The vaccination with DNA encoding T cell epitope on the Der p inhibited allergic responses in mice

S. S. Kwon, S. Y. Lee, S. J. Kim, Y. K. Kim, K. H. Kim, H. S. Moon, J. S. Song, S. H. Park, T. J. Yoo (Sechogu, South Korea; Memphis, United States Of America)

Source: Annual Congress 2002 - Cellular reactions in allergy in humans and animals
Session: Cellular reactions in allergy in humans and animals
Session type: Poster Discussion
Number: 302
Disease area: Airway diseases

Congress or journal article abstract

Abstract

Immunization with naked plasmid DNA leads to strong and persistent cell-mediated and humoral immune response to the antigen encoded by plasmid. Recently vaccines based on plasmid DNA encoding T cell epitopes on Der p induced immunoprotective effect on allergic response. However, little information is currently available on the therapeutic efficacy of DNA encoding the T cell epitope in the allergic disease. The purpose of this study was to evaluate whether the therapeutic effect of DNA vaccination with T cell epitope on allergic responses. To address this issue, on 4 weeks after immunization of Der p allergen extract, the vaccination group was injected with the mixed naked DNA plasmids encoding the murine T cell epitope on Der p 2, on three successive weeks into muscle of BALB/c mice. The control mice group was injected with the pcDNA 3.1 blank vector. On 9 weeks after immunization, all mice were challenged with the Der p extracts on 3 successive days. The vaccination group(1.96±]0.67 mg/ml) inhibited significantly the level of the Immunoglobulin E antibody response than the control mice group (5.96±]1.96 mg/ml). These result suggest that gene therapy using T-cell epitope encoding DNA could be an ideal way of combating allergic disease in future.


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S. S. Kwon, S. Y. Lee, S. J. Kim, Y. K. Kim, K. H. Kim, H. S. Moon, J. S. Song, S. H. Park, T. J. Yoo (Sechogu, South Korea; Memphis, United States Of America). The vaccination with DNA encoding T cell epitope on the Der p inhibited allergic responses in mice. Eur Respir J 2002; 20: Suppl. 38, 302

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