Schneider H G, Rutherford D, Kotsimbos T
Clinical Biochemistry Unit, Alfred Pathology Service, Commercial Road, Victoria 3181, Prahran, Australia.
Clin Chim Acta. 2001 Nov;313(1-2):221-9. doi: 10.1016/s0009-8981(01)00676-3.
Laboratory services for the support of heart and lung transplantation in Australia have adapted to the special needs of the clinicians looking after the heart and lung transplantation patients.
Pre-transplantation standardized tests encompassing a wide variety of different parameters are carried out both to establish the suitability of patients for a transplant and to maximize the chance of success following this procedure. Potential solid organ recipients routinely have blood samples sent to a number of centers Australia-wide so that human leukocyte antigen (HLA) presensitization can be checked for at the time a donor becomes available in any state in Australia. Although prospective HLA matching is not performed for thoracic organ transplant recipients, pre-existing antibodies to donor HLA antigens are a contra-indication to transplantation. Following transplantation, the predominant roles of the laboratory are in the monitoring of immunosuppressive drug levels, in the detection of allograft rejection, and in the detection of bacterial infection or viral reactivation. While a number of markers have been proposed in the detection of rejection, we currently rely on interpretation of the histological analysis of biopsies. The treatment with immune suppressive agents, in particular cyclosporin A, has made organ transplantation from non-HLA identical donors possible. As cyclosporin A and other immune suppressive drugs have significant side effects, their concentrations need to be carefully followed to guarantee sufficient immune suppression while avoiding renal failure and other complications including excessive immunosuppression and infectious disease risk. Recently, the role of viral reactivation with the human cytomegalovirus (HCMV) has attained more prominence. HCMV is a potential pathogen in up to 90% of thoracic organ transplant recipients and in the pre-gancyclovir era, it was a major cause of morbidity and mortality in at-risk lung transplant recipients. New PCR-based assays that measure the viral load levels of HCMV allow earlier intervention and more appropriate treatment strategies to prevent the HCMV disease syndromes and optimize the HCMV prophylaxis strategy.
Diagnostic pathology testing to support heart and lung transplantation is a combination of routine testing and specialized testing. Depending on the time-critical nature of the tests, this testing has to be done on site or in more centralized testing facilities. Further developments in the laboratory support of heart and lung transplantation will hopefully continue to improve both the short- and long-term outcomes of thoracic organ transplant recipients.
澳大利亚为支持心脏和肺移植提供的实验室服务已适应了照顾心脏和肺移植患者的临床医生的特殊需求。
移植前进行涵盖多种不同参数的标准化测试,以确定患者是否适合移植,并使该手术后的成功几率最大化。潜在的实体器官接受者通常会将血样送往澳大利亚各地的多个中心,以便在澳大利亚任何一个州有供体可用时检查人类白细胞抗原(HLA)致敏情况。虽然不对胸器官移植受者进行前瞻性HLA配型,但预先存在的针对供体HLA抗原的抗体是移植的禁忌证。移植后,实验室的主要作用是监测免疫抑制药物水平、检测同种异体移植排斥反应以及检测细菌感染或病毒再激活。虽然在检测排斥反应方面已经提出了一些标志物,但我们目前依靠活检组织学分析的解读。免疫抑制剂的使用,特别是环孢素A,使得从非HLA匹配的供体进行器官移植成为可能。由于环孢素A和其他免疫抑制药物有显著的副作用,需要仔细监测它们的浓度,以确保足够的免疫抑制,同时避免肾衰竭和其他并发症,包括过度免疫抑制和感染性疾病风险。最近,人类巨细胞病毒(HCMV)病毒再激活的作用变得更加突出。HCMV是高达90%的胸器官移植受者中的潜在病原体,在使用更昔洛韦之前的时代,它是高危肺移植受者发病和死亡的主要原因。基于PCR的新检测方法可测量HCMV的病毒载量水平,从而能更早地进行干预并采取更合适的治疗策略,以预防HCMV疾病综合征并优化HCMV预防策略。
支持心脏和肺移植的诊断病理学检测是常规检测和专门检测的结合。根据检测的时间紧迫性,这种检测必须在现场或更集中的检测设施中进行。心脏和肺移植实验室支持方面的进一步发展有望继续改善胸器官移植受者的短期和长期预后。