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艾滋病患者中由细小病毒B19引起的慢性纯红细胞再生障碍性贫血:静脉注射免疫球蛋白的应用——8例报告

Chronic pure red cell aplasia caused by parvovirus B19 in AIDS: use of intravenous immunoglobulin--a report of eight patients.

作者信息

Koduri P R, Kumapley R, Valladares J, Teter C

机构信息

Department of Medicine, Cook County Hospital, Chicago, Illinois, USA.

出版信息

Am J Hematol. 1999 May;61(1):16-20. doi: 10.1002/(sici)1096-8652(199905)61:1<16::aid-ajh4>3.0.co;2-y.

Abstract

The optimal management of chronic pure red cell aplasia caused by parvovirus B19 (B19-PRCA) in patients with AIDS is unclear. Our purpose was to determine the effects of intravenous immunoglobulin (IVIg) in the treatment of B19-PRCA in patients with AIDS. The patients were eight adults with AIDS admitted during the period 1993-1997. A diagnosis of B19-PRCA was made if all the following criteria were met: 1. Bone marrow biopsy finding of pure red cell aplasia; 2. Detection of parvovirus B19 DNA in serum; and 3. No alternative explanation for PRCA. Initial (induction) therapy was with IVIg 1 g/kg daily for 1-2 days. Relapses were treated with IVIg 1 g/kg for 2 days. Maintenance therapy with IVIg 0.4-1.0 g/kg q 4 weeks was given to those patients who developed a second or subsequent relapse. The patients were followed for a mean of 27 months (range 8-38 months). All patients responded to initial therapy with IVIg. Six patients with CD4 counts < 80 cells/mm3 relapsed. The response was short lived in two patients with a CD4 count < 80 cells/mm3 who were given a single infusion of IVIg 1 g/kg as initial therapy. Four patients were given regular maintenance IVIg therapy following a second or subsequent relapse and remain in remission. Two patients whose CD4 counts were > 300 cells/mm3 remain in continuous unmaintained remission from B19-PRCA for over 8 and 11 months, respectively, following induction therapy with IVIg. AIDS patients with B19-PRCA respond well to therapy with IVIg 2 g/kg given over 2 days. Most patients with CD4 counts of < or = 80 cells/mm3 suffer relapse within six months necessitating retreatment with IVIg; maintenance therapy with IVIg 0.4 g/kg q 4 weeks is effective in preventing relapse of B19-PRCA, and may be cost effective. Routine maintenance therapy is probably not indicated in patients with CD4 counts over 300 cells/mm3. Prospective studies are needed to confirm these findings.

摘要

艾滋病患者中由细小病毒B19(B19-PRCA)引起的慢性纯红细胞再生障碍性贫血的最佳治疗方法尚不清楚。我们的目的是确定静脉注射免疫球蛋白(IVIg)对艾滋病患者B19-PRCA的治疗效果。研究对象为1993年至1997年期间收治的8例成年艾滋病患者。若满足以下所有标准,则诊断为B19-PRCA:1. 骨髓活检发现纯红细胞再生障碍;2. 血清中检测到细小病毒B19 DNA;3. 无PRCA的其他解释。初始(诱导)治疗为每日静脉注射IVIg 1 g/kg,持续1 - 2天。复发时给予IVIg 1 g/kg治疗2天。对于出现第二次或后续复发的患者,给予IVIg 0.4 - 1.0 g/kg每4周一次的维持治疗。对患者平均随访27个月(范围8 - 38个月)。所有患者对IVIg初始治疗均有反应。6例CD4细胞计数<80个/mm³的患者复发。2例CD4细胞计数<80个/mm³且初始治疗仅单次输注IVIg 1 g/kg的患者,反应持续时间较短。4例患者在第二次或后续复发后接受常规IVIg维持治疗,目前仍处于缓解状态。2例CD4细胞计数>300个/mm³的患者,在接受IVIg诱导治疗后,分别持续8个月和11个月以上未接受维持治疗而处于持续缓解状态。艾滋病合并B19-PRCA患者对2天内给予2 g/kg的IVIg治疗反应良好。大多数CD4细胞计数≤80个/mm³的患者在6个月内复发,需要再次接受IVIg治疗;IVIg 0.4 g/kg每4周一次的维持治疗可有效预防B19-PRCA复发,且可能具有成本效益。CD4细胞计数超过300个/mm³的患者可能无需常规维持治疗。需要进行前瞻性研究以证实这些发现。

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