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Exogenous interleukin-16 inhibits antigen-induced airway hyper-reactivity, eosinophilia and Th2-type cytokine production in mice.

AbstractBACKGROUND:
IL-16 has been described as a natural soluble CD4-ligand with immunosuppressive effects in vitro. However, little is known about the effect of IL-16 on immune responses in vivo.
OBJECTIVE:
In the present study, we examined the effect of IL-16 administration in a murine model of allergic asthma. Next, we determined whether these effects were mediated by modulation of CD4+ T lymphocytes.
METHODS AND RESULTS:
Intraperitoneal administration of IL-16 completely inhibits antigen-induced airway hyper-responsiveness and largely decreases the number of eosinophils in bronchoalveolar lavage fluid (> 90%) and airway tissue of ovalbumin-sensitized and challenged mice. Firstly, it appears that thoracic lymph node cells isolated from in vivo IL-16-treated ovalbumin-challenged animals produce less IL-4 (77%) and IL-5 (85%) upon antigenic re-stimulation, when compared to vehicle-treated mice. Secondly, pre-incubation of lymphocytes with IL-16 in vitro reduces antigen-induced proliferation (55%) and Th2-type cytokine production (IL-4; 56%, IL-5; 77%). Thirdly, the presence of IL-16 during priming cultures of TCR transgenic T cells (DO11.10), reduces IL-4 (33%) and IL-5 (35%), but not IL-10 and IFNgamma levels upon re-stimulation.
CONCLUSION:
It can be concluded that IL-16 has potent immunosuppressive effects on a Th2dominated allergic airway response.
AuthorsJ J De Bie, E H Jonker, P A J Henricks, J Hoevenaars, F F Little, W W Cruikshank, F P Nijkamp, A J M Van Oosterhout
JournalClinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology (Clin Exp Allergy) Vol. 32 Issue 11 Pg. 1651-8 (Nov 2002) ISSN: 0954-7894 [Print] England
PMID12569988 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antigens
  • Cytokines
  • Interleukin-16
  • Immunoglobulin E
  • Interferon-gamma
  • Ovalbumin
Topics
  • Animals
  • Antigens
  • Asthma (immunology)
  • Bronchial Hyperreactivity (immunology)
  • Cell Differentiation (drug effects)
  • Cytokines (biosynthesis)
  • Eosinophilia (immunology)
  • Immunoglobulin E (blood)
  • Interferon-gamma (immunology)
  • Interleukin-16 (pharmacology)
  • Lung (immunology)
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Models, Animal
  • Ovalbumin
  • Th2 Cells (immunology)

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