Anti-nuclear envelope antibodies: Clinical associations

被引:40
作者
Nesher, G
Margalit, R
Ashkenazi, YJ
机构
[1] Shaare Zedek Med Ctr, Dept Internal Med, IL-91031 Jerusalem, Israel
[2] Shaare Zedek Med Ctr, Dept Hematol, IL-91031 Jerusalem, Israel
[3] Hebrew Univ Jerusalem, Sch Med, Dept Rheumatol Serv, IL-91010 Jerusalem, Israel
关键词
antinuclear antibody; systemic lupus erythematosus; lupus anticoagulant; autoimmune liver diseases; antilamin antibodies;
D O I
10.1053/sarh.2001.20266
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Objectives: Characterization of the clinical associations and clinical implications of antibodies reacting with antigens of the nuclear envelope. Methods: Description of an illustrative case and a MEDLINE search-assisted literature review of relevant cases. Results: With indirect immunofluorescence, autoantibodies directed against various antigens of the nuclear envelope stain the nucleus in a ring-like (rim) pattern. Autoantibodies against 5 antigenic components of the nuclear envelope have been described: anti-gp210, p62, lamina, lamina-associated polypeptides, and lamin B receptor. Antibodies to antigens of the nuclear pore complex, such as gp210 and p62, are highly specific (>95%) for primary biliary cirrhosis and may aid in the serologic diagnosis of this condition, especially in cases in which antimitochondrial antibodies are not detectable. In contrast, antilamin antibodies are not disease-specific but seem to be associated with lupus anticoagulant or anticardiolipin antibodies, antiphospholipid syndrome, thrombocytopenia, autoimmune liver diseases, and arthralgia. High-titered antilamin antibodies help to define a subset of lupus patients with antiphospholipid antibodies who are at a lower risk of developing thrombotic events. In addition, preliminary data suggest that the presence of antilamin antibodies may be helpful in the diagnosis of chronic fatigue syndrome. Conclusions: Each of the antibodies reacting with nuclear membrane antigens has its own spectrum of disease associations. Relevance: Determination of anti-nuclear envelope antibody pattern by indirect immunofluorescence, with subsequent determination of the specific antibody, carries important diagnostic and prognostic implications in various autoimmune conditions. Semin Arthritis Rheum 30:313-320. Copyright (C) 2001 by W.B. Saunders Company.
引用
收藏
页码:313 / 320
页数:8
相关论文
共 43 条
[1]
Bandin O, 1996, HEPATOLOGY, V23, P1020
[2]
BRITO J, 1994, J IMMUNOL, V153, P2268
[3]
ONSET AND REGULATION OF ANTI-LAMIN-B AUTOANTIBODY PRODUCTION IS INDEPENDENT OF THE LEVEL OF POLYCLONAL ACTIVATION [J].
CHOU, CH ;
ALI, SA ;
ROUBEY, R ;
BUYON, J ;
REEVES, WH .
AUTOIMMUNITY, 1991, 8 (04) :297-305
[4]
CHOU CH, 1992, MOL IMMUNOL, V29, P1055
[5]
Nuclear envelope protein autoantibodies in primary biliary cirrhosis [J].
Courvalin, JC ;
Worman, HJ .
SEMINARS IN LIVER DISEASE, 1997, 17 (01) :79-90
[6]
IDENTIFICATION AND CHARACTERIZATION OF AUTOANTIBODIES AGAINST THE NUCLEAR-ENVELOPE LAMIN-B RECEPTOR FROM PATIENTS WITH PRIMARY BILIARY-CIRRHOSIS [J].
COURVALIN, JC ;
LASSOUED, K ;
WORMAN, HJ ;
BLOBEL, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (03) :961-967
[7]
A NOVEL AUTOANTIBODY CAUSING A PERIPHERAL FLUORESCENT ANTINUCLEAR ANTIBODY PATTERN IS SPECIFIC FOR NUCLEAR-PORE COMPLEXES [J].
DAGENAIS, A ;
BIBORHARDY, V ;
SENECAL, JL .
ARTHRITIS AND RHEUMATISM, 1988, 31 (10) :1322-1327
[8]
The tail domain of lamin Dm0 binds histones H2A and H2B [J].
Goldberg, M ;
Harel, A ;
Brandeis, M ;
Rechsteiner, T ;
Richmond, TJ ;
Weiss, AM ;
Gruenbaum, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) :2852-2857
[9]
GUILLY MN, 1987, EUR J CELL BIOL, V43, P266
[10]
Clinical associations of anti-lamin autoantibodies [J].
Hill, C ;
Gillis, D ;
RobertsThomson, P ;
Kirkham, B ;
Pollard, A .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE, 1996, 26 (02) :162-166