2018
DOI: 10.1097/qad.0000000000001926
|View full text |Cite
|
Sign up to set email alerts
|

Inhibition of HIV-1 infection by human pegivirus type 1-derived peptides is affected by human pegivirus type 1 genotype and HIV-1 coreceptor tropism

Abstract: Our data indicate that the inhibitory effect of peptides derived from HPgV-1 E2 protein is dependent on the genotype, suggesting that coinfection with HPgV-1 GT1 is less likely to confer a beneficial effect on HIV-1 disease progression than GT2. The preferential suppression of more pathogenic CXCR4-tropic HIV-1 by peptides derived from HPgV-1 GT2 may explain the favorable effect in patients harboring these HIV-1 isolates. Consequently, HPgV-1 genotype and HIV-1 coreceptor tropism are likely determinants for th… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
4
0

Year Published

2019
2019
2022
2022

Publication Types

Select...
4
1

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(4 citation statements)
references
References 63 publications
0
4
0
Order By: Relevance
“…Subtype 2b and genotype 5 were already related to higher rates of CD4+ T-cells compared to subtype 2a and genotype 1 [19, 33], and genotype 7 has already been associated with slower progression to AIDS [34]. It is thought that the different HPgV-1 genotypes have different tropisms to the CXCR4 and CCR5 coreceptors used by HIV-1 for entry into host cells, which would be determinant in the evolution of HIV-1 infection [35]. The competition for these coreceptors has also been suggested [36], since both viruses present cell tropism to CD4+ T-cells [37].…”
Section: Discussionmentioning
confidence: 99%
“…Subtype 2b and genotype 5 were already related to higher rates of CD4+ T-cells compared to subtype 2a and genotype 1 [19, 33], and genotype 7 has already been associated with slower progression to AIDS [34]. It is thought that the different HPgV-1 genotypes have different tropisms to the CXCR4 and CCR5 coreceptors used by HIV-1 for entry into host cells, which would be determinant in the evolution of HIV-1 infection [35]. The competition for these coreceptors has also been suggested [36], since both viruses present cell tropism to CD4+ T-cells [37].…”
Section: Discussionmentioning
confidence: 99%
“…Antibodies directed toward the envelope HPgV glycoprotein E2, which is thought to be the immunodominant antigenic site, are detected as viremia is cleared [ 18 ]. While the pathogenicity of this virus remains unclear, HPgV-1 has a propensity to co-infect individuals with other viral infections, particularly human immunodeficiency virus (HIV) [ 19 , 20 ] and HCV [ 6 , 21 ]. HPgV interferes with the pathogenicity of HIV [ 22 ] and slows disease progression [ 7 , 9 , 19 , 23 , 24 ].…”
Section: Introductionmentioning
confidence: 99%
“…While the pathogenicity of this virus remains unclear, HPgV-1 has a propensity to co-infect individuals with other viral infections, particularly human immunodeficiency virus (HIV) [ 19 , 20 ] and HCV [ 6 , 21 ]. HPgV interferes with the pathogenicity of HIV [ 22 ] and slows disease progression [ 7 , 9 , 19 , 23 , 24 ]. Indeed, epidemiological evidence showed that longer period of HPgV viremia is associated with greater survival among HIV-positive individuals [ 7 ].…”
Section: Introductionmentioning
confidence: 99%
“…While the pathogenicity of this virus remains unclear, HPgV-1 has a propensity to co-infect individuals with other viral infections, particularly human immunodeficiency virus (HIV) (19,20) and HCV (6,21). HPgV interferes with the pathogenicity of HIV (22) and slows disease progression (7,9,19,23,24).…”
Section: Introductionmentioning
confidence: 99%