Genetic and Clinical Factors Associated with Olokizumab Treatment in Russian Patients with Rheumatoid Arthritis

被引:1
|
作者
Mikhaylenko, Dmitry S. [1 ,2 ]
Kuznetsova, Ekaterina B. [1 ]
Musatova, Viktoria V. [2 ]
Bure, Irina, V [1 ]
Deryagina, Tatiana A. [2 ]
Alekseeva, Ekaterina A. [1 ,2 ]
Tarasov, Vadim V. [3 ]
Zamyatnin, Andrey A. [1 ,4 ,5 ,6 ]
Nemtsova, Marina, V [1 ,2 ]
机构
[1] IM Sechenov First Moscow State Med Univ, Lab Med Genet, Sechenov Univ, Moscow 119991, Russia
[2] Res Ctr Med Genet, Lab Epigenet, Moscow 115522, Russia
[3] IM Sechenov First Moscow State Med Univ, Inst Translat Med & Biotechnol, Moscow 119991, Russia
[4] Lomonosov Moscow State Univ, Belozersky Inst Phys Chem Biol, Moscow 119992, Russia
[5] Sirius Univ Sci & Technol, Dept Biotechnol, 1 Olymp Ave, Soci 354340, Russia
[6] Univ Surrey, Fac Hlth & Med Sci, Guildford GU2 7X, Surrey, England
来源
JOURNAL OF PERSONALIZED MEDICINE | 2022年 / 12卷 / 04期
关键词
rheumatoid arthritis; olokizumab; genetic predisposition; genotyping; NGS; response to therapy; POLYMORPHISMS; INTERLEUKIN-6; REPLICATION; ANTIBODY; SAFETY; PADI4;
D O I
10.3390/jpm12040641
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Rheumatoid arthritis (RA) is a chronic systemic inflammatory disease and its treatment is an urgent problem of rheumatology. Olokizumab (OKZ) is a new humanized monoclonal antibody targeting IL-6 and is one of the few promising drugs for RA therapy. One-hundred-and-twenty-five DNA samples from Russian patients with RA, treated with olokizumab, were genotyped with an NGS panel containing 60 single nucleotide polymorphisms (SNPs) and the whole coding sequences of IL6, IL6R, TNFRSF1A, CTLA4, IL10, IL23R, and PADI4; and by RT-PCR for HLA-DRB1 and HLA-B. Associations of polymorphic variants with olokizumab efficacy according to the scores ACR20, ACR50, and DAS28-CRP were determined. We analyzed the obtained data by using logistic regression, ROC curves, and multivariate ANOVA. A high predictive value of the response to olokizumab therapy at 24 weeks was found for the combination of HLA-DRB1*04 and HLA-B*27 alleles with SNPs located in non-HLA genes (IL1B, IL17A, PADI4, DHODH, GLCCI1, IL23R, and TNFAIP3), and clinical characteristics (age, RA duration, and intensity) according to ACR20. Thus, the comprehensive assessment of polymorphic variants of HLA and non-HLA genes considering population characteristics in combination with clinical parameters allows for the elaboration of an RA prognostic panel.
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页数:12
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