Literature DB >> 29045069

Association of Natural Killer Cell Ligand Polymorphism HLA-C Asn80Lys With the Development of Anti-SSA/Ro-Associated Congenital Heart Block.

Hannah C Ainsworth1, Miranda C Marion1, Tiziana Bertero2, Antonio Brucato3, Rolando Cimaz4, Nathalie Costedoat-Chalumeau5, Micaela Fredi6, Patrick Gaffney7, Jennifer Kelly7, Kateri Levesque5, Alice Maltret5, Nathalie Morel5, Veronique Ramoni3, Amelia Ruffatti8, Carl D Langefeld1, Jill P Buyon9, Robert M Clancy9.   

Abstract

OBJECTIVE: Fetal exposure to maternal anti-SSA/Ro antibodies is necessary but not sufficient for the development of autoimmune congenital heart block (CHB), suggesting that other factors, such as fetal genetic predisposition, are important. Given the previously described association between major histocompatibility complex alleles and CHB risk, we undertook the present study to test the hypothesis that a variant form of HLA-C Asn80Lys, which binds with high affinity to an inhibitory killer cell immunoglobulin-like receptor (KIR) and thus renders natural killer (NK) cells incapable of restricting inflammation, contributes to the development of CHB.
METHODS: Members of 192 pedigrees in the US and Europe (194 cases of CHB, 91 unaffected siblings, 152 fathers, 167 mothers) and 1,073 out-of-study controls were genotyped on the Immunochip single-nucleotide polymorphism microarray. Imputation was used to identify associations at HLA-C Asn80Lys (Asn, C1; Lys, C2) and KIR. Tests for association were performed using logistic regression. McNemar's test and the pedigree disequilibrium test (PDT) were used for matched analyses between affected and unaffected children.
RESULTS: Compared with out-of-study controls of the same sex, the C2 allele was less frequent in the mothers (odds ratio [OR] 0.63, P = 0.0014) and more frequent in the fathers (OR 1.40, P = 0.0123), yielding a significant sex-by-C2 interaction (P = 0.0002). The C2 allele was more frequent in affected siblings than in unaffected siblings (OR 3.67, P = 0.0025), which was consistent with the PDT results (P = 0.016); these results were observed in both sexes and across the US and European cohorts. There was no difference in the frequency of the inhibitory KIR genotype (KIR AA) between affected and unaffected children (P = 0.55).
CONCLUSION: These data establish C2 as a novel genetic risk factor associated with CHB. This observation supports a model in which fetuses with C2 ligand expression and maternal anti-SSA/Ro positivity may have impaired NK cell surveillance, resulting in unchecked cardiac inflammation and scarring.
© 2017, American College of Rheumatology.

Entities:  

Mesh:

Substances:

Year:  2017        PMID: 29045069      PMCID: PMC5679096          DOI: 10.1002/art.40228

Source DB:  PubMed          Journal:  Arthritis Rheumatol        ISSN: 2326-5191            Impact factor:   10.995


  15 in total

1.  The interaction of human natural killer cells with either unpolarized or polarized macrophages results in different functional outcomes.

Authors:  Francesca Bellora; Roberta Castriconi; Alessandra Dondero; Giorgio Reggiardo; Lorenzo Moretta; Alberto Mantovani; Alessandro Moretta; Cristina Bottino
Journal:  Proc Natl Acad Sci U S A       Date:  2010-11-30       Impact factor: 11.205

2.  Anatomical and pathological findings in hearts from fetuses and infants with cardiac manifestations of neonatal lupus.

Authors:  Carolina Llanos; Deborah M Friedman; Amit Saxena; Peter M Izmirly; Chung-E Tseng; Renata Dische; Rosanna G Abellar; Marc Halushka; Robert M Clancy; Jill P Buyon
Journal:  Rheumatology (Oxford)       Date:  2012-02-03       Impact factor: 7.580

3.  Multidirectional interactions are bridging human NK cells with plasmacytoid and monocyte-derived dendritic cells during innate immune responses.

Authors:  Mariella Della Chiesa; Chiara Romagnani; Andreas Thiel; Lorenzo Moretta; Alessandro Moretta
Journal:  Blood       Date:  2006-07-27       Impact factor: 22.113

4.  The HLA locus contains novel foetal susceptibility alleles for congenital heart block with significant paternal influence.

Authors:  S Meisgen; T Östberg; S Salomonsson; B Ding; H Eliasson; A Mälarstig; L Alfredsson; L Klareskog; A Hamsten; T Olsson; T Axelsson; F Gadler; A Jonzon; S-E Sonesson; I Kockum; M Wahren-Herlenius
Journal:  J Intern Med       Date:  2014-01-20       Impact factor: 8.989

5.  Specific combinations of HLA-DR2 and DR3 class II haplotypes contribute graded risk for disease susceptibility and autoantibodies in human SLE.

Authors:  Robert R Graham; Ward Ortmann; Peter Rodine; Karl Espe; Carl Langefeld; Ethan Lange; Adrienne Williams; Stephanie Beck; Chieko Kyogoku; Kathy Moser; Patrick Gaffney; Peter K Gregersen; Lindsey A Criswell; John B Harley; Timothy W Behrens
Journal:  Eur J Hum Genet       Date:  2007-04-04       Impact factor: 4.246

6.  A single amino acid in the p58 killer cell inhibitory receptor controls the ability of natural killer cells to discriminate between the two groups of HLA-C allotypes.

Authors:  C C Winter; E O Long
Journal:  J Immunol       Date:  1997-05-01       Impact factor: 5.422

7.  Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus.

Authors:  Robert M Clancy; Miranda C Marion; Kenneth M Kaufman; Paula S Ramos; Adam Adler; John B Harley; Carl D Langefeld; Jill P Buyon
Journal:  Arthritis Rheum       Date:  2010-11

8.  KIR ligand C2 is associated with increased susceptibility to childhood ALL and confers an elevated risk for late relapse.

Authors:  Florian Babor; Angela R Manser; Johannes C Fischer; Nadine Scherenschlich; Jürgen Enczmann; Olympe Chazara; Ashley Moffett; Arndt Borkhardt; Roland Meisel; Markus Uhrberg
Journal:  Blood       Date:  2014-08-27       Impact factor: 22.113

9.  Transancestral mapping and genetic load in systemic lupus erythematosus.

Authors:  Carl D Langefeld; Hannah C Ainsworth; Deborah S Cunninghame Graham; Jennifer A Kelly; Mary E Comeau; Miranda C Marion; Timothy D Howard; Paula S Ramos; Jennifer A Croker; David L Morris; Johanna K Sandling; Jonas Carlsson Almlöf; Eduardo M Acevedo-Vásquez; Graciela S Alarcón; Alejandra M Babini; Vicente Baca; Anders A Bengtsson; Guillermo A Berbotto; Marc Bijl; Elizabeth E Brown; Hermine I Brunner; Mario H Cardiel; Luis Catoggio; Ricard Cervera; Jorge M Cucho-Venegas; Solbritt Rantapää Dahlqvist; Sandra D'Alfonso; Berta Martins Da Silva; Iñigo de la Rúa Figueroa; Andrea Doria; Jeffrey C Edberg; Emőke Endreffy; Jorge A Esquivel-Valerio; Paul R Fortin; Barry I Freedman; Johan Frostegård; Mercedes A García; Ignacio García de la Torre; Gary S Gilkeson; Dafna D Gladman; Iva Gunnarsson; Joel M Guthridge; Jennifer L Huggins; Judith A James; Cees G M Kallenberg; Diane L Kamen; David R Karp; Kenneth M Kaufman; Leah C Kottyan; László Kovács; Helle Laustrup; Bernard R Lauwerys; Quan-Zhen Li; Marco A Maradiaga-Ceceña; Javier Martín; Joseph M McCune; David R McWilliams; Joan T Merrill; Pedro Miranda; José F Moctezuma; Swapan K Nath; Timothy B Niewold; Lorena Orozco; Norberto Ortego-Centeno; Michelle Petri; Christian A Pineau; Bernardo A Pons-Estel; Janet Pope; Prithvi Raj; Rosalind Ramsey-Goldman; John D Reveille; Laurie P Russell; José M Sabio; Carlos A Aguilar-Salinas; Hugo R Scherbarth; Raffaella Scorza; Michael F Seldin; Christopher Sjöwall; Elisabet Svenungsson; Susan D Thompson; Sergio M A Toloza; Lennart Truedsson; Teresa Tusié-Luna; Carlos Vasconcelos; Luis M Vilá; Daniel J Wallace; Michael H Weisman; Joan E Wither; Tushar Bhangale; Jorge R Oksenberg; John D Rioux; Peter K Gregersen; Ann-Christine Syvänen; Lars Rönnblom; Lindsey A Criswell; Chaim O Jacob; Kathy L Sivils; Betty P Tsao; Laura E Schanberg; Timothy W Behrens; Earl D Silverman; Marta E Alarcón-Riquelme; Robert P Kimberly; John B Harley; Edward K Wakeland; Robert R Graham; Patrick M Gaffney; Timothy J Vyse
Journal:  Nat Commun       Date:  2017-07-17       Impact factor: 14.919

10.  HIBAG--HLA genotype imputation with attribute bagging.

Authors:  X Zheng; J Shen; C Cox; J C Wakefield; M G Ehm; M R Nelson; B S Weir
Journal:  Pharmacogenomics J       Date:  2013-05-28       Impact factor: 3.550

View more
  1 in total

1.  Auxilin is a novel susceptibility gene for congenital heart block which directly impacts fetal heart function.

Authors:  Sabrina Meisgen; Malin Hedlund; Aurelie Ambrosi; Lasse Folkersen; Vijole Ottosson; David Forsberg; Gudny Ella Thorlacius; Luca Biavati; Linn Strandberg; Johannes Mofors; Daniel Ramskold; Sabrina Ruhrmann; Lauro Meneghel; William Nyberg; Alexander Espinosa; Robert Murray Hamilton; Anders Franco-Cereceda; Anders Hamsten; Tomas Olsson; Lois Greene; Per Eriksson; Kristina Gemzell-Danielsson; Stina Salomonsson; Vijay K Kuchroo; Eric Herlenius; Ingrid Kockum; Sven-Erik Sonesson; Marie Wahren-Herlenius
Journal:  Ann Rheum Dis       Date:  2022-04-25       Impact factor: 27.973

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.