Ferguson A C
J Pediatr. 1978 Jul;93(1):52-6. doi: 10.1016/s0022-3476(78)80599-x.
Cellular immunity was studied in 17 newborn infants, in eight children aged 1 to 5 years with intrauterine growth retardation, and in age-matched control subjects. At birth T and B peripheral blood lymphocytes were decreased, and delayed cutaneous hypersensitivity to phytohemagglutinin was diminished. In vitro PHA-induced lymphocyte proliferation was similar to that in control subjects but was greater than in healthy adults. In later childhood the numbers of T lymphocytes were normal, but their proliferative capacity was significantly reduced and cutaneous hypersensitivity was minimal or absent. Prolonged impairment of cellular immunity in these children may explain their increased susceptibility to infection and inadequate response to immunization, and predispose to the development of allergic, autoimmune, and neoplastic disease.
对17名新生儿、8名年龄在1至5岁的宫内生长迟缓儿童以及年龄匹配的对照受试者进行了细胞免疫研究。出生时,外周血T和B淋巴细胞减少,对植物血凝素的迟发型皮肤超敏反应减弱。体外PHA诱导的淋巴细胞增殖与对照受试者相似,但高于健康成年人。在儿童后期,T淋巴细胞数量正常,但其增殖能力显著降低,皮肤超敏反应轻微或不存在。这些儿童细胞免疫的长期损害可能解释了他们对感染易感性增加、对免疫接种反应不足,以及易患过敏性、自身免疫性和肿瘤性疾病的原因。