Jørgensen F, Kristensen T, Lamm L U, Kissmeyer-Nielsen F
Tissue Antigens. 1977 Nov;10(5):379-93. doi: 10.1111/j.1399-0039.1977.tb00774.x.
The genetics of five HLA-D specificities (Dw1, Dw2, Dw3, Dw4 and Dw6) have been assessed in 21 normal families with four or more children. The HLA-D traits, as defined by typing response against homozygous typing cells, normally behave as dominant characters. The data support the concept of allelic factors. The locial flaw in the basic algorithm of MLC typing (HLA-D typing), i.e. to draw positive conclusions from negative observations, has been amply reinforced in the following studies. Five assignments could not be verified genetically under the assumption of dominant traits. Homozygous lack of specific response genes is among the mechanisms proposed as a cause for the phenomenon which has not yet been fully explained. The estimated magnitude of the frequency of false assignments is approximately 10%.
在21个有4个或更多孩子的正常家庭中,对5种HLA - D特异性(Dw1、Dw2、Dw3、Dw4和Dw6)的遗传学进行了评估。根据对纯合分型细胞的分型反应所定义的HLA - D性状,通常表现为显性性状。这些数据支持等位基因因子的概念。混合淋巴细胞培养分型(HLA - D分型)基本算法中的逻辑缺陷,即从阴性观察结果得出阳性结论,在以下研究中得到了充分强化。在显性性状的假设下,有5种分型结果无法通过遗传学验证。纯合缺乏特异性反应基因是被提出作为尚未完全解释的这一现象的原因之一的机制。估计错误分型频率的大小约为10%。