ABSTRACT
Describe a case of a female patient having anti-Ro/SSA antibodies without any other risk factor or collagen disease. In her first pregnancy a congenital heart block and hydrops in the fetus were diagnosed, and these caused stillbirth. In a second pregnancy an in utero treatment resulted in the succesful delivery of a normal child.
Subject(s)
Antibodies, Antinuclear , Fetal Diseases/immunology , Heart Block/congenital , Adult , Female , Heart Block/immunology , Humans , PregnancySubject(s)
Humans , Male , Female , Infant, Newborn , Heart Block/complications , Heart Block/congenital , Heart Block/epidemiology , Heart Block/immunology , Lupus Erythematosus, Systemic/complications , Lupus Erythematosus, Systemic/diagnosis , Lupus Erythematosus, Systemic/therapy , Autoimmune Diseases/complications , Autoimmune Diseases/congenitalABSTRACT
OBJECTIVE: Noninvasive cardiac assessment of newborns and infants of women with systemic lupus erythematosus. The children had no congenital total atrioventricular block and were compared with the children of healthy women. METHODS: We prospectively assessed 13 newborns and infants aged 1 to 60 days, children of women with systemic lupus erythematosus and without congenital total atrioventricular block. These children were compared with 30 children of women who had no lupus or anti-Ro/SSA antibodies, and no risk factors for congenital heart disease either. Their age groups matched. The following examinations were performed: cardiological physical examination, electrocardiography, echocardiography, and signal-averaged electrocardiography. RESULTS: The statistical analysis showed no significant difference in ventricular function or in the cardiac conduction system between the groups. CONCLUSION: In regard to the conduction system and ventricular function in the absence of total atrioventricular block, no statistically significant difference was observed between the children of women with systemic lupus erythematosus and children of healthy women.
Subject(s)
Child of Impaired Parents , Heart Block/diagnosis , Lupus Erythematosus, Systemic , Antibodies, Antinuclear/blood , Echocardiography, Doppler, Color , Electrocardiography , Female , Heart Block/diagnostic imaging , Heart Block/immunology , Heart Rate , Humans , Infant , Infant, Newborn , Male , Prospective Studies , Statistics, NonparametricABSTRACT
OBJECTIVE: Noninvasive cardiac assessment of newborns and infants of women with systemic lupus erythematosus. The children had no congenital total atrioventricular block and were compared with the children of healthy women. METHODS: We prospectively assessed 13 newborns and infants aged 1 to 60 days, children of women with systemic lupus erythematosus and without congenital total atrioventricular block. These children were compared with 30 children of women who had no lupus or anti-Ro/SSA antibodies, and no risk factors for congenital heart disease either. Their age groups matched. The following examinations were performed: cardiological physical examination, electrocardiography, echocardiography, and signal-averaged electrocardiography. RESULTS: The statistical analysis showed no significant difference in ventricular function or in the cardiac conduction system between the groups. CONCLUSION: In regard to the conduction system and ventricular function in the absence of total atrioventricular block, no statistically significant difference was observed between the children of women with systemic lupus erythematosus and children of healthy women
Subject(s)
Humans , Male , Female , Infant, Newborn , Infant , Electrocardiography , Heart Block/diagnosis , Lupus Erythematosus, Systemic/diagnosis , Antibodies, Antinuclear/blood , Echocardiography, Doppler, Color , Heart Rate , Heart Block/immunology , Heart Block , Lupus Erythematosus, Systemic/immunology , Lupus Erythematosus, Systemic , Prospective Studies , Statistics, NonparametricABSTRACT
OBJECTIVE: Neonatal lupus erythematosus (NLE) is characterized by complete congenital heart block (CCHB), cutaneous rash, and laboratory abnormalities in infants born to mothers with autoantibodies directed against SSA/Ro, SSB/La, or both. We carried out a prospective study to determine the incidence of individual NLE features. STUDY DESIGN: The study was performed in two centers: Toronto, Canada, and Milano, Italy. Mothers had been referred for the presence of anti-SSA/Ro autoantibodies, regardless of their diagnosis. All the children were seen at least once within the first 6 months of life for clinical evaluation and laboratory testing. The study group consisted of 128 infants born from 124 pregnancies in 112 women with anti-Ro antibodies with or without anti-La antibodies. RESULTS: There were two cases of CCHB for an overall percentage of 1.6%. Twenty-one children (16%) developed cutaneous NLE. Laboratory testing showed hematologic abnormalities in 27% of the babies and elevation of liver enzymes in 26%. CONCLUSIONS: Mothers with autoimmune diseases and anti-Ro antibodies are at risk of delivering a child with NLE but at a low risk of delivering a child with CCHB. Infants born to mothers with anti-Ro or anti-La antibodies should be monitored for other features of NLE in addition to CCHB.
Subject(s)
Autoantigens/immunology , Autoimmune Diseases/immunology , Heart Block/congenital , Lupus Erythematosus, Systemic/epidemiology , Pregnancy Complications/immunology , RNA, Small Cytoplasmic , Ribonucleoproteins/immunology , Adolescent , Adult , Autoantibodies/immunology , Female , Heart Block/immunology , Humans , Incidence , Infant, Newborn , Male , Pregnancy , Prospective StudiesSubject(s)
Antibodies, Antinuclear/blood , Heart Block/congenital , Heart Block/diagnosis , Adult , Female , Heart Block/immunology , Humans , Infant, NewbornABSTRACT
Isolated congenital heart block may be associated with autoimmune disorder such as Sjögren Syndrome and systemic lupus erythematosus. In this work we demonstrate circulating autoantibodies against neonatal heart M1 muscarinic acetylcholine receptor (mAChR) in the sera of children with congenital heart block. This antibody were able to react with the second extracellular loop of the human M1 mAChR as demonstrated using a synthetic peptide in enzyme immune assay and binding assay. Affinity purified anti-peptide IgG as well as total IgG from children with congenital heart block, interfered with the specific radioligand occupancy from neonatal heart M1 mAChR, interacting irreversibly. The antipeptide antibodies also displayed an 'agonist-like' activity, i.e. decreased contractility, activated nitric oxide synthase activity and increased production of cyclic GMP. All of these effects were selectively blunted by pirenzepine and neutralized by the synthetic M1 peptide. Both binding and biological effects were obtained using neonatal rat heart instead adult heart and were independent of Ro/SS-A and La/SS-B antibodies and were also absent in the sera of normal children. A clinical relevance of these findings is demonstrated by a strong association between the existence of circulating M1 mAChR antipeptide antibodies and the presence of isolated congenital heart block, making these antibodies a proper marker of this disease.
Subject(s)
Autoantibodies/immunology , Autoantigens/immunology , Heart Block/immunology , Receptors, Muscarinic/immunology , Amino Acid Sequence , Animals , Autoantibodies/blood , Child , Child, Preschool , Cyclic GMP/immunology , Heart , Heart Block/blood , Heart Block/complications , Heart Defects, Congenital/blood , Heart Defects, Congenital/immunology , Humans , Infant , Lupus Erythematosus, Systemic/complications , Lupus Erythematosus, Systemic/immunology , Molecular Sequence Data , Nitric Oxide Synthase/immunology , Peptides/immunology , Rats , Receptor, Muscarinic M1ABSTRACT
Neonatal lupus erythematosus (NLE) is an auto-immune disease related to systemic lupus erythematosus (SLE). Unlike SLE it is not a spontaneous syndrome but rather an acquired one. In NLE the most common disease manifestations are a transient cutaneous lesion and cardiac conduction disturbances. The cutaneous lesions and other non-cardiac manifestations of NLE are transient and disappear about six months after birth, at the time when maternal antibodies disappear from the neonatal circulation. This fact suggests that maternal antibodies may cross the placenta leading to an inflammatory reaction in the fetal tissues. NLE is the principal cause of atria-ventricular block, when it is not associated with congenital birth defects. All the clinical studies to date correlate the heart block in NLE with the presence of certain types of circulating maternal antibodies, against the Ro/SSA nuclear proteins, in the serum of the newborn. In this paper we discuss animal models that have been developed by our and others groups to study the participation of the anti-Ro/SSA antibodies in the pathogenesis of the cardiac conduction blockades that occur in NLE.
Subject(s)
Heart Block/congenital , Immunity, Maternally-Acquired , Lupus Erythematosus, Systemic/congenital , Animals , Antibodies, Antinuclear/immunology , Autoantibodies/immunology , Autoimmune Diseases/immunology , Disease Models, Animal , Heart Block/immunology , Lupus Erythematosus, Systemic/immunology , SyndromeABSTRACT
Neonatal lupus erythematosus (NLE) is an auto-immune disease related to systemic lupus erythematosus (SLE). Unlike SLE it is not a spontaneous syndrome but rather an acquired one. In NLE the most common disease manifestations are a transient cutaneous lesion and cardiac conduction disturbances. The cutaneous lesions and other non-cardiac manifestations of NLE are transient and disappear about six months after birth, at the time when maternal antibodies disappear from the neonatal circulation. This fact suggests that maternal antibodies may cross the placenta leading to an inflamatory reaction in the fetal tissues. NLE is the principal cause of atria-ventricular block, when it is not associated with congenial birth defects. All the clinical studies to date correlate the heart block in NLE with the presence of certain types of circulating maternal antibodies, against the Ro/SSA nuclear proteins, in the serum of the newborn. In this paper we discuss animal models that have been developed by our and other groups to study the participation of the anti-Ro/SSA antibodies in the pathogenesis of the cardiac conduction blockades that occur in NLE.
Subject(s)
Animals , Antibodies, Antinuclear/immunology , Heart Block/congenital , Heart Block/immunology , Immunity, Maternally-Acquired , Lupus Erythematosus, Systemic/congenital , Lupus Erythematosus, Systemic/immunology , Autoantibodies/immunology , Disease Models, Animal , SyndromeABSTRACT
BACKGROUND: Immune dysfunction has long been proposed as a mechanism for the etiopathogenesis of the chronic phase of Chagas' disease. Antibodies of chagasic patients have been shown to interfere with electric and mechanical activity of embryonic myocardial cells in culture. Here, we demonstrate that antibodies derived from a group of chronic chagasic patients are able to induce disturbances in the electrogenesis and conduction in isolated adult rabbit hearts. METHODS AND RESULTS: Sera from chronic chagasic patients with complex cardiac arrhythmias (ChA+) decreased heart rate (from 131+/-26 to 98+/-37 bpm [mean+/-SD]; n=6; P<.05) in isolated rabbit hearts when perfused at a dilution of 1:100 (vol:vol) by the Langendorff method. Sera from another experimental group of four chronic chagasic patients without complex arrhythmias (ChA-) and two control groups composed of five Wolff-Parkinson-White (WPW) syndrome patients and five orthopedic surgery patients did not affect heart rate when tested under similar conditions. In addition, sera from five of six ChA+ patients and from one WPW patient induced AV conduction blockade. Effects of the sera from ChA+ patients are due to their IgG fractions. Both serum and IgG effects are blocked by atropine (10 micromol/L). CONCLUSIONS: Antibodies of ChA+ patients decrease heart rate and induce AV conduction block in isolated adult rabbit hearts through activation of muscarinic receptors.
Subject(s)
Antibodies, Protozoan/immunology , Cardiomyopathy, Dilated/physiopathology , Chagas Cardiomyopathy/immunology , Chagas Disease/immunology , Heart Block/physiopathology , Wolff-Parkinson-White Syndrome/physiopathology , Adult , Animals , Atrioventricular Node/drug effects , Atrioventricular Node/immunology , Atrioventricular Node/physiopathology , Atropine/pharmacology , Cardiomyopathy, Dilated/immunology , Cardiomyopathy, Dilated/parasitology , Chagas Cardiomyopathy/physiopathology , Chagas Disease/blood , Chronic Disease , Electrocardiography , Electrophysiology , Female , Heart Block/immunology , Heart Block/parasitology , Heart Rate , Humans , Immunoglobulin G/pharmacology , In Vitro Techniques , Male , Middle Aged , Muscarinic Antagonists/pharmacology , Rabbits , Wolff-Parkinson-White Syndrome/immunology , Wolff-Parkinson-White Syndrome/parasitologyABSTRACT
A young girl born to a mother with systemic lupus erythematosus (SLE) had congenital heart block and developed symptoms of a connective tissue disorder at the age of 13 y. When first seen at the age of 15 y she was found to have an unclassified connective tissue disorder and to be seropositive for anti Ro/SSA and U1 RNP. This constellation of clinical/serological features has not been described among the reported handful of patients with congenital heart block and subsequent development of a connective tissue disorder.
Subject(s)
Antibodies, Antinuclear/immunology , Autoimmune Diseases/genetics , Connective Tissue Diseases/genetics , Heart Block/congenital , RNA, Small Cytoplasmic , Adolescent , Adult , Antibodies, Antinuclear/blood , Autoantigens/immunology , Autoimmune Diseases/immunology , Connective Tissue Diseases/immunology , Female , HLA Antigens/analysis , Heart Block/immunology , Humans , Immunity, Maternally-Acquired , Lupus Erythematosus, Systemic/genetics , Pregnancy , Pregnancy Complications/immunology , Raynaud Disease/etiology , Ribonucleoprotein, U1 Small Nuclear/immunology , Ribonucleoproteins/immunology , Scleroderma, Localized/etiologyABSTRACT
OBJECTIVE: To study the association of maternal antibodies to Ro(SSA) and/or La(SSB) with isolated complete congenital heart block (CCHB) in children according to the child's age at detection. METHODS: Sera from 17 mothers of 18 children with CCHB of unidentified cause were studied. Autoantibodies were measured by double immunodiffusion, enzyme linked immunosorbent assay (ELISA), Western blot, and immunoprecipitation from cell extracts. Statistical analysis used the chi 2 test with Yates' correction. RESULTS: CCHB was diagnosed in 12 children of 11 mothers before the age of 3 mo (Group A) and in 6 children of 6 mothers after the age of 17 mo (Group B). Seven Group A mothers and no Group B mother had connective tissue disorders; autoantibodies were found in 9/11 Group A and in 1/6 Group B mothers (p < 0.01). Eight Group A children needed a pacemaker and one other died of cardiac insufficiency, whereas only one of the 6 Group B children needed a pacemaker. Interestingly, this latter child was the only one from Group B whose mother's serum contained autoantibodies. Irrespective of their age at diagnosis, the children with CCHB who needed a pacemaker and the one who died were born to mothers with autoantibodies (p < 0.001). CONCLUSION: CCHB detected before the age of 3 mo is highly associated with the presence of anti-Ro(SSA)/La(SSB) in the mothers, while CCHB diagnosed later is generally not. For epidemiological studies, the former type should be considered early onset as opposed to late onset CCHB in the latter type. Establishing this clinicoserological distinction is also important for the children, since it alerts the clinician to a more severe prognosis (necessity of a pacemaker), even in the rare occurrence of late diagnosed CCHB.
Subject(s)
Autoantibodies/blood , Autoantigens/immunology , Heart Block/diagnosis , RNA, Small Cytoplasmic , Ribonucleoproteins/immunology , Adolescent , Blotting, Western , Child , Child, Preschool , Enzyme-Linked Immunosorbent Assay , Female , Heart Block/congenital , Heart Block/immunology , Humans , Immunodiffusion , Infant , Male , Precipitin Tests , Prognosis , SS-B AntigenABSTRACT
In this work we demonstrated that IgG present in the sera of patients with congenital heart block (CHB) and their mothers could bind and activate beta adrenoceptors and muscarinic cholinergic receptors of neonatal heart. These antibodies were able to inhibit in a noncompetitive manner the binding of [3H]QNB and [3H]CGP to muscarinic cholinergic and beta adrenoceptors of purified neonatal rat myocardial membranes, respectively. Moreover, IgG from children with CHB and their mothers could modify biological effects mediated by these neurotransmitter receptors, i.e., heart contractility and cAMP production. Neither binding nor biological effects were obtained using adult instead of neonatal rat atria. Both reactivities (adrenergic and cholinergic) were independent of Ro/SS-A and La/SS-B antibodies and were absent in the sera of normal women of childbearing age and of normal children. It could be concluded that antibodies against cardiac neurotransmitter receptors may be another serum factor (or factors) to be considered in the pathophysiology of the development of CHB.
Subject(s)
Autoantibodies/blood , Heart Block/immunology , Receptors, Adrenergic, beta/immunology , Receptors, Muscarinic/immunology , Adult , Animals , Female , Heart Atria/physiopathology , Heart Block/congenital , Humans , Immunoglobulin G/metabolism , In Vitro Techniques , Infant , Mothers , Myocardial Contraction , Myocardium/metabolism , RatsABSTRACT
To determine whether antibodies against beta adrenergic activity interact with neonatal cardiac cell receptors and alter their physiological behaviour. An "in vitro" experimental model measuring the frequency of contraction, the production of cAMP and binding assay on neonatal and adult rat atria was employed. Sera and IgG fraction from mothers of infants with congenital heart block (CHB) interact with neonatal rat atria increasing the frequency of contraction and cAMP production. These effects were abolished by propranolol, pointing to a beta adrenergic participation. IgG also competed with 3H-CGP to beta adrenergic receptors on neonatal cardiac membranes. Neither the contractile nor the cAMP effects or binding assay were obtained using adult instead of neonatal rat atria. Reactivity against cardiac neurotransmitter receptors may be another serum factor(s) to be considered in the pathophysiology of the development of CHB.
Subject(s)
Autoantibodies/physiology , Heart Block/congenital , Receptors, Adrenergic, beta/immunology , Animals , Chi-Square Distribution , Cyclic AMP/biosynthesis , Female , Heart/drug effects , Heart Atria/physiopathology , Heart Block/immunology , Humans , Immunoglobulin G/physiology , In Vitro Techniques , Infant, Newborn , Mothers , Myocardial Contraction/drug effects , Propranolol/pharmacology , RatsABSTRACT
En este trabajo se empleó un modelo experimental "in vitro" en el cual se midió la frecuencia de las contracciones, la producción de AMPc y la la unión de ligandos específicos al receptor ß adrenérgicos en las aurículas de ratas neonatales y adultas; a fin de, determinar si anticuerpos con actividad ß adrenérgica interactuaban con receptores ß adrenérgicos cardíacos y alteraban su compartimiento fisiológico. Los sueros y la fracción IgG de madres de infantes con bloqueo cardíaco neonatal congénito incrementaron la frecuencia de las contracciones y la producciín de AMPc en el miocardio auricular neonato. Este efecto fue inhibido por propranolol, puntalizando una participación ß adrenérgica. La IgG también compitió con el radiologando específico por los receptores ß adrenérgicos (3H-CGP) en las membranas purificadas de miocardio neonatal. Ni los efectos biológicos ni los ensayos de unión específica fueron modificados cuando se usó miocardio de rata adulta. La reactividad contra adrenoreceptores cardíacos por parte de anticuerpos provenientes de madres de niños con bloqueo neonatal congénito, podría ser otro factor sérico que debería considerarse en la patofisiología del desarrollo del bloqueo neonatal congénito
Subject(s)
Humans , Animals , Female , Infant, Newborn , Rats , Autoantibodies/physiology , Heart Block/congenital , Receptors, Adrenergic, beta/immunology , Cyclic AMP/biosynthesis , Heart Block/immunology , Chi-Square Distribution , Chromatography, DEAE-Cellulose , Myocardial Contraction , Heart Atria/physiopathology , Immunoglobulin G/physiology , Mothers , Propranolol/pharmacologyABSTRACT
En este trabajo se empleó un modelo experimental "in vitro" en el cual se midió la frecuencia de las contracciones, la producción de AMPc y la la unión de ligandos específicos al receptor ß adrenérgicos en las aurículas de ratas neonatales y adultas; a fin de, determinar si anticuerpos con actividad ß adrenérgica interactuaban con receptores ß adrenérgicos cardíacos y alteraban su compartimiento fisiológico. Los sueros y la fracción IgG de madres de infantes con bloqueo cardíaco neonatal congénito incrementaron la frecuencia de las contracciones y la producciín de AMPc en el miocardio auricular neonato. Este efecto fue inhibido por propranolol, puntalizando una participación ß adrenérgica. La IgG también compitió con el radiologando específico por los receptores ß adrenérgicos (3H-CGP) en las membranas purificadas de miocardio neonatal. Ni los efectos biológicos ni los ensayos de unión específica fueron modificados cuando se usó miocardio de rata adulta. La reactividad contra adrenoreceptores cardíacos por parte de anticuerpos provenientes de madres de niños con bloqueo neonatal congénito, podría ser otro factor sérico que debería considerarse en la patofisiología del desarrollo del bloqueo neonatal congénito (AU)
Subject(s)
Humans , Animals , Female , Comparative Study , Infant, Newborn , Rats , Receptors, Adrenergic, beta/immunology , Autoantibodies/physiology , Heart Block/congenital , Heart Block/immunology , Cyclic AMP/biosynthesis , Propranolol/pharmacology , Immunoglobulin G/physiology , Myocardial Contraction/drug effects , Heart Atria/physiopathology , Chromatography, DEAE-Cellulose , Mothers , Chi-Square DistributionABSTRACT
We report 3 patients with congenital A-V block whose mothers had anti-Ro or anti-La antibodies. One of them had systemic lupus with serum anti-Ro antibodies; the other had anti-Ro antibodies and no clinical manifestations; the third had an undifferentiated connective tissue disorder with anti-La antibodies in the serum. The epidemiology of this association is discussed as well as some therapeutic options.
Subject(s)
Connective Tissue Diseases/immunology , Heart Block/congenital , Adult , Autoimmune Diseases/immunology , Female , Heart Block/immunology , Humans , Immunity, Maternally-Acquired , Infant, NewbornABSTRACT
Antibodies to SS-A/Ro have been proposed to be a serologic marker for the neonatal lupus syndrome, which is characterized by congenital heart block or cutaneous lupus or both. The antibodies occur in the mother and are transiently found in the child's serum. We examined an unselected series of 12 children with idiopathic CHB, isolated in 10 children and with cutaneous lupus lesions in two. Six of these children and their mothers were studied during the child's neonatal period, and six were studied retrospectively. All six neonates had SS-A/Ro autoantibodies. Nine of 12 mothers had SS-A/Ro autoantibodies. Of the seropositive mothers, one had systemic lupus erythematosus, two had sicca syndrome, one had photosensitivity, one had arthralgias, and four were asymptomatic. We propose that congenital heart block may be related to transplacental passage of maternal SS-A/Ro antibodies and that neonatal lupus may be the most common cause.