Lortholary O, Dupont B
Service de Médecine Interne, Hôpital Avicenne, Université Paris-Nord, Bobigny, France.
Clin Microbiol Rev. 1997 Jul;10(3):477-504. doi: 10.1128/CMR.10.3.477.
Fungal infections represent a major source of morbidity and mortality in patients with almost all types of immunodeficiencies. These infections may be nosocomial (aspergillosis) or community acquired (cryptococcosis), or both (candidiasis). Endemic mycoses such as histoplasmosis, coccidioidomycosis, and penicilliosis may infect many immunocompromised hosts in some geographic areas and thereby create major public health problems. With the wide availability of oral azoles, antifungal prophylactic strategies have been extensively developed. However, only a few well-designed studies involving strict criteria have been performed, mostly in patients with hematological malignancies or AIDS. In these situations, the best dose and duration of administration of the antifungal drug often remain to be determined. In high-risk neutropenic or bone marrow transplant patients, fluconazole is effective for the prevention of superficial and/or systemic candidal infections but is not always able to prolong overall survival and potentially selects less susceptible or resistant Candida spp. Primary prophylaxis against aspergillosis remains investigative. At present, no standard general recommendation for primary antifungal prophylaxis can be proposed for AIDS patients or transplant recipients. However, for persistently immunocompromised patients who previously experienced a noncandidal systemic fungal infection, prolonged suppressive antifungal therapy is often indicated to prevent a relapse. Better strategies for controlling immune deficiencies should also help to avoid some potentially life-threatening deep mycoses. When prescribing antifungal prophylaxis, physicians should be aware of the potential emergence of resistant strains, drug-drug interactions, and the cost. Well-designed, randomized, multicenter clinical trials in high-risk immunocompromised hosts are urgently needed to better define how to prevent severe invasive mycoses.
真菌感染是几乎所有类型免疫缺陷患者发病和死亡的主要原因。这些感染可能是医院获得性(曲霉病)或社区获得性(隐球菌病),或两者皆有(念珠菌病)。地方性真菌病,如组织胞浆菌病、球孢子菌病和青霉病,在某些地理区域可能感染许多免疫功能低下的宿主,从而造成重大的公共卫生问题。随着口服唑类药物的广泛应用,抗真菌预防策略得到了广泛发展。然而,仅进行了少数涉及严格标准的精心设计的研究,主要针对血液系统恶性肿瘤患者或艾滋病患者。在这些情况下,抗真菌药物的最佳剂量和给药持续时间往往仍有待确定。在高危中性粒细胞减少或骨髓移植患者中,氟康唑对预防浅表和/或系统性念珠菌感染有效,但并不总能延长总生存期,且可能会选择出较不易感或耐药的念珠菌属。针对曲霉病的一级预防仍在研究中。目前,无法为艾滋病患者或移植受者提出标准的抗真菌一级预防通用建议。然而,对于先前经历过非念珠菌系统性真菌感染的持续免疫功能低下患者,通常需要延长抗真菌抑制治疗以预防复发。更好地控制免疫缺陷的策略也应有助于避免一些潜在的危及生命的深部真菌病。在开具抗真菌预防药物处方时,医生应意识到耐药菌株的潜在出现、药物相互作用以及成本问题。迫切需要在高危免疫功能低下宿主中开展精心设计、随机、多中心的临床试验,以更好地确定如何预防严重的侵袭性真菌病。