Combinatorial Crispr/Cas9 For Suppression Of Latent Hiv-1 Provirus In Vitro
Although HAART effectively suppresses HIV-1 replication, its compromised effectiveness against non-B subtypes, the challenge of eliminating latent proviruses, life-long treatment, and viral resistance complicates the cure for HIV-1. CRISPR/Cas9, the latest genome editing tool, can overcome the limit...
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my-usm-ep.521242022-03-31T07:08:35Z Combinatorial Crispr/Cas9 For Suppression Of Latent Hiv-1 Provirus In Vitro 2020-11 Ravichantar, Nithya R5-920 Medicine (General) Although HAART effectively suppresses HIV-1 replication, its compromised effectiveness against non-B subtypes, the challenge of eliminating latent proviruses, life-long treatment, and viral resistance complicates the cure for HIV-1. CRISPR/Cas9, the latest genome editing tool, can overcome the limitations seen with HAART. By targeting the promoter of HIV-1 (LTR), CRISPR/Cas9 can disrupt the latent reservoirs. Here, we designed an improved CRISPR/Cas9 system, combinatorial CRISPR/Cas9 to concurrently knockdown multiple HIV-1 genes: structural (Pol and Gag), regulatory (Rev and Tat) and accessory genes (Vif). We investigated the efficacy of this tool as a therapy against different viral subtypes in a subset population . Our preliminary data, showed a huge decrease in viral load and we verified the safety of CRISPR/Cas9 in human cell lines. 2020-11 Thesis http://eprints.usm.my/52124/ http://eprints.usm.my/52124/1/Pages%20from%20Combinatorial%20CrisprCas9%20ForSuppression%20Of%20Latent%20Hiv-1%20Provirus%20In%20Vitro.pdf application/pdf en public phd doctoral Universiti Sains Malaysia Institut Perubatan & Pergigian Termaju |
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R5-920 Medicine (General) |
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R5-920 Medicine (General) Ravichantar, Nithya Combinatorial Crispr/Cas9 For Suppression Of Latent Hiv-1 Provirus In Vitro |
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Although HAART effectively suppresses HIV-1 replication, its compromised effectiveness against non-B subtypes, the challenge of eliminating latent proviruses, life-long treatment, and viral resistance complicates the cure for HIV-1. CRISPR/Cas9, the latest genome editing tool, can overcome the limitations seen with HAART. By targeting the promoter of HIV-1 (LTR), CRISPR/Cas9 can disrupt the latent reservoirs. Here, we designed an improved CRISPR/Cas9 system, combinatorial CRISPR/Cas9 to concurrently knockdown multiple HIV-1 genes: structural (Pol and Gag), regulatory (Rev and Tat) and accessory genes (Vif). We investigated the efficacy of this tool as a therapy against different viral subtypes in a subset population . Our preliminary data, showed a huge decrease in viral load and we verified the safety of CRISPR/Cas9 in human cell lines. |
format |
Thesis |
qualification_name |
Doctor of Philosophy (PhD.) |
qualification_level |
Doctorate |
author |
Ravichantar, Nithya |
author_facet |
Ravichantar, Nithya |
author_sort |
Ravichantar, Nithya |
title |
Combinatorial Crispr/Cas9 For Suppression Of Latent Hiv-1 Provirus In Vitro |
title_short |
Combinatorial Crispr/Cas9 For Suppression Of Latent Hiv-1 Provirus In Vitro |
title_full |
Combinatorial Crispr/Cas9 For Suppression Of Latent Hiv-1 Provirus In Vitro |
title_fullStr |
Combinatorial Crispr/Cas9 For Suppression Of Latent Hiv-1 Provirus In Vitro |
title_full_unstemmed |
Combinatorial Crispr/Cas9 For Suppression Of Latent Hiv-1 Provirus In Vitro |
title_sort |
combinatorial crispr/cas9 for suppression of latent hiv-1 provirus in vitro |
granting_institution |
Universiti Sains Malaysia |
granting_department |
Institut Perubatan & Pergigian Termaju |
publishDate |
2020 |
url |
http://eprints.usm.my/52124/1/Pages%20from%20Combinatorial%20CrisprCas9%20ForSuppression%20Of%20Latent%20Hiv-1%20Provirus%20In%20Vitro.pdf |
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1747822136102223872 |