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 inAutoimmunity reviews Vol. 14; no. 1; pp. 75 - 79
Main Authors Yaniv, Gal, Twig, Gilad, Shor, Dana Ben-Ami, Furer, Ariel, Sherer, Yaniv, Mozes, Oshry, Komisar, Orna, Slonimsky, Einat, Klang, Eyal, Lotan, Eyal, Welt, Mike, Marai, Ibrahim, Shina, Avi, Amital, Howard, Shoenfeld, Yehuda
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.01.2015
Subjects
Online AccessGet full text
ISSN1568-9972
1873-0183
DOI10.1016/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.
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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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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https://www.clinicalkey.es/playcontent/1-s2.0-S1568997214002158
https://www.ncbi.nlm.nih.gov/pubmed/25449682
https://www.proquest.com/docview/1647003154
Volume 14
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