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Neoself Antigens Presented on MHC Class II Molecules in Autoimmune Diseases. | LitMetric

Neoself Antigens Presented on MHC Class II Molecules in Autoimmune Diseases.

Adv Exp Med Biol

Department of Immunochemistry, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.

Published: March 2024

AI Article Synopsis

  • * When the body's tolerance to self-antigens is disrupted, immune cells can mistakenly attack healthy tissues, resulting in autoimmune diseases, with MHC class II genes being strongly linked to these conditions.
  • * Misfolded self-antigens, known as neoself antigens, interact with MHC class II molecules and can trigger autoimmune responses, making their study vital for understanding the mechanisms behind autoimmune diseases.

Article 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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Source
http://dx.doi.org/10.1007/978-981-99-9781-7_4DOI Listing

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