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Lack of association of CCR2-64I and CCR5-Delta 32 with type 1 diabetes and latent autoimmune diabetes in adults

Gambelunghe, G. (author)
Ghaderi, M. (author)
Karolinska Institutet
Brozzetti, A. (author)
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Del Sindaco, P. (author)
Gharizadeh, B. (author)
Nyrén, Pål (author)
KTH,Biokemi och biokemisk teknologi
Hjelmstrom, P. (author)
Karolinska Institutet
Nikitina-Zake, L. (author)
Sanjeevi, C. B. (author)
Karolinska Institutet
Falorni, A. (author)
Umbria Type 1 Diabetes, Registry (author)
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 (creator_code:org_t)
2003
2003
English.
In: Human Immunology. - 0198-8859 .- 1879-1166. ; 64:6, s. 629-632
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • It is well known that type I diabetes mellitus (T1DM) is a complex genetic disease resulting from the autoimmune destruction of pancreatic beta cells. Several genes have been associated with susceptibility and/or protection for T1DM, but the disease risk is mostly influenced by genes located in the class II region of the major histocompatibility complex. The attraction of leukocytes to tissues is essential for inflammation and the beginning of autoimmune reaction. The process is controlled by chemokines, which are chemotactic cytolines. Some studies have shown that CCR2-64I and CCR5-Delta32 might be important for protection of susceptibility to some immunologically-mediated disorders. In the present study, we demonstrate the lack of association between CCR2-64I and CCR5-Delta32 gene polymorphism and TIDM and we desrcibe a new method for a simple and more precise genotyping of the CCR2 gene.

Keyword

chemokine
CCR2-641 gene
CCR5-Delta 32 gene
type 1 diabetes
latent autoimmune diabetes of the adult
disease progression
gene polymorphism
ccr5
mellitus
onset
hla

Publication and Content Type

ref (subject category)
art (subject category)

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