Güngör T, Funk M, Linde R, Kynast I, Allendorf A, Lotz C, Ehrenforth S, Hofmann D, Kornhuber B, Kreuz W
Department of Haematology/Oncology, J. W. Goethe University, Frankfurt am Main, Germany.
Eur J Pediatr. 1993 Aug;152(8):650-4. doi: 10.1007/BF01955241.
From 1988 to 1991 the long-term efficacy of a combined therapy with a polyvalent immunoglobulin/cytomegalovirus (CMV) hyperimmunoglobulin, oral low dose zidovudine, oral cotrimoxazole or inhaled pentamidine was investigated in three groups of human immunodeficiency virus (HIV)-infected children. Group 1A consisted of three perinatally infected children with a CD4 cell decrease of > 400 cells/microliters per year. Group 1B were 17 perinatally infected children with a CD4 cell decrease of < 400 cells/microliters per year. Group 2 comprised eight haemophilic children infected by clotting factors. Despite combined therapy none of group 1A survived longer than 12 months showing a rapid loss of CD4 cell counts, progressive encephalopathy, wasting syndrome and severe bacterial, fungal and CMV reactivation. Under pure intravenous immunoglobulin (IVIG) therapy severe bacterial infections were seen in 1 of 12 children in group 1B. The majority of these patients showed increases or stabilisation of length and weight percentiles. In this group low dose zidovudine therapy was of benefit in HIV-associated neurological symptoms. Nevertheless combined therapy could not prevent further deterioration of CD4 cell counts. In group 2 severe bacterial infections were not seen under IVIG therapy. In this group a temporary increase (6 months) of CD4 cell counts under IVIG/zidovudine combined therapy occurred. Pneumocystis carinii pneumonia (PCP) prophylaxis with oral cotrimoxazole or inhaled pentamidine successfully prevented PCP in all three groups. Under CMV hyperimmunoglobulin (n = 22), ten out of ten patients did not acquire primary CMV infection, whereas CMV reactivations mainly located in the CNS could not be prevented in 5 of 12 patients.(ABSTRACT TRUNCATED AT 250 WORDS)
1988年至1991年,在三组感染人类免疫缺陷病毒(HIV)的儿童中研究了多价免疫球蛋白/巨细胞病毒(CMV)高免疫球蛋白、口服低剂量齐多夫定、口服复方新诺明或吸入喷他脒联合治疗的长期疗效。1A组由3名围产期感染儿童组成,其CD4细胞每年减少>400个/微升。1B组是17名围产期感染儿童,其CD4细胞每年减少<400个/微升。2组包括8名因凝血因子感染的血友病儿童。尽管进行了联合治疗,1A组中没有一名患者存活超过12个月,表现为CD4细胞计数迅速下降、进行性脑病、消瘦综合征以及严重的细菌、真菌和CMV再激活。在单纯静脉注射免疫球蛋白(IVIG)治疗下,1B组12名儿童中有1名出现严重细菌感染。这些患者中的大多数身长和体重百分位数增加或稳定。在该组中,低剂量齐多夫定治疗对HIV相关神经症状有益。然而,联合治疗无法阻止CD4细胞计数的进一步恶化。在2组中,IVIG治疗下未出现严重细菌感染。在该组中,IVIG/齐多夫定联合治疗使CD4细胞计数暂时增加(6个月)。口服复方新诺明或吸入喷他脒预防卡氏肺孢子虫肺炎(PCP)在所有三组中均成功预防了PCP。在CMV高免疫球蛋白治疗下(n = 22),10名患者中有10名未发生原发性CMV感染,而12名患者中有5名无法预防主要位于中枢神经系统的CMV再激活。(摘要截短于250字)