Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1980 Jan;27(1):158–167. doi: 10.1128/iai.27.1.158-167.1980

Effect of prostaglandins and cyclic adenosine 3',5'-monophosphate modulators on herpes simplex virus growth and interferon response in human cells.

K F Trofatter Jr, C A Daniels
PMCID: PMC550738  PMID: 6244226

Abstract

Mechanisms whereby prostaglandins and other cyclic adenosine 3',5'-monophosphate (cAMP) modulators might enhance the growth of herpes simplex virus (HSV) in human skin fibroblasts were explored. Prostaglandins A1, B1, E1, E2, and F2 alpha, as well as isoproterenol, imidazole, carbamylcholine, and dibutyryl cAMP had no effect on HSV growth. On the other hand, the phosphodiesterase inhibitors 1-methyl-3-isobutylxanthine and theophylline delayed the growth, suppressed the cell-to-cell spread, but inhibited neither the adsorption nor the penetration of the virus. Although none of the cAMP-elevating reagents directly enhanced HSV growth, they were found to inhibit dose dependently the antiviral action of both type I and HSV antigen-induced human interferon preparations. Furthermore, these reagents suppressed the production of HSV antigen-induced interferon by immune human mononuclear leukocytes. These data support the hypothesis that prostaglandin elaboration in vivo could contribute to exacerbations of HSV infections by compromising the host's interferon defense system.

Full text

PDF
158

Selected References

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

  1. AURELIAN L., ROIZMAN B. ABORTIVE INFECTION OF CANINE CELLS BY HERPES SIMPLEX VIRUS. II. ALTERNATIVE SUPPRESSION OF SYNTHESIS OF INTERFERON AND VIRAL CONSTITUENTS. J Mol Biol. 1965 Mar;11:539–548. doi: 10.1016/s0022-2836(65)80009-2. [DOI] [PubMed] [Google Scholar]
  2. Arturson G., Hamberg M., Jonsson C. E. Prostaglandins in human burn blister fluid. Acta Physiol Scand. 1973 Feb;87(2):270–276. doi: 10.1111/j.1748-1716.1973.tb05390.x. [DOI] [PubMed] [Google Scholar]
  3. Baringer J. R., Swoveland P. Recovery of herpes-simplex virus from human trigeminal ganglions. N Engl J Med. 1973 Mar 29;288(13):648–650. doi: 10.1056/NEJM197303292881303. [DOI] [PubMed] [Google Scholar]
  4. Blyth W. A., Hill T. J., Field H. J., Harbour D. A. Reactivation of herpes simplex virus infection by ultraviolet light and possible involvement of prostaglandins. J Gen Virol. 1976 Dec;33(3):547–550. doi: 10.1099/0022-1317-33-3-547. [DOI] [PubMed] [Google Scholar]
  5. Böyum A. A one-stage procedure for isolation of granulocytes and lymphocytes from human blood. General sedimentation properties of white blood cells in a 1g gravity field. Scand J Clin Lab Invest Suppl. 1968;97:51–76. [PubMed] [Google Scholar]
  6. CARTON C. A. Effect of previous sensory loss on the appearance of herpes simplex following trigeminal sensory root section. J Neurosurg. 1953 Sep;10(5):463–468. doi: 10.3171/jns.1953.10.5.0463. [DOI] [PubMed] [Google Scholar]
  7. Coceani F., Pace-Asciak C., Volta F., Wolfe L. S. Effect of nerve stimulation on prostaglandin formation and release from the rat stomach. Am J Physiol. 1967 Oct;213(4):1056–1064. doi: 10.1152/ajplegacy.1967.213.4.1056. [DOI] [PubMed] [Google Scholar]
  8. Cooper J. A., Jr, Daniels C. A., Trofatter E. F., Jr The effect of prednisolone on antibody-dependent cell-mediated cytotoxicity and the growth of type I herpes simplex virus in human cells. Invest Ophthalmol Vis Sci. 1978 Apr;17(4):381–385. [PubMed] [Google Scholar]
  9. Degré M. Cholera toxin inhibits antiviral and growth inhibitory activities of human interferon. Proc Soc Exp Biol Med. 1978 Feb;157(2):253–255. [PubMed] [Google Scholar]
  10. Dianzani F., Neri P., Zucca M. Effect of dibutyryl cyclic AMP on interferon production by cells treated with viral or nonviral inducers. 1. Proc Soc Exp Biol Med. 1972 Sep;140(4):1375–1378. doi: 10.3181/00379727-140-36677. [DOI] [PubMed] [Google Scholar]
  11. Dingfelder J. R., Brenner W. E. The thermogenic activity of exogenous E and F prostaglandins in humans. Acta Obstet Gynecol Scand. 1978;57(1):35–40. doi: 10.3109/00016347809154196. [DOI] [PubMed] [Google Scholar]
  12. FRUITSTONE M. J., WADDELL G. H., SIGEL M. M. AN INTERFERON PRODUCED IN RESPONSE TO INFECTION BY HERPES SIMPLEX VIRUS. Proc Soc Exp Biol Med. 1964 Dec;117:804–807. doi: 10.3181/00379727-117-29703. [DOI] [PubMed] [Google Scholar]
  13. Feldberg W. The Ferrier Lecture, 1974. Body temperature and fever: changes in our views during the last decade. Proc R Soc Lond B Biol Sci. 1975 Nov 18;191(1103):199–229. doi: 10.1098/rspb.1975.0124. [DOI] [PubMed] [Google Scholar]
  14. Forghani B., Klassen T., Baringer J. R. Radioimmunoassay of herpes simplex virus antibody: correlation with ganglionic infection. J Gen Virol. 1977 Sep;36(3):371–375. doi: 10.1099/0022-1317-36-3-371. [DOI] [PubMed] [Google Scholar]
  15. Greaves M. W., Sondergaard J. Pharmacologic agents released in ultraviolet inflammation studied by continuous skin pefusion. J Invest Dermatol. 1970 May;54(5):365–367. doi: 10.1111/1523-1747.ep12259058. [DOI] [PubMed] [Google Scholar]
  16. Gresser I., Tovey M. G., Maury C., Bandu M. T. Role of interferon in the pathogenesis of virus diseases in mice as demonstrated by the use of anti-interferon serum. II. Studies with herpes simplex, Moloney sarcoma, vesicular stomatitis, Newcastle disease, and influenza viruses. J Exp Med. 1976 Nov 2;144(5):1316–1323. doi: 10.1084/jem.144.5.1316. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Guillon J. C., Gresser I. Rôle de l'interféron dans la pathogenèse d'une infection herpétique expérimentale chez la souris. Ann Microbiol (Paris) 1978 Feb-Mar;129(2):207–216. [PubMed] [Google Scholar]
  18. Haahr S., Rasmussen L., Merigan T. C. Lymphocyte transformation and interferon production in human mononuclear cell microcultures for assay of cellular immunity to herpes simplex virus. Infect Immun. 1976 Jul;14(1):47–54. doi: 10.1128/iai.14.1.47-54.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Hampar B., Notkins A. L., Mage M., Keehn M. A. Heterogeneity in the properties of 7 S and 19S rabbit-neutralizing antibodies to herpes simplex virus. J Immunol. 1968 Mar;100(3):586–593. [PubMed] [Google Scholar]
  20. Harbour D. A., Blyth W. A., Hill T. J. Prostanglandins enhance spread of herpes simplex virus in cell cultures. J Gen Virol. 1978 Oct;41(1):87–95. doi: 10.1099/0022-1317-41-1-87. [DOI] [PubMed] [Google Scholar]
  21. Hill T. J., Blyth W. A. An alternative theory of herpes-simplex recurrence and a possible role for prostaglandins. Lancet. 1976 Feb 21;1(7956):397–399. doi: 10.1016/s0140-6736(76)90220-8. [DOI] [PubMed] [Google Scholar]
  22. Hill T. J., Blyth W. A., Harbour D. A. Trauma to the skin causes recurrence of herpes simplex in the mouse. J Gen Virol. 1978 Apr;39(1):21–28. doi: 10.1099/0022-1317-39-1-21. [DOI] [PubMed] [Google Scholar]
  23. Hoyt C. S., Billson F. A. Herpes-simplex infection after blow-out fractures. Lancet. 1976 Dec 18;2(7999):1364–1365. doi: 10.1016/s0140-6736(76)92024-9. [DOI] [PubMed] [Google Scholar]
  24. Johnson H. M., Blalock J. E., Baron S. Separation of mitogen-induced suppressor and helper cell activities during inhibition of interferon production by cyclic AMP. Cell Immunol. 1977 Sep;33(1):170–179. doi: 10.1016/0008-8749(77)90144-7. [DOI] [PubMed] [Google Scholar]
  25. Lion G., Mombaerts-Servais M., Mouton R. F. Increased detection and yield of adenovirus in caffeine-stabilised KB cell monolayers. Arch Virol. 1976;52(3):263–268. doi: 10.1007/BF01348024. [DOI] [PubMed] [Google Scholar]
  26. Lodmell D. L., Notkins A. L. Cellular immunity to herpes simplex virus mediated by interferon. J Exp Med. 1974 Sep 1;140(3):764–778. doi: 10.1084/jem.140.3.764. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Mathur G. P., Wadia A. S. Epidermal prostaglandin and histamine in UV-induced erythema reaction. Indian J Med Res. 1976 Dec;64(12):1799–1806. [PubMed] [Google Scholar]
  28. Meldolesi M. F., Friedman R. M., Kohn L. D. An interferon-induced increase in cyclic AMP levels precedes the establishment of the antiviral state. Biochem Biophys Res Commun. 1977 Nov 7;79(1):239–246. doi: 10.1016/0006-291x(77)90086-9. [DOI] [PubMed] [Google Scholar]
  29. Merigan T. C., Rand K. H., Pollard R. B., Abdallah P. S., Jordan G. W., Fried R. P. Human leukocyte interferon for the treatment of herpes zoster in patients with cancer. N Engl J Med. 1978 May 4;298(18):981–987. doi: 10.1056/NEJM197805042981801. [DOI] [PubMed] [Google Scholar]
  30. Milton A. S., Wendlandt S. A possible role for prostaglandin E1 as a modulator for temperature regulation in the central nervous system of the cat. J Physiol. 1970 Apr;207(2):76P–77P. [PubMed] [Google Scholar]
  31. Nahmias A. J., Roizman B. Infection with herpes-simplex viruses 1 and 2. 3. N Engl J Med. 1973 Oct 11;289(15):781–789. doi: 10.1056/NEJM197310112891505. [DOI] [PubMed] [Google Scholar]
  32. Newton A. A. Inhibitors of prostaglandin synthesis as inhibitors of herpes simplex virus replication. Adv Ophthalmol. 1979;38:58–63. [PubMed] [Google Scholar]
  33. Pelus L. M., Strausser H. R. Prostaglandins and the immune response. Life Sci. 1977 Mar 15;20(6):903–913. doi: 10.1016/0024-3205(77)90274-0. [DOI] [PubMed] [Google Scholar]
  34. Rand K. H., Rasmussen L. E., Pollard R. B., Arvin A., Merigan T. C. Cellular immunity and herpesvirus infections in cardiac-transplant patients. N Engl J Med. 1977 Jun 16;296(24):1372–1377. doi: 10.1056/NEJM197706162962402. [DOI] [PubMed] [Google Scholar]
  35. Rasmussen L. E., Jordan G. W., Stevens D. A., Merigan T. C. Lymphocyte interferon production and transformation after Herpes simplex infections in humans. J Immunol. 1974 Feb;112(2):728–736. [PubMed] [Google Scholar]
  36. Rasmussen L., Merigan T. C. Role of T lymphocytes in cellular immune responses during herpes simplex virus infection in humans. Proc Natl Acad Sci U S A. 1978 Aug;75(8):3957–3961. doi: 10.1073/pnas.75.8.3957. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Reizin F. N., Roikhel V. M., Chumakov M. P. The influence of substances changing the intracellular concentration of cyclic adenosine 3'5'-monophosphate on interferon synthesis in chick embryo cell culture. Arch Virol. 1975;49(4):307–315. doi: 10.1007/BF01318239. [DOI] [PubMed] [Google Scholar]
  38. Stanwick T. L., Anderson R. W., Nahmias A. J. Interaction between cyclic nucleotides and herpes simplex viruses: productive infection. Infect Immun. 1977 Nov;18(2):342–347. doi: 10.1128/iai.18.2.342-347.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Steiner A. L., Parker C. W., Kipnis D. M. Radioimmunoassay for cyclic nucleotides. I. Preparation of antibodies and iodinated cyclic nucleotides. J Biol Chem. 1972 Feb 25;247(4):1106–1113. [PubMed] [Google Scholar]
  40. Stevens J. G. Latent herpes simplex virus and the nervous system,. Curr Top Microbiol Immunol. 1975;70:31–50. doi: 10.1007/978-3-642-66101-3_2. [DOI] [PubMed] [Google Scholar]
  41. Thion C., Green M. Cyclic AMP-amplified replication of RNA tumour virus-like particles in Chinese hamster ovary cells. Nat New Biol. 1973 Aug 22;244(138):227–231. doi: 10.1038/newbio244227a0. [DOI] [PubMed] [Google Scholar]
  42. Trofatter K. F., Jr, Daniels C. A. Interaction of human cells with prostaglandins and cyclic AMP modulators. I. Effects on complement-mediated lysis and antibody-dependent cell-mediated cytolysis of herpes simplex virus-infected human fibroblasts. J Immunol. 1979 Apr;122(4):1363–1370. [PubMed] [Google Scholar]
  43. Valle M. J., Jordan G. W., Haahr S., Merigan T. C. Characteristics of immune interferon produced by human lymphocyte cultures compared to other human interferons. J Immunol. 1975 Jul;115(1):230–233. [PubMed] [Google Scholar]
  44. Vilcek J., Ng M. H. Post-transcriptional control of interferon synthesis. J Virol. 1971 May;7(5):588–594. doi: 10.1128/jvi.7.5.588-594.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Wheeler C. E., Jr Pathogenesis of recurrent herpes simplex infections. J Invest Dermatol. 1975 Oct;65(4):341–346. doi: 10.1111/1523-1747.ep12607603. [DOI] [PubMed] [Google Scholar]
  46. Yamanishi K., Fogel M., Rapp F. Effect of caffeine on the replication of nonirradiated and ultraviolet-irradiated cytomegalovirus. Intervirology. 1978;10(4):241–253. doi: 10.1159/000148987. [DOI] [PubMed] [Google Scholar]
  47. Yang J., Nandi S. Cyclic AMP regulation of mammary tumor virus production. J Virol. 1977 Feb;21(2):815–819. doi: 10.1128/jvi.21.2.815-819.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Yaron M., Yaron I., Gurari-Rotman D., Revel M., Lindner H. R., Zor U. Stimulation of prostaglandin E production in cultured human fibroblasts by poly(I)-poly(C) and human interferon. Nature. 1977 Jun 2;267(5610):457–459. doi: 10.1038/267457a0. [DOI] [PubMed] [Google Scholar]
  49. Youngner J. S., Salvin S. B. Production and properties of migration inhibitory factor and interferon in the circulation of mice with delayed hypersensitivity. J Immunol. 1973 Dec;111(6):1914–1922. [PubMed] [Google Scholar]

Articles from Infection and Immunity are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES