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Peptide-based Identification of Functional Motifs and their Binding Partners
Published on: June 30, 2013
The Complement Pathway Is Activated in People With Human Immunodeficiency Virus and Is Associated With Non-AIDS
Ivan Vujkovic-Cvijin1, Ornella Sortino2,3, Eveline Verheij4
1Metaorganism Immunity Section, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Insights
The complement cascade, a key immune pathway, is elevated in people with human immunodeficiency virus (PWH). Specifically, complement component C5 shows a strong link to non-AIDS related health issues in PWH.
Area of Science:
- Immunology
- Proteomics
- HIV Medicine
Background:
- Human immunodeficiency virus (HIV) infection impacts various biological systems.
- Understanding the molecular underpinnings of comorbidities in people with HIV (PWH) is crucial for improving long-term health outcomes.
Purpose of the Study:
- To identify novel plasma protein biomarkers associated with health status in treated PWH.
- To investigate the role of the complement system in PWH.
Main Methods:
- Utilized unbiased plasma proteomics in a matched case-control study design.
- Analyzed plasma samples from treated individuals with HIV and controls.
Main Results:
- The complement cascade was identified as a significantly enriched pathway in PWH.
- Complement component C5 demonstrated a strong association with the prevalence of non-AIDS comorbidities.
- C5 showed a stronger association than established predictive biomarkers.
Conclusions:
- The complement cascade, particularly C5, represents a potential therapeutic target and predictive biomarker for non-AIDS comorbidities in PWH.
- These findings highlight the importance of immune system dysregulation in the long-term health of PWH.
Abstract:
Unbiased plasma proteomics in a matched case-control study of treated people with human immunodeficiency virus (PWH) revealed the complement cascade as being among the top pathways enriched in PWH. Specific complement components, namely C5, associated significantly with non-AIDS comorbidity prevalence, and did so more strongly than previously established predictive biomarkers.
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