No Association Between Ljungan Virus Seropositivity and the Beta-cell Damaging Process in the Finnish Type 1 Diabetes Prediction and Prevention Study Cohort

被引:5
|
作者
Jaaskelainen, Anne J. [1 ,2 ]
Nurminen, Noora [3 ]
Kolehmainen, Pekka [1 ,2 ,4 ]
Smura, Teemu [1 ,2 ]
Tauriainen, Sisko [4 ]
Toppari, Jorma [5 ,6 ]
Ilonen, Jorma [7 ,8 ]
Veijola, Riitta [9 ,10 ]
Knip, Mikael [11 ,12 ,13 ,14 ,15 ]
Hyoty, Heikki [3 ,16 ]
Vapalahti, Olli [1 ,2 ,9 ]
Kallio-Kokko, Hannimari [1 ,2 ]
机构
[1] Univ Helsinki, Dept Virol, POB 21,Haartmaninkatu 3, FIN-00014 Helsinki, Finland
[2] Helsinki Univ Hosp, HUSLAB, Helsinki, Finland
[3] Univ Tampere, Sch Med, Dept Virol, Tampere, Finland
[4] Univ Turku, Dept Virol, Turku, Finland
[5] Univ Turku, Inst Biomed, Dept Physiol, Turku, Finland
[6] Turku Univ Hosp, Dept Pediat, Turku, Finland
[7] Univ Turku, Immunogenet Lab, Turku, Finland
[8] Turku Univ Hosp, Turku, Finland
[9] Oulu Univ Hosp, Dept Pediat, PEDEGO Res Unit, Med Res Ctr, Oulu, Finland
[10] Univ Oulu, Oulu, Finland
[11] Univ Helsinki, Childrens Hosp, Helsinki, Finland
[12] Helsinki Univ Hosp, POB 21,Haartmaninkatu 3, FIN-00014 Helsinki, Finland
[13] Univ Helsinki, Res Programs Unit, Diabet & Obes, Helsinki, Finland
[14] Folkhalsan Res Ctr, Helsinki, Finland
[15] Tampere Univ Hosp, Tampere Ctr Child Hlth Res, Tampere, Finland
[16] Pirkanmaa Hosp Dist, Fimlab Labs, Tampere, Finland
基金
芬兰科学院;
关键词
Ljungan virus; LV; human parechovirus; HPeV; DIPP; diabetes; type; 1; PARECHOVIRUS; ANTIBODIES;
D O I
10.1097/INF.0000000000002201
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Ljungan virus (LV) has not confirmed to associate with any human disease, but a possible connection with type 1 diabetes has been suggested. LV is a rodent-borne picornavirus that induces a diabetes-like condition in rodents. Approximately 30% of adults and 60% of children are seropositive in Finland. The Finnish Type 1 Diabetes Prediction and Prevention study enabled the use of very well characterized sample panels from children seroconverted to positivity for multiple islet autoantibodies during their prospective observation from birth; in addition, samples from age, sex, human leukocyte antigen (HLA), and residence area matched control children. Methods: We analyzed LV IgG seroprevalence in 102 case children (65 had also developed type 1 diabetes), in addition to nondiabetic control children. LV and human parechovirus (HPeV) immunofluorescence assays were used to analyze LV and HPeV-specific IgG from 102 plasma samples taken at the time of islet autoantibody appearance and from 204 samples from the matched control children. Results: Altogether 46.1% of the case and 50.7% of the control children were positive for LV IgG (odds ratio 0.8; 95% confidence interval, 0.47-1.36; P = 0.416) and 67.6% versus 79.8% were positive for HPeV IgG, respectively (odds ratio 0.49, 0.27-0.9, P = 0.023). Conclusions: Thus, no risk associations between LV or HPeV-specific IgG and islet autoimmunity were observed. However, a trend for significantly higher prevalence of HPeV antibodies in control children (P = 0.023) suggests a possible protective association of this virus with islet autoimmunity.
引用
收藏
页码:314 / 316
页数:3
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