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The Influence of CCL3L1 Gene- Containing Segmental Duplications on HIV-1/AIDS Susceptibility Gonzalez et al. Mar 4, 2005 :307 Science Presenter: Braydon Burgess Dept. Of Pathology and Laboratory Medicine, Masters Program
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Estimated number of adults and children living with HIV by region, 1985—2004 0 10 20 30 40 50 19851986198719881989199019911992199319941995199619971998199920002001200220032004 Caribbean North Africa & Middle East Eastern Europe & Central Asia Western and Central Europe & North America Latin America Asia Sub-Saharan Africa Number of people living with HIV Millions Source: UNAIDS/WHO AIDS Epidemic Update, Dec 2004
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HIV Epidemiology People newly infected with HIV in 2004 Total4.9 million (4.3 – 6.4 million) AIDS deaths in 2004 Total3.1 million (2.8 – 3.5 million)
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Institutional spending for HIV and AIDS 1996−2002 (US$ disbursements in millions) 0 500 1,000 1,500 2,000 2,500 3,000 1996199719981999200020012002 Domestic Private UN System Bilateral US$ millions Source: UNAIDS Resource Tracking Consortium 2004 Report on the Global AIDS Epidemic (Fig 37)
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Human Immunodeficiency Virus-1 Transmission: Horizontal: Adult Adult Vertical: Mother Child Cell Binding: Host Receptor: CD4 Co-receptor: CCR5 Membrane fusion Viral replication & cell death
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Background CD4 Cell signalling molecule Cell signalling molecule A defining feature of T-helper cells A defining feature of T-helper cells The REQUIRED receptor for HIV entry The REQUIRED receptor for HIV entry Chemokine Receptor 5 (CCR5) Highly expressed on memory T-cells Highly expressed on memory T-cells Major co-receptor for HIV entry Major co-receptor for HIV entry Chemokine Ligand 3-like-1 (CCL3L1) Released following immunological challenge Released following immunological challenge CCL3L1 strongest ligand for CCR5 CCL3L1 strongest ligand for CCR5 Known to be a dominant suppressor of HIV Known to be a dominant suppressor of HIV
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Background CCL3L1 gene contained on a hotspot for segmental duplication Copy # was known to be variable in human populations Gene dose is proportionate to chemokine levels
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Research Question Can segmental duplications causing dosage effects of host defence genes be associated with phenotypic effects in vivo? Do extra gene copies of CCL3L1 decrease HIV susceptibility?
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Study Populations Human Diversity Cell Line Panel Tissue samples from ancestral populations Tissue samples from ancestral populations Wilford Hall Medical Centre (WHMC) Cohort of 1330 HIV + USAF Military Personnel & matched controls Cohort of 1330 HIV + USAF Military Personnel & matched controlsNon-WHMC HIV - civilian cohort, 1300 individuals matched to the WHMC cohort HIV - civilian cohort, 1300 individuals matched to the WHMC cohort Argentinean Children Composed of 450 HIV + children and controls all exposed perinatally to HIV Composed of 450 HIV + children and controls all exposed perinatally to HIV
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Q: What is the Global Variation in CCL3L1 Copy # Conclusion: CCL3L1 gene copy # is variable between populations but similarly dispersed within populations. ANOVA indicates that geography accounts for 35% of copy# variance.
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Q: Is CCL3L1 Copy # Associated with HIV Acquisition Conclusion: There is a significant correlation between copy # and HIV prevalence in all populations Each CCL3L1 copy decreases risk of HIV infection by 4.5%-10.5%
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Clinical Answer Biochemical Answer Q: Does CCL3L1 Copy # Affect Progression to AIDS Conclusion: 1: Progression to AIDS is accelerated in low copy # individuals. 2: Low CCL3L1 copy # elevates CCR5 exposure, increasing accessibility to HIV 3: Low copy # is associated with a poorer clinical prognosis Epidemiology Answer
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Q: Is Copy # an Absolute Determinant of HIV Progression Conclusion: Copy # in the context of genetic background determines which copy #s are beneficial
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Q: Are Copy # Phenotypes Affected by Genetic Interactions Conclusion: CCL3L1 copy # effect is stronger than CCR5 genotype and copy # enhances CCR5 defects
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CCR5 and CCL3L1 Are Major Contributors to HIV Susceptibility
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Summary CCL3L1 copy number shows inter- and intra- population variation (0-10+ copies) CCL3L1 copy # is positively associated with a dose-dependant protection from HIV acquisition and progression to AIDS. Low CCL3L1 copy # and detrimental CCR5 mutations have harmful interactions and account for variability in disease progression (~30%) and in transmission (~20-40%)
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