Autoimmune disease (AID) refers to the disease caused by the body's immune response to self-antigens, resulting in damage to its own tissues. The global prevalence of autoimmune diseases ranges from 5% to 20%. Incidence and prevalence have increased significantly over the past 30 years. Autoimmune diseases are one of the top 10 leading causes of death in women under the age of 64.
Rheumatism |
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Digestive System Related |
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Kidney Disease Related |
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Nervous System Related |
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Skin Related |
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Blood Disease Related |
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Endocrine System Related |
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Detecting autoimmune disease at an early stage can prevent or delay irreparable damage to the target organ or tissue, so early diagnosis is important for managing autoimmune disease. Since the production of autoantibodies is one of the basic characteristics of autoimmune diseases, autoantibodies themselves become the serological markers of most autoimmune diseases.
Rheumatic disease-related autoantibodies include antinuclear antibodies (ANA), anti-neutrophil cytoplasmic autoantibodies (ANCA), antiphospholipid antibodies, and rheumatoid arthritis-related antibodies.
The available detection method is indirect immunofluorescence testing (IIFT). In addition, the target antigen can be confirmed by methods such as line immunoassay (LIA), enzyme linked immunosorbent assay (ELISA), and molecular diagnostic technology based on CRISPR-Cas system.
Among them, ASMA can be detected by IIFT with rat stomach as standard matrix, LKM-1 and LC-1 can be detected by ELISA or IIFT with rat kidney and rat liver as matrix, and AMA can be detected by IIFT with rat kidney as standard matrix The AMA subtypes were distinguished by ELISA or LIA with reference to the fluorescence results of rat stomach, rat liver, HEp-2 cells and other matrices.
Autoimmune nephropathy-related autoantibodies include anti-glomerular basement membrane (GBM) antibodies and anti-phospholipase A2 receptor (PLA2R) antibodies. Among them, anti-GBM antibody can be detected by ELISA or IIFT with primate kidney and lung as standard matrix, and anti-PLA2R antibody can be detected by ELISA and IIFT with transfected cells as matrix. In addition, molecular diagnostic technology based on CRISPR-Cas system can also detect related antibodies.
Autoimmune enteropathy-related autoantibodies include anti-saccharomyces cerevisiae antibodies (ASCA), anti-parietal cell autoantibodies (PCA), intrinsic factor antibodies, and anti-gliadin antibodies (anti-gliadin antibodies, AGA), anti-tissue transglutaminase (tTG) antibodies, and anti-endomysia antibodies (EMA). Among them, ASCA can be detected by ELISA, PCA can be detected by ELISA or IIFT with primate stomach as standard matrix, AGA and anti-tTG antibody can be detected by ELISA.
Among them, autoantibodies related to thyroid diseases include anti-thyroid peroxidase antibody (TPOAb), anti-thyroid microsomal antibody, anti-thyroglobulin antibody, anti-thyrotropin receptor antibody, etc. Diabetes-related autoantibodies include anti-islet cell autoantibodies (ICA), anti-tyrosine phosphatase (insulinoma associated antigen 2, IA2) antibodies, anti-GAD antibodies, and anti-insulin autoimmune antibodies (IAA). These antibodies can be detected by electrochemiluminescence immunoassay, ELISA and molecular diagnostic technology based on CRISPR-Cas system.
Utilizing the DeteCasTM platform based on the CRISPR-Cas system, CD BioSciences can provide various services in autoimmune diseases diagnosis, such as nucleic acids detection service, protein biomarker detection service and small molecule detection service. If you are interested in these services, please contact us.
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