4.7 Article

MICA*019 Allele and Soluble MICA as Biomarkers for Ankylosing Spondylitis in Taiwanese

Journal

JOURNAL OF PERSONALIZED MEDICINE
Volume 11, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/jpm11060564

Keywords

MICA; AS; soluble MICA; HLA-B27; syndesmophyte

Funding

  1. Chang Gung Memorial Hospital [CMRPG 5H0022, CMRPG 3J1422, CMRPG 5I0061]
  2. Ministry of Science and Technology, Taiwan [MOST 105-2314-B-182-068-MY3, 107-2314-B-182-059-MY3]
  3. NIH [R21AI149395]

Ask authors/readers for more resources

The MICA*019 allele is significantly associated with an increased susceptibility to ankylosing spondylitis (AS) in Taiwanese populations, as well as with syndesmophyte formation and HLA-B27 positivity in AS patients. Elevated levels of soluble MICA (sMICA) in serum are also linked to AS, with MICA*019 homozygous individuals showing the highest sMICA production. In vitro experiments further demonstrated that cells expressing MICA*019 produced the highest levels of sMICA compared to other major MICA alleles.
MICA (major histocompatibility complex class I chain-related gene A) interacts with NKG2D on immune cells to regulate host immune responses. We aimed to determine whether MICA alleles are associated with AS susceptibility in Taiwanese. MICA alleles were determined through haplotype analyses of major MICA coding SNP (cSNP) data from 895 AS patients and 896 normal healthy controls in Taiwan. The distributions of MICA alleles were compared between AS patients and normal healthy controls and among AS patients, stratified by clinical characteristics. ELISA was used to determine soluble MICA (sMICA) levels in serum of AS patients and healthy controls. Stable cell lines expressing four major MICA alleles (MICA*002, MICA*008, MICA*010 and MICA*019) in Taiwanese were used for biological analyses. We found that MICA*019 is the only major MICA allele significantly associated with AS susceptibility (P-FDR = 2.25 x 10(-115); OR, 14.90; 95% CI, 11.83-18.77) in Taiwanese. In addition, the MICA*019 allele is associated with syndesmophyte formation (P-FDR = 0.0017; OR, 1.69; 95% CI, 1.29-2.22) and HLA-B27 positivity (P-FDR = 1.45 x 10(-33); OR, 28.79; 95% CI, 16.83-49.26) in AS patients. Serum sMICA levels were significantly increased in AS patients as compared to healthy controls. Additionally, MICA*019 homozygous subjects produced the highest levels of sMICA, compared to donors with other genotypes. Furthermore, in vitro experiments revealed that cells expressing MICA*019 produced the highest level of sMICA, as compared to other major MICA alleles. In summary, the MICA*019 allele, producing the highest levels of sMICA, is a significant risk factor for AS and syndesmophyte formation in Taiwanese. Our data indicate that a high level of sMICA is a biomarker for AS.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available