Department of Biomedicine, Aarhus University, Aarhus C, Denmark.
PLoS One. 2013 Sep 16;8(9):e74063. doi: 10.1371/journal.pone.0074063. eCollection 2013.
We recently described that the autoimmune, central nervous system disease, multiple sclerosis (MS), is genetically associated with the human endogenous retroviral locus, HERV-Fc1, in Scandinavians. A number of dominant human genes encoding factors that restrict retrovirus replication have been known for a long time. Today human restriction genes for retroviruses include amongst others TRIMs, APOBEC3s, BST2 and TREXs. We have therefore looked for a role of these retroviral restriction genes in MS using genetic epidemiology. We here report that markers in two TRIMs, TRIM5 and TRIM22 and a marker in BST2, associated statistically with the risk of getting MS, while markers in or near APOBEC3s and TREXs showed little or no effect. This indicates that the two TRIMs and BST2 influence the risk of disease and thus supports the hypothesis of a viral involvement.
我们最近描述了自身免疫性中枢神经系统疾病多发性硬化症(MS)与斯堪的纳维亚人群中的人类内源性逆转录病毒基因座 HERV-Fc1 在遗传上有关。长期以来,人们已经知道许多编码限制逆转录病毒复制的因子的显性人类基因。如今,人类针对逆转录病毒的限制基因包括 TRIMs、APOBEC3s、BST2 和 TREXs 等。因此,我们使用遗传流行病学来寻找这些逆转录病毒限制基因在 MS 中的作用。我们在这里报告,两个 TRIM 基因(TRIM5 和 TRIM22)中的标记物以及 BST2 中的一个标记物与 MS 的发病风险呈统计学相关,而 APOBEC3s 和 TREXs 中的或附近的标记物则几乎没有影响。这表明这两个 TRIM 基因和 BST2 影响疾病的风险,从而支持病毒参与的假说。