Abstract | BACKGROUND:
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.
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Authors | J 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 |
Journal | Clinical 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 |
PMID | 12569988
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antigens
- Cytokines
- Interleukin-16
- Immunoglobulin E
- Interferon-gamma
- Ovalbumin
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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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