Biomaterial‐based gene therapy DOI Creative Commons
Yi Yu, Yijun Gao,

Liming He

et al.

MedComm, Journal Year: 2023, Volume and Issue: 4(3)

Published: June 1, 2023

Gene therapy, a medical approach that involves the correction or replacement of defective and abnormal genes, plays an essential role in treatment complex refractory diseases, such as hereditary cancer, rheumatic immune diseases. Nucleic acids alone do not easily enter target cells due to their easy degradation vivo structure cell membranes. The introduction genes into biological is often dependent on gene delivery vectors, adenoviral which are commonly used therapy. However, traditional viral vectors have strong immunogenicity while also presenting potential infection risk. Recently, biomaterials attracted attention for use efficient vehicles, because they can avoid drawbacks associated with vectors. Biomaterials improve stability nucleic efficiency intracellular delivery. This review focused biomaterial-based systems therapy disease treatment. Herein, we recent developments modalities Additionally, discuss acid strategies, focus systems. Furthermore, current applications summarized.

Language: Английский

From structural design to delivery: mRNA therapeutics for cancer immunotherapy DOI Creative Commons
Feng Zhou, Lujia Huang,

Shiqin Li

et al.

Exploration, Journal Year: 2023, Volume and Issue: 4(2)

Published: Nov. 17, 2023

Abstract mRNA therapeutics have emerged as powerful tools for cancer immunotherapy in accordance with their superiority expressing all sequence‐known proteins vivo. In particular, a small dosage of delivered mRNA, antigen‐presenting cells (APCs) can synthesize mutant neo‐antigens and multi‐antigens present epitopes to T lymphocytes elicit antitumor effects. addition, receptors like chimeric antigen receptor (CAR), T‐cell (TCR), CD134, immune‐modulating factors including cytokines, interferons, antibodies specific enhance immunological response against tumors. With the maturation vitro transcription (IVT) technology, large‐scale pure encoding be synthesized quickly. However, clinical translation mRNA‐based anticancer strategies is restricted by delivering into target organs or inadequate endosomal escape efficiency mRNA. Recently, there been some advances immunotherapy, which roughly classified modifications structure development delivery systems, especially lipid nanoparticle platforms. this review, latest overcoming limitations immunotherapies recent are summarized. Challenges opportunities applications also discussed.

Language: Английский

Citations

55

Lipid Nanoparticles as Promising Carriers for mRNA Vaccines for Viral Lung Infections DOI Creative Commons
Mena Hajiaghapour Asr, Fatemeh Dayani,

Fatemeh Saedi Segherloo

et al.

Pharmaceutics, Journal Year: 2023, Volume and Issue: 15(4), P. 1127 - 1127

Published: April 3, 2023

In recent years, there has been an increase in deaths due to infectious diseases, most notably the context of viral respiratory pathogens. Consequently, focus shifted search for new therapies, with attention being drawn use nanoparticles mRNA vaccines targeted delivery improve efficacy these vaccines. Notably, vaccine technologies denote as a era vaccination their rapid, potentially inexpensive, and scalable development. Although they do not pose risk integration into genome are produced from elements, challenges, including exposing naked mRNAs extracellular endonucleases. Therefore, development nanotechnology, we can further efficacy. Nanoparticles, nanometer dimensions, move more freely body and, small size, have unique physical chemical properties. The best candidates transfer lipid (LNPs), which stable biocompatible contain four components: cationic lipids, ionizable polyethylene glycols (PEGs), cholesterol, used facilitate cytoplasmic delivery. this article, components system mRNA-LNP against lung infections such influenza, coronavirus, syncytial virus reviewed. Moreover, provide succinct overview current challenges potential future directions field.

Language: Английский

Citations

46

Nanoparticle technology for mRNA: Delivery strategy, clinical application and developmental landscape DOI Creative Commons
Xiang Li, Jing Qi, Juan Wang

et al.

Theranostics, Journal Year: 2024, Volume and Issue: 14(2), P. 738 - 760

Published: Jan. 1, 2024

The mRNA vaccine, a groundbreaking advancement in the field of immunology, has garnered international recognition by being awarded prestigious Nobel Prize, which emerged as promising prophylactic and therapeutic modality for various diseases, especially cancer, rare disease, infectious disease such COVID-19, wherein successful treatment can be achieved improving stability introducing safe effective delivery system. Nanotechnology-based systems, lipid nanoparticles, lipoplexes, polyplexes, lipid-polymer hybrid nanoparticles others, have attracted great interest been explored delivery. Nanoscale platforms protect from extracellular degradation while promoting endosome escape after endocytosis, hence efficacy. This review provides an overview diverse nanoplatforms utilized preclinical clinical stages, including formulation, preparation process, transfection efficiency, administration route. Furthermore, market situation prospects vaccines are discussed here.

Language: Английский

Citations

33

Exosome for mRNA delivery: strategies and therapeutic applications DOI Creative Commons

Zoya Iqbal,

Khurrum Rehman,

Ayesha Mahmood

et al.

Journal of Nanobiotechnology, Journal Year: 2024, Volume and Issue: 22(1)

Published: July 4, 2024

Abstract Messenger RNA (mRNA) has emerged as a promising therapeutic molecule with numerous clinical applications in treating central nervous system disorders, tumors, COVID-19, and other diseases. mRNA therapies must be encapsulated into safe, stable, effective delivery vehicles to preserve the cargo from degradation prevent immunogenicity. Exosomes have gained growing attention because of their good biocompatibility, low immunogenicity, small size, unique capacity traverse physiological barriers, cell-specific tropism. Moreover, these exosomes can engineered utilize natural carriers target specific cells or tissues. This targeted approach will enhance efficacy reduce side effects mRNAs. However, difficulties such lack consistent reliable methods for exosome purification efficient encapsulation large mRNAs addressed. article outlines current breakthroughs cell-derived vesicle-mediated its biomedical applications. Graphical

Language: Английский

Citations

30

mRNA vaccine platforms: linking infectious disease prevention and cancer immunotherapy DOI Creative Commons
Dariush Haghmorad, Majid Eslami,

Niloufar Orooji

et al.

Frontiers in Bioengineering and Biotechnology, Journal Year: 2025, Volume and Issue: 13

Published: March 12, 2025

The advent of mRNA vaccines, accelerated by the global response to COVID-19 pandemic, marks a transformative shift in vaccine technology. In this article, we discuss development, current applications, and prospects vaccines for both prevention treatment infectious diseases oncology. By leveraging capacity encode antigens within host cells directly, provide versatile scalable platform suitable addressing broad spectrum pathogens tumor-specific antigens. We highlight recent advancements design, innovative delivery mechanisms, ongoing clinical trials, with particular emphasis on their efficacy combating diseases, such as COVID-19, Zika, influenza, well emerging potential cancer immunotherapy. also address critical challenges, including stability, optimization immune responses, broader issue accessibility. Finally, review strategies advancing next-generation aim overcoming limitations technology enhancing preventive therapeutic approaches oncological diseases.

Language: Английский

Citations

3

Polymeric and lipid nanoparticles for delivery of self-amplifying RNA vaccines DOI Creative Commons
Anna K. Blakney, Paul F. McKay, Kai Hu

et al.

Journal of Controlled Release, Journal Year: 2021, Volume and Issue: 338, P. 201 - 210

Published: Aug. 18, 2021

Self-amplifying RNA (saRNA) is a next-generation vaccine platform, but like all nucleic acids, requires delivery vehicle to promote cellular uptake and protect the saRNA from degradation. To date, platforms for have included lipid nanoparticles (LNP), polyplexes cationic nanoemulsions; of these LNP are most clinically advanced with recent FDA approval COVID-19 based-modified mRNA vaccines. While effect on immunogenicity well studied, role biomaterials in effectiveness under investigated. Here, we tested formulated either pABOL, bioreducible polymer, or LNP, characterized protein expression both platforms. We observed that pABOL-formulated resulted higher magnitude expression, formulations were overall more immunogenic. Furthermore, helper phospholipid route administration (intramuscular versus intranasal) impacted two model antigens (influenza hemagglutinin SARS-CoV-2 spike protein). administered intramuscularly, not pABOL intranasally, increased acute interleukin-6 after vaccination. Overall, results indicate systems routes may fulfill different niches within field genetic medicines.

Language: Английский

Citations

97

Gold-Nanostar-Chitosan-Mediated Delivery of SARS-CoV-2 DNA Vaccine for Respiratory Mucosal Immunization: Development and Proof-of-Principle DOI Open Access
Uday Kumar Sukumar, Rayhaneh Afjei, Katherine W. Ferrara

et al.

ACS Nano, Journal Year: 2021, Volume and Issue: 15(11), P. 17582 - 17601

Published: Oct. 27, 2021

The COVID-19 pandemic is caused by the coronavirus SARS-CoV-2 (SC2). A variety of anti-SC2 vaccines have been approved for human applications, including those using messenger RNA (mRNA), adenoviruses expressing SC2 spike (S) protein, and inactivated virus. protective periods immunization afforded these intramuscularly administered are currently unknown. An alternative self-administrable vaccine capable mounting long-lasting immunity via sterilizing neutralizing antibodies would be hugely advantageous in tackling emerging mutant variants. This could also diminish possibility vaccinated individuals acting as passive carriers COVID-19. Here, we investigate potential an intranasal (IN)-delivered DNA encoding S protein BALB/c C57BL/6J immunocompetent mouse models. immune response to IN delivery this SC2-spike transported on a modified gold-chitosan nanocarrier shows strong consistent surge (IgG, IgA, IgM) effective neutralization pseudoviruses proteins different variants (Wuhan, beta, D614G). Immunophenotyping histological analyses reveal chronological events involved recognition antigen resident dendritic cells alveolar macrophages, which prime draining lymph nodes spleen peak SC2-specific cellular humoral responses. attainable high levels IgA lung mucosa tissue-resident memory T can efficiently inhibit its at site entry provide immunity.

Language: Английский

Citations

79

Application of microneedle patches for drug delivery; doorstep to novel therapies DOI Creative Commons

Fateme Nazary Abrbekoh,

Leila Salimi,

Sepideh Saghati

et al.

Journal of Tissue Engineering, Journal Year: 2022, Volume and Issue: 13

Published: Jan. 1, 2022

In the past decade, microneedle-based drug delivery systems showed promising approaches to become suitable and alternative for hypodermic injections can control agent without side effects compared conventional approaches. Despite these advantages, procedure of microfabrication is facing some difficulties. For instance, loading method, stability drugs, retention time are subjects debate. Besides, application novel refining fabrication methods, types materials, instruments other issues that need further attention. Herein, we tried summarize recent achievements in controllable (microneedle patches) vitro vivo settings. addition, discussed influence delivered drugs on cellular mechanism immunization molecular signaling pathways through intradermal route. Understanding putative efficiency microneedle patches human medicine help us develop design sophisticated therapeutic modalities.

Language: Английский

Citations

56

Advances in Nanoparticles for Effective Delivery of RNA Therapeutics DOI Open Access
Min Ji Byun, Jaesung Lim, Se−Na Kim

et al.

BioChip Journal, Journal Year: 2022, Volume and Issue: 16(2), P. 128 - 145

Published: March 3, 2022

Language: Английский

Citations

47

Enzyme-Catalyzed One-Step Synthesis of Ionizable Cationic Lipids for Lipid Nanoparticle-Based mRNA COVID-19 Vaccines DOI
Zhongyu Li, Xue‐Qing Zhang, William Ho

et al.

ACS Nano, Journal Year: 2022, Volume and Issue: 16(11), P. 18936 - 18950

Published: Oct. 21, 2022

Ionizable cationic lipid-containing lipid nanoparticles (LNPs) are the most clinically advanced non-viral gene delivery platforms, holding great potential for therapeutics. This is exemplified by two COVID-19 vaccines employing mRNA-LNP technology from Pfizer/BioNTech and Moderna. Herein, we develop a chemical library of ionizable lipids through one-step chemical-biological enzyme-catalyzed esterification method, synthesized were further prepared to be LNPs mRNA delivery. Through orthogonal design experiment methodology screening, top-performing AA3-DLin show outstanding efficacy long-term storage capability. Furthermore, LNP encapsulating SARS-CoV-2 spike mRNAs successfully induced strong immunogenicity in BALB/c mouse model demonstrated antibody titers, virus challenge, T cell immune response studies. The developed an excellent platform, this study provides overall perspective lipids, aspects design, synthesis, optimization, fabrication, characterization, application.

Language: Английский

Citations

46