DeArmond B
Department of Immunology and Antiviral Therapy II, Syntex Research, Palo Alto, California 94303.
J Acquir Immune Defic Syndr (1988). 1991;4 Suppl 1:S53-6.
Ganciclovir currently is the only agent approved for use in the treatment of cytomegalovirus (CMV) retinitis in immunocompromised patients, including those with the acquired immune deficiency syndrome (AIDS). Its effect against CMV in vitro and in vivo suggests its usefulness in other types of CMV infection as well. Investigations of the use of this agent in the treatment of AIDS patients with CMV gastrointestinal disease and in the treatment or prevention of CMV disease in transplant recipients are ongoing. In other studies, issues important to the management of patients receiving ganciclovir therapy are being addressed. Particular objectives include characterizing the scope of ganciclovir resistance in CMV, detailing the prospects for the tolerance of coadministered ganciclovir and zidovudine, and determining the plausibility of enhancing drug delivery through the concomitant use of recombinant human granulocyte-macrophage colony-stimulating factor and through oral administration of the agent.
更昔洛韦目前是唯一被批准用于治疗免疫功能低下患者,包括获得性免疫缺陷综合征(艾滋病)患者巨细胞病毒(CMV)视网膜炎的药物。它在体外和体内对CMV的作用表明它在其他类型的CMV感染中也有用。关于该药物用于治疗患有CMV胃肠道疾病的艾滋病患者以及用于治疗或预防移植受者CMV疾病的研究正在进行中。在其他研究中,正在探讨对接受更昔洛韦治疗的患者管理至关重要的问题。具体目标包括确定CMV中更昔洛韦耐药性的范围,详细说明同时使用更昔洛韦和齐多夫定的耐受性前景,以及确定通过同时使用重组人粒细胞-巨噬细胞集落刺激因子和口服该药物来增强药物递送的可行性。