Associations between early-life and in utero infections and cytomegalovirus-positive acute lymphoblastic leukemia in children

被引:2
|
作者
Gallant, Rachel E. [1 ,2 ,3 ]
Arroyo, Katti [3 ]
Metayer, Catherine [4 ]
Kang, Alice Y. [4 ]
de Smith, Adam J. [3 ]
Wiemels, Joseph L. [3 ]
机构
[1] Univ Southern Calif, Childrens Hosp Los Angeles, Los Angeles, CA 90089 USA
[2] Univ Southern Calif, Keck Sch Med, Los Angeles, CA 90089 USA
[3] Univ Southern Calif, Keck Sch Med, Ctr Genet Epidemiol, Dept Populat & Publ Hlth Sci, 1450 Biggy St,NRT 1506, Los Angeles, CA 90089 USA
[4] Univ Calif Berkeley, Sch Publ Hlth, Div Epidemiol & Biostat, Berkeley, CA 94720 USA
关键词
childhood infection; cytomegalovirus; leukemia etiology; maternal infection; pediatric acute lymphoblastic leukemia; CHILDHOOD LEUKEMIA; RISK; RESPONSES;
D O I
10.1002/ijc.34292
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Childhood infections and cytomegalovirus (CMV) are associated with pediatric acute lymphoblastic leukemia (ALL). CMV dysregulates the host immune system and alters the immune response to subsequent antigenic exposures. We suspect that this immune dysregulation contributes to increased numbers of symptomatic infections in childhood allowing for expansion of pre-leukemic clones. We explored the association between childhood infections, maternal infections during pregnancy and CMV-positive ALL. Using a droplet digital PCR assay, we screened diagnostic ALL bone marrow samples from the California Childhood Leukemia Study (1995-2015) for the presence of CMV DNA identifying CMV-positive and CMV-negative cases. We performed a case-only analysis (n = 524) comparing the number and types of childhood infections and maternal infections during pregnancy between CMV-positive and CMV-negative ALL cases using logistic regression. With increasing numbers of infections in the first 12 months of life, children were more likely to classify to the highest tertile of CMV DNA in the bone marrow at diagnosis (OR: 1.04, 95% CI: 1.01-1.08). Specifically, those reporting cough or flu in the first 12 months were more likely to be CMV-positive at ALL diagnosis (OR: 2.15, 95% CI: 1.06-4.37 and OR: 2.06, 95% CI: 1.17-3.63 respectively). Furthermore, those with a history of maternal infection during pregnancy were more likely to be CMV-positive (OR: 2.12, 95% CI: 1.24-3.62). We hypothesize that children with underlying immune dysregulation develop more symptomatic infections in childhood and ultimately CMV-positive ALL; this underlying immune dysregulation may be due to early immune system alterations via CMV exposure (in utero or early infancy) proposing a potential link between CMV and ALL etiology.
引用
收藏
页码:845 / 853
页数:9
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