Abstract | OBJECTIVE: METHODS: RESULTS:
MICA*008 allele frequency was lower in patients with chronic granulocytic leukemia than in the control group (22.2% vs 34.3%, Chi(2)=4.98, P<0.05). The infection rate of HCMV was significantly higher in those individuals with genotype of MICA*008 (-) than in those with MICA*008 (+), and moderate correlation was suggested between MICA*008 and HCMV infection (C=0.5829, 0.6142). CONCLUSION: Individuals with MICA*008 positivity is not liable to HCMV infection, but those with MICA*008 (-) can be vulnerable to HCMV infection, suggesting an inverse correlation between MICA*008 allele with HCMV.
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Authors | Bai-sheng Huang, Qi-zhi Luo, Bing Mei, Ping Yu |
Journal | Nan fang yi ke da xue xue bao = Journal of Southern Medical University
(Nan Fang Yi Ke Da Xue Xue Bao)
Vol. 27
Issue 4
Pg. 509-11
(Apr 2007)
ISSN: 1673-4254 [Print] China |
PMID | 17545046
(Publication Type: English Abstract, Journal Article)
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Chemical References |
- Histocompatibility Antigens Class I
- MHC class I-related chain A
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Topics |
- Alleles
- Cytomegalovirus Infections
(genetics)
- Gene Frequency
- Genetic Predisposition to Disease
- Genotype
- Histocompatibility Antigens Class I
(genetics)
- Humans
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive
(genetics, virology)
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