HLA association with the susceptibility to anti-synthetase syndrome

•HLA typing may help to identify patients with ASSD.•HLA-DRB1*03:01 and HLA-B1*08:01 are predisposition markers of ASSD.•HLA-DRB1*07:01 is a protective allele against ASSD.•HLA-DRB1*03:01 increases the risk of developing anti-Jo-1 autoantibodies in ASSD.•Smoking does not seem to influence anti-Jo-1...

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Veröffentlicht in:Joint, bone, spine : revue du rhumatisme bone, spine : revue du rhumatisme, 2021-05, Vol.88 (3), p.105115-105115, Article 105115
Hauptverfasser: Remuzgo-Martínez, Sara, Atienza-Mateo, Belén, Ocejo-Vinyals, J. Gonzalo, Pulito-Cueto, Verónica, Prieto-Peña, Diana, Genre, Fernanda, Marquez, Ana, Llorca, Javier, Mora Cuesta, Víctor M., Fernández, David Iturbe, Riesco, Laura, Ortego-Centeno, Norberto, Gómez, Nair Pérez, Mera, Antonio, Martínez-Barrio, Julia, López-Longo, Francisco Javier, Lera-Gómez, Leticia, Moriano, Clara, Díez, Elvira, Tomero, Eva, Calvo-Alén, Jaime, Romero-Bueno, Fredeswinda, Sanchez-Pernaute, Olga, Nuño, Laura, Bonilla, Gema, Grafia, Ignacio, Prieto-González, Sergio, Narvaez, Javier, Trallero-Araguas, Ernesto, Selva-O’Callaghan, Albert, Gualillo, Oreste, Martín, Javier, Cavagna, Lorenzo, Castañeda, Santos, Cifrian, José M., Renzoni, Elisabetta A., López-Mejías, Raquel, González-Gay, Miguel A.
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Zusammenfassung:•HLA typing may help to identify patients with ASSD.•HLA-DRB1*03:01 and HLA-B1*08:01 are predisposition markers of ASSD.•HLA-DRB1*07:01 is a protective allele against ASSD.•HLA-DRB1*03:01 increases the risk of developing anti-Jo-1 autoantibodies in ASSD.•Smoking does not seem to influence anti-Jo-1 antibody positivity in ASSD. To investigate the human leukocyte antigen (HLA) association with anti-synthetase syndrome (ASSD). We conducted the largest immunogenetic HLA-DRB1 and HLA-B study to date in a homogeneous cohort of 168 Caucasian patients with ASSD and 486 ethnically matched healthy controls by sequencing-based-typing. A statistically significant increase of HLA-DRB1*03:01 and HLA-B*08:01 alleles in patients with ASSD compared to healthy controls was disclosed (26.2% versus 12.2%, P=1.56E–09, odds ratio–OR [95% confidence interval–CI]=2.54 [1.84–3.50] and 21.4% versus 5.5%, P=18.95E–18, OR [95% CI]=4.73 [3.18–7.05]; respectively). Additionally, HLA-DRB1*07:01 allele was significantly decreased in patients with ASSD compared to controls (9.2% versus 17.5%, P=0.0003, OR [95% CI]=0.48 [0.31–0.72]). Moreover, a statistically significant increase of HLA-DRB1*03:01 allele in anti-Jo-1 positive compared to anti-Jo-1 negative patients with ASSD was observed (31.8% versus 15.5%, P=0.001, OR [95% CI]=2.54 [1.39–4.81]). Similar findings were observed when HLA carrier frequencies were assessed. The HLA-DRB1*03:01 association with anti-Jo-1 was unrelated to smoking history. No HLA differences in patients with ASSD stratified according to the presence/absence of the most representative non-anti-Jo-1 anti-synthetase autoantibodies (anti-PL-12 and anti-PL-7), arthritis, myositis or interstitial lung disease were observed. Our results support the association of the HLA complex with the susceptibility to ASSD.
ISSN:1297-319X
1778-7254
DOI:10.1016/j.jbspin.2020.105115