BIOLOGICAL BASIS OF THE HLA-B8, DR3-ASSOCIATED PROGRESSION OF ACQUIRED-IMMUNE-DEFICIENCY-SYNDROME

Citation
G. Candore et al., BIOLOGICAL BASIS OF THE HLA-B8, DR3-ASSOCIATED PROGRESSION OF ACQUIRED-IMMUNE-DEFICIENCY-SYNDROME, Pathobiology, 66(1), 1998, pp. 33-37
Citations number
44
Categorie Soggetti
Cell Biology",Pathology
Journal title
ISSN journal
10152008
Volume
66
Issue
1
Year of publication
1998
Pages
33 - 37
Database
ISI
SICI code
1015-2008(1998)66:1<33:BBOTHD>2.0.ZU;2-P
Abstract
The factors influencing the evolution of human immunodeficiency virus (HN) infection are not fully known, but the host genotype undoubtedly plays a role in determining the outcome of the disease by affecting th e immune response to HIV. The role of the host human leukocyte antigen (HLA) genotype in the regulation of susceptibility to HIV infection a nd expression has been studied extensively in different major risk gro ups. Certain HLA alleles and haplotypes, being associated with aberran t immune responses independently from HIV infection, have been reporte d to facilitate the rapid progression of disorders related to HIV infe ction. Particularly, the association of rapid acquired immunodeficienc y syndrome (AIDS) progression with genes from the HLA-B8,DR3 haplotype has been reported by different research groups. It is well known that this haplotype is associated in all Caucasian populations with a wide variety of diseases with autoimmune features and in healthy subjects with a number of immune system dysfunctions, as a reduced production o f T helper (Th)1 type cytokine. HIV infection may act on this genetic background triggering immunopathogenetic mechanisms leading to AIDS wi th a dominant Th2 profile as a common feature.