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CD4+ T cell-mimicking nanoparticles encapsulating DIABLO/SMAC mimetics broadly neutralize HIV-1 and selectively kill HIV-1-infected cells

HIV-1 is a major global health challenge. The development of an effective vaccine and a therapeutic cure are top priorities. The creation of vaccines that focus an antibody response toward a particular epitope of a protein has shown promise, but the genetic diversity of HIV-1 stymies this progress....

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Autores principales: Campbell, Grant R., Zhuang, Jia, Zhang, Gang, Landa, Igor, Kubiatowicz, Luke J., Dehaini, Diana, Fang, Ronnie H., Zhang, Liangfang, Spector, Stephen A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419049/
https://www.ncbi.nlm.nih.gov/pubmed/34522224
http://dx.doi.org/10.7150/thno.59728
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author Campbell, Grant R.
Zhuang, Jia
Zhang, Gang
Landa, Igor
Kubiatowicz, Luke J.
Dehaini, Diana
Fang, Ronnie H.
Zhang, Liangfang
Spector, Stephen A.
author_facet Campbell, Grant R.
Zhuang, Jia
Zhang, Gang
Landa, Igor
Kubiatowicz, Luke J.
Dehaini, Diana
Fang, Ronnie H.
Zhang, Liangfang
Spector, Stephen A.
author_sort Campbell, Grant R.
collection PubMed
description HIV-1 is a major global health challenge. The development of an effective vaccine and a therapeutic cure are top priorities. The creation of vaccines that focus an antibody response toward a particular epitope of a protein has shown promise, but the genetic diversity of HIV-1 stymies this progress. Therapeutic strategies that provide effective and broad‐spectrum neutralization against HIV-1 infection are highly desirable. Methods: We investigated the potential of nanoengineered CD4+ T cell membrane-coated nanoparticles (TNP) encapsulating the DIABLO/SMAC mimetics LCL-161 or AT-406 (also known as SM-406 or Debio 1143) to both neutralize HIV-1 and selectively kill HIV-1-infected resting CD4+ T cells and macrophages. Results: DIABLO/SMAC mimetic-loaded TNP displayed outstanding neutralizing breadth and potency, and selectively kill HIV-1-infected cells via autophagy-dependent apoptosis while having no drug-induced off-target or cytotoxic effects on bystander cells. Genetic inhibition of early stages of autophagy abolishes this effect. Conclusion: DIABLO/SMAC mimetic loaded TNP have the potential to be used as therapeutic agents to neutralize cell-free HIV-1 and to kill specifically HIV-1-infected cells as part of an HIV-1 cure strategy.
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spelling pubmed-84190492021-09-13 CD4+ T cell-mimicking nanoparticles encapsulating DIABLO/SMAC mimetics broadly neutralize HIV-1 and selectively kill HIV-1-infected cells Campbell, Grant R. Zhuang, Jia Zhang, Gang Landa, Igor Kubiatowicz, Luke J. Dehaini, Diana Fang, Ronnie H. Zhang, Liangfang Spector, Stephen A. Theranostics Research Paper HIV-1 is a major global health challenge. The development of an effective vaccine and a therapeutic cure are top priorities. The creation of vaccines that focus an antibody response toward a particular epitope of a protein has shown promise, but the genetic diversity of HIV-1 stymies this progress. Therapeutic strategies that provide effective and broad‐spectrum neutralization against HIV-1 infection are highly desirable. Methods: We investigated the potential of nanoengineered CD4+ T cell membrane-coated nanoparticles (TNP) encapsulating the DIABLO/SMAC mimetics LCL-161 or AT-406 (also known as SM-406 or Debio 1143) to both neutralize HIV-1 and selectively kill HIV-1-infected resting CD4+ T cells and macrophages. Results: DIABLO/SMAC mimetic-loaded TNP displayed outstanding neutralizing breadth and potency, and selectively kill HIV-1-infected cells via autophagy-dependent apoptosis while having no drug-induced off-target or cytotoxic effects on bystander cells. Genetic inhibition of early stages of autophagy abolishes this effect. Conclusion: DIABLO/SMAC mimetic loaded TNP have the potential to be used as therapeutic agents to neutralize cell-free HIV-1 and to kill specifically HIV-1-infected cells as part of an HIV-1 cure strategy. Ivyspring International Publisher 2021-08-25 /pmc/articles/PMC8419049/ /pubmed/34522224 http://dx.doi.org/10.7150/thno.59728 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Campbell, Grant R.
Zhuang, Jia
Zhang, Gang
Landa, Igor
Kubiatowicz, Luke J.
Dehaini, Diana
Fang, Ronnie H.
Zhang, Liangfang
Spector, Stephen A.
CD4+ T cell-mimicking nanoparticles encapsulating DIABLO/SMAC mimetics broadly neutralize HIV-1 and selectively kill HIV-1-infected cells
title CD4+ T cell-mimicking nanoparticles encapsulating DIABLO/SMAC mimetics broadly neutralize HIV-1 and selectively kill HIV-1-infected cells
title_full CD4+ T cell-mimicking nanoparticles encapsulating DIABLO/SMAC mimetics broadly neutralize HIV-1 and selectively kill HIV-1-infected cells
title_fullStr CD4+ T cell-mimicking nanoparticles encapsulating DIABLO/SMAC mimetics broadly neutralize HIV-1 and selectively kill HIV-1-infected cells
title_full_unstemmed CD4+ T cell-mimicking nanoparticles encapsulating DIABLO/SMAC mimetics broadly neutralize HIV-1 and selectively kill HIV-1-infected cells
title_short CD4+ T cell-mimicking nanoparticles encapsulating DIABLO/SMAC mimetics broadly neutralize HIV-1 and selectively kill HIV-1-infected cells
title_sort cd4+ t cell-mimicking nanoparticles encapsulating diablo/smac mimetics broadly neutralize hiv-1 and selectively kill hiv-1-infected cells
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419049/
https://www.ncbi.nlm.nih.gov/pubmed/34522224
http://dx.doi.org/10.7150/thno.59728
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