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齐多夫定治疗获得性免疫缺陷综合征儿童

Zidovudine therapy in children with acquired immunodeficiency syndrome.

作者信息

Blanche S, Caniglia M, Fischer A, Rouzioux C, Burgard M, Tardieu M, Duhamel G, Griscelli C

机构信息

Département de Pédiatrie, Hôpital Necker, Paris, France.

出版信息

Am J Med. 1988 Aug 29;85(2A):203-7.

PMID:3165604
Abstract

Eight children with acquired immunodeficiency syndrome (AIDS), aged four months to 12 years, were treated with zidovudine (azidothymidine) 100 mg/m2 intravenously every six hours for 14 days, followed by oral zidovudine at the same dose for a total of six months. Of the eight, six were infected at birth and two were contaminated by blood transfusion at ages eight and nine years, respectively; seven of the eight showed specific neurologic impairment consisting of encephalopathy (six children) and myelopathy (one child). In two children, a dramatic improvement of clinical status occurred, including neurologic progress in one; in three, the improvement was dissociate or transient and in the other three, no modification was observed. A marked increase of total lymphocyte and CD4(+) cell counts occurred in four children but was transient without modification of in vitro antigen-induced lymphocyte proliferation; p24 human immunodeficiency virus serum antigens were detected in seven of eight children, then transiently disappeared in all children during intravenous therapy but reappeared progressively during the oral regimen in all but one. Progressive modification of human immunodeficiency virus serology was noted in five children, mainly characterized by the finding of anti-core antibodies. The hematologic toxicity of zidovudine was comparable with that observed in adults. These preliminary results support the need for further studies in order to delineate the optimal regimen of zidovudine in children with AIDS.

摘要

八名患有获得性免疫缺陷综合征(艾滋病)的儿童,年龄从4个月至12岁,接受了齐多夫定(叠氮胸苷)治疗,剂量为每平方米体表面积100毫克,静脉注射,每6小时一次,共14天,随后口服相同剂量的齐多夫定,为期6个月。这八名儿童中,六名在出生时即被感染,另外两名分别在8岁和9岁时因输血而被感染;八名儿童中有七名表现出特定的神经功能损害,包括脑病(六名儿童)和脊髓病(一名儿童)。两名儿童的临床状况显著改善,其中一名在神经功能方面取得进展;三名儿童的改善是分离性的或短暂的,另外三名儿童则未观察到变化。四名儿童的总淋巴细胞和CD4(+)细胞计数显著增加,但为短暂性,体外抗原诱导的淋巴细胞增殖未改变;八名儿童中有七名检测到p24人类免疫缺陷病毒血清抗原,在静脉治疗期间所有儿童的该抗原均短暂消失,但除一名儿童外,在口服治疗期间又逐渐重新出现。五名儿童的人类免疫缺陷病毒血清学出现渐进性变化,主要表现为抗核心抗体的出现。齐多夫定对血液系统的毒性与在成人中观察到的情况相当。这些初步结果支持需要进一步研究,以确定齐多夫定在艾滋病儿童中的最佳治疗方案。

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