Identification of two novel bullous pemphigoid- associated alleles, HLA-DQA1*05:05 and -DRB1*07:01, in Germans

German AIBD Study Group

doi:10.1186/s13023-021-01863-9

Identification of two novel bullous pemphigoid- associated alleles, HLA-DQA105:05 and -DRB107:01, in Germans

German AIBD Study Group

Abstract

Bullous pemphigoid (BP) is the most common autoimmune skin blistering disease characterized by autoimmunity against the hemidesmosomal proteins BP180, type XVII collagen, and BP230. To elucidate the genetic basis of susceptibility to BP, we performed the first genome-wide association study (GWAS) in Germans. This GWAS was combined with HLA locus targeted sequencing in an additional independent BP cohort. The strongest association with BP in Germans tested in this study was observed in the two HLA loci, HLA-DQA1*05:05 and HLA-DRB1*07:01. Further studies with increased sample sizes and complex studies integrating multiple pathogenic drivers will be conducted.

Originalsprache	Englisch
Aufsatznummer	228
Zeitschrift	Orphanet Journal of Rare Diseases
Jahrgang	16
Ausgabenummer	1
Seiten (von - bis)	228
ISSN	1750-1172
DOIs	https://doi.org/10.1186/s13023-021-01863-9
Publikationsstatus	Veröffentlicht - 19.05.2021

Strategische Forschungsbereiche und Zentren

Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)
Zentren: Center for Research on Inflammation of the Skin (CRIS)

DFG-Fachsystematik

204-05 Immunologie
205-19 Dermatologie
201-05 Allgemeine Genetik und funktionelle Genomforschung

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

Zugriff auf Dokument

10.1186/s13023-021-01863-9

Andere Dateien und Links

KFO 303: Pemphigoid Diseases - Molecular Pathways and their Therapeutic Potential
Sadik, C., Zillikens, D., Ibrahim, S., Baines, J. F., Schmidt, E., Köhl, J., Ehlers, M., Hirose, M., König, P., Ludwig, R., Manz, R., Schwaninger, M., Beek, N., Erdmann, J., König, I. R., Verschoor, A., Karsten, C., Bieber, K. & Busch, H. S.
01.04.15 → 31.12.23
Projekt: DFG-Projekte › DFG-Verbundforschung: Forschergruppen/Klinische Forschergruppen

Zitieren

@article{1c4645b4712345ca8fa7dfd2583d2a87,

title = "Identification of two novel bullous pemphigoid- associated alleles, HLA-DQA1*05:05 and -DRB1*07:01, in Germans",

abstract = "Bullous pemphigoid (BP) is the most common autoimmune skin blistering disease characterized by autoimmunity against the hemidesmosomal proteins BP180, type XVII collagen, and BP230. To elucidate the genetic basis of susceptibility to BP, we performed the first genome-wide association study (GWAS) in Germans. This GWAS was combined with HLA locus targeted sequencing in an additional independent BP cohort. The strongest association with BP in Germans tested in this study was observed in the two HLA loci, HLA-DQA1*05:05 and HLA-DRB1*07:01. Further studies with increased sample sizes and complex studies integrating multiple pathogenic drivers will be conducted.",

author = "Christian Schwarm and {German AIBD Study Group} and Damian Gola and Holtsche, {Maike M.} and Anabelle Dieterich and Anita Bhandari and Miriam Freitag and Peter N{\"u}rnberg and Mohammad Toliat and Wolfgang Lieb and Michael Wittig and Andr{\'e} Franke and Margitta Worm and Michael Sticherling and Jan Ehrchen and Claudia G{\"u}nther and Regine Gl{\"a}ser and Peitsch, {Wiebke K.} and Mikl{\'o}s S{\'a}rdy and R{\"u}diger Eming and Michael Hertl and Sandrine Benoit and Matthias Goebeler and Claudia Pf{\"o}hler and Manfred Kunz and Alexander Kreuter and {van Beek}, Nina and Jeanette Erdmann and Hauke Busch and Detlef Zillikens and Sadik, {Christian D.} and Misa Hirose and K{\"o}nig, {Inke R.} and Enno Schmidt and Ibrahim, {Saleh M.}",

note = "Publisher Copyright: {\textcopyright} 2021, The Author(s).",

year = "2021",

month = may,

day = "19",

doi = "10.1186/s13023-021-01863-9",

language = "English",

volume = "16",

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journal = "Orphanet Journal of Rare Diseases",

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TY - JOUR

T1 - Identification of two novel bullous pemphigoid- associated alleles, HLA-DQA1*05:05 and -DRB1*07:01, in Germans

AU - Schwarm, Christian

AU - German AIBD Study Group

AU - Gola, Damian

AU - Holtsche, Maike M.

AU - Dieterich, Anabelle

AU - Bhandari, Anita

AU - Freitag, Miriam

AU - Nürnberg, Peter

AU - Toliat, Mohammad

AU - Lieb, Wolfgang

AU - Wittig, Michael

AU - Franke, André

AU - Worm, Margitta

AU - Sticherling, Michael

AU - Ehrchen, Jan

AU - Günther, Claudia

AU - Gläser, Regine

AU - Peitsch, Wiebke K.

AU - Sárdy, Miklós

AU - Eming, Rüdiger

AU - Hertl, Michael

AU - Benoit, Sandrine

AU - Goebeler, Matthias

AU - Pföhler, Claudia

AU - Kunz, Manfred

AU - Kreuter, Alexander

AU - van Beek, Nina

AU - Erdmann, Jeanette

AU - Busch, Hauke

AU - Zillikens, Detlef

AU - Sadik, Christian D.

AU - Hirose, Misa

AU - König, Inke R.

AU - Schmidt, Enno

AU - Ibrahim, Saleh M.

PY - 2021/5/19

Y1 - 2021/5/19

N2 - Bullous pemphigoid (BP) is the most common autoimmune skin blistering disease characterized by autoimmunity against the hemidesmosomal proteins BP180, type XVII collagen, and BP230. To elucidate the genetic basis of susceptibility to BP, we performed the first genome-wide association study (GWAS) in Germans. This GWAS was combined with HLA locus targeted sequencing in an additional independent BP cohort. The strongest association with BP in Germans tested in this study was observed in the two HLA loci, HLA-DQA1*05:05 and HLA-DRB1*07:01. Further studies with increased sample sizes and complex studies integrating multiple pathogenic drivers will be conducted.

AB - Bullous pemphigoid (BP) is the most common autoimmune skin blistering disease characterized by autoimmunity against the hemidesmosomal proteins BP180, type XVII collagen, and BP230. To elucidate the genetic basis of susceptibility to BP, we performed the first genome-wide association study (GWAS) in Germans. This GWAS was combined with HLA locus targeted sequencing in an additional independent BP cohort. The strongest association with BP in Germans tested in this study was observed in the two HLA loci, HLA-DQA1*05:05 and HLA-DRB1*07:01. Further studies with increased sample sizes and complex studies integrating multiple pathogenic drivers will be conducted.

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U2 - 10.1186/s13023-021-01863-9

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M3 - Letters

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AN - SCOPUS:85106287801

SN - 1750-1172

VL - 16

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JO - Orphanet Journal of Rare Diseases

JF - Orphanet Journal of Rare Diseases

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