Zaia J A
Int J Cell Cloning. 1986;4 Suppl 1:135-54. doi: 10.1002/stem.5530040715.
Human cytomegalovirus (HCMV) infection remains the most common infectious cause of morbidity after bone marrow transplantation (BMT). In a prospective study of 127 BMT recipients who received blood cultures for HCMV between days 28 to 105 after marrow grafting, HCMV viremia occurred in 68 patients (53.4%). Twenty patients (15.7%) had one or two positive cultures, and 48 (37.7%) had greater than or equal to three positive cultures. Fifty-nine patients (46.4%) had no viremia. HCMV-associated interstitial pneumonia (HCMV-IP) occurred in one-third of the viremic patients. Quantitative measurements of infectious HCMV or of HCMV DNA in lung tissue were made to determine whether HCMV replication correlated with clinical disease. Using DNA probes, viral DNA was measured by dot-blot hybridization, and this correlated with infectious HCMV. However, neither HCMV DNA nor HCMV viral titer correlated with time from the onset of pneumonia to death. The hypothesis is presented that HCMV-IP is caused by immunologic events induced after HCMV infection. In this model HCMV alterations in recipient cell surfaces induce donor alloreactivity to minor histocompatibility differences and lead to the subsequent pneumonitis which we term HCMV-IP. This model suggests that prevention of HCMV-IP will require early use of antiviral therapy or late use of immune response modification.
人巨细胞病毒(HCMV)感染仍然是骨髓移植(BMT)后发病的最常见感染原因。在一项对127名骨髓移植受者的前瞻性研究中,这些受者在骨髓移植后第28天至105天接受了HCMV血培养,68名患者(53.4%)出现了HCMV病毒血症。20名患者(15.7%)有一两次培养结果呈阳性,48名患者(37.7%)有三次或三次以上培养结果呈阳性。59名患者(46.4%)没有病毒血症。三分之一的病毒血症患者发生了HCMV相关性间质性肺炎(HCMV-IP)。对肺组织中感染性HCMV或HCMV DNA进行定量测量,以确定HCMV复制是否与临床疾病相关。使用DNA探针,通过斑点杂交法测量病毒DNA,其与感染性HCMV相关。然而,HCMV DNA和HCMV病毒滴度均与肺炎发病至死亡的时间无关。本文提出假说,即HCMV-IP是由HCMV感染后诱导的免疫事件引起的。在这个模型中,受体细胞表面的HCMV改变诱导供体对次要组织相容性差异产生同种异体反应性,并导致随后的肺炎,我们称之为HCMV-IP。该模型表明,预防HCMV-IP将需要早期使用抗病毒治疗或晚期使用免疫反应调节剂。