PIG TONSIL CELLS AS A MODEL TO EVALUATE ORAL, LOW-DOSE CYTOKINE TREATMENTS

Abstract

Cytokines are low molecular weight mediators of the immune system. Because of their properties and biological roles, they have been used as diagnostic reagents for human and animal diseases, as well as for prognostic tests and prophylactic treatments. Concerning this kind of treatments, there is uncertainty as to how cytokines are effective after oral administration. They probably act on the oral lymphoid tissues (palatine and pharyngeal tonsils) and trigger a cascade of events leading to activation of the immune system and control of the inflammatory cascade in tissues and organs. Owing to above, the aim of our project was to develop a reliable in vitro model related to the crucial interactions between cytokines and oral lymphoid cells, in terms of homeostatic regulation of the inflammatory response and antibody production. In this project, we focused our attention on the IFN-α system. The study was divided into 4 steps: 1) Isolation and culture of pig tonsil lymphocytes; 2) evaluation of IPEC-J2 cells as a reporter system of the anti-inflammatory control actions of interferon-alpha; 3) A pig tonsil cell culture model for evaluating oral, low-dose IFN-α treatments; 4) Disease-dependent modulation of tonsil cell phenotypes. In the first steps we develop reliable procedures for isolation and culture of pig tonsil cells, which were validated for use in functional immunoassays. Our results indicate that pig tonsil cells can be employed within 2 months from freezing to maintain suitable conditions in terms of recovery, vitality and release of antibody in vitro. Tonsil mononuclear cells also showed the ability to secrete antimicrobial peptides and to respond in vitro to immunological stimuli. In the second part of the project, IPEC-J2 (a continuous cell line of porcine intestinal epithelial cells) was validated as reporter system of the biological properties of IFN-α. Three different experimental conditions (oxidative stress, inflammatory response, and amplification of lymphoid cell signals) were selected to evaluate the effects of porcine recombinant IFN-α1 (rIFN-α) and 2 natural porcine IFN-α preparations (nIFN-α). The IFNs under study showed significantly different control actions in IPEC-J2 cells. In particular, rIFN-α was shown to down-regulate interleukin (IL)-8, IL-1β, tumor necrosis factor (TNF)-α, and β-defensin 1 genes either directly, or indirectly through second messengers released by IFN-α-treated lymphoid cells. With regard to IL-6, only second messengers from IFN-α-treated lymphoid cells could regulate the expression of this cytokine. Our results indicate that IPEC-J2 cells can be a useful tool for investigating the regulatory actions of type I IFNs and second messengers thereof. In the third step we developed an in vitro model of interaction between different types of human and porcine IFNs-α at low / moderate concentrations and pig tonsil cells. The IFNs-α under study showed different properties with respect to three fundamental control actions: 1) IgA release in culture (up and down-regulation,…