HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Characterization of self-T-cell response and antigenic determinants of U1A protein with bone marrow-derived dendritic cells in NZB x NZW F1 mice.

Abstract
Systemic lupus erythematosus (SLE) is characterized by the existence of a heterogeneous group of autoantibodies directed against nuclear intact structures, such as nucleosomes and small nuclear ribonucleoproteins (snRNPs). Autoantibodies against snRNPs are of special interest because they are detectable in the majority of SLE patients. Although the B-cell antigenic determinants have been well characterized, very limited data have been reported in regard to the T-cell epitopes of snRNPs. Furthermore, several studies have demonstrated that determination of the auto-T-cell epitopes recognized by freshly isolated T cells is difficult from unprimed lupus mice when self-antigen-pulsed B cells or macrophages are used as antigen-presenting cells (APCs) in vitro. In the present study, we showed a novel approach for determining the auto-T-cell epitopes, using bone marrow-derived dendritic cells (BMDCs) pulsed with the murine U1A protein - an immunodominant antigen of the U1 snRNPs - which is capable of activating freshly isolated T cells from unprimed (NZB x NZW) F1 (BWF1) mice in vitro. The T-cell epitope area was found to be located at the C-terminus of U1A, overlapping the T-cell epitope of human U1A that has been reported in human SLE. Identification of the autoreactive T-cell epitope(s) in snRNPs will help to elucidate how reciprocal T-B determinant spreading of snRNPs emerges in lupus. The results presented here also indicate that it is feasible to use this approach to further explore strategies to design immunotherapy for patients with lupus.
AuthorsJ L Suen, C H Wu, Y Y Chen, W M Wu, B L Chiang
JournalImmunology (Immunology) Vol. 103 Issue 3 Pg. 301-9 (Jul 2001) ISSN: 0019-2805 [Print] England
PMID11454059 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Autoantibodies
  • Cytokines
  • Epitopes, T-Lymphocyte
  • Histocompatibility Antigens Class II
  • RNA-Binding Proteins
  • Ribonucleoprotein, U1 Small Nuclear
  • U1A protein
Topics
  • Animals
  • Autoantibodies (biosynthesis)
  • Autoimmunity (immunology)
  • Bone Marrow Cells (immunology)
  • Cell Culture Techniques
  • Cell Division (immunology)
  • Cytokines (biosynthesis)
  • Dendritic Cells (immunology)
  • Dose-Response Relationship, Immunologic
  • Epitopes, T-Lymphocyte (immunology)
  • Female
  • Histocompatibility Antigens Class II (immunology)
  • Lupus Erythematosus, Systemic (immunology)
  • Lymphocyte Activation (immunology)
  • Mice
  • Mice, Inbred DBA
  • Mice, Inbred NZB
  • Mice, Inbred Strains
  • RNA-Binding Proteins (immunology)
  • Ribonucleoprotein, U1 Small Nuclear (immunology)
  • T-Lymphocyte Subsets (immunology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: