A volcanic explosion of autoantibodies in systemic lupus erythematosus: A diversity of 180 different antibodies found in SLE patients
Recent research in systemic lupus erythematosus (SLE) yielded new antigens and antibodies in SLE patients. We describe the various autoantibodies that can be detected in patients with SLE. A literature review, using the terms “autoantibody” and “systemic lupus erythematosus”, was conducted to search...
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Published in | Autoimmunity reviews Vol. 14; no. 1; pp. 75 - 79 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.01.2015
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Subjects | |
Online Access | Get full text |
ISSN | 1568-9972 1873-0183 |
DOI | 10.1016/j.autrev.2014.10.003 |
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Abstract | Recent research in systemic lupus erythematosus (SLE) yielded new antigens and antibodies in SLE patients. We describe the various autoantibodies that can be detected in patients with SLE.
A literature review, using the terms “autoantibody” and “systemic lupus erythematosus”, was conducted to search for articles on autoantibodies in SLE, their target antigens, association with disease activity and other clinical manifestations.
One hundred and eighty autoantibodies were so far described in SLE patients. These include autoantibodies that target nuclear antigens, cytoplasmic antigens, cell membrane antigens, phospholipid-associated antigens, blood cells, endothelial cells, and nervous system antigens, plasma proteins, matrix proteins, and miscellaneous antigens. The target of an autoantibody, the autoantigen properties, autoantibody frequencies in SLE, as well as clinical associations, and correlation with disease activity are described for all 180 autoantibodies.
SLE is so far the autoimmune disease with the largest number of detectable autoantibodies. Their production could be antigen-driven, the result of a polyclonal B cell activation, impaired apoptotic pathways, or the outcome of an idiotypic network dysregulation. |
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AbstractList | Recent research in systemic lupus erythematosus (SLE) yielded new antigens and antibodies in SLE patients. We describe the various autoantibodies that can be detected in patients with SLE. A literature review, using the terms "autoantibody" and "systemic lupus erythematosus", was conducted to search for articles on autoantibodies in SLE, their target antigens, association with disease activity and other clinical manifestations. One hundred and eighty autoantibodies were so far described in SLE patients. These include autoantibodies that target nuclear antigens, cytoplasmic antigens, cell membrane antigens, phospholipid-associated antigens, blood cells, endothelial cells, and nervous system antigens, plasma proteins, matrix proteins, and miscellaneous antigens. The target of an autoantibody, the autoantigen properties, autoantibody frequencies in SLE, as well as clinical associations, and correlation with disease activity are described for all 180 autoantibodies. SLE is so far the autoimmune disease with the largest number of detectable autoantibodies. Their production could be antigen-driven, the result of a polyclonal B cell activation, impaired apoptotic pathways, or the outcome of an idiotypic network dysregulation. Recent research in systemic lupus erythematosus (SLE) yielded new antigens and antibodies in SLE patients. We describe the various autoantibodies that can be detected in patients with SLE. A literature review, using the terms “autoantibody” and “systemic lupus erythematosus”, was conducted to search for articles on autoantibodies in SLE, their target antigens, association with disease activity and other clinical manifestations. One hundred and eighty autoantibodies were so far described in SLE patients. These include autoantibodies that target nuclear antigens, cytoplasmic antigens, cell membrane antigens, phospholipid-associated antigens, blood cells, endothelial cells, and nervous system antigens, plasma proteins, matrix proteins, and miscellaneous antigens. The target of an autoantibody, the autoantigen properties, autoantibody frequencies in SLE, as well as clinical associations, and correlation with disease activity are described for all 180 autoantibodies. SLE is so far the autoimmune disease with the largest number of detectable autoantibodies. Their production could be antigen-driven, the result of a polyclonal B cell activation, impaired apoptotic pathways, or the outcome of an idiotypic network dysregulation. Abstract Recent research in systemic lupus erythematosus (SLE) yielded new antigens and antibodies in SLE patients. We describe the various autoantibodies that can be detected in patients with SLE. A literature review, using the terms “autoantibody” and “systemic lupus erythematosus”, was conducted to search for articles on autoantibodies in SLE, their target antigens, association with disease activity and other clinical manifestations. One hundred and eighty autoantibodies were so far described in SLE patients. These include autoantibodies that target nuclear antigens, cytoplasmic antigens, cell membrane antigens, phospholipid-associated antigens, blood cells, endothelial cells, and nervous system antigens, plasma proteins, matrix proteins, and miscellaneous antigens. The target of an autoantibody, the autoantigen properties, autoantibody frequencies in SLE, as well as clinical associations, and correlation with disease activity are described for all 180 autoantibodies. SLE is so far the autoimmune disease with the largest number of detectable autoantibodies. Their production could be antigen-driven, the result of a polyclonal B cell activation, impaired apoptotic pathways, or the outcome of an idiotypic network dysregulation. |
Author | Shor, Dana Ben-Ami Welt, Mike Slonimsky, Einat Twig, Gilad Lotan, Eyal Mozes, Oshry Klang, Eyal Sherer, Yaniv Amital, Howard Furer, Ariel Komisar, Orna Yaniv, Gal Marai, Ibrahim Shoenfeld, Yehuda Shina, Avi |
Author_xml | – sequence: 1 givenname: Gal surname: Yaniv fullname: Yaniv, Gal organization: Department of Imaging, The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel – sequence: 2 givenname: Gilad surname: Twig fullname: Twig, Gilad organization: Department of Medicine ‘B’, The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel – sequence: 3 givenname: Dana Ben-Ami surname: Shor fullname: Shor, Dana Ben-Ami organization: Department of Medicine ‘B’, The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel – sequence: 4 givenname: Ariel surname: Furer fullname: Furer, Ariel organization: The Israel Defense Forces Medical Corps, Israel – sequence: 5 givenname: Yaniv surname: Sherer fullname: Sherer, Yaniv organization: The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel – sequence: 6 givenname: Oshry surname: Mozes fullname: Mozes, Oshry organization: Department of Imaging, The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel – sequence: 7 givenname: Orna surname: Komisar fullname: Komisar, Orna organization: Department of Imaging, The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel – sequence: 8 givenname: Einat surname: Slonimsky fullname: Slonimsky, Einat organization: Department of Imaging, The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel – sequence: 9 givenname: Eyal surname: Klang fullname: Klang, Eyal organization: Department of Imaging, The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel – sequence: 10 givenname: Eyal surname: Lotan fullname: Lotan, Eyal organization: Department of Imaging, The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel – sequence: 11 givenname: Mike surname: Welt fullname: Welt, Mike organization: Department of Medicine ‘B’, The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel – sequence: 12 givenname: Ibrahim surname: Marai fullname: Marai, Ibrahim organization: Department of Cardiology, Rambam Medical Center, Haifa, Israel – sequence: 13 givenname: Avi surname: Shina fullname: Shina, Avi organization: Department of Obstetrics and Gynecology, Sheba Medical Center, Tel Hashomer, Israel – sequence: 14 givenname: Howard surname: Amital fullname: Amital, Howard organization: Department of Medicine ‘B’, The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel – sequence: 15 givenname: Yehuda surname: Shoenfeld fullname: Shoenfeld, Yehuda email: shoenfel@post.tau.ac.il organization: The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25449682$$D View this record in MEDLINE/PubMed |
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Keywords | Autoantibodies Systemic lupus erythematosus |
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Snippet | Recent research in systemic lupus erythematosus (SLE) yielded new antigens and antibodies in SLE patients. We describe the various autoantibodies that can be... Abstract Recent research in systemic lupus erythematosus (SLE) yielded new antigens and antibodies in SLE patients. We describe the various autoantibodies that... |
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SubjectTerms | Allergy and Immunology Animals Autoantibodies Autoantibodies - analysis Autoantibodies - immunology Autoantigens - immunology Humans Lupus Erythematosus, Systemic - immunology Systemic lupus erythematosus |
Title | A volcanic explosion of autoantibodies in systemic lupus erythematosus: A diversity of 180 different antibodies found in SLE patients |
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