Lima Suelen Cristina, Gomes da Silva Isaura Isabelle Fonseca, Nascimento Denise de Queiroga, de Moura Ronald Rodrigues, Mesquita Matheus da Silva, Asano Nadja Maria Jorge, Fernandes Gisele Vagjel, Valente Lucila Maria, Rushansky Eliezer, Mariano Maria Helena Queiroz de Araújo, Xavier Ricardo Machado, Chies José Artur Bogo, Crovella Sergio, Sandrin-Garcia Paula
Laboratory of Immunopathology Keizo Asami, Recife, Brazil.
PostGraduate Program in Genetics, Federal University of Pernambuco, Recife, Brazil.
Int J Immunogenet. 2021 Oct;48(5):429-434. doi: 10.1111/iji.12548. Epub 2021 Jun 27.
Systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA) are influenced by genetic variants in immune system HLA genes. The Class II Major Histocompatibility Complex Transactivator (CIITA) is an important co-activator of the HLA transcriptional complex; the single nucleotide variant (SNV) rs3087456 localized in the gene promoter region (-168 A/G) has been reported as able to modify its transcription level. In our study, we assessed CIITA rs3087456 SNV in 1,044 Brazilians from two Brazilian regions (Northeast and South) to verify the association with susceptibility and clinical manifestations of (SLE) and (RA) using TaqMan SNP Genotyping Assays System. We observed a protection for a recessive model (GG x AA+AG) for RA susceptibility and increased risk for erosion development in AG genotype patients. No significant association was observed for SLE susceptibility; however, we observed significant increased risk for Class IV and V nephritis development in G allele and GG genotype patients. In conclusion, we showed the contribution of CIITA rs3087456 to SLE or RA clinical features and RA susceptibility in the studied populations.
系统性红斑狼疮(SLE)和类风湿性关节炎(RA)受免疫系统HLA基因中的遗传变异影响。II类主要组织相容性复合体反式激活因子(CIITA)是HLA转录复合体的重要共激活因子;据报道,位于基因启动子区域(-168 A/G)的单核苷酸变异(SNV)rs3087456能够改变其转录水平。在我们的研究中,我们使用TaqMan SNP基因分型检测系统,对来自巴西两个地区(东北部和南部)的1044名巴西人进行了CIITA rs3087456 SNV评估,以验证其与SLE和RA易感性及临床表现的关联。我们观察到,对于RA易感性,隐性模型(GG x AA+AG)具有保护作用,而AG基因型患者发生侵蚀的风险增加。未观察到SLE易感性存在显著关联;然而,我们观察到G等位基因和GG基因型患者发生IV级和V级肾炎的风险显著增加。总之,我们证明了CIITA rs3087456对所研究人群中SLE或RA临床特征及RA易感性的影响。