| Literature DB >> 17493711 |
Shoshana Frankenburg1, Igor Grinberg, Ziva Bazak, Lena Fingerut, Jacob Pitcovski, Raphael Gorodetsky, Tamar Peretz, Ram M Spira, Yehuda Skornik, Ronald S Goldstein.
Abstract
Transcutaneous immunization aims at taking advantage of the skin's immune system for the purpose of immunoprotection. In the present study, we evaluated the potential of topical delivery of a recombinant melanoma protein, HR-gp100, derived from a shortened sequence of the native gp100 gene. The protein was applied on the skin, with and without the addition of two forms of heat labile enterotoxin (nLT and LTB). HR-gp100 fused to Haptide, a cell penetrating 20mer peptide (HR-gp100H) was also tested. Topical HR-gp100 and HR-gp100H application on the ears of mice elicited the production of specific antibodies, and transcutaneous delivery to intact human skin induced dose-dependent LC activation. nLT and LTB also activated LC, but did not further increase the activation induced by HR-gp100. These results show that HR-gp100, an antigenic tumor-derived protein, activates the immune system following transcutaneous delivery, as shown by both Langerhans cell activation and induction of antibody production.Entities:
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Year: 2007 PMID: 17493711 PMCID: PMC2702702 DOI: 10.1016/j.vaccine.2007.04.025
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641