Chhaya S U
Dhirubhai Ambani Life Sciences Centre, Molecular Diagnostics & Genetics, Rabale, Navi Mumbai, 400701, India.
Leuk Lymphoma. 2006 Feb;47(2):291-5. doi: 10.1080/10428190500287117.
In chronic myeloid leukemia (CML), experimental studies using synthetic peptides identical to the bcr-abl fusion region have revealed the capability of specific peptides to bind to human leukocyte antigen (HLA) class I molecules (HLA-A2, A3, A11, B8) and class II molecules (HLA-DR1, DR2, DR3, DR4 and DR11). Individuals expressing HLA-A3, B8 or DR4 have a diminished risk for the development of CML in Caucasian populations. A statistically significant increase in the frequency of Cw3 and Cw4 antigens in Caucasians and European CML patients has been reported. However, HLA associations in CML have not been reported in India. In lieu of the allelic diversity of HLA in the Indian population, the present study assessed the possibility of an association of HLA molecules in Indian patients with CML. HLA A, B, C and DRB1 antigen associations in 180 clinically diagnosed Indian CML patients (aged 17 - 54 years) were analysed and compared with age-matched (n = 100) healthy individuals from the same ethnic background. In the HLA class I antigen distribution, a significant decrease was observed in HLA-A11 (25.6% versus 39%; P = 0.027, odds ratio (OR) = 0.54, 95% confidence interval (CI) = 0.31 - 0.94) and HLA-Cw6 (7.8% versus 20%; P = 0.005, OR = 0.34, 95% CI = 0.15 - 0.74). Among the DRB1 alleles, HLA-DRB113 (7.8% versus 17%; P = 0.031, OR = 0.41, 95% CI = 0.18 - 0.93) was decreased in CML patients. However, the differences for HLA-A11 (P(c) = 0.351) and DRB113 (P(c) = 0.403) did not remain significant after the application of a correction factor for the P-value. These results suggest that the development of CML is apparently associated with HLA phenotypes specific to each population and indicate that expression of HLA-Cw6 may result in a protective effect on CML acquisition in the Indian population.
在慢性粒细胞白血病(CML)中,使用与bcr-abl融合区域相同的合成肽进行的实验研究表明,特定肽能够与人白细胞抗原(HLA)I类分子(HLA-A2、A3、A11、B8)和II类分子(HLA-DR1、DR2、DR3、DR4和DR11)结合。在高加索人群中,表达HLA-A3、B8或DR4的个体患CML的风险降低。据报道,白种人和欧洲CML患者中Cw3和Cw4抗原的频率有统计学意义的增加。然而,在印度尚未报道CML与HLA的关联。鉴于印度人群中HLA的等位基因多样性,本研究评估了印度CML患者中HLA分子关联的可能性。分析了180例临床诊断的印度CML患者(年龄17 - 54岁)的HLA A、B、C和DRB1抗原关联,并与来自相同种族背景的年龄匹配(n = 100)健康个体进行比较。在HLA I类抗原分布中,观察到HLA-A11(25.6%对39%;P = 0.027,优势比(OR) = 0.54,95%置信区间(CI) = 0.31 - 0.94)和HLA-Cw6(7.8%对20%;P = 0.005,OR = 0.34,95% CI = 0.15 - 0.74)显著降低。在DRB1等位基因中,CML患者中HLA-DRB113(7.8%对17%;P = 0.031,OR = 0.41,95% CI = 0.18 - 0.93)降低。然而,在应用P值校正因子后,HLA-A11(P(c) = 0.351)和DRB113(P(c) = 0.403)的差异不再显著。这些结果表明,CML的发生显然与每个群体特有的HLA表型相关,并表明HLA-Cw6的表达可能对印度人群中CML的获得产生保护作用。