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. 1973 Oct 31;138(5):1033–1043. doi: 10.1084/jem.138.5.1033

INDUCTION OF SKIN RESISTANCE TO VACCINIA VIRUS IN RABBITS BY VACCINIA-SOLUBLE EARLY ANTIGENS

Y Ueda 1, I Tagaya 1
PMCID: PMC2139429  PMID: 4744920

Abstract

The immunological role of vaccinia-soluble early antigen was examined in rabbits. The antigens were prepared from HeLa cells infected with a conditional lethal mutant of vaccinia virus, which induces in these cells early antigens including those responsible for surface immunofluorescence of infected cells, but not viral DNA and late protein syntheses. Immunization of rabbits with the antigens in Freund's complete adjuvant induced complement-fixing antibody but neither detectable circulating neutralizing antibody nor any detectable level of inhibitory substance or interferon in the skin of the animals. When immunized animals were inoculated intradermally with vaccinia virus, multiplication of virus in the skin was greatly inhibited, being accompanied by an earlier appearance as well as an accelerated wane of the local reactions. The resistance could not be transferred passively by the serum of immunized animals to normal rabbits. Immunization of rabbits with the antigens without the adjuvant not only failed to inhibit but, contrariwise, enhanced the multiplication of intradermally inoculated vaccinia virus, inducing heavy skin lesions and exalted virus multiplication.

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Selected References

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  1. Allison A. C. Cell-mediated immune responses to virus infections and virus-induced tumours. Br Med Bull. 1967 Jan;23(1):60–65. doi: 10.1093/oxfordjournals.bmb.a070518. [DOI] [PubMed] [Google Scholar]
  2. Appleyard G., Hapel A. J., Boulter E. A. An antigenic difference between intracellular and extracellular rabbitpox virus. J Gen Virol. 1971 Oct;13(1):9–17. doi: 10.1099/0022-1317-13-1-9. [DOI] [PubMed] [Google Scholar]
  3. Blanden R. V. Mechanisms of recovery from a generalized viral infection: mousepox. 3. Regression infectious foci. J Exp Med. 1971 May 1;133(5):1090–1104. doi: 10.1084/jem.133.5.1090. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. 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]
  5. Blanden R. V. Mechanisms of recovery from a generalized viral infection: mousepox. II. Passive transfer of recovery mechanisms with immune lymphoid cells. J Exp Med. 1971 May 1;133(5):1074–1089. doi: 10.1084/jem.133.5.1074. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Boulter E. A., Zwartouw H. T., Titmuss D. H., Maber H. B. The nature of the immune state produced by inactivated vaccinia virus in rabbits. Am J Epidemiol. 1971 Dec;94(6):612–620. doi: 10.1093/oxfordjournals.aje.a121360. [DOI] [PubMed] [Google Scholar]
  7. Hansson O., Johansson S. G., Vahlquist B. Vaccinia Gangrenosa with normal humoral antibodies. A case possibly due to deficient cellular immunity treated with N-methylisatin beta-thiosemicarbazone (Compound 33T57, Marboran). Acta Paediatr Scand. 1966 May;55(3):264–272. doi: 10.1111/j.1651-2227.1966.tb17653.x. [DOI] [PubMed] [Google Scholar]
  8. Hirsch M. S., Nahmias A. J., Murphy F. A., Kramer J. H. Cellular immunity in vaccinia infection of mice. Anti-thymocyte serum effects on primary and secondary responsiveness. J Exp Med. 1968 Jul 1;128(1):121–132. doi: 10.1084/jem.128.1.121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. KEMPE C. H. Studies smallpox and complications of smallpox vaccination. Pediatrics. 1960 Aug;26:176–189. [PubMed] [Google Scholar]
  10. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  11. McNeill T. A. The development of skin resistance and hypersensitivity following inactivated vaccinia virus vaccines in rabbits. J Hyg (Lond) 1966 Mar;64(1):23–31. doi: 10.1017/s0022172400040304. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Miyamoto H., Kato S. Immune hemadsorption by cells infected with poxviruses. Biken J. 1968 Dec;11(4):343–353. [PubMed] [Google Scholar]
  13. Rocklin R. E., Meyers O. L., David J. R. An in vitro assay for cellular hypersensitivity in man. J Immunol. 1970 Jan;104(1):95–102. [PubMed] [Google Scholar]
  14. TAGAYA I., KITAMURA T., SANO Y. A new mutant of dermovaccinia virus. Nature. 1961 Oct 28;192:381–382. doi: 10.1038/192381a0. [DOI] [PubMed] [Google Scholar]
  15. TURK J. L., ALLISON A. C., OXMAN M. N. Delayed hypersensitivity in relation to vaccination and multiplication of vaccinia virus in the guineapig. Lancet. 1962 Feb 24;1(7226):405–407. doi: 10.1016/s0140-6736(62)91362-4. [DOI] [PubMed] [Google Scholar]
  16. Ueda S., Nozima T. Delayed hypersensitivity in vaccinia-infected mice. I. Antigen(s) responsible for developing delayed hypersensitivity. Acta Virol. 1969 Nov;13(6):532–537. [PubMed] [Google Scholar]
  17. Ueda Y., Ito M., Tagaya I. A specific surface antigen induced by poxvirus. Virology. 1969 May;38(1):180–182. doi: 10.1016/0042-6822(69)90141-x. [DOI] [PubMed] [Google Scholar]
  18. Ueda Y., Tagaya I., Amano H., Ito M. Studies on the early antigens induced by vaccinia virus. Virology. 1972 Sep;49(3):794–800. doi: 10.1016/0042-6822(72)90535-1. [DOI] [PubMed] [Google Scholar]
  19. Ueda Y., Tgaya I., Shiroki K. Immunological relationship between herpes simplex virus and B virus. Arch Gesamte Virusforsch. 1968;24(3):231–244. doi: 10.1007/BF01241295. [DOI] [PubMed] [Google Scholar]
  20. Worthington M., Rabson A. S., Baron S. Mechanism of recovery from systemic vaccinia virus infection. I. The effects of cyclophosphamide. J Exp Med. 1972 Aug 1;136(2):277–290. doi: 10.1084/jem.136.2.277. [DOI] [PMC free article] [PubMed] [Google Scholar]

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