Medical Journals

Therapeutic Vaccination of Active Arthritis with a Glycosylated Collagen Type Ii Peptide in Complex with Mhc Class Ii Molecules.

Authors:
  • Dzhambazov Balik
  • Nandakumar Kutty Selva
  • Kihlberg Jan
  • Fugger Lars
  • Holmdahl Rikard
  • Vestberg Mikael

From: Medical Inflammation Research, Lund University, Lund, Sweden.

Journal of immunology (Baltimore, Md. : 1950)

  • Publish Date: Feb 2006
  • ISSN: 0022-1767
  • Volume: 176
  • Issue: 3
  • Pages: 1525-33
  • Medium: Print
  • Language: English
  • Citation (JAMA): Dzhambazov Balik, Nandakumar Kutty Selva, Kihlberg Jan, et al. Therapeutic Vaccination of Active Arthritis with a Glycosylated Collagen Type Ii Peptide in Complex with Mhc Class Ii Molecules.. J. Immunol. Feb 2006;176:1525-33

Abstract

In both collagen-induced arthritis (CIA) and rheumatoid arthritis, T cells recognize a galactosylated peptide from type II collagen (CII). In this study, we demonstrate that the CII259-273 peptide, galactosylated at lysine 264, in complex with Aq molecules prevented development of CIA in mice and ameliorated chronic relapsing disease. In contrast, nonglycosylated CII259-273/Aq complexes had no such effect. CIA dependent on other MHC class II molecules (Ar/Er) was also down-regulated, indicating a bystander vaccination effect. T cells could transfer the amelioration of CIA, showing that the protection is an active process. Thus, a complex between MHC class II molecules and a posttranslationally modified peptide offers a new possibility for treatment of chronically active autoimmune inflammation such as rheumatoid arthritis.

Mesh Headings (Keywords): Animals, Arthritis, Experimental, Bystander Effect, Cattle, Chronic Disease, Collagen Type II, Galactose, Glycosylation, Histocompatibility Antigens Class II, Hybridomas, Immunodominant Epitopes, Immunotherapy, Active, Lymphocyte Activation, Male, Mice, Mice, Inbred BALB C, Multiprotein Complexes, Peptides, Rats, Solubility, T-Lymphocytes, Vaccines


Check for Full Text / PubMed Unique Identifier (PMID): 16424181


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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