Donnelly J P
Department of Haematology, University Hospital Nijmegen, The Netherlands.
J Antimicrob Chemother. 1995 Oct;36 Suppl B:59-72. doi: 10.1093/jac/36.suppl_b.59.
Bacterial complications develop mainly after transplantation during the period before engraftment takes place. Wound infections, urinary tract infection and pneumonia are the commonest complications of solid organ transplantation and generally involve Gram-negative bacilli and Staphylococcus aureus. However, Gram-positive cocci will predominate when selective oral antimicrobial prophylaxis is given as is frequently the case in bone marrow transplant recipients. Oromucositis, induced by total body irradiation or anthracyclines, result in more bacteraemia due to oral viridans streptococci. The use of central intravenous catheters leads to an increase in bacteraemia and infection due to coagulase-negative staphylococci. Patients requiring intensive care are also at risk of nosocomial infections including legionellosis. Once engraftment has occurred, there is much less risk of bacterial infection but patients remain vulnerable to the intracellular pathogens Listeria monocytogenes, non-typhoid salmonellae, Norcardia spp. and mycobacteria for as long as they require immunosuppression. Any rejection crisis must be treated aggressively with high-dose steroids or other agents which further undermine an already fragile immunity. In bone marrow transplant recipients, graft versus host disease and its treatment exerts a more profound effect on immunity and often coincides with cytomegalovirus infection which compromises the patient even further. Such patients are again at risk of infection with the same range of pathogens encountered during neutropenia since the oral mucosa, gut and catheter, if one is present, provide the same portals of entry. Immunosuppressive therapy, in some centres, is discontinued once the risk of graft versus host disease is reduced, although the reconstitution of the immune system is a lengthy process and there is a continued deficiency of IgG which renders patients unable to opsonise the encapsulated bacteria Streptococcus pneumonia and Haemophilus influenzae. In contrast to bone marrow transplant recipients, those with a solid organ transplant require life-long immunosuppression and so remain susceptible to infections with intracellular pathogens and, even with minimal immunosuppression, there will always be the risk that common bacteria will cause infection in unusual places and that uncommon organisms will be involved in apparently straightforward infections.
细菌并发症主要发生在移植后植入前的这段时间。伤口感染、尿路感染和肺炎是实体器官移植最常见的并发症,通常涉及革兰氏阴性杆菌和金黄色葡萄球菌。然而,在骨髓移植受者中,经常进行选择性口服抗菌预防时,革兰氏阳性球菌将占主导地位。全身照射或蒽环类药物引起的口腔黏膜炎,会导致更多由口腔草绿色链球菌引起的菌血症。中心静脉导管的使用会导致凝固酶阴性葡萄球菌引起的菌血症和感染增加。需要重症监护的患者也有医院感染的风险,包括军团病。一旦发生植入,细菌感染的风险就会大大降低,但只要患者需要免疫抑制,他们仍然易受细胞内病原体单核细胞增生李斯特菌、非伤寒沙门氏菌、诺卡氏菌属和分枝杆菌的感染。任何排斥危机都必须用大剂量类固醇或其他药物积极治疗,这会进一步削弱本已脆弱的免疫力。在骨髓移植受者中,移植物抗宿主病及其治疗对免疫力有更深远的影响,并且常常与巨细胞病毒感染同时发生,这会使患者的情况更加糟糕。这类患者再次面临与中性粒细胞减少期间遇到的相同病原体感染的风险,因为口腔黏膜、肠道和导管(如果存在)提供了相同的入口途径。在一些中心,一旦移植物抗宿主病的风险降低,免疫抑制治疗就会停止,尽管免疫系统的重建是一个漫长的过程,并且存在持续的IgG缺乏,这使得患者无法调理肺炎链球菌和流感嗜血杆菌等包膜细菌。与骨髓移植受者不同,实体器官移植受者需要终身免疫抑制,因此仍然易受细胞内病原体感染,而且即使免疫抑制程度最低,常见细菌也总是有可能在不寻常的部位引起感染,不常见的病原体也可能参与明显简单的感染。