Abstract 3499: Extracellular Loop (Domain I, S5-S6) of α1D L-type Ca Channel is an Antigenic Site in Autoimmune Associated Congenital Heart Block

Circulation ◽  
2008 ◽  
Vol 118 (suppl_18) ◽  
Author(s):  
Eddy Karnabi ◽  
Yongxia Qu ◽  
Raj Wadgaonkar ◽  
Salvatore Mancarella ◽  
Yunkun Yue ◽  
...  

Congenital heart block (CHB) is an autoimmune disease associated with autoantibodies against intracellular ribonucleoproteins SSB/La and SSA/Ro. The hallmark of CHB is complete atrioventricular block. We have established that anti-SSA/Ro -SSB/La autoantibodies inhibit L-type α 1D Ca current, I Ca-L and cross-react with the α 1D Ca channel protein. This study aims at identifying the possible binding sites on α 1D protein for autoantibodies from sera of mothers with CHB children. GST fusion proteins of the extracellular regions between the transmembrane segments (S5-S6) of each of the four α 1D Ca channel protein domains I–IV were prepared and tested for reactivity with sera from mothers with CHB children and controls using ELISA. Sera from 118 mothers with CHB children and 28 control healthy sera were used in this study. Seventeen of 118 (14.4%) maternal CHB sera reacted with the extracellular loop of Domain I S5-S6 region (E1). In contrast, 2 of 28 (7%) healthy control sera reacted with the E1 loop. Preincubation of E1 loop with the positive sera decreased the O.D. reading of the positive sera establishing the specificity of the response. Electrophysiological characterization of the ELISA positive sera demonstrated inhibition (44.1%) of the α 1D I Ca-L expressed in tsA201 cells. The inhibition was abolished when the sera were pre-incubated with E1 extracellular loop fusion protein. The results identified the extracellular loop of domain I S5-S6 of L-type Ca channel α 1D subunit as a target for autoantibodies from mothers with CHB children. This novel finding provides insights into the development of therapeutic peptides that could bind to the pathogenic antibodies.

2010 ◽  
Vol 34 (2) ◽  
pp. 80-86 ◽  
Author(s):  
Eddy Karnabi ◽  
Yongxia Qu ◽  
Raj Wadgaonkar ◽  
Salvatore Mancarella ◽  
Yuankun Yue ◽  
...  

Circulation ◽  
2008 ◽  
Vol 118 (suppl_18) ◽  
Author(s):  
Eddy Karnabi ◽  
Yongxia Qu ◽  
Mohamed Boutjdir

Congenital Heart Block (CHB) is a passively acquired autoimmune disease associated with the transfer of maternal autoantibodies anti-SSA/Ro -SSB/La through the placenta causing AV block and sinus bradycardia. We previously established a murine model for CHB in which pups born to wild type (WT) mothers immunized with Ro and/or La recombinant proteins developed conduction abnormalities similar to those seen in the clinical settings and inhibited L-type Ca channels (LTCC) responsible for electrogenesis at the AV and SA node. Here, we hypothesized that overexpression of cardiac LTCC should prevent or reduce the electrocardiographic abnormalities seen in the pups, whereas LTCC knockout should exhibit severe conduction abnormalities and increased mortality. Transgenic (TG) mice overexpressing LTCC and LTCC knockouts were immunized with Ro and La antigens. Following the immunization and boosters, a high antibody titer was demonstrated both in mothers and pups. ECG parameters were measured from pups born to immunized and to WT mothers. Ca channel overexpressing pups had significantly lesser sinus bradycardia and AV block compared to their non-TG (NTG) litter mates and WT pups. Sinus bradycardia was seen in 10% (n= 90) of TG pups v.s. 19.7% in WT (n=76, p<0.05) vs. 22% NTG littermates (n=109, p<0.05) and AV block in 8.8% of TG (n=90) v.s. 25% in WT (n= 76, p<0.05) v.s. 27.5% in NTG (n=109, p<0.05). On the other hand, Ca channel knockout pups had a significantly higher sinus bradycardia and a higher percentage of AV bock; 100% in knockout pups (n=16, p<0.05), 42.3% in heterozygotes (n=52, p<0.05), and 18.2% in NTG (n=33, p<0.05). No electrocardiographic abnormalities were observed in control WT pups (nonimmunized). Cardiac specific overexpression of LTCC significantly rescues the incidence of AV block and sinus bradycardia in pups exposed to circulating maternal anti-Ro/La autoantibodies. Whereas exposure of LTCC knockout pups to anti-Ro/La autoantibodies significantly worsened the conduction abnormalities. This finding support the hypothesis that maternal antibodies’ inhibition of LTCC contributes to the development of CHB. Altogether the results are relevant for future novel therapies for CHB.


2020 ◽  
Vol 2 (4) ◽  
pp. e204-e205 ◽  
Author(s):  
Nathalie Costedoat-Chalumeau ◽  
Nathalie Morel

2015 ◽  
Vol 53 (3) ◽  
pp. 269-278 ◽  
Author(s):  
Amelia Ruffatti ◽  
Maria Favaro ◽  
Antonio Brucato ◽  
Veronique Ramoni ◽  
Myriam Facchinetti ◽  
...  

1995 ◽  
Vol 4 (2) ◽  
pp. 63-65 ◽  
Author(s):  
Brian K. O'Connor ◽  
Christopher L. Case ◽  
Paul C. Gillette

2000 ◽  
Vol 43 (5) ◽  
pp. 1049 ◽  
Author(s):  
Rolando Cimaz ◽  
Marco Stramba-Badiale ◽  
Antonio Brucato ◽  
Luca Catelli ◽  
Paola Panzeri ◽  
...  

Autoimmunity ◽  
1999 ◽  
Vol 30 (2) ◽  
pp. 81-83 ◽  
Author(s):  
Nathalie De Parseval ◽  
Graham Forrest ◽  
Patrick J.W. Venables ◽  
Thierry Heidmann

1989 ◽  
Vol 169 (5) ◽  
pp. 1583-1588 ◽  
Author(s):  
K K Gaither ◽  
J B Harley

Idiotypes and antiidiotypes are thought to be important immune regulators and have provided clues for the origin and pathogenicity of autoantibodies. Many lupus and Sjögren's syndrome patients, as well as most neonatal lupus infants with congenital heart block or dermatitis, have antibodies to the ribonucleoprotein Ro/SSA, which is one of a group of RNA-protein autoantigens commonly found in human lupus sera. To characterize the fine specificity of anti-Ro/SSA antibodies, a rabbit antidiotypic serum was prepared against polyclonal affinity purified anti-Ro/SSA F(ab')2. The resulting antiidiotype, anti-Id-Rol, is specific for the F(ab')2 fraction of the anti-Ro/SSA immunogen and its binding to anti-Ro/SSA is inhibited by purified Ro/SSA. These data indicate that the Id-Rol epitope on anti-Ro/SSA is associated with the antigen binding site of these same antibodies. The Id-Rol idiotype was present by ELISA in 3 of 12 additional anti-Ro/SSA preparations from precipitin-positive donor sera and in anti-Ro/SSA from one normal donor with low level antibody. This is the first shared idiotype to be found in the human autoantibodies binding to this RNA-protein antigen. Idiotypic differences between anti-Ro/SSA autoantibodies have the potential to explain the variation in pathologic associations found in individuals who develop this autoantibody specificity.


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