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Frequencies of immune hypersensitivity reaction-associated HLA class I alleles in healthy South African Indian and mixed ancestry populations determined by a novel real-time PCR assay

机译:通过新型实时荧光定量PCR测定的健康南非非裔和混合血统人群中与免疫超敏反应相关的HLA I类等位基因的频率

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We have determined the frequencies of human leucocyte antigen (HLA)-B*57:01, HLA-B*35:05, HLA-CW4 and HLA-C*08 in healthy individuals of South African Indian (SAI) ethnicity (n = 50) and South African mixed (SAM) ancestry (n = 50) using real-time allele-specific polymerase chain reaction (AS-PCR) assay. HLA-B*57:01 associates with immune hypersensitivity reaction (IHR) in individuals exposed to abacavir (ABC), while nevirapine (NVP) IHR associates with HLA-B*35:05, HLA-C*04 and HLA-C*08. Real-time AS-PCR assays typically use less DNA, are more cost-effective and rapid compared with conventional genotyping methods, such as sequence-based typing (SBT). The assay was developed using samples of known HLA class I genotype and subsequently applied to the SAI and SAM samples. HLA-B*57:01 was detected in SAM and SAI populations at frequencies of 8.0% and 12.0%, respectively, while HLA-B*35:05 was not found in SAI individuals, but was present in 6.0% of SAM individuals. HLA-C*04 was detected in 22.0% and 24.0% of SAM and SAI individuals, respectively, while 10.0% and 8.0% of SAM and SAI individuals, respectively, were HLA-C*08 positive. This study reports the development of a novel real-time AS-PCR assay to identify HLA class I alleles associated with ABC and NVP IHR and has established the frequencies of these alleles present in healthy SAI and SAM populations. Using South African demographic data, our hypothetical analysis suggests that a substantial number of individuals would benefit from the assay.
机译:我们已经确定了南非印度裔(SAI)种族健康个体中人白细胞抗原(HLA)-B * 57:01,HLA-B * 35:05,HLA-CW4和HLA-C * 08的频率(n = 50)和南非混合(SAM)血统(n = 50),使用实时等位基因特异性聚合酶链反应(AS-PCR)分析。 HLA-B * 57:01与暴露于阿巴卡韦(ABC)的个体的免疫超敏反应(IHR)相关,而奈韦拉平(NVP)IHR与HLA-B * 35:05,HLA-C * 04和HLA-C *相关08。与传统的基因分型方法(例如基于序列的分型(SBT))相比,实时AS-PCR分析通常使用较少的DNA,具有更高的成本效益和速度。该测定是使用已知的HLA I类基因型的样本开发的,随后应用于SAI和SAM样本。在SAM和SAI人群中分别以8.0%和12.0%的频率检测到HLA-B * 57:01,而在SAI个体中未发现HLA-B * 35:05,但在6.0%的SAM个体中存在。在SAM和SAI个体中分别检测到22.0%和24.0%的HLA-C * 04,而在SAM和SAI个体中分别检测到HLA-C * 08阳性的10.0%和8.0%。这项研究报告了一种新型实时AS-PCR分析方法的开发,以鉴定与ABC和NVP IHR相关的HLA I类等位基因,并确定了健康SAI和SAM人群中这些等位基因的频率。使用南非的人口统计数据,我们的假设分析表明,大量个体将从该检测中受益。

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