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Effects of interferon-gamma treatment on the cutaneous DTH reaction in rats.

Abstract
The capacity of interferon-gamma (IFN-gamma) to induce class II histocompatibility antigens on different cell types including keratinocytes, is well known, but the impact of IFN-gamma on the immune response is still unclear. Lewis rats sensitized with dinitrofluorobenzene (DNFB) were injected with recombinant rat IFN-gamma (10(5) U) or phosphate-buffered saline (PBS) once daily on 3 successive days at the bases of the ears either before or after they were challenged on the ears. As expected, the PBS-treated animals showed about a 30% increase in ear thickness and there was an induced expression of class II antigens on the keratinocytes as judged by immunohistochemistry 72 h after challenge. Exogenously added IFN-gamma prior to DNFB challenge resulted in a significantly reduced ear swelling at 24 (p less than 0.01) and 48 h (p less than 0.05) after challenge. In this case the keratinocytes expressed class II antigens already at the time of challenge. When IFN-gamma injections were given during the contact allergic reaction there was no significant reduction of ear swelling until 72 h (p less than 0.01). At that time point there was a more pronounced expression of class II antigens on the keratinocytes compared with PBS-injected animals, due to the IFN-gamma treatment. These in vivo data support our previous observations that IFN-gamma may play a self-limiting role in certain immune responses.
AuthorsC Skoglund, A Scheynius
JournalArchives of dermatological research (Arch Dermatol Res) Vol. 282 Issue 5 Pg. 318-24 ( 1990) ISSN: 0340-3696 [Print] Germany
PMID2121107 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Recombinant Proteins
  • Interferon-gamma
  • Dinitrofluorobenzene
Topics
  • Animals
  • Dermatitis, Contact (drug therapy, etiology)
  • Dinitrofluorobenzene
  • Female
  • Immunoenzyme Techniques
  • Interferon-gamma (therapeutic use)
  • Male
  • Rats
  • Rats, Inbred Lew
  • Recombinant Proteins

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