Froom P, Aghai E, Dobinsky J B, Quitt M, Lahat N
Leuk Res. 1987;11(2):197-9. doi: 10.1016/0145-2126(87)90026-9.
Natural killer (NK) activity was measured in the peripheral blood of a family with Fanconi's anemia (FA) and compared to normal controls. One of two children with FA, and 6 of 11 family members had reduced NK activity (less than 30% with an E:T ratio of 25:1) compared to none of 40 controls (p less than 0.001). On retesting 5 of 8 family members and both children with FA had reduced endogenous NK activity compared to 0 of 5 controls (p less than 0.02). The number of NK cells determined by Leu 11b antibody was not reduced in any of the family members. Augmentation with interleukin-2 (IL-2) and alpha interferon (IFN) in those with low endogenous activity was variable. Three demonstrated no response to the 2 immunomodulators, while the 4 others increased to low normal levels. We conclude that some patients with FA and their apparently healthy relatives have reduced NK activity, which appears to be secondary to an intrinsic cell defect.
对一个患有范可尼贫血(FA)的家族的外周血进行自然杀伤(NK)活性检测,并与正常对照组进行比较。两个患有FA的孩子中的一个,以及11名家族成员中的6名,其NK活性降低(在E:T比例为25:1时低于30%),而40名对照组中无一例降低(p<0.001)。再次检测时,8名家族成员中的5名以及两名患有FA的孩子的内源性NK活性降低,而5名对照组中无一例降低(p<0.02)。通过Leu 11b抗体测定的NK细胞数量在任何家族成员中均未减少。内源性活性低的患者使用白细胞介素-2(IL-2)和α干扰素(IFN)进行增强治疗的效果各不相同。3例对这两种免疫调节剂无反应,而另外4例则升至低正常水平。我们得出结论,一些FA患者及其表面健康的亲属的NK活性降低,这似乎是由内在细胞缺陷所致。