Kuzushima K, Yamamoto M, Kimura H, Ando Y, Kudo T, Tsuge I, Morishima T
Department of Paediatrics, Nagoya University, School of Medicine, Japan.
Clin Exp Immunol. 1996 Feb;103(2):192-8. doi: 10.1046/j.1365-2249.1996.d01-619.x.
We describe an experience of a specific immune transfer treatment in a patient with chronic active EBV infection. The patient had low anti-EBV T cell-mediated cytotoxic activity in his peripheral blood mononuclear cells (PBMC), which may have been the primary cause of the disease. An EBV-specific cytotoxic T lymphocyte (CTL) line was established from PBMC obtained from the patient's sister whose human leucocyte antigens (HLA) are identical to patient's. The patient received three courses of intravenously administered CTL at 3-week intervals. The number of the cells was increased with each course of treatment. After infusion of the T cell line, anti-EBV CTL activity was detected in the patient's PBMC. CTL activity increased markedly after the second course of immune transfer therapy. The amount of EBV DNA in the patient's plasma showed transient but repeated decreases. Serum levels of tumour necrosis factor-alpha (TNF-alpha), which had elevated before treatment, began to decrease after initiation of treatment. No adverse effects were directly associated with CTL infusions. Despite having previously received a pneumococcal vaccine and prophylactic antibiotics, the patient died of infection caused by Streptococcus pneumoniae bacteraemia 27 days after the third infusion. Although the long-term efficacy and safety of this therapy remains to be established, our findings suggest that adoptive transfer of CTL specific for EBV obtained from an HLA-matched donor might be a promising treatment for patients with chronic active EBV infection.
我们描述了一名慢性活动性EB病毒感染患者接受特异性免疫转移治疗的经历。该患者外周血单个核细胞(PBMC)中抗EB病毒T细胞介导的细胞毒性活性较低,这可能是该疾病的主要原因。从患者姐姐的PBMC中建立了EB病毒特异性细胞毒性T淋巴细胞(CTL)系,其人类白细胞抗原(HLA)与患者相同。患者每隔3周静脉注射3个疗程的CTL。每次治疗后细胞数量均增加。输注T细胞系后,在患者的PBMC中检测到抗EB病毒CTL活性。免疫转移治疗第二个疗程后,CTL活性显著增加。患者血浆中EB病毒DNA含量出现短暂但反复下降。治疗前升高的肿瘤坏死因子-α(TNF-α)血清水平在治疗开始后开始下降。未发现与CTL输注直接相关的不良反应。尽管患者此前已接种肺炎球菌疫苗并接受预防性抗生素治疗,但在第三次输注后27天死于肺炎链球菌菌血症引起的感染。虽然这种治疗的长期疗效和安全性仍有待确定,但我们的研究结果表明,从HLA匹配供体获得的EB病毒特异性CTL的过继转移可能是慢性活动性EB病毒感染患者的一种有前景的治疗方法。