Human cytomegalovirus seroprevalence and titres in solid organ transplant recipients and transplant donors in Seoul, South Korea

被引:10
|
作者
La, Yeonju [1 ]
Kwon, Da Eun [1 ]
Yoo, Seul Gi [1 ]
Lee, Kyoung Hwa [1 ]
Han, Sang Hoon [1 ]
Song, Yong Goo [1 ]
机构
[1] Yonsei Univ, Coll Med, Div Infect Dis, Dept Internal Med, Seoul, South Korea
关键词
Age; Human cytomegalovirus; Seroprevalence; Solid organ transplantation; INFECTION; RISK; TRANSMISSION; POPULATION; MANAGEMENT; DISEASE; LATENCY; PREDICT; AGE;
D O I
10.1186/s12879-019-4607-x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background Human cytomegalovirus (HCMV) can cause poor outcomes in solid organ transplant (SOT) recipients; moreover, it is associated with cardiovascular diseases (CVD) in the general population. Accordingly, anti-HCMV immunoglobulin G (IgG) seroepidemiology may be useful in identifying the risk of post-SOT HCMV infection or disease as well as immunosenescence or CVD. However, HCMV seroprevalence and titre have not been fully evaluated with regard to age distribution or compared between SOT recipients and healthy individuals in South Korea. Methods We retrospectively retrieved all unduplicated anti-HCMV IgG results of individuals aged > 1 year evaluated between July 2006 and November 2017 at Severance Hospital in Seoul. The cohort, excluding haematopoietic stem cell transplant recipients and subjects with equivocal values, included 2184 SOT recipients and 3015 healthy transplant donors. All IgG results in the SOT recipients were measured during the pre-transplant period. Results The overall IgG seroprevalence and titres were significantly higher among SOT recipients than among healthy donors (98.7% vs. 88.6%, p < 0.001, and 64.7 +/- 44.3 vs. 49.8 +/- 20.6 arbitrary units/mL, p < 0.001, respectively). The lowest seropositive rate in the SOT group was observed in recipients aged between 11 and 15 years (70.6%). The frequency of seropositivity among adults aged >= 41 years increased to >= 90% in SOT recipients and healthy donors. Age was independently associated with higher HCMV seroprevalence (41-60 years, OR, 76.4, 95% CI, 24.5-238.9, p < 0.001; >= 61 years, OR, 4.4, 95% CI, 1.3-14.9, p < 0.001, compared to <= 40 years). The healthy donor group had an independently low HCMV seropositive rate (OR, 0.1, 95% CI, 0.1-0.2, p < 0.001). Conclusions HCMV seropositivity was the lowest among school-aged children and adolescents. IgG testing revealed an intermediate serostatus risk of post-transplant HCMV infection and disease for most adult SOT recipients in South Korea.
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