Till M M, Jones L H, Pentycross C R, Hardisty R M, Lawler S D, Harvey B A, Soothill J F
Br J Haematol. 1975 Apr;29(4):575-86. doi: 10.1111/j.1365-2141.1975.tb02744.x.
Seven of 500 children with acute leukaemia seen over a 15-year period were known to have a close relative with leukaemia or lymphoma. In each case the affected relative was a grandparent of the child, six of the seven being paternal grandparents. Investigation of thses six families showed that the fathers, who had two affected first-degree relatives, had lower lymphocyte counts and higher serum IgA concentrations than paired controls. Atopy, repeated infections and rheumatic disease were common amongst the parents and their sibs. The findings suggest a possible immunodeficiency basis for leukaemia in these families and perhaps also for acute lymphoblastic leukaemia of childhood in general. In the only family in which three generations, including both leukaemic patients, were available for HL-A typing, the affected grandson had not inherited either of his affected grandmother's haplotypes.
在15年期间诊治的500例急性白血病患儿中,有7例患儿的白血病或淋巴瘤近亲。每例中,患病亲属均为患儿的祖父母,7例中有6例是患儿父亲的父母。对这6个家庭的调查显示,有两名一级亲属患病的父亲,其淋巴细胞计数低于配对对照组,血清IgA浓度高于配对对照组。特应性、反复感染和风湿性疾病在患儿父母及其同胞中很常见。这些发现提示这些家庭中的白血病,或许还有儿童急性淋巴细胞白血病,可能存在免疫缺陷基础。在唯一一个三代人均可供进行HL - A分型的家庭中,患病的孙子并未遗传其患病祖母的任何一种单倍型。