传染病信息
傳染病信息
전염병신식
INFECTIOUS DISEASE INFORMATION
2014年
5期
279-281
,共3页
刘立明%李永利%马洪滨%王雪飞%王嫣%王志富%毛远丽%王海滨
劉立明%李永利%馬洪濱%王雪飛%王嫣%王誌富%毛遠麗%王海濱
류립명%리영리%마홍빈%왕설비%왕언%왕지부%모원려%왕해빈
白细胞介素-2%丙型肝炎%多态现象,单核苷酸%基因型
白細胞介素-2%丙型肝炎%多態現象,單覈苷痠%基因型
백세포개소-2%병형간염%다태현상,단핵감산%기인형
interleukin-2%hepatitis C%polymorphism,single nucleotide%genotype
目的:建立一种适合临床常规检测白细胞介素28B(interleukin-28B, IL-28B)rs12979860基因多态性的快速实验方法。方法随机收集我院223例丙型肝炎住院患者外周血标本,设计针对IL-28B rs12979860基因多态性位点的特异性引物和荧光探针,直接通过双色荧光PCR法检测IL-28B rs12979860基因多态性,以基因测序法进行验证,同时初步探讨IL-28B rs12979860不同基因型在本研究人群中的分布频率。结果双色荧光PCR法能很好地鉴别IL-28B rs129798603种基因型,与测序法结果一致率为100%。IL-28B rs12979860基因多态性中T/T、C/T和C/C基因型在本研究人群中的分布频率分别为1.79%(4/223)、23.32%(52/223)和74.89%(167/223)。结论根据IL-28B rs12979860单核苷酸多态性基因型特异性探针和引物所建立的双色荧光PCR法能快速有效地进行rs12979860基因多态性分型,方法快速、可靠,为丙型肝炎患者抗病毒个体化治疗效果的预测提供了一种有效的检测方法。
目的:建立一種適閤臨床常規檢測白細胞介素28B(interleukin-28B, IL-28B)rs12979860基因多態性的快速實驗方法。方法隨機收集我院223例丙型肝炎住院患者外週血標本,設計針對IL-28B rs12979860基因多態性位點的特異性引物和熒光探針,直接通過雙色熒光PCR法檢測IL-28B rs12979860基因多態性,以基因測序法進行驗證,同時初步探討IL-28B rs12979860不同基因型在本研究人群中的分佈頻率。結果雙色熒光PCR法能很好地鑒彆IL-28B rs129798603種基因型,與測序法結果一緻率為100%。IL-28B rs12979860基因多態性中T/T、C/T和C/C基因型在本研究人群中的分佈頻率分彆為1.79%(4/223)、23.32%(52/223)和74.89%(167/223)。結論根據IL-28B rs12979860單覈苷痠多態性基因型特異性探針和引物所建立的雙色熒光PCR法能快速有效地進行rs12979860基因多態性分型,方法快速、可靠,為丙型肝炎患者抗病毒箇體化治療效果的預測提供瞭一種有效的檢測方法。
목적:건립일충괄합림상상규검측백세포개소28B(interleukin-28B, IL-28B)rs12979860기인다태성적쾌속실험방법。방법수궤수집아원223례병형간염주원환자외주혈표본,설계침대IL-28B rs12979860기인다태성위점적특이성인물화형광탐침,직접통과쌍색형광PCR법검측IL-28B rs12979860기인다태성,이기인측서법진행험증,동시초보탐토IL-28B rs12979860불동기인형재본연구인군중적분포빈솔。결과쌍색형광PCR법능흔호지감별IL-28B rs129798603충기인형,여측서법결과일치솔위100%。IL-28B rs12979860기인다태성중T/T、C/T화C/C기인형재본연구인군중적분포빈솔분별위1.79%(4/223)、23.32%(52/223)화74.89%(167/223)。결론근거IL-28B rs12979860단핵감산다태성기인형특이성탐침화인물소건립적쌍색형광PCR법능쾌속유효지진행rs12979860기인다태성분형,방법쾌속、가고,위병형간염환자항병독개체화치료효과적예측제공료일충유효적검측방법。
Objective To establish a rapid method suitable for routine clinical detection of interleukin (IL)-28B rs12979860 gene polymorphisms. Methods A total of 223 peripheral blood samples from hospitalized patients with hepatitis C in our hospital were randomly collected. The specific primers and fluorescent probe sequences in the sites of IL-28B rs12979860 gene polymor-phisms were designed, and IL-28B rs12979860 gene polymorphisms were detected by two-color fluorescent PCR directly, and vali-dated by gene sequencing method. The frequencies of different HCV IL-28B rs12979860 genotypes in this population were dis-cussed as well. Results The two-color fluorescent PCR technology could identify 3 genotypes of IL-28B rs12979860 single nu-cleotide polymorphisms, achieving 100%consistence with sequencing method. The frequencies of T/T, C/T and C/C genotypes in IL-28B rs12979860 gene polymorphisms were 1.79% (4/223), 23.32% (52/223) and 74.89% (167/223), respectively. Conclusions The two-color fluorescent PCR technology based on the specific probe and primer of IL-28B rs12979860 single nucleotide polymor-phisms is effective, rapid and reliable in identifying genotypes of rs12979860 gene polymorphisms. It is an effective detection method for the prediction of antiviral individualized treatment in patients with hepatitis C.