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. 1988 Sep;56(9):2412–2416. doi: 10.1128/iai.56.9.2412-2416.1988

Modulation of infection by gamma interferon treatment following trauma.

M J Hershman 1, H C Polk Jr 1, J D Pietsch 1, R E Shields 1, S R Wellhausen 1, G Sonnenfeld 1
PMCID: PMC259581  PMID: 3137168

Abstract

Gamma interferon (IFN-gamma) has been shown to be able to modulate several microbiol infections, perhaps as a result of the immunoregulatory properties of this interferon. The present study was designed to determine the efficacy of IFN-gamma treatment in a mouse model of infection that simulates clinical conditions occurring following abdominal trauma. In this model, mice were first infected intraperitoneally with Escherichia coli and then underwent immediate surgical laparotomy. Finally the mice were secondarily infected intramuscularly with Klebsiella pneumoniae. Groups of CBA/J mice received either IFN-gamma or RPMI 1640 medium (controls) subcutaneously. IFN-gamma was administered daily at a dose of 7,500 U, commencing 1 h postlaparotomy and continuing until the second bacterial challenge. Mice treated with IFN-gamma survived significantly longer than controls. The Ia antigen expression of peripheral blood monocytes was severely reduced in animals for 3 days after laparotomy and for 5 days after laparotomy and infection. This drop in Ia antigen expression was prevented in animals treated with IFN-gamma. These data indicate that IFN-gamma had a beneficial effect in a model simulating bacterial infection after trauma and that maintenance of Ia antigen expression in interferon-treated mice may have contributed to the observed therapeutic effect.

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Selected References

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

  1. Bukholm G., Berdal B. P., Haug C., Degré M. Mouse fibroblast interferon modifies Salmonella typhimurium infection in infant mice. Infect Immun. 1984 Jul;45(1):62–66. doi: 10.1128/iai.45.1.62-66.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Faist E., Mewes A., Strasser T., Walz A., Alkan S., Baker C., Ertel W., Heberer G. Alteration of monocyte function following major injury. Arch Surg. 1988 Mar;123(3):287–292. doi: 10.1001/archsurg.1988.01400270021002. [DOI] [PubMed] [Google Scholar]
  3. Fil'chakov I. V., Spivak N. Ia, Zaritskii A. M., Zueva V. S., Kuznetsov V. P. Vliianie interferona tipa I na persistentsiiu Salmonella typhimurium in vivo. Zh Mikrobiol Epidemiol Immunobiol. 1986 Feb;(2):24–27. [PubMed] [Google Scholar]
  4. Goris R. J., Draaisma J. Causes of death after blunt trauma. J Trauma. 1982 Feb;22(2):141–146. doi: 10.1097/00005373-198202000-00011. [DOI] [PubMed] [Google Scholar]
  5. Gould C. L., Sonnenfeld G. Effect of treatment with interferon-gamma and concanavalin A on the course of infection of mice with Salmonella typhimurium strain LT-2. J Interferon Res. 1987 Jun;7(3):255–260. doi: 10.1089/jir.1987.7.255. [DOI] [PubMed] [Google Scholar]
  6. Harned C. L., Nerland D. E., Sonnenfeld G. Effects of passive transfer and induction of gamma (type II immune) interferon preparations on the metabolism of diphenylhydantoin by murine cytochrome P-450. J Interferon Res. 1982;2(1):5–10. doi: 10.1089/jir.1982.2.5. [DOI] [PubMed] [Google Scholar]
  7. Izadkhah Z., Mandel A. D., Sonnenfeld G. Effect of treatment of mice with sera containing gamma interferon on the course of infection with Salmonella typhimurium strain LT-2. J Interferon Res. 1980 Fall;1(1):137–145. doi: 10.1089/jir.1980.1.137. [DOI] [PubMed] [Google Scholar]
  8. Kierszenbaum F., Sonnenfeld G. Characterization of the antiviral activity produced during Trypanosoma cruzi infection and protective effects of exogenous interferon against experimental Chagas' disease. J Parasitol. 1982 Apr;68(2):194–198. [PubMed] [Google Scholar]
  9. Polk H. C., Jr, George C. D., Wellhausen S. R., Cost K., Davidson P. R., Regan M. P., Borzotta A. P. A systematic study of host defense processes in badly injured patients. Ann Surg. 1986 Sep;204(3):282–299. [PMC free article] [PubMed] [Google Scholar]
  10. Schwartz D. E., Vetter W., Englert G. Trimethoprim metabolites in rat, dog and man: qualitative and quantitative studies. Arzneimittelforschung. 1970 Dec;20(12):1867–1871. [PubMed] [Google Scholar]
  11. Stephan R. N., Saizawa M., Conrad P. J., Dean R. E., Geha A. S., Chaudry I. H. Depressed antigen presentation function and membrane interleukin-1 activity of peritoneal macrophages after laparotomy. Surgery. 1987 Aug;102(2):147–154. [PubMed] [Google Scholar]
  12. Zueva V. S., Kuznetsov V. P., Spivak N. Ia, Avakian L. M. Podavlenie interferonom razvitiia stafilokokkovoi infektsii. Antibiot Med Biotekhnol. 1985 Nov;30(11):863–868. [PubMed] [Google Scholar]
  13. de Gee A. L., Sonnenfeld G., Mansfield J. M. Genetics of resistance to the African trypanosomes. V. Qualitative and quantitative differences in interferon production among susceptible and resistant mouse strains. J Immunol. 1985 Apr;134(4):2723–2726. [PubMed] [Google Scholar]

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