Genetic polymorphisms associated with psoriasis, methods of detection and uses thereof
View Patent ↗The present invention is based on the discovery of genetic polymorphisms that are associated with psoriasis and related pathologies. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, including groups of nucleic acid molecules that may be used as a signature marker set, such as a haplotype, a diplotype, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.
1. A method of administering an anti-IL-12p40 antibody to a human, the method comprising:
testing nucleic acid from said human to determine the nucleotide content of a polymorphism in gene IL23R at position 101 of SEQ ID NO:38 or the complement of SEQ ID NO:38, wherein the presence of G at position 101 of SEQ ID NO: 38 or C at position 101 of the complement of SEQ ID NO:38 is detected;
correlating the presence of said G or said C with said human having an increased risk for developing psoriasis; and
administering said anti-IL-12p40 antibody to said human.
2. The method of claim 1 , wherein said testing is performed using sequencing, 5′ nuclease digestion, molecular beacon assay, oligonucleotide ligation assay, size analysis, and single-stranded conformation polymorphism analysis, or denaturing gradient gel electrophoresis (DGGE).
3. The method of claim 1 , wherein said nucleic acid is a nucleic acid extract from a biological sample from said human.
4. The method of claim 3 , wherein said biological sample is blood, saliva, or buccal cells.
5. The method of claim 3 , further comprising preparing said nucleic acid extract from said biological sample prior to said testing.
6. The method of claim 5 , further comprising obtaining said biological sample from said human prior to said preparing.
7. The method of claim 1 , wherein said testing comprises nucleic acid amplification.
8. The method of claim 7 , wherein said nucleic acid amplification is carried out by polymerase chain reaction.
9. The method of claim 1 , wherein said testing is performed using an allele-specific method.
10. The method of claim 9 , wherein said allele-specific method is allele-specific probe hybridization, allele-specific primer extension, or allele-specific amplification.
11. A method of determining that a human has an increased risk for developing psoriasis, the method comprising:
a) testing nucleic acid from said human to determine the nucleotide content of a polymorphism in gene IL23R at position 101 of SEQ ID NO:38 or the complement of SEQ ID NO:38; and
b) correlating the presence of G at position 101 of SEQ ID NO:38 or C at position 101 of the complement of SEQ ID NO:38 with said human having said increased risk for developing psoriasis.
12. The method of claim 11 , wherein said nucleic acid is a nucleic acid extract from a biological sample from said human.
13. The method of claim 12 , wherein said biological sample is blood, saliva, or buccal cells.
14. The method of claim 12 , further comprising preparing said nucleic acid extract from said biological sample prior to said testing.
15. The method of claim 14 , further comprising obtaining said biological sample from said human prior to said preparing.
16. The method of claim 11 , wherein said testing comprises nucleic acid amplification.
17. The method of claim 16 , wherein said nucleic acid amplification is carried out by polymerase chain reaction.
18. The method of claim 11 , wherein said testing is performed using sequencing, 5′ nuclease digestion, molecular beacon assay, oligonucleotide ligation assay, size analysis, single-stranded conformation polymorphism analysis, or denaturing gradient gel electrophoresis (DGGE).
19. The method of claim 11 , wherein said testing is performed using an allele-specific method.
20. The method of claim 19 , wherein said allele-specific method is allele-specific probe hybridization, allele-specific primer extension, or allele-specific amplification.
21. The method of claim 1 , wherein said human is homozygous for said G or said C.
22. The method of claim 1 , wherein said human is heterozygous for said G or said C.
23. The method of claim 11 , wherein said human is homozygous for said G or said C.
24. The method of claim 11 , wherein said human is heterozygous for said G or said C.