Mohammed G S, Taylor C E, Dickinson A M, Craft A W, Kernahan J, Reid M M, Proctor S J, Toms G L
Br J Haematol. 1986 Dec;64(4):789-98. doi: 10.1111/j.1365-2141.1986.tb02241.x.
Human peripheral blood mononuclear cell cultures (PBMC) stimulated with Sendai virus or K562 cells produce a mixture of interferons. Temperature and pH stability characteristics and reactions with monospecific antibodies indicate that PBMC cultures from adults produce interferons alpha and gamma in approximately equal proportions. PBMC cultures from children produce lower levels of interferons with a higher proportion of type alpha. The ability of PBMC cultures from children with acute lymphoblastic leukaemia (ALL) to produce interferon was determined. Little or no gamma interferon was induced by either Sendai virus or K562 cells. Cultures from some children with ALL produced alpha interferon but mean levels were significantly lower than from normal children. A group of older children with ALL who had completed their course of therapy and were off treatment produced levels of interferon indistinguishable from those of normal children. This in vitro deficit, possibly induced by chemotherapy, may reflect an in vivo deficit and may contribute to the impaired handling of viruses seen in children being treated for ALL.
用仙台病毒或K562细胞刺激的人外周血单个核细胞培养物(PBMC)可产生多种干扰素。温度和pH稳定性特征以及与单特异性抗体的反应表明,来自成年人的PBMC培养物产生的α干扰素和γ干扰素比例大致相等。来自儿童的PBMC培养物产生的干扰素水平较低,其中α型比例较高。测定了急性淋巴细胞白血病(ALL)患儿的PBMC培养物产生干扰素的能力。仙台病毒或K562细胞几乎不诱导或不诱导γ干扰素产生。一些ALL患儿的培养物产生α干扰素,但平均水平明显低于正常儿童。一组完成治疗疗程且已停止治疗的大龄ALL患儿产生的干扰素水平与正常儿童无异。这种可能由化疗引起的体外缺陷可能反映了体内缺陷,并且可能导致ALL患儿在处理病毒时出现障碍。