Department of Preventive Medicine, Center for Genetic Epidemiology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Cigna Health and Life Insurance Company (Cigna), Bloomfield, CT, USA.
Cancer Causes Control. 2020 May;31(5):451-462. doi: 10.1007/s10552-020-01266-4. Epub 2020 Mar 2.
We explored the interaction between non-Hodgkin lymphoma (NHL), infectious mononucleosis (IM) history, and immune-related genotypes in a pooled case-control analysis.
A total of 7,926 NHL patients and 10,018 controls from 12 case-control studies were included. Studies were conducted during various time periods between 1988 and 2008, and participants were 17-96 years of age at the time of ascertainment/recruitment. Self-reported IM history and immune response genotypes were provided by the InterLymph Data Coordinating Center at Mayo Clinic. Odds ratios (OR) were estimated using multivariate logistic regression, and interactions were estimated using the empirical Bayes method. P was used to account for multiple comparisons.
There was evidence of an interaction effect between IM history and two variants on T-cell lymphoma (TCL) risk: rs1143627 in interleukin-1B (IL1B) (p = 0.04, OR = 0.09, 95% confidence interval [CI] 0.01, 0.87) and rs1800797 in interleukin-6 (IL6) (p = 0.03, OR = 0.08, 95% CI 0.01, 0.80). Neither interaction effect withstood adjustment for multiple comparisons. There were no statistically significant interactions between immune response genotypes and IM on other NHL subtypes.
Genetic risk variants in IL1B and IL6 may affect the association between IM and TCL, possibly by influencing T-cell activation, growth, and differentiation in the presence of IM, thereby decreasing risk of immune cell proliferation.
我们通过汇总病例对照分析,探讨了非霍奇金淋巴瘤(NHL)、传染性单核细胞增多症(IM)病史与免疫相关基因型之间的相互作用。
共纳入了来自 12 项病例对照研究的 7926 例 NHL 患者和 10018 例对照。这些研究分别在 1988 年至 2008 年期间的不同时间段内开展,参与者在确定/招募时的年龄为 17-96 岁。自我报告的 IM 病史和免疫反应基因型由梅奥诊所的 InterLymph 数据协调中心提供。使用多变量逻辑回归估计比值比(OR),并使用经验贝叶斯法估计相互作用。P 用于校正多重比较。
IM 病史与两种 T 细胞淋巴瘤(TCL)风险变体之间存在交互作用:白细胞介素 1B(IL1B)中的 rs1143627(p=0.04,OR=0.09,95%置信区间 [CI] 0.01,0.87)和白细胞介素 6(IL6)中的 rs1800797(p=0.03,OR=0.08,95% CI 0.01,0.80)。这两种交互作用在经过多重比较校正后均无统计学意义。免疫反应基因型与 IM 之间的其他 NHL 亚型没有统计学上显著的相互作用。
IL1B 和 IL6 中的遗传风险变异可能会影响 IM 与 TCL 之间的关联,可能是通过影响 T 细胞在 IM 存在时的激活、生长和分化,从而降低免疫细胞增殖的风险。