Genetic insights into the disease mechanisms of type II mixed cryoglobulinemia induced by hepatitis C virus
Autor: | Laura Caggiari, M. Lenzi, Riccardo Dolcetti, S. De Vita, F. Dammacco, Massimo Galli, G. Monti, Anna Linda Zignego, Clodoveo Ferri, D. Sansonno, R. Talamini, Massimo Libra, V. De Re, Cesare Mazzaro, R. Cannizzaro, Alessandro Gabrielli, N. Sacchi, Michele Spina, M. Guidoboni |
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Přispěvatelé: | De Re V, Caggiari L, De Vita S, Mazzaro C, Lenzi M, Galli M, Monti G, Ferri C, Zignego AL, Gabrielli A, Sansonno D, Dammacco F, Libra M, Sacchi N, Talamini R, Spina M, Cannizzaro R, Guidoboni M, Dolcetti R. |
Jazyk: | angličtina |
Rok vydání: | 2007 |
Předmět: |
mixed cryoglobulinemia
Settore MED/17 - Malattie Infettive Hepatitis C virus B-cell lymphoma (NHL) Hepatitis C virus (HCV) Human leukocyte antigen (HLA) molecules Type II mixed cryoglobulinemia (MC) Human leukocyte antigen Biology medicine.disease_cause HLA-DR5 Antigen Epitope Autoimmune Diseases Autoimmunity Immune system Autoimmune Process HLA Antigens HLA-DQ Antigens medicine Cluster Analysis Humans genetics hepatitis C Autoimmune disease Hepatology Histocompatibility Testing Gastroenterology Hepatitis C Chronic medicine.disease Cryoglobulinemia Virology Immunology |
Popis: | The ability of the immune system to distinguish between self and non-self is critical to the functioning of the immune response. A breakdown in these mechanisms can lead to the onset of autoimmune disease. Clinical and molecular data suggest that shared immunogenetic mechanisms lead to the autoimmune process. The most studied part of the autoimmune process is the human leukocyte antigen (HLA) region. Recently, progress has been made in narrowing down HLA cluster classifications based on structural and functional features of HLA alleles. Using this approach we have investigated 175 patients with hepatitis C virus (HCV)-induced type II cryoglobulinemia (MC), and compared them to a control group of 14,923 bone marrow donors. Additionally, we investigated the frequency of HLA homozygosity in the same groups of subjects. Our results provide evidence of a role for DR5 and DQ3 HLA class II clusters and a higher frequency of HLA homozygous leading to the clinical outcome of type II mixed cryoglobulinemic autoimmune disease. The DR5 cluster is characterized by a Glu in β9 and its polymorphism is connected with preferred anchors at β9 of the binding peptide, while the DQ3 cluster is characterized by Glu B86 and Leu B87, which allows the binding of large hydrophobic amino acids at p1 of the binding peptide. The mechanisms by which variations in HLA lead to autoimmunity remain unknown, although they are likely to be mediated by continuous presentation of HCV epitopes to T cells and a genetic background that limits the effective clearance of HCV. The results presented in this paper have increased our knowledge of the mechanism of autoimmune disease and B-cell lymphoproliferation during HCV infection. The work was performed in accordance with the principles of the 1983 Declaration of Helsinki. There is no conflict of interest. |
Databáze: | OpenAIRE |
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