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Treatment of autoimmune disease by adoptive cellular gene therapyTarner, Ingo H. ...Autoimmune disorders represent inappropriate immune responses directed at self-tissue. Antigen-specific CD4+ T cells and antigen-presenting dendritic cells (DCs) are important mediators in the ... pathogenesis of auto-immune diseaseand thus are ideal candidates for adoptive cellular gene therapy, an exvivo approach to therapeutic gene transfer. Using retrovirally transduced cells and luciferase bioluminescence, we have demonstrated that primary T cells, T cell hybridomas, and DCs rapidly and preferentially home to the sitesof inflammation in animal models of multiple sclerosis, arthritis, and diabetes. These cells, transduced with retroviral vectors to drive expression of various "regulatory proteins" such as IL-4, IL-10, IL-12p40, and anti-TNF scFv, deliver these immunoregulatory proteins to the inflamed lesions, providing therapy for experimental autoimmune encephalitis (EAE), collagen-induced arthritis (CIA), and nonobese diabetic mice (NOD).Vir: Annals of the New York Academy of Sciences. - ISSN 0077-8923 (Letn. 998, št. 1, 2003, str. 512-519)Vrsta gradiva - članek, sestavni delLeto - 2003Jezik - angleškiCOBISS.SI-ID - 21488089
Avtor
Tarner, Ingo H. |
Levičnik, Alenka-Uršula
Teme
Adoptive Transfer |
Autoimmune Diseases |
Therapy |
Dendritic Cells |
Metabolism |
Gene Therapy |
Genetic Vectors |
Luminescence |
Retroviridae |
Genetics |
T-Lymphocytes |
Metabolism |
Adoptivni prenos |
Avtoimunske bolezni |
Dendritične celice |
Genetski vektorji |
Gensko zdravljenje |
Limfociti T |
Luminiscenca |
Retroviridae
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Tarner, Ingo H. | ![]() |
Levičnik, Alenka-Uršula | 28085 |
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