplement (Royal College of Pathologists) logoLink to Journal of Clinical Pathology. Supplement (Royal College of Pathologists)
. 1972;6:121–131.

Immune responses in persistent virus infections

A C Allison 1
PMCID: PMC1347261  PMID: 4376149

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Allison A. C., Denman A. M., Barnes R. D. Cooperating and controlling functions of thymus-derived lymphocytes in relation to autoimmunity. Lancet. 1971 Jul 17;2(7716):135–140. doi: 10.1016/s0140-6736(71)92306-3. [DOI] [PubMed] [Google Scholar]
  2. Alpert E., Isselbacher K. J., Schur P. H. The pathogenesis of arthritis associated with viral hepatitis. Complement-component studies. N Engl J Med. 1971 Jul 22;285(4):185–189. doi: 10.1056/NEJM197107222850401. [DOI] [PubMed] [Google Scholar]
  3. Blanden R. V. Mechanisms of recovery from a generalized viral infection: mousepox. I. The effects of anti-thymocyte serum. J Exp Med. 1970 Nov;132(5):1035–1054. doi: 10.1084/jem.132.5.1035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bloom B. R., Jimenez L., Marcus P. I. A plaque assay for enumerating antigen-sensitive cells in delayed-type hypersensitivity. J Exp Med. 1970 Jul 1;132(1):16–30. doi: 10.1084/jem.132.1.16. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Brunell P. A., Ross A., Miller L. H., Kuo B. Prevention of varicella by zoster immune globulin. N Engl J Med. 1969 May 29;280(22):1191–1194. doi: 10.1056/NEJM196905292802201. [DOI] [PubMed] [Google Scholar]
  6. Buser F. Side reaction to measles vaccination suggesting the Arthus phenomenon. N Engl J Med. 1967 Aug 3;277(5):250–251. doi: 10.1056/NEJM196708032770507. [DOI] [PubMed] [Google Scholar]
  7. Cangir A., Sullivan M. P. The occurrence of cytomegalovirus infections in childhood leukemia. JAMA. 1966 Feb 21;195(8):616–622. [PubMed] [Google Scholar]
  8. Cole G. A., Gilden D. H., Monjan A. A., Nathanson N. Lymphocytic choriomeningitis virus: pathogenesis of acute central nervous system disease. Fed Proc. 1971 Nov-Dec;30(6):1831–1841. [PubMed] [Google Scholar]
  9. Combes B., Shorey J., Barrera A., Stastny P., Eigenbrodt E. H., Hull A. R., Carter N. W. Glomerulonephritis with deposition of Australia antigen-antibody complexes in glomerular basement membrane. Lancet. 1971 Jul 31;2(7718):234–237. doi: 10.1016/s0140-6736(71)92572-4. [DOI] [PubMed] [Google Scholar]
  10. Craighead J. E. Immunologic response to cytomegalovirus infection in renal allograft recipients. Am J Epidemiol. 1969 Dec;90(6):506–513. doi: 10.1093/oxfordjournals.aje.a121096. [DOI] [PubMed] [Google Scholar]
  11. Dixon F. J., Oldstone M. B., Tonietti G. Pathogenesis of immune complex glomerulonephritis of New Zealand mice. J Exp Med. 1971 Sep 1;134(3 Pt 2):65s–71s. [PubMed] [Google Scholar]
  12. ELLISON S. A., CARTON C. A., ROSE H. M. Studies of recurrent herpes simplex infections following section of the trigeminal nerve. J Infect Dis. 1959 Sep-Oct;105:161–167. doi: 10.1093/infdis/105.2.161. [DOI] [PubMed] [Google Scholar]
  13. Evans R., Salaman M. H. Studies on the mechanism of action of Riley virus. 3. Replication of Riley's plasma enzyme-elevating virus in vitro. J Exp Med. 1965 Nov 1;122(5):993–1002. doi: 10.1084/jem.122.5.993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Gerson K. L., Haslam R. H. Subtle immunologic abnormalities in four boys with subacute sclerosing panencephalitis. N Engl J Med. 1971 Jul 8;285(2):78–82. doi: 10.1056/NEJM197107082850203. [DOI] [PubMed] [Google Scholar]
  15. Gibbons R. A., Hunter G. D. Nature of the scrapie agent. Nature. 1967 Sep 2;215(5105):1041–1043. doi: 10.1038/2151041a0. [DOI] [PubMed] [Google Scholar]
  16. Gibbs R. C., Shapiro E., Cassidy H., Brunell P. A. Possible mechanisms for maintaining immunity to varicella-zoster virus. Clinical observations. Am J Dis Child. 1970 Nov;120(5):456–457. doi: 10.1001/archpedi.1970.02100100120015. [DOI] [PubMed] [Google Scholar]
  17. Gocke D. J., Hsu K., Morgan C., Bombardieri S., Lockshin M., Christian C. L. Vasculitis in association with Australia antigen. J Exp Med. 1971 Sep 1;134(3 Pt 2):330s–336s. [PubMed] [Google Scholar]
  18. Gudnadóttir M., Pálsson P. A. Host-virus interaction in visna infected sheep. J Immunol. 1965 Dec;95(6):1116–1120. [PubMed] [Google Scholar]
  19. Haworth J. C., Hoogstraten J., Taylor H. Thymic alymphoplasia. Arch Dis Child. 1967 Feb;42(221):40–54. doi: 10.1136/adc.42.221.40. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Hayes J. A., Been T. E., Valentine E. J., Bras G. A case of fatal dissemination of varicella. J Pathol Bacteriol. 1965 Jul;90(1):328–333. doi: 10.1002/path.1700900139. [DOI] [PubMed] [Google Scholar]
  21. Jabbour J. T., Roane J. A., Sever J. L. Studies of delayed dermal hypersensitivity in patients with subacute sclerosing panencephalitis. Neurology. 1969 Oct;19(10):929–931. doi: 10.1212/wnl.19.10.929. [DOI] [PubMed] [Google Scholar]
  22. Kaufman H. E., Brown D. C., Ellison E. M. Recurrent herpes in the rabbit and man. Science. 1967 Jun 23;156(3782):1628–1629. doi: 10.1126/science.156.3782.1628. [DOI] [PubMed] [Google Scholar]
  23. Kolar O. Measles and subacute sclerosing panencephalitis. Lancet. 1968 Dec 7;2(7580):1242–1242. doi: 10.1016/s0140-6736(68)91719-4. [DOI] [PubMed] [Google Scholar]
  24. Kretschmer R., August C. S., Rosen F. S., Janeway C. A. Recurrent infections, episodic lymphopenia and impaired cellular immunity. N Engl J Med. 1969 Aug 7;281(6):285–290. doi: 10.1056/NEJM196908072810602. [DOI] [PubMed] [Google Scholar]
  25. Latarjet R., Muel B., Haig D. A., Clarke M. C., Alper T. Inactivation of the scrapie agent by near monochromatic ultraviolet light. Nature. 1970 Sep 26;227(5265):1341–1343. doi: 10.1038/2271341a0. [DOI] [PubMed] [Google Scholar]
  26. Leonard L. L., Schmidt N. J., Lennette E. H. Demonstration of viral antibody activity in two immunoglobulin G subclasses in patients with varicella-zoster virus infection. J Immunol. 1970 Jan;104(1):23–27. [PubMed] [Google Scholar]
  27. Lundstedt C. Interaction between antigenically different cells. Virus-induced cytotoxicity by immune lymphoid cells in vitro. Acta Pathol Microbiol Scand. 1969;75(1):139–152. [PubMed] [Google Scholar]
  28. McFarlin D. E., Raff M. C., Simpson E., Nehlsen S. H. Scrapie in immunologically deficient mice. Nature. 1971 Oct 1;233(5318):336–336. doi: 10.1038/233336a0. [DOI] [PubMed] [Google Scholar]
  29. McGuire T. C., Crawford T. B., Henson J. B. Immunofluorescent localization of equine infectious anemia virus in tissue. Am J Pathol. 1971 Feb;62(2):283–294. [PMC free article] [PubMed] [Google Scholar]
  30. Miller L. H., Brunell P. A. Zoster, reinfection or activation of latent virus? Observations on the antibody response. Am J Med. 1970 Oct;49(4):480–483. doi: 10.1016/s0002-9343(70)80042-0. [DOI] [PubMed] [Google Scholar]
  31. Miller M. E., Schieken R. M. Thymic dysplasia. A separable entity from "swiss agammaglobulinemia". Am J Med Sci. 1967 Jun;253(6):741–750. doi: 10.1097/00000441-196706000-00012. [DOI] [PubMed] [Google Scholar]
  32. Montgomerie J. Z., Becroft D. M., Croxson M. C., Doak P. B., North J. D. Herpes-simplex-virus infection after renal transplantation. Lancet. 1969 Oct 25;2(7626):867–871. doi: 10.1016/s0140-6736(69)92327-7. [DOI] [PubMed] [Google Scholar]
  33. Nahmias A. J., Griffith D., Salsbury C., Yoshida K. Thymic aplasia with lymphopenia, plasma cells, and normal immunoglobulins. Relation to measles virus infection. JAMA. 1967 Sep 4;201(10):729–734. [PubMed] [Google Scholar]
  34. Nathanson N., Cole G. A. Immunosuppression and experimental virus infection of the nervous system. Adv Virus Res. 1970;16:397–448. doi: 10.1016/S0065-3527(08)60028-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Notkins A. L., Mahar S., Scheele C., Goffman J. Infectious virus-antibody complex in the blood of chronically infected mice. J Exp Med. 1966 Jul 1;124(1):81–97. doi: 10.1084/jem.124.1.81. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. O'CONNELL C. J., KARZON D. T., BARRON A. L., PLAUT M. E., ALI V. M. PROGRESSIVE VACCINIA WITH NORMAL ANTIBODIES. A CASE POSSIBLY DUE TO DEFICIENT CELLULAR IMMUNITY. Ann Intern Med. 1964 Feb;60:282–289. doi: 10.7326/0003-4819-60-2-282. [DOI] [PubMed] [Google Scholar]
  37. Oldstone M. B., Dixon F. J. Immune complex disease in chronic viral infections. J Exp Med. 1971 Sep 1;134(3 Pt 2):32s–40s. [PubMed] [Google Scholar]
  38. Oldstone M. B., Dixon F. J. Pathogenesis of chronic disease associated with persistent lymphocytic choriomeningitis viral infection. I. Relationship of antibody production to disease in neonatally infected mice. J Exp Med. 1969 Mar 1;129(3):483–505. doi: 10.1084/jem.129.3.483. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Porter D. D., Larsen A. E., Porter H. G. The pathogenesis of Aleutian disease of mink. I. In vivo viral replication and the host antibody response to viral antigen. J Exp Med. 1969 Sep 1;130(3):575–593. doi: 10.1084/jem.130.3.575. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Porter D. D., Porter H. G. Deposition of immune complexes in the kidneys of mice infected with lactic dehydrogenase virus. J Immunol. 1971 May;106(5):1264–1266. [PubMed] [Google Scholar]
  41. Rifkind D. The activation of varicella-zoster virus infections by immunosuppressive therapy. J Lab Clin Med. 1966 Sep;68(3):463–474. [PubMed] [Google Scholar]
  42. SMITH M. G., VELLIOS F. Inclusion disease or generalized salivary gland virus infection. AMA Arch Pathol. 1950 Dec;50(6):862–884. [PubMed] [Google Scholar]
  43. Saunders M., Chambers M. E., Knowles M., Caspary E. A., Gardner-Medwin D., Walker P. Cellular and humoral responses to measles in subacute sclerosing panencephalitis. Lancet. 1969 Jan 11;1(7585):72–74. doi: 10.1016/s0140-6736(69)91090-3. [DOI] [PubMed] [Google Scholar]
  44. Schur P. H., Borel H., Gelfand E. W., Alper C. A., Rosen F. S. Selective gamma-g globulin deficiencies in patients with recurrent pyogenic infections. N Engl J Med. 1970 Sep 17;283(12):631–634. doi: 10.1056/NEJM197009172831205. [DOI] [PubMed] [Google Scholar]
  45. Scott T. F., Bonanno D. E. Reactions to live-measles-virus vaccine in children previously inoculated with killed-virus vaccine. N Engl J Med. 1967 Aug 3;277(5):248–250. doi: 10.1056/NEJM196708032770506. [DOI] [PubMed] [Google Scholar]
  46. Speel L. F., Osborn J. E., Walker D. L. An immuno-cytopathogenic interaction between sensitized leukocytes and epithelial cells carrying a persistent noncytocidal myxovirus infection. J Immunol. 1968 Sep;101(3):409–417. [PubMed] [Google Scholar]
  47. Stevens J. G., Nesburn A. B., Cook M. L. Latent herpes simplex virus from trigeminal ganglia of rabbits with recurrent eye infection. Nat New Biol. 1972 Feb 16;235(59):216–217. doi: 10.1038/newbio235216a0. [DOI] [PubMed] [Google Scholar]
  48. Trepo C., Thivolet J. Hepatitis associated antigen and periarteritis nodosa (PAN). Vox Sang. 1970 Sep-Oct;19(3):410–411. [PubMed] [Google Scholar]
  49. Wear D. J., Rapp F. Latent measles virus infection of the hamster central nervous system. J Immunol. 1971 Dec;107(6):1593–1598. [PubMed] [Google Scholar]
  50. Weiner L. P., Cole G. A., Nathanson N. Virus-specific immunologic depression in mice following combined immunization and cyclophosphamide-induced immunosuppression. J Immunol. 1971 Feb;106(2):427–430. [PubMed] [Google Scholar]
  51. Wiktor T. J., Kuwert E., Koprowski H. Immune lysis of rabies virus-infected cells. J Immunol. 1968 Dec;101(6):1271–1282. [PubMed] [Google Scholar]
  52. Zisman B., Wheelock E. F., Allison A. C. Role of macrophages and antibody in resistance of mice against yellow fever virus. J Immunol. 1971 Jul;107(1):236–243. [PubMed] [Google Scholar]
  53. Zlotnik I., Smith C. E., Grant D. P., Peacock S. The effect of immunosuppression on viral encephalitis, with special reference to cyclophosphamide. Br J Exp Pathol. 1970 Aug;51(4):434–439. [PMC free article] [PubMed] [Google Scholar]

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