Academic Journal

During the early prediabetic period in NOD mice, the pathogenic CD8(+) T-cell population comprises multiple antigenic specificities.

التفاصيل البيبلوغرافية
العنوان: During the early prediabetic period in NOD mice, the pathogenic CD8(+) T-cell population comprises multiple antigenic specificities.
المؤلفون: DiLorenzo, T P, Lieberman, S M, Takaki, T, Honda, S, Chapman, H D, Santamaria, P, Serreze, D V, Nathenson, S G
المصدر: Faculty Research 2000 - 2009
بيانات النشر: The Mouseion at the JAXlibrary
سنة النشر: 2002
المجموعة: The Jackson Laboratory: The Mouseion at the JAXlibrary
مصطلحات موضوعية: CD8-Positive-T-Lymphocytes, Cell-Line-Transformed, Clone-Cells, Diabetes-Mellitus-Insulin-Dependent, Epitopes, Histocompatibility-Antigens-Class-I, Insulin, Islets-of-Langerhans, Mice, Mice-Inbred-NOD, Mice-Transgenic, Prediabetic-State, SUPPORT-NON-U-S-GOVT, SUPPORT-U-S-GOVT-P-H-S, T-Lymphocytes-Cytotoxic
الوصف: In the NOD mouse model of type 1 diabetes, major histocompatibilitycomplex (MHC) class I-restricted CD8(+) T cells are essential for disease development. However, the extent of diversity of their antigenic specificities during early pathogenesis remains unclear. An insulin-derived peptide was recently identified as the epitope for the NOD-derived diabetogenic T-cell clone G9C8. To explore the possibility that the early pathogenic CD8(+) T-cell population comprises additional antigenic specificities, we employed the T-cell clones AI4 and NY8.3, both of which are pathogenic and represent specificities present in early insulitic lesions. The clones responded to distinct fractions of chromatographically separated class I MHC-bound peptides purified from NOD-derived NIT-1 beta cells, and neither clone recognized the insulin-derived peptide. NIT-1 cells represent an unlimited peptide source that will allow for the future isolation and sequencing of the novel multiple epitopes targeted early in the autoimmune response by pathogenic CD8(+) T cells.
نوع الوثيقة: text
اللغة: unknown
Relation: https://mouseion.jax.org/stfb2000_2009/450; http://linkinghub.elsevier.com/retrieve/pii/S1521661602952988
الاتاحة: https://mouseion.jax.org/stfb2000_2009/450
http://linkinghub.elsevier.com/retrieve/pii/S1521661602952988
رقم الانضمام: edsbas.EA70FBBC
قاعدة البيانات: BASE