[Association of TLR3-1377C/T gene polymorphisms and expression with susceptibility to enterovirus 71 encephalitis in children].

Zhongguo Dang Dai Er Ke Za Zhi

Department of Neurological Rehabilitation, Qingdao Women and Children's Hospital, Qingdao University, Qingdao, Shandong 266034, China.

Published: January 2017

AI Article Synopsis

  • The study explored the relationship between TLR3 gene polymorphisms and susceptibility to enterovirus 71 (EV71) encephalitis in children, comparing those with and without encephalitis.
  • While genotype frequencies for TLR3-1377C/T were similar between groups, both encephalitis and non-encephalitis patients showed higher serum TLR3 levels than controls, with non-encephalitis patients having the highest levels.
  • The encephalitis group had a greater EV71 viral load, and children over 1 year had higher TLR3 levels compared to younger children within the same group, indicating age-related differences in immune response.

Article Abstract

Objective: To investigate the association of gene polymorphisms of Toll-like receptor 3 (TLR3)-1377C/T and expression of TLR3 with the susceptibility to enterovirus 71 (EV71) encephalitis in children.

Methods: A total of 187 children with EV71 infection (59 children in the encephalitis group and 128 in the non-encephalitis group) and 232 children who underwent physical examination were enrolled in the case-control study. Polymerase chain reaction-restriction fragment length polymorphism was used to detect the TLR3-1377C/T gene polymorphisms. ELISA was used to measure the serum level of TLR3.

Results: There were no significant differences in the genotype and allele frequencies of TLR3-1377C/T between the non-encephalitis group and the encephalitis group. Compared with the control group, the encephalitis group and the non-encephalitis group had significant increases in the serum level of TLR3 (P<0.05), and the non-encephalitis group had the highest level (P<0.05). The encephalitis group had a significantly higher EV71 viral load than the non-encephalitis group (P<0.01). The children aged <1 year or ≥1 year in the encephalitis group and the non-encephalitis group had significant increases in the serum level of TLR3 compared with their counterparts in the control group (P<0.05), and the children aged <1 year or ≥1 year in the non-encephalitis group had a significantly higher serum level of TLR3 than those in the encephalitis group (P<0.05). In the encephalitis group, the children aged ≥1 year had a significantly higher TLR3 concentration than those aged <1 year (P<0.05), and there were no significant differences in the TLR3 concentration between the children aged ≥1 year and <1 year in the non-encephalitis group and the control group. In the encephalitis group, the proportion of children aged <1 year was significantly higher than those aged ≥1 year (P<0.05).

Conclusions: The TLR3-1377C/T gene polymorphisms are not significantly associated with the development of EV71 encephalitis. Low expression of TLR3 might weaken the inhibitory effect on virus replication and promote the development of EV71 encephalitis. The deficiency in the expression of TLR3 in serum after EV71 infection might be an important factor for the development of encephalitis in infants.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7390130PMC
http://dx.doi.org/10.7499/j.issn.1008-8830.2017.01.005DOI Listing

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