Division of Hematology/Oncology, Department of Pediatrics, The Seventh Affiliated Hospital, Sun Yat-Sen University, Shenzhen, China.
Department of Pediatrics, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, Guangzhou, China.
Pediatr Blood Cancer. 2021 Aug;68(8):e29097. doi: 10.1002/pbc.29097. Epub 2021 May 24.
Cytokine storms are central to the development of Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis (EBV-HLH). Previous studies have shown that single-nucleotide polymorphisms (SNPs) of cytokine genes may be associated with the development of EBV-HLH in children. As such, we investigated the association between susceptibility to EBV-HLH in children and SNPs and haplotypes of genes encoding interleukin-2 receptor subunit alpha (IL2RA), interleukin-10 (IL10), interferon gamma (IFNG), interferon regulatory factor 5 (IRF5), and C-C chemokine receptor 2 (CCR2).
Sixty-six children with EBV-HLH and 58 healthy EBV-seropositive controls were enrolled in this study. SNPs of IL2RA rs2104286, rs12722489, and rs11594656; IL10 rs1800896, rs1800871, and rs1800872; IFNG rs2430561, IRF5 rs2004640, and CCR2 rs1799864 were assayed and genotyped using the SNaPshot technique.
Frequencies of the A allele of IL2RA rs2104286 and IL10 rs1800896, and C allele of IL-10 rs1800872 were significantly higher in the EBV-HLH group than in the control group. The AA genotype of IL2RA rs2104286 and IL10 rs1800896, and the CC genotype of IL10 rs1800872 might be associated with a significantly high risk of EBV-HLH. However, the frequencies of genotypes and alleles of IL2RA rs2104286, IL10 rs1800871, IFNG rs2430561, IRF5 rs2004640, and CCR2 rs1799864 were similar in both groups. Additionally, IL2RA AGT (rs2104286-rs12722489-rs11594656) and IL10 ACC (rs1800896-rs1800871-rs1800872) haplotypes were also associated with an increased risk of EBV-HLH.
SNPs of IL2RA rs2104286, IL10 rs1800896 and rs1800872 and the haplotypes of IL2RA AGT and IL10 ACC were highly associated with susceptibility to EBV-HLH in children.
细胞因子风暴是 Epstein-Barr 病毒相关噬血细胞性淋巴组织细胞增生症(EBV-HLH)发展的核心。先前的研究表明,细胞因子基因的单核苷酸多态性(SNPs)可能与儿童 EBV-HLH 的发展有关。因此,我们研究了儿童易患 EBV-HLH 与白细胞介素 2 受体亚单位 α(IL2RA)、白细胞介素 10(IL10)、干扰素 γ(IFNG)、干扰素调节因子 5(IRF5)和 C-C 趋化因子受体 2(CCR2)编码基因的 SNPs 和单倍型之间的关系。
本研究纳入了 66 例 EBV-HLH 患儿和 58 例 EBV 血清阳性健康对照者。采用 SNaPshot 技术检测 IL2RA rs2104286、rs12722489 和 rs11594656;IL10 rs1800896、rs1800871 和 rs1800872;IFNG rs2430561、IRF5 rs2004640 和 CCR2 rs1799864 的 SNPs,并进行基因分型。
与对照组相比,EBV-HLH 组 IL2RA rs2104286 的 A 等位基因和 IL10 rs1800896 的频率以及 IL10 rs1800872 的 C 等位基因明显较高。IL2RA rs2104286 的 AA 基因型和 IL10 rs1800896 的基因型以及 IL10 rs1800872 的 CC 基因型可能与 EBV-HLH 的高风险显著相关。然而,两组 IL2RA rs2104286、IL10 rs1800871、IFNG rs2430561、IRF5 rs2004640 和 CCR2 rs1799864 的基因型和等位基因频率相似。此外,IL2RA AGT(rs2104286-rs12722489-rs11594656)和 IL10 ACC(rs1800896-rs1800871-rs1800872)单倍型也与 EBV-HLH 的高风险相关。
IL2RA rs2104286、IL10 rs1800896 和 rs1800872 的 SNPs 以及 IL2RA AGT 和 IL10 ACC 单倍型与儿童易患 EBV-HLH 高度相关。