1988
DOI: 10.1016/s0140-6736(88)92009-0
|View full text |Cite
|
Sign up to set email alerts
|

Hla Haplotype A1 B8 Dr3 as a Risk Factor for Hiv-Related Disease

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4

Citation Types

3
69
0

Year Published

1989
1989
2001
2001

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 191 publications
(73 citation statements)
references
References 19 publications
3
69
0
Order By: Relevance
“…In the patients studied by Steel et al [5], the HLA haplotype Al B8 DR3 was weakly associated with an increased risk of seroconversion and our data for Italian population [6] suggested a possible role of class I HLA antigens in susceptibility to HIV infection.…”
Section: Introductionsupporting
confidence: 59%
See 2 more Smart Citations
“…In the patients studied by Steel et al [5], the HLA haplotype Al B8 DR3 was weakly associated with an increased risk of seroconversion and our data for Italian population [6] suggested a possible role of class I HLA antigens in susceptibility to HIV infection.…”
Section: Introductionsupporting
confidence: 59%
“…At present recent data suggest that several HLA alleles influence both the rapidity and the type of HIV-1 infection [3][4][5][6][7][8][9][10][11][12]. We have much less information about HLA-linked genetic control of HIV susceptibility.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…[8][9][10] Recently, for some viral infections, associations have been reported between HLA polymorphism and the clinical outcome of infected patients. [11][12][13][14] However, it remains uncertain whether HLA polymorphisms are involved in the pathogenesis of liver injury in chronic HCV infection.…”
mentioning
confidence: 99%
“…The DRl antigen was associated with an increased risk of rapid progression from an asymptomatic state to AIDS [8]. Especially the Caucasian haplotype Al B8 DR3 was consistently found to be associated with rapid progression to AIDS [9] and rapid decline in CD4 helper cells [10]. Complement C4 null alleies [11] and several ancestral haplotypes that carry them have also been shown to be Correspondence: F. Hentges MD, Department of Immuno-Allergology.…”
Section: Introductionmentioning
confidence: 99%