Kariuki Silvia N, Franek Beverly S, Mikolaitis Rachel A, Utset Tammy O, Jolly Meenakshi, Skol Andrew D, Niewold Timothy B
Section of Rheumatology and Gwen Knapp Center for Lupus and Immunology Research, University of Chicago, 5841 S. Maryland Ave. MC 0930, Chicago, IL 60637, USA.
J Biomed Biotechnol. 2010;2010:826434. doi: 10.1155/2010/826434. Epub 2010 Jul 4.
The PIK3C3 locus was implicated in case-case genome-wide association study of systemic lupus erythematosus (SLE) which we had performed to detect genes associated with autoantibodies and serum interferon-alpha (IFN-alpha). Herein, we examine a PIK3C3 promoter variant (rs3813065/-442 C/T) in an independent multiancestral cohort of 478 SLE cases and 522 controls. rs3813065 C was strongly associated with the simultaneous presence of both anti-Ro and anti-Sm antibodies in African-American patients [OR = 2.24 (1.34-3.73), P = 2.0 x 10(-3)]. This autoantibody profile was associated with higher serum IFN-alpha (P = 7.6 x 10(-6)). In the HapMap Yoruba population, rs3813065 was associated with differential expression of ERAP2 (P = 2.0 x 10(-5)), which encodes an enzyme involved in MHC class I peptide processing. Thus, rs3813065 C is associated with a particular autoantibody profile and altered expression of an MHC peptide processing enzyme, suggesting that this variant modulates serologic autoimmunity in African-American SLE patients.
在我们为检测与自身抗体和血清干扰素-α(IFN-α)相关的基因而进行的系统性红斑狼疮(SLE)病例对照全基因组关联研究中,PIK3C3基因座被牵涉其中。在此,我们在一个由478例SLE病例和522例对照组成的独立多祖先队列中检测了PIK3C3启动子变体(rs3813065/-442 C/T)。rs3813065 C与非裔美国患者中抗Ro和抗Sm抗体同时存在密切相关[比值比(OR)=2.24(1.34 - 3.73),P = 2.0×10⁻³]。这种自身抗体谱与较高的血清IFN-α相关(P = 7.6×10⁻⁶)。在国际人类基因组单体型图计划(HapMap)的约鲁巴人群中,rs3813065与内质网氨肽酶2(ERAP2)的差异表达相关(P = 2.0×10⁻⁵),ERAP2编码一种参与MHC I类肽加工的酶。因此,rs3813065 C与特定的自身抗体谱以及MHC肽加工酶的表达改变相关,这表明该变体调节了非裔美国SLE患者的血清学自身免疫。