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Esmaeili Gouvarchin Ghaleh, Hadi, Mahabadi, Mostafa, Farzanehpour, Mahdieh, Zahiri, Ali, Mirzaei Nodoushan, Majid. (1404). Virus-Like Particles (Vlps) from Synthesis to Targeted Drug Delivery, Vaccine Approaches, and Gene Therapy. سامانه مدیریت نشریات علمی, 80(4), 833-842. doi: 10.32592/ARI.2025.80.4.833
Hadi Esmaeili Gouvarchin Ghaleh; Mostafa Mahabadi; Mahdieh Farzanehpour; Ali Zahiri; Majid Mirzaei Nodoushan. "Virus-Like Particles (Vlps) from Synthesis to Targeted Drug Delivery, Vaccine Approaches, and Gene Therapy". سامانه مدیریت نشریات علمی, 80, 4, 1404, 833-842. doi: 10.32592/ARI.2025.80.4.833
Esmaeili Gouvarchin Ghaleh, Hadi, Mahabadi, Mostafa, Farzanehpour, Mahdieh, Zahiri, Ali, Mirzaei Nodoushan, Majid. (1404). 'Virus-Like Particles (Vlps) from Synthesis to Targeted Drug Delivery, Vaccine Approaches, and Gene Therapy', سامانه مدیریت نشریات علمی, 80(4), pp. 833-842. doi: 10.32592/ARI.2025.80.4.833
Esmaeili Gouvarchin Ghaleh, Hadi, Mahabadi, Mostafa, Farzanehpour, Mahdieh, Zahiri, Ali, Mirzaei Nodoushan, Majid. Virus-Like Particles (Vlps) from Synthesis to Targeted Drug Delivery, Vaccine Approaches, and Gene Therapy. سامانه مدیریت نشریات علمی, 1404; 80(4): 833-842. doi: 10.32592/ARI.2025.80.4.833

Virus-Like Particles (Vlps) from Synthesis to Targeted Drug Delivery, Vaccine Approaches, and Gene Therapy

Archives of Razi Institute
مقاله 3، دوره 80، شماره 4، مهر و آبان 2025، صفحه 833-842    اصل مقاله (560.74 K)
نوع مقاله: Review Article
شناسه دیجیتال (DOI): 10.32592/ARI.2025.80.4.833
نویسندگان
Hadi Esmaeili Gouvarchin Ghaleh1؛ Mostafa Mahabadi1؛ Mahdieh Farzanehpour* 1؛ Ali Zahiri2؛ Majid Mirzaei Nodoushan1
1Applied Virology Research Center, Biomedicine Technologeis Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran.
2Students Research Committee, Baqiyatallah University of Medical Sciences, Tehran, Iran.
چکیده
VLPs are spontaneously generated from viral capsid proteins. VLPs imitate genuine viruses visually and physiologicallybut lack viral DNA. Various VLP designs provide structural and functional appeal. Spontaneous polymerization of viral capsid proteins may result in VLPs with geometrical symmetry, which are often icosahedral, spherical, or rod-like.Moreover, functionalized VLPs may precisely target cancer cells and recruit macrophages to destroy them. The ability to target tumors for therapeutic drug delivery through using VLP-based delivery platforms in novel and intriguing aspects related to cancer treatment is the primary goal of VLP design. Cancer therapies require precise targeting of diagnostic or therapeutic elements to tumor cells while avoiding healthy cells and tissues. VLPs offer an innovative approachas site-specific drug delivery systems reducing systemic toxicity and injury to healthy cells. Immunotherapy, which boosts the host's immune system, has fewer side effects. Cancer vaccines aim to induce an immune response that provides protection against tumor cells. Due to their naturally fitted particle size and repetitive structural order, VLPs may be employed as a vaccine without any adjuvant. This review aims to provide basic information on VLPs and outline current studies on their use as drug and vaccine delivery systems in different cancers, highlighting their potential as a promising cancer treatment strategy. This review aims to provide basic information on VLPs and outline current studies on their use as drug and vaccine delivery systems in different cancers, highlighting their potential as a promising cancer treatment strategy. This review aims to provide basic information on VLPs and outline current studies on their use as drug and vaccine delivery systems in different cancers, highlighting their potential as a promising cancer treatment strategy.
کلیدواژه‌ها
Drug delivery؛ Gene therapy؛ Multi-capsid VLPs؛ Virus-like particles (VLPs )
عنوان مقاله [English]
Virus-Like Particles (Vlps) from Synthesis to Targeted Drug Delivery, Vaccine Approaches, and Gene Therapy
چکیده [English]
VLPs are spontaneously generated from viral capsid proteins. VLPs imitate genuine viruses visually and physiologicallybut lack viral DNA. Various VLP designs provide structural and functional appeal. Spontaneous polymerization of viral capsid proteins may result in VLPs with geometrical symmetry, which are often icosahedral, spherical, or rod-like.Moreover, functionalized VLPs may precisely target cancer cells and recruit macrophages to destroy them. The ability to target tumors for therapeutic drug delivery through using VLP-based delivery platforms in novel and intriguing aspects related to cancer treatment is the primary goal of VLP design. Cancer therapies require precise targeting of diagnostic or therapeutic elements to tumor cells while avoiding healthy cells and tissues. VLPs offer an innovative approachas site-specific drug delivery systems reducing systemic toxicity and injury to healthy cells. Immunotherapy, which boosts the host's immune system, has fewer side effects. Cancer vaccines aim to induce an immune response that provides protection against tumor cells. Due to their naturally fitted particle size and repetitive structural order, VLPs may be employed as a vaccine without any adjuvant. This review aims to provide basic information on VLPs and outline current studies on their use as drug and vaccine delivery systems in different cancers, highlighting their potential as a promising cancer treatment strategy. Recombinant VLP structures can be enhanced by including antigenic epitopes of viruses or different disease-related antigens and targeting peptides to the interior and exterior surfaces,making them potential tools for future immunizations with preventive and regenerative qualities. Additionally, VLP-based delivery strategies may enhance immunogenicity and provide a more effective and safer approach to managing solid cancers with fewer side effects compare to chemotherapy or radiation. However, the production of chimeric VLPs still faces challenges, such as the need for more reliable preclinical animal models and associated costs Despite these obstacles, ongoing research will improve VLP-based technologies and increase their potential advantages.
کلیدواژه‌ها [English]
Drug delivery, Gene therapy, Multi-capsid VLPs, Virus-like particles (VLPs )
سایر فایل های مرتبط با مقاله
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آمار
تعداد مشاهده مقاله: 192
تعداد دریافت فایل اصل مقاله: 195


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