Styczynski Jan
Department of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University in Toruń, Bydgoszcz, Poland.
Infect Dis Ther. 2018 Mar;7(1):1-16. doi: 10.1007/s40121-017-0180-z. Epub 2017 Dec 4.
Cytomegalovirus (CMV) is an agent of global infection, and its acquisition in a population is characterized by an age-dependent rise in seropositivity. After primary infection, CMV remains in the host cells in latent form, and it can reactivate in the case of immune suppression. The risk of CMV recurrence is dependent on the level of incompetency of the immune system, manifested as an impairment of T-cell immunity, including the presence and function of CMV-specific cytotoxic T lymphocytes. This article presents data on the incidence of CMV recurrence in groups of immunocompromised patients, including allogeneic hematopoietic stem cell transplantation (HSCT) patients and other groups of patients, based on a summary of reported data. The median rate of CMV recurrence in HSCT recipients was estimated as 37% after allogeneic transplant and 12% after autologous transplant, 5% in patients with nontransplant hematological malignancies, 14% in recipients of anti-CD52 therapy, 30% in solid organ transplant recipients, 21% in patients with primary immunodeficiencies, 20% during active replication in HIV-positive patients and 3.3% during antiretroviral therapy, 7% in patients with chronic kidney disease, 0.6% in patients with congenital infection, and 0.6% in neonates with primary infection. The highest risk of CMV recurrence and CMV disease is reported for HSCT CMV-seropositive recipients, regardless of donor serostatus. The odds ratio (OR) for CMV recurrence is higher for recipient-positive versus recipient-negative CMV serostatus transplants (OR 8.0), donor-negative/recipient-positive versus donor-positive/recipient-positive CMV serostatus transplants (OR 1.2), unrelated/mismatched versus matched-family donor transplants (OR 1.6), and acute graft-versus-host-disease versus other diseases (OR 3.2). Other risk factors have minor significance.
巨细胞病毒(CMV)是一种全球感染性病原体,其在人群中的感染特征是血清阳性率随年龄增长而升高。初次感染后,CMV以潜伏形式存在于宿主细胞中,在免疫抑制情况下可重新激活。CMV复发风险取决于免疫系统功能不全的程度,表现为T细胞免疫受损,包括CMV特异性细胞毒性T淋巴细胞的存在和功能。本文基于已报道数据的总结,呈现了免疫功能低下患者群体中CMV复发率的数据,包括异基因造血干细胞移植(HSCT)患者及其他患者群体。HSCT受者中CMV复发的中位率估计为:异基因移植后为37%,自体移植后为12%;非移植血液系统恶性肿瘤患者为5%;抗CD52治疗受者为14%;实体器官移植受者为30%;原发性免疫缺陷患者为21%;HIV阳性患者病毒活跃复制期为20%,抗逆转录病毒治疗期间为3.3%;慢性肾病患者为7%;先天性感染患者为0.6%;原发性感染新生儿为0.6%。无论供体血清学状态如何,HSCT CMV血清阳性受者的CMV复发和CMV疾病风险最高。CMV血清阳性受者与血清阴性受者移植相比,CMV复发的比值比(OR)更高(OR 8.0);供体阴性/受者阳性与供体阳性/受者阳性CMV血清学状态移植相比(OR 1.2);无关/不匹配与匹配家族供体移植相比(OR 1.6);急性移植物抗宿主病与其他疾病相比(OR 3.2)。其他风险因素意义较小。