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早期莱姆病患者人类白细胞抗原II类等位基因与伯氏疏螺旋体基因型之间的关联

Association between human leukocyte antigen class II alleles and genotype of Borrelia burgdorferi in patients with early lyme disease.

作者信息

Wormser Gary P, Kaslow Richard, Tang Jianming, Wade Karen, Liveris Dionysios, Schwartz Ira, Klempner Mark

机构信息

Department of Medicine, Division of Infectious Diseases, New York Medical College, Valhalla, NY 10595, USA.

出版信息

J Infect Dis. 2005 Dec 1;192(11):2020-6. doi: 10.1086/497693. Epub 2005 Oct 28.

Abstract

BACKGROUND

On the basis of a polymerase chain reaction-restriction fragment-length polymorphism analysis of the 16S-23S ribosomal DNA intergenic spacer, clinical isolates of Borrelia burgdorferi can be classified into 3 genotypes designated as RST1, RST2, and RST3. RST1 strains are the most pathogenic, and RST3 strains are the least pathogenic.

METHODS

Human leukocyte antigen (HLA) class II alleles were determined for a group of culture-positive patients with Lyme disease-associated erythema migrans and were evaluated for an association with the genotype of the infecting B. burgdorferi strain.

RESULTS

The DRB10101 allele carriage rate was higher in patients infected with RST3 strains (9/25 [36.0%]) than in patients infected with RST1 strains (2/28 [7.1%]) or RST2 strains (7/36 [19.4%]) (P=.010). The same relationship was found for carriage of the DRB10101-DQB1*0501 haplotype (P=.018), because of tight linkage disequilibrium. Similar associations could not be demonstrated for any of the other DRB1 and DQB1 alleles or haplotypes that were assessed.

CONCLUSION

The DRB10101 allele and the DRB10101-DQB1*0501 haplotype may be relevant to the development of infection with strains from the least invasive genotypes of B. burgdorferi.

摘要

背景

基于对16S - 23S核糖体DNA基因间隔区的聚合酶链反应 - 限制性片段长度多态性分析,伯氏疏螺旋体的临床分离株可分为3种基因型,分别命名为RST1、RST2和RST3。RST1菌株致病性最强,RST3菌株致病性最弱。

方法

对一组培养阳性的莱姆病相关游走性红斑患者测定人类白细胞抗原(HLA)II类等位基因,并评估其与感染的伯氏疏螺旋体菌株基因型的相关性。

结果

感染RST3菌株的患者中DRB10101等位基因携带率(9/25 [36.0%])高于感染RST1菌株的患者(2/28 [7.1%])或RST2菌株的患者(7/36 [19.4%])(P = 0.010)。由于紧密连锁不平衡,DRB10101 - DQB1*0501单倍型的携带情况也呈现相同关系(P = 0.018)。对于所评估的任何其他DRB1和DQB1等位基因或单倍型,均未显示出类似的相关性。

结论

DRB10101等位基因和DRB10101 - DQB1*0501单倍型可能与感染致病性最弱的伯氏疏螺旋体基因型菌株的发病有关。

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