Kim Sung-Han, Lee Ho-Su, Lee Hyun-Jung, Kim Sun-Mi, Shin Sung, Park Sang-Hyoung, Kim Kyung-Jo, Kim Young-Hoon, Sung Heungsup, Lee Sang-Oh, Choi Sang-Ho, Yang Suk-Kyun, Kim Yang Soo, Woo Jun Hee, Han Duck-Jong
Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Department of Gastroenterology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Korean J Intern Med. 2017 Sep;32(5):900-909. doi: 10.3904/kjim.2015.354. Epub 2017 Aug 23.
BACKGROUND/AIMS: We evaluated the proposed clinical application of the combined interpretation of host factors and viral factors in two different cytomegalovirus (CMV) co-infection models.
We prospectively enrolled all human immunodeficiency virus non-infected patients with confirmed pneumonia (PCP) and those with suspected gastrointestinal CMV disease in a tertiary hospital. All patients underwent CMV interferon-γ releasing assay (IGRA) for CMV (T-track CMV, Lophius Biosciences). We created the 2-axis model with the CMV IGRA results as the x-axis and the results for CMV virus replication as the y-axis, and hypothesized that cases falling in the left upper quadrant (high viral load and low CMV-specific immunity) of the model would be true CMV infections. The CMV IGRA results were concealed from the attending physicians.
Of 39 patients with PCP, four (10%) were classified as combined CMV pneumonia, 13 (33%) as bystander activation, and the remaining 22 (56%) as no CMV infection. The data for all four patients with PCP and CMV pneumonia fell in the left upper quadrant of the 2-axis model. Of 24 patients with suspected gastrointestinal CMV disease, 12 (50%) were classified as gastrointestinal CMV disease and the remaining 12 (50%) as bystander activation with no gastrointestinal CMV disease. The data for 11 of the 12 patients (92%) with gastrointestinal CMV disease were located in the left upper quadrant of the 2-axis model.
Cases yielding low CMV IGRA results and high CMV viral replication appear to be true CMV infections. Further studies with large number of cases in different types of CMV disease should be proposed.
背景/目的:我们在两种不同的巨细胞病毒(CMV)合并感染模型中评估了宿主因素和病毒因素联合解读的临床应用前景。
我们前瞻性纳入了一家三级医院中所有确诊为肺孢子菌肺炎(PCP)且未感染人类免疫缺陷病毒的患者以及疑似胃肠道CMV疾病的患者。所有患者均接受了针对CMV的CMV干扰素-γ释放试验(IGRA)(T-track CMV,Lophius Biosciences公司)。我们以CMV IGRA结果为x轴、CMV病毒复制结果为y轴构建了二维模型,并假设模型左上象限(高病毒载量和低CMV特异性免疫)的病例为真正的CMV感染。CMV IGRA结果对主治医生保密。
在39例PCP患者中,4例(10%)被归类为合并CMV肺炎,13例(33%)为旁观者激活,其余22例(56%)为无CMV感染。所有4例PCP合并CMV肺炎患者的数据均落在二维模型的左上象限。在24例疑似胃肠道CMV疾病的患者中,12例(50%)被归类为胃肠道CMV疾病,其余12例(50%)为无胃肠道CMV疾病的旁观者激活。12例胃肠道CMV疾病患者中有11例(92%)的数据位于二维模型的左上象限。
CMV IGRA结果低且CMV病毒复制高的病例似乎为真正的CMV感染。应开展针对不同类型CMV疾病的大量病例的进一步研究。