
BMC Infectious Diseases, Journal Year: 2024, Volume and Issue: 24(1)
Published: Sept. 9, 2024
Language: Английский
BMC Infectious Diseases, Journal Year: 2024, Volume and Issue: 24(1)
Published: Sept. 9, 2024
Language: Английский
Nature Reviews Neurology, Journal Year: 2023, Volume and Issue: 19(11), P. 668 - 687
Published: Oct. 10, 2023
Language: Английский
Citations
32Virology Journal, Journal Year: 2024, Volume and Issue: 21(1)
Published: Feb. 23, 2024
Abstract HIV infection compromises both the peripheral and central immune systems due to its pathogenic neuropathogenic features. The mechanisms driving HIV-1 pathogenesis neuropathogenesis involve a series of events, including metabolic dysregulation. Furthermore, HIV-subtype-specific variations, particularly alterations in amino acid sequences key viral proteins, are known influence severity clinical outcomes people living with HIV. However, impact sequence variations specific such as Viral protein R (Vpr), on metabolites within Tryptophan (Trp)-kynurenine (Kyn) pathway remains unclear. Our research aimed explore relationship between Vpr (specifically at positions 22, 41, 45, 55, these have been previously linked neurocognitive function) Trp-Kyn metabolites. Additionally, we sought clarify biology variation by examining link metabolism inflammation, mechanism. In this preliminary study, analyzed unique cohort thirty-two ( n = 32) South African cART naïve We employed Sanger sequencing ascertain blood-derived targeted LC-MS/MS metabolomics platform assess metabolites, Trp, Kyn, kynurenic (KA), quinolinic (QUIN). Particle-enhanced turbidimetric assay Enzyme-linked immunosorbent assays were used measure markers, hsCRP, IL-6, suPAR, NGAL sCD163. After applying Bonferroni corrections p =.05/3) adjusting for covariates (age sex), only G41 A55 groups was nearing significance higher levels QUIN compared S41 T55 groups, respectively (all =.023). Multiple regression results revealed that position 41 (adj 2 0.049, β 0.505; =.023), 55 0.126, 0.444; =.023) displayed significant associations after age sex. Lastly, observed group found be correlated suPAR r =.588, =.005). These collectively underscore importance substitutions influencing inflammation levels), potentially contributing our understanding their roles HIV-1.
Language: Английский
Citations
1Open Forum Infectious Diseases, Journal Year: 2024, Volume and Issue: 11(3)
Published: Feb. 27, 2024
Subtype-specific amino acid variations in viral proteins of human immunodeficiency virus type 1 (HIV-1) influence disease progression. Furthermore, Vpr sequence variation correlates with chronic inflammation, a central mechanism HIV-1 (neuro)pathogenesis. Nevertheless, no clinical study has investigated the link between and peripheral inflammation people HIV (PWH). The aim this pilot was to ascertain whether specific variants were associated immune markers PWH.
Language: Английский
Citations
1European Journal of Clinical Investigation, Journal Year: 2022, Volume and Issue: 53(5)
Published: Dec. 29, 2022
The HIV viral protein R (Vpr) is a multifunction involved in the pathophysiology of HIV-1. Recent evidence has suggested that Vpr amino acid substitutions influence HIV-1 and clinical outcomes people living with (PLWH). Several studies have linked to PLWH; however, there no clear consensus as which acids or are most important PLWH. We, therefore, conducted systematic review investigating PLWH.PubMed, Scopus Web Science databases were searched according PRISMA guidelines using search protocol designed specifically for this study.A total 22 included data extraction, comprising 14 cross-sectional 8 longitudinal studies. Results indicated associated specific outcomes, including disease progressions, neurological treatment status. Studies consistently showed substitution 63T was slower progression, whereas 77H 85P significant contribution progression.Vpr-specific may be contributors PLWH, future should consider highlighted review.
Language: Английский
Citations
6Elsevier eBooks, Journal Year: 2024, Volume and Issue: unknown, P. 179 - 207
Published: Jan. 1, 2024
Language: Английский
Citations
0BMC Infectious Diseases, Journal Year: 2024, Volume and Issue: 24(1)
Published: Sept. 9, 2024
Language: Английский
Citations
0