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Neoself Antigens Presented on MHC Class II Molecules in Autoimmune Diseases.
Jin, Hui; Arase, Hisashi.
Afiliación
  • Jin H; Department of Immunochemistry, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.
  • Arase H; Department of Immunochemistry, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan. arase@biken.osaka-u.ac.jp.
Adv Exp Med Biol ; 1444: 51-65, 2024.
Article en En | MEDLINE | ID: mdl-38467972
ABSTRACT
Major histocompatibility complex (MHC) class II molecules play a crucial role in immunity by presenting peptide antigens to helper T cells. Immune cells are generally tolerant to self-antigens. However, when self-tolerance is broken, immune cells attack normal tissues or cells, leading to the development of autoimmune diseases. Genome-wide association studies have shown that MHC class II is the gene most strongly associated with the risk of most autoimmune diseases. When misfolded self-antigens, called neoself antigens, are associated with MHC class II molecules in the endoplasmic reticulum, they are transported by the MHC class II molecules to the cell surface without being processed into peptides. Moreover, neoself antigens that are complexed with MHC class II molecules of autoimmune disease risk alleles exhibit distinct antigenicities compared to normal self-antigens, making them the primary targets of autoantibodies in various autoimmune diseases. Elucidation of the immunological functions of neoself antigens presented on MHC class II molecules is crucial for understanding the mechanism of autoimmune diseases.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Autoinmunes / Estudio de Asociación del Genoma Completo Límite: Humans Idioma: En Revista: Adv Exp Med Biol Año: 2024 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Autoinmunes / Estudio de Asociación del Genoma Completo Límite: Humans Idioma: En Revista: Adv Exp Med Biol Año: 2024 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos