Expression of human leukocyte antigens (HLA) is important for the immune re
sponse against infectious agents and malignant cells. Association of single
HLA antigens or HLA haplotypes with disease has been investigated previous
ly, and positive correlations between HLA and some cancers, such as cervica
l or nasopharyngeal carcinomas have been reported. In the present study, HL
A antigen frequencies of 65 adult Caucasian patients with low-grade, anapla
stic, or malignant astrocytic glioma (WHO grades II-IV) were compared with
157 racially similar, asymptomatic control individuals. Both standard serol
ogic and PCR techniques for HLA typing were employed for all patients and c
ontrols.
Our results suggest a positive association between single HLA antigens and
presence of symptomatic cerebral glioma. Compared with the control populati
on, patients positive for HLA-A*25 had a 3.0-fold increased risk of glioma
(p = 0.04), patients positive for HLA-B*27, a 2.7-fold risk (p = 0.03), and
patients positive for HLA-DRB1*15, a 2.2-fold risk (p = 0.03), whereas HLA
-DRB1*07 was associated with a 0.4-fold decreased risk of glioma (p = 0.02)
. Occurrence rate of some HLA antigen combinations and estimated haplotypes
was also different in glioma patients. Thus, HLA-DRB1*15:DRB5*(51) occurre
nce in combination with HLA-DRB1*11 was associated with a 13.4-fold increas
ed risk of glioma (p = 0.001), and the incidence of HLA-Cw*6:DRB1*07 with a
0.2-fold decreased risk of glioma (p = 0.03).
In conclusion, single HLA antigens and their combinations and estimated hap
lotypes are possibly significantly more or less frequent in persons develop
ing symptomatic cerebral glioma during their adult life, compared with asym
ptomatic individuals.