Molecular mechanisms of congenital heart block

被引:61
作者
Ambrosi, Aurelie [1 ]
Sonesson, Sven-Erik [2 ]
Wahren-Herlenius, Marie [1 ]
机构
[1] Karolinska Inst, Dept Med, Unit Expt Rheumatol, S-17176 Stockholm, Sweden
[2] Karolinska Inst, Dept Women & Child Hlth, S-17176 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Congenital heart block; Atrioventricular block; Neonatal lupus erythematosus; Autoantibodies; Ro/SSA; La/SSB; MHC; ANTI-RO/SSA ANTIBODIES; AMINO-ACID; 200-239; CARDIAC L-TYPE; CALCIUM-CHANNELS; NEONATAL LUPUS; RECURRENCE RATES; SSA/RO-SSB/LA; TNF-ALPHA; IN-UTERO; CHILDREN;
D O I
10.1016/j.yexcr.2014.01.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Autoantibody-associated congenital heart block (CHB) is a passively acquired autoimmune condition associated with maternal anti-R0/SSA antibodies and primarily affecting electric signal conduction at the atrioventricular node in the fetal heart. CHB occurs in 1-2% of anti-Ro/SSA antibody-positive pregancies and has a recurrence rate of 12-20% in a subsequent pregnancy. Despite the long-recognized association between maternal anti-Ro/SSA autoantibodies and CHB, the molecular mechanisms underlying CHB pathogenesis are not fully understood, but several targets for the maternal autoantibodies in the fetal heart have been suggested. Recent studies also indicate that fetal susceptibility genes determine whether an autoantibody-exposed fetus will develop CHB or not, and begin to identify such genes. In this article, we review the different lines of investigation undertaken to elucidate the molecular pathways involved in CHB development and reflect on the hypotheses put forward to explain CHB pathogenesis as well as on the questions left unanswered and that should guide future studies. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:2 / 9
页数:8
相关论文
共 67 条
[11]   CONGENITAL COMPLETE HEART-BLOCK [J].
BUYON, JP .
LUPUS, 1993, 2 (05) :291-295
[12]   AUTOANTIGENS TARGETED IN SYSTEMIC LUPUS-ERYTHEMATOSUS ARE CLUSTERED IN 2 POPULATIONS OF SURFACE-STRUCTURES ON APOPTOTIC KERATINOCYTES [J].
CASCIOLAROSEN, LA ;
ANHALT, G ;
ROSEN, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (04) :1317-1330
[13]   The Ro 60 kDa autoantigen: insights into cellular function and role in autoimmunity [J].
Chen, XG ;
Wolin, SL .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2004, 82 (04) :232-239
[14]  
Clancy R.M., 2010, ARTHRITIS RHEUM, V62
[15]   Maternal antibody responses to the 52-kd SSA/Ro p200 peptide and the development of fetal conduction defects [J].
Clancy, RM ;
Buyon, JP ;
Ikeda, K ;
Nozawa, K ;
Argyle, DA ;
Friedman, DM ;
Chan, EKL .
ARTHRITIS AND RHEUMATISM, 2005, 52 (10) :3079-3086
[16]   Immunohistologic evidence supports apoptosis, IgG deposition, and novel macrophage/fibroblast crosstalk in the pathologic cascade leading to congenital heart block [J].
Clancy, RM ;
Kapur, RP ;
Molad, Y ;
Askanase, AD ;
Buyon, JP .
ARTHRITIS AND RHEUMATISM, 2004, 50 (01) :173-182
[17]   Cytokine polymorphisms and histologic expression in autopsy studies:: Contribution of TNF-α and TGF-β1 to the pathogenesis of autoimmune-associated congenital heart block [J].
Clancy, RM ;
Backer, CB ;
Yin, XM ;
Kapur, RP ;
Molad, Y ;
Buyon, JP .
JOURNAL OF IMMUNOLOGY, 2003, 171 (06) :3253-3261
[18]   Transdifferentiation of cardiac fibroblasts, a fetal factor in anti-SSA/Ro-SSB/La antibody-mediated congenital heart block [J].
Clancy, RM ;
Askanase, AD ;
Kapur, RP ;
Chiopelas, E ;
Azar, N ;
Miranda-Carus, ME ;
Buyon, JP .
JOURNAL OF IMMUNOLOGY, 2002, 169 (04) :2156-2163
[19]   Impaired clearance of apoptotic cardiocytes is linked to anti-SSA/Ro and -SSB/La antibodies in the pathogenesis of congenital heart block [J].
Clancy, Robert M. ;
Neufing, Petra J. ;
Zheng, Ping ;
O'Mahony, Marguerita ;
Nimmerjahn, Falk ;
Gordon, Tom P. ;
Buyon, Jill P. .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (09) :2413-2422
[20]   Relationship of maternal autoimmune response to clinical manifestations in children with congenital complete heart block [J].
Eronen, M ;
Miettinen, A ;
Walle, TK ;
Chan, EKL ;
Julkunen, H .
ACTA PAEDIATRICA, 2004, 93 (06) :803-809