Project Details
Abstract
Neuroinflammatory diseases are clinically heterogeneous and one of the major causes of
acquired neurological disability. An underlying complex genetic susceptibility may play an
important role in their etiologies; however, the role of genetic factors in determining their
clinical features is still unclear. Neuroinflammation disease included multiple sclerosis, Acute
disseminated encephalomyelitis, Acute necrotizing encephalopathy and nonparaneoplastic
limbic encephalitis. The etiology of neuroinflammation diseases were still unknown, but
immunogenetic mechanism has been suggested.
The human leukocyte antigen system (HLA) is the name of the major histocompatibility
complex (MHC) in humans. The super locus contains a large number of genes related to
immune system function in humans. This group of genes reside on chromosome 6, and
encode cell-surface antigen-presenting proteins and many other genes. The major HLA
antigens are essential elements for immune function. Different classes have different functions.
HLA typing divided into two group: type I (HLA-A, B & C) and type II ( HLA- DP, DQ &
DR). HLA have other roles. Diversity of HLA in human population is one aspect of disease
defense. They may protect against or fail to protect (if down regulated by an infection). They
may mediate autoimmune disease (examples: type I diabetes, coeliac disease).
Therefore we studied HLA determinants in children consecutively diagnosed with
neuroinflammatory disease to study the immunogenetic peculiarities of neuroinflammatory
diseases in children.
Project IDs
Project ID:PC10107-0358
External Project ID:NSC101-2314-B182-034
External Project ID:NSC101-2314-B182-034
Status | Finished |
---|---|
Effective start/end date | 01/08/12 → 31/07/13 |
Keywords
- neuroinflammation disease
- HLA
- Genetic Susceptibility
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