Association of KIR Genes with Middle East Respiratory Syndrome Coronavirus Infection in South Koreans

被引:0
|
作者
Baek, In-Cheol [1 ]
Choi, Eun-Jeong [1 ]
Kim, Hyoung-Jae [1 ]
Choi, Haeyoun [1 ,2 ]
Shin, Hyoung-Shik [3 ]
Lim, Dong-Gyun [4 ]
Kim, Tai-Gyu [1 ,2 ]
机构
[1] Catholic Univ Korea, Coll Med, Catholic Hematopoiet Stem Cell Bank, Seoul 06591, South Korea
[2] Catholic Univ Korea, Coll Med, Dept Microbiol, Seoul 06591, South Korea
[3] Eulji Univ, Coll Med, Dept Radiol, Div Infect Dis, Daejeon 34824, South Korea
[4] Natl Med Ctr, Translat Res Ctr, Res Inst Publ Hlth, 245 Eulji Ro, Seoul 04564, South Korea
关键词
KIR; HLA; polymorphism; MERS; immunogenetics; Koreans; KILLER-CELL RECEPTOR; CHAIN-RELATED-GENE; MERS-COV OUTBREAK; SARS-COV; MHC; POLYMORPHISM; HEALTH; CANCER; MICA; SUSCEPTIBILITY;
D O I
10.3390/jcm13010258
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Middle East respiratory syndrome (MERS) is a lower respiratory tract disease caused by a beta coronavirus (CoV) called MERS-CoV, characterized by a high mortality rate. We aimed to evaluate the association between genetic variation in killer cell immunoglobulin-like receptors (KIRs) and the risk of MERS in South Koreans. Methods: KIR genes were genotyped by multiplex polymerase chain reaction with sequence-specific primers (PCR-SSP). A case-control study was performed to identify the odds ratios (OR) of KIR genes for MERS and the association of KIR genes and their ligands, human leukocyte antigens (HLA) genes. Results: KIR2DS4D and KIR3DP1F showed higher frequencies in the group of all patients infected with MERS-CoV than in the control group (p = 0.023, OR = 2.4; p = 0.039, OR = 2.7). KIR2DL1, KIR2DP1, and KIR3DP1D were significantly associated with moderate/mild (Mo/Mi) cases. KIR2DL2, KIR2DS1, and KIR3DP1F were affected in severe cases. When we investigated the association between KIR genes and their ligands in MERS patient and control groups, KIR3DL1+/Bw4(80I)+, KIR3DL1+/Bw6+, KIR3DL1+/Bw6-, KIR2DS1+/C2+, and KIR3DS+/Bw4(80I)+ were associated with MERS. KIR3DL1+/Bw6- was found in Mo/Mi cases. KIR2DS1+/C2+ and KIR2DS2+/C1+ were found in severe cases. Conclusion: Further investigations are needed to prove the various immune responses of MERS-CoV-infected cells according to variations in the KIR gene and ligand gene. A treatment strategy based on current research on the KIR gene and MERS-CoV will suggest potential treatment targets.
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