Appraisal for the Potential of Viral and Nonviral Vectors in Gene Therapy: A Review.

gene delivery gene expression gene therapy nonviral vectors transgene viral vectors

Journal

Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097

Informations de publication

Date de publication:
30 07 2022
Historique:
received: 17 06 2022
revised: 24 07 2022
accepted: 26 07 2022
entrez: 26 8 2022
pubmed: 27 8 2022
medline: 30 8 2022
Statut: epublish

Résumé

Over the past few decades, gene therapy has gained immense importance in medical research as a promising treatment strategy for diseases such as cancer, AIDS, Alzheimer's disease, and many genetic disorders. When a gene needs to be delivered to a target cell inside the human body, it has to pass a large number of barriers through the extracellular and intracellular environment. This is why the delivery of naked genes and nucleic acids is highly unfavorable, and gene delivery requires suitable vectors that can carry the gene cargo to the target site and protect it from biological degradation. To date, medical research has come up with two types of gene delivery vectors, which are viral and nonviral vectors. The ability of viruses to protect transgenes from biological degradation and their capability to efficiently cross cellular barriers have allowed gene therapy research to develop new approaches utilizing viruses and their different genomes as vectors for gene delivery. Although viral vectors are very efficient, science has also come up with numerous nonviral systems based on cationic lipids, cationic polymers, and inorganic particles that provide sustainable gene expression without triggering unwanted inflammatory and immune reactions, and that are considered nontoxic. In this review, we discuss in detail the latest data available on all viral and nonviral vectors used in gene delivery. The mechanisms of viral and nonviral vector-based gene delivery are presented, and the advantages and disadvantages of all types of vectors are also given.

Identifiants

pubmed: 36011281
pii: genes13081370
doi: 10.3390/genes13081370
pmc: PMC9407213
pii:
doi:

Substances chimiques

Cations 0
Nucleic Acids 0

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Muhammad Hammad Butt (MH)

Department of Pharmaceutics, Faculty of Pharmacy, University of Central Punjab, Lahore 54000, Pakistan.

Muhammad Zaman (M)

Department of Pharmaceutics, Faculty of Pharmacy, University of Central Punjab, Lahore 54000, Pakistan.

Abrar Ahmad (A)

Department of Pharmaceutics, Faculty of Pharmacy, University of Central Punjab, Lahore 54000, Pakistan.

Rahima Khan (R)

Department of Pharmaceutics, Faculty of Pharmacy, University of Central Punjab, Lahore 54000, Pakistan.

Tauqeer Hussain Mallhi (TH)

Department of Clinical Pharmacy, College of Pharmacy, Jouf University, Sakaka 72341, Saudi Arabia.

Mohammad Mehedi Hasan (MM)

Department of Biochemistry and Molecular Biology, Faculty of Life Science, Mawlana Bhashani Science and Technology University, Tangail 1902, Bangladesh.

Yusra Habib Khan (YH)

Department of Clinical Pharmacy, College of Pharmacy, Jouf University, Sakaka 72341, Saudi Arabia.

Sara Hafeez (S)

Department of Biotechnology, Quaid-i-Azam University, Islamabad 45320, Pakistan.

Ehab El Sayed Massoud (EES)

Biology Department, Faculty of Science and Arts in Dahran Aljnoub, King Khalid University, Abha 62529, Saudi Arabia.
Research Center for Advanced Materials Science (RCAMS), King Khalid University, Abha 61413, Saudi Arabia.
Agriculture Research Centre, Soil, Water and Environment Research Institute, Giza 3725004, Egypt.

Md Habibur Rahman (MH)

Department of Global Medical Science, Wonju College of Medicine, Yonsei University, Wonju 26426, Korea.

Simona Cavalu (S)

Faculty of Medicine and Pharmacy, University of Oradea, Pta 1 Decembrie 10, 410087 Oradea, Romania.

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