Siadak M F, Kopecky K, Sullivan K M
Fred Hutchinson Cancer Research Center, University of Washington School of Medicine, Seattle 98104.
Clin Exp Immunol. 1994 Jul;97 Suppl 1(Suppl 1):53-7.
Bone marrow transplantation renders patients immunocompetent due to the need for supralethal doses of chemoradiotherapy prior to infusion of the donor stem cells. Multiple immunological deficiencies are seen and patients are at high risk of developing a variety of infections. This period of immunological incompetence usually lasts from 6 to 12 months. In some subsets of patients [those with chronic graft-versus-host disease (GVHD); recipients of unrelated transplants; increasing patient age] persistent T and B cell abnormalities may be seen for years, despite normal serum immunoglobulin levels. This review summarizes a number of trials of intravenous immune globulin (IVIG) therapy to prevent infection following bone marrow transplantation. IVIG has shown benefit in reducing septicaemia, interstitial pneumonia, fatal cytomegalovirus (CMV) disease, acute GVHD and transplant-related mortality in adult recipients of related marrow transplants. Further investigation into dose, schedule and duration of IVIG prophylaxis needs to be conducted.
由于在输注供体干细胞之前需要进行超致死剂量的放化疗,骨髓移植使患者具备免疫能力。患者会出现多种免疫缺陷,并有发生各种感染的高风险。这段免疫无反应期通常持续6至12个月。在某些患者亚组中(患有慢性移植物抗宿主病[GVHD]的患者;无关供体移植的受者;患者年龄增加),尽管血清免疫球蛋白水平正常,但可能多年持续存在T和B细胞异常。本综述总结了多项静脉注射免疫球蛋白(IVIG)治疗以预防骨髓移植后感染的试验。IVIG已显示出在降低相关骨髓移植成年受者的败血症、间质性肺炎、致命性巨细胞病毒(CMV)疾病、急性GVHD和移植相关死亡率方面的益处。需要对IVIG预防的剂量、方案和持续时间进行进一步研究。