» Articles » PMID: 24253260

Site-specific Genome Editing in PBMCs With PLGA Nanoparticle-delivered PNAs Confers HIV-1 Resistance in Humanized Mice

Overview
Publisher Cell Press
Date 2013 Nov 21
PMID 24253260
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

Biodegradable poly (lactic-co-glycolic acid) (PLGA) nanoparticles (NPs) encapsulating triplex-forming peptide nucleic acids (PNAs) and donor DNAs for recombination-mediated editing of the CCR5 gene were synthesized for delivery into human peripheral blood mononuclear cells (PBMCs). NPs containing the CCR5-targeting molecules efficiently entered PBMCs with low cytotoxicity. Deep sequencing revealed that a single treatment with the formulation resulted in a targeting frequency of 0.97% in the CCR5 gene and a low off-target frequency of 0.004% in the CCR2 gene, a 216-fold difference. NP-treated PBMCs efficiently engrafted immunodeficient NOD-scid IL-2rγ(-/-) mice, and the targeted CCR5 modification was detected in splenic lymphocytes 4 weeks posttransplantation. After infection with an R5-tropic strain of HIV-1, humanized mice with CCR5-NP-treated PBMCs displayed significantly higher levels of CD4(+) T cells and significantly reduced plasma viral RNA loads compared with control mice engrafted with mock-treated PBMCs. This work demonstrates the feasibility of PLGA-NP-encapsulated PNA-based gene-editing molecules for the targeted modification of CCR5 in human PBMCs as a platform for conferring HIV-1 resistance.Molecular Therapy-Nucleic Acids (2013) 2, e135; doi:10.1038/mtna.2013.59; published online 19 November 2013.

Citing Articles

Navigating Latency-Inducing Viral Infections: Therapeutic Targeting and Nanoparticle Utilization.

Vasukutty A, Jang Y, Han D, Park H, Park I Biomater Res. 2024; 28:0078.

PMID: 39416703 PMC: 11480834. DOI: 10.34133/bmr.0078.


Next generation triplex-forming PNAs for site-specific genome editing of the F508del CFTR mutation.

Gupta A, Barone C, Quijano E, Piotrowski-Daspit A, Perera J, Riccardi A J Cyst Fibros. 2024; 24(1):142-148.

PMID: 39107154 PMC: 11788067. DOI: 10.1016/j.jcf.2024.07.009.


DNA recognition and induced genome modification by a hydroxymethyl-γ tail-clamp peptide nucleic acid.

Oyaghire S, Quijano E, Perera J, Mandl H, Saltzman W, Bahal R Cell Rep Phys Sci. 2023; 4(10).

PMID: 37920723 PMC: 10621889. DOI: 10.1016/j.xcrp.2023.101635.


Cationic Calix[4]arene Vectors to Efficiently Deliver AntimiRNA Peptide Nucleic Acids (PNAs) and miRNA Mimics.

Gasparello J, Papi C, Zurlo M, Volpi S, Gambari R, Corradini R Pharmaceutics. 2023; 15(8).

PMID: 37631335 PMC: 10460053. DOI: 10.3390/pharmaceutics15082121.


In vivo correction of cystic fibrosis mediated by PNA nanoparticles.

Piotrowski-Daspit A, Barone C, Lin C, Deng Y, Wu D, Binns T Sci Adv. 2022; 8(40):eabo0522.

PMID: 36197984 PMC: 9534507. DOI: 10.1126/sciadv.abo0522.


References
1.
Park M, Chung S, Park Y, Lee S . Pro-inflammatory effect of leptin on peripheral blood mononuclear cells of patients with ankylosing spondylitis. Joint Bone Spine. 2008; 76(2):170-5. DOI: 10.1016/j.jbspin.2008.04.018. View

2.
Schleifman E, Bindra R, Leif J, del Campo J, Rogers F, Uchil P . Targeted disruption of the CCR5 gene in human hematopoietic stem cells stimulated by peptide nucleic acids. Chem Biol. 2011; 18(9):1189-98. PMC: 3183429. DOI: 10.1016/j.chembiol.2011.07.010. View

3.
Zhou J, Patel T, Fu M, Bertram J, Saltzman W . Octa-functional PLGA nanoparticles for targeted and efficient siRNA delivery to tumors. Biomaterials. 2011; 33(2):583-91. PMC: 4204797. DOI: 10.1016/j.biomaterials.2011.09.061. View

4.
Jain A, Bacolla A, Chakraborty P, Grosse F, Vasquez K . Human DHX9 helicase unwinds triple-helical DNA structures. Biochemistry. 2010; 49(33):6992-9. PMC: 2949957. DOI: 10.1021/bi100795m. View

5.
Allain J, Laurian Y, Paul D, Verroust F, Leuther M, Gazengel C . Long-term evaluation of HIV antigen and antibodies to p24 and gp41 in patients with hemophilia. Potential clinical importance. N Engl J Med. 1987; 317(18):1114-21. DOI: 10.1056/NEJM198710293171804. View