Aloui Chaker, Sut Caroline, Prigent Antoine, Fagan Jocelyne, Cognasse Fabrice, Granados-Herbepin Viviana, Touraine Renaud, Pozzetto Bruno, Aouni Mahjoub, Fendri Chedlia, Hassine Mohsen, Chakroun Tahar, Jemni-Yacoub Saloua, Garraud Olivier, Laradi Sandrine
1] University of Lyon GIMAP-EA3064, Saint-Etienne, France [2] French Blood Establishment, EFS Auvergne-Loire, Saint-Etienne, France.
University of Lyon GIMAP-EA3064, Saint-Etienne, France.
Sci Rep. 2014 Nov 28;4:7239. doi: 10.1038/srep07239.
The CD40 ligand (CD40L/CD154), a member of TNF superfamily, is notably expressed on activated CD4+ T-cells and stimulated platelets. CD40L is linked to a variety of pathologies and to acute transfusion reactions (ATR). Mutations in this gene (CD40LG) lead to X-linked hyper-IgM syndrome. Some CD40LG polymorphisms are associated with variable protein expression. The rationale behind this study is that CD40L protein has been observed to be involved in ATR. We wondered whether genetic polymorphisms are implicated. We investigated genetic diversity in the CD40LG using DHPLC and capillary electrophoresis for screening and genotyping (n = 485 French and Tunisian blood donors). We identified significant difference in the CD40LG linkage pattern between the two populations. Variant minor alleles were significantly over-represented in Tunisian donors (P<0.0001 to 0.0270). We found higher heterogeneity in the Tunisian, including three novel low frequency variants. As there was not a particular pattern of CD40LG in single apheresis donors whose platelet components induced an ATR, we discuss how this information may be useful for future disease association studies on CD40LG.
CD40配体(CD40L/CD154)是肿瘤坏死因子超家族的成员,在活化的CD4+T细胞和受刺激的血小板上显著表达。CD40L与多种病理状况及急性输血反应(ATR)相关。该基因(CD40LG)的突变会导致X连锁高IgM综合征。一些CD40LG多态性与蛋白质表达的变化有关。本研究的理论依据是,已观察到CD40L蛋白参与ATR。我们想知道遗传多态性是否与之有关。我们使用变性高效液相色谱法(DHPLC)和毛细管电泳进行筛选和基因分型,研究了CD40LG中的遗传多样性(n = 485名法国和突尼斯献血者)。我们发现这两个人群在CD40LG连锁模式上存在显著差异。突尼斯献血者中变异的次要等位基因显著过多(P<0.0001至0.0270)。我们发现突尼斯人群中存在更高的异质性,包括三个新的低频变异。由于在血小板成分引发ATR的单采献血者中没有特定的CD40LG模式,我们讨论了这些信息如何可能对未来关于CD40LG的疾病关联研究有用。