Author/Authors :
Khosravi, Farideh Department of Immunology - Medical School - Medical Sciences/University of Tehran, Tehran , Amirzargar, Aliakbar Department of Immunology - Medical School - Medical Sciences/University of Tehran, Tehran , Sarafnejad, Abdolfatah Department of Pathobiology - Immunology Division - School of Public Health - Medical Sciences/University of Tehran, Tehran , Nicknam, Mohammad Hossein Department of Immunology - Medical School - Medical Sciences/University of Tehran, Tehran , Alimoghadam, Kamran Department of Hematology - Oncology and Bone Marrow Transplantation - Shariaty Hospital - Medical Sciences/University of Tehran, Tehran , Dianat, Saied Department of Immunology - Medical School - Medical Sciences/University of Tehran, Tehran , Solgi, Ghasem Department of Immunology - Medical School - Medical Sciences/University of Tehran, Tehran , Nikbin, Behrouz Department of Immunology - Medical School - Medical Sciences/University of Tehran, Tehran
Abstract :
Previous studies demonstrated significant differences in a number of HLA allele
frequencies in leukemia patients and normal subjects.
In this study, we have analyzed HLA class II alleles and haplotypes in 110 leukemia
patients (60 acute myelogenous leukemia “AML”, 50 chronic myelogenous leukemia”CML”)
and 180 unrelated normal subjects. Blood samples were collected from all of the patients and
control subjects. DNA was extracted by salting out method and HLA typing was performed
using PCR-SSP method.
Significant positive association with AML was obtained for HLA-DRB1*11allele (35% vs.
24.7%, P=0.033). Two alleles including HLA-DRB4 and –DQB1*0303 were significantly less
frequent in AML patients than in controls. HLA-DQB1*0303 allele was never observed in CML
patients compared with allele frequency in controls (4.2%). According to haplotype analysis,
HLA-DRB1*0101/DQA1*0104/-DQB1*0501 frequencies were significantly higher and –
DRB1*16/-DQA1*01021/-DQB1*0501 frequencies were significantly lower in CML patients
than in controls .In conclusion it is suggested that HLA-DRB1*16 allele and HLA-DRB1*15/-
DQA1*0103/-DQB1*06011 and –DRB1*16/-DQA1*01021/-DQB1*0501 haplotypes
predispose individuals to AML and HLA-DRB4 allele predispose to CML.
Future studies are needed to confirm these results and establish the role of these associations
in AML and CML.
Keywords :
Acute myelogenous leukemia (AML) , Chronic myelogenous leukemia (CML) , HLA class II , Polymorphism