DIAGNOSTIC AUTO-ANTIBODIES APPEAR MANY YEARS BEFORE SYMPTOM ONSET IN LYMPHOMA-PRONE SJOGREN’S SYNDROME (ВОЗМОЖНОСТЬ РАННЕЙ ДИАГНОСТИКИ СИНДРОМА ШЕГРЕНА КАК ПРЕДШЕСТВЕННИКА ЛИМФОМЫ НА ОСНОВЕ АУТОАНТИТЕЛ)

Sjogren’s syndrome (SS) is a non-hereditary and relatively common disease  with adult onset. It is characterized by extreme tiredness, diminished  exocrine  glandular function, specific auto-antibody production and focal infiltration of B and T lymphocytes. The disease may be also complicated by mal...

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Bibliographic Details
Main Author: A. Bredberg
Format: Article
Language:English
Published: Bashkir State Medical University 2017-02-01
Series:Креативная хирургия и онкология
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Online Access:https://www.surgonco.ru/jour/article/view/165
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Summary:Sjogren’s syndrome (SS) is a non-hereditary and relatively common disease  with adult onset. It is characterized by extreme tiredness, diminished  exocrine  glandular function, specific auto-antibody production and focal infiltration of B and T lymphocytes. The disease may be also complicated by malignant lymphoma. Most SS patients have high serum levels of anti-nuclear antibodies (ANA), and the ANA subtypes SS-A and SS-B (autoantibodies to RNA-modifying spliceosome components) are used as diagnostic markers of SS. Antibodies to chromatin make  cancer  cells more  sensitive  to DNA-binding  cytostatic drugs  suggests that  indeed  the  ANA in SS may  have  some  influence on  cellular functions, and  perhaps contribute to SS patients’ symptoms.A most recent  report from our department has demonstrated that  ANA including SS-A and SS-B are present at high titres in sera obtained from SS patients many years before the onset  of symptoms, and even longer times before the diagnosis was established.
ISSN:2076-3093
2307-0501