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Lack of association of human chemokine receptor gene polymorphisms CCR2-64I and CCR5-Delta 32 with autoimmune Addison's disease

Gambelunghe, G. (author)
Ghaderi, M. (author)
Karolinska Institutet
Gharizadeh, Baback (author)
KTH,Bioteknologi
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Brozzetti, A. (author)
Tortoioli, C. (author)
Del Sindaco, P. (author)
Sanjeevi, C. B. (author)
Karolinska Institutet
Hjelmstrom, P. (author)
Karolinska Institutet
Sirsjo, A. (author)
Nyrén, Pål (author)
KTH,Biokemi och biokemisk teknologi
Santeusanio, F. (author)
Falorni, A. (author)
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 (creator_code:org_t)
Wiley, 2004
2004
English.
In: European journal of immunogenetics. - : Wiley. - 0960-7420 .- 1365-2370. ; 31:2, s. 73-76
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The attraction of leukocytes to tissues is essential for inflammation and the initiation of the autoimmune reaction. The process is controlled by chemokines, which are chemotactic cytokines. We investigated whether human chemokine receptor gene polymorphisms, namely CCR5-Delta32 and CCR2-64I, are associated with susceptibility to autoimmune Addison's disease. Genotyping was performed in 56 patients and 127 healthy controls by a new method using pyrosequencing for CCR2-64I and by polymerase chain reaction and detecting gel for CCR5-Delta32. None of the CCR2 or CCR5 alleles was found to be associated, either positively or negatively, with disease risk. Our results indicate that the CCR2-64I and CCR5-Delta32 gene polymorphisms do not play a major role in conferring genetic risk for, and/or protection against, autoimmune Addison's disease.

Subject headings

NATURVETENSKAP  -- Biologi -- Genetik (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Genetics (hsv//eng)

Keyword

adrenal insufficiency
progression
infection
genotype
alleles
risk

Publication and Content Type

ref (subject category)
art (subject category)

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