Nudeosomal DNA fragments in autoimmune diseases

被引:45
作者
Holdenrieder, Stefan [1 ]
Eichhorn, Peter
Beuers, Ulrich
Samtleben, Walter
Schoenermarck, Ulf
Zachoval, Reinhart
Nagel, Dorothea
Stieber, Petra
机构
[1] Univ Hosp Munich Grosshadern, Inst Clin Chem, Munich, Germany
[2] Univ Hosp Munich Grosshadern, Med Clin 2, Munich, Germany
[3] Univ Hosp Munich Grosshadern, Med Clin 1, Munich, Germany
来源
CIRCULATING NUCLEIC ACIDS IN PLASMA AND SERUM IV | 2006年 / 1075卷
关键词
DNA; nucleosomes; caspases; serum; plasma; autoimmune disease; connective tissue disease; vasculitis; AIH; PSC; PBC; SLE;
D O I
10.1196/annals.1368.043
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The inadequate response of immune cells to circulating apoptotic products, such as nucleosomal DNA fragments, is assumed to be a potent stimulus for the production of autoantibodies during the pathogenesis and progression of systemic lupus erythematosus (SLE). Here, we analyzed the levels of circulating nucleosomes, caspases, and C-reactive protein in sera of 244 individuals with various autoimmune diseases (155 with autoimmune hepatic disorders, 25 with ANCA-associated vasculitis, and 64 with various connective tissue diseases), and 32 healthy controls. Nucleosomes and caspase activities were significantly elevated in sera of patients with hepatic autoimmune diseases, connective tissue diseases, and particularly in ANCA-associated vasculitis when compared with healthy individuals. Nucleosomes showed a correlation with caspases, and caspases with C-reactive protein, but nucleosomes did not correlate with C-reactive protein. Serum levels of the apoptotic products, nucleosomes, and caspases are increased in various autoimmune diseases but may not be solely responsible for antinucleosome antibody production in SLE patients. It remains to be clarified whether qualitative changes in nucleosomes are linked with pathogenesis and disease progression in SLE.
引用
收藏
页码:318 / 327
页数:10
相关论文
共 49 条
[41]  
Sozzi G, 2001, CANCER RES, V61, P4675
[42]   The language of covalent histone modifications [J].
Strahl, BD ;
Allis, CD .
NATURE, 2000, 403 (6765) :41-45
[43]  
Stroun M, 2000, ANN NY ACAD SCI, V906, P161
[44]   Autoantibodies in SLE but not in scleroderma react with protein-stripped nucleosornes [J].
Suer, W ;
Dähnrich, C ;
Schlumberger, W ;
Stöcker, W .
JOURNAL OF AUTOIMMUNITY, 2004, 22 (04) :325-334
[45]   Circulating nucleosomes and response to chemotherapy:: An in vitro, in vivo and clinical study on cervical cancer patients [J].
Trejo-Becerril, C ;
Pérez-Cárdenas, E ;
Treviño-Cuevas, H ;
Taja-Chayeb, L ;
García-López, P ;
Segura-Pacheco, B ;
Chávez-Blanco, AC ;
Lizano-Soberon, M ;
González-Fierro, A ;
Mariscal, I ;
Wegman-Ostrosky, T ;
Dueñas-González, A .
INTERNATIONAL JOURNAL OF CANCER, 2003, 104 (06) :663-668
[46]   Time between onset of apoptosis and release of nucleosomes from apoptotic cells: putative implications for systemic lupus erythematosus [J].
van Nieuwenhuijze, AEM ;
van Lopik, T ;
Smeenk, RJT ;
Aarden, LA .
ANNALS OF THE RHEUMATIC DISEASES, 2003, 62 (01) :10-14
[47]   ANTIBODIES TO HISTONE (H2A-H2B) DNA COMPLEXES IN THE ABSENCE OF ANTIBODIES TO DOUBLE-STRANDED DNA OR TO (H2A-H2B) COMPLEXES ARE MORE SENSITIVE AND SPECIFIC FOR SCLERODERMA-RELATED DISORDERS THAN FOR LUPUS [J].
WALLACE, DJ ;
LIN, HC ;
SHEN, GQ ;
PETER, JB .
ARTHRITIS AND RHEUMATISM, 1994, 37 (12) :1795-1797
[48]  
Williams RC, 2001, J RHEUMATOL, V28, P81
[49]   Elevated nucleosome levels in systemic inflammation and sepsis [J].
Zeerleder, S ;
Zwart, B ;
Wuillemin, WA ;
Aarden, LA ;
Groeneveld, ABJ ;
Caliezi, C ;
van Nieuwenhuijze, AEM ;
van Mierlo, GJ ;
Eerenberg, AJM ;
Lämmle, B ;
Hack, CE .
CRITICAL CARE MEDICINE, 2003, 31 (07) :1947-1951