The next-generation DNA vaccine platforms and delivery systems: advances, challenges and prospects
Vaccines have proven effective in the treatment and prevention of numerous diseases. However, traditional attenuated and inactivated vaccines suffer from certain drawbacks such as complex preparation, limited efficacy, potential risks and others. These limitations restrict their widespread use, espe...
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Published in | Frontiers in immunology Vol. 15; p. 1332939 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
01.02.2024
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Online Access | Get full text |
ISSN | 1664-3224 1664-3224 |
DOI | 10.3389/fimmu.2024.1332939 |
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Abstract | Vaccines have proven effective in the treatment and prevention of numerous diseases. However, traditional attenuated and inactivated vaccines suffer from certain drawbacks such as complex preparation, limited efficacy, potential risks and others. These limitations restrict their widespread use, especially in the face of an increasingly diverse range of diseases. With the ongoing advancements in genetic engineering vaccines, DNA vaccines have emerged as a highly promising approach in the treatment of both genetic diseases and acquired diseases. While several DNA vaccines have demonstrated substantial success in animal models of diseases, certain challenges need to be addressed before application in human subjects. The primary obstacle lies in the absence of an optimal delivery system, which significantly hampers the immunogenicity of DNA vaccines. We conduct a comprehensive analysis of the current status and limitations of DNA vaccines by focusing on both viral and non-viral DNA delivery systems, as they play crucial roles in the exploration of novel DNA vaccines. We provide an evaluation of their strengths and weaknesses based on our critical assessment. Additionally, the review summarizes the most recent advancements and breakthroughs in pre-clinical and clinical studies, highlighting the need for further clinical trials in this rapidly evolving field. |
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AbstractList | Vaccines have proven effective in the treatment and prevention of numerous diseases. However, traditional attenuated and inactivated vaccines suffer from certain drawbacks such as complex preparation, limited efficacy, potential risks and others. These limitations restrict their widespread use, especially in the face of an increasingly diverse range of diseases. With the ongoing advancements in genetic engineering vaccines, DNA vaccines have emerged as a highly promising approach in the treatment of both genetic diseases and acquired diseases. While several DNA vaccines have demonstrated substantial success in animal models of diseases, certain challenges need to be addressed before application in human subjects. The primary obstacle lies in the absence of an optimal delivery system, which significantly hampers the immunogenicity of DNA vaccines. We conduct a comprehensive analysis of the current status and limitations of DNA vaccines by focusing on both viral and non-viral DNA delivery systems, as they play crucial roles in the exploration of novel DNA vaccines. We provide an evaluation of their strengths and weaknesses based on our critical assessment. Additionally, the review summarizes the most recent advancements and breakthroughs in pre-clinical and clinical studies, highlighting the need for further clinical trials in this rapidly evolving field. Vaccines have proven effective in the treatment and prevention of numerous diseases. However, traditional attenuated and inactivated vaccines suffer from certain drawbacks such as complex preparation, limited efficacy, potential risks and others. These limitations restrict their widespread use, especially in the face of an increasingly diverse range of diseases. With the ongoing advancements in genetic engineering vaccines, DNA vaccines have emerged as a highly promising approach in the treatment of both genetic diseases and acquired diseases. While several DNA vaccines have demonstrated substantial success in animal models of diseases, certain challenges need to be addressed before application in human subjects. The primary obstacle lies in the absence of an optimal delivery system, which significantly hampers the immunogenicity of DNA vaccines. We conduct a comprehensive analysis of the current status and limitations of DNA vaccines by focusing on both viral and non-viral DNA delivery systems, as they play crucial roles in the exploration of novel DNA vaccines. We provide an evaluation of their strengths and weaknesses based on our critical assessment. Additionally, the review summarizes the most recent advancements and breakthroughs in pre-clinical and clinical studies, highlighting the need for further clinical trials in this rapidly evolving field.Vaccines have proven effective in the treatment and prevention of numerous diseases. However, traditional attenuated and inactivated vaccines suffer from certain drawbacks such as complex preparation, limited efficacy, potential risks and others. These limitations restrict their widespread use, especially in the face of an increasingly diverse range of diseases. With the ongoing advancements in genetic engineering vaccines, DNA vaccines have emerged as a highly promising approach in the treatment of both genetic diseases and acquired diseases. While several DNA vaccines have demonstrated substantial success in animal models of diseases, certain challenges need to be addressed before application in human subjects. The primary obstacle lies in the absence of an optimal delivery system, which significantly hampers the immunogenicity of DNA vaccines. We conduct a comprehensive analysis of the current status and limitations of DNA vaccines by focusing on both viral and non-viral DNA delivery systems, as they play crucial roles in the exploration of novel DNA vaccines. We provide an evaluation of their strengths and weaknesses based on our critical assessment. Additionally, the review summarizes the most recent advancements and breakthroughs in pre-clinical and clinical studies, highlighting the need for further clinical trials in this rapidly evolving field. |
Author | Bonam, Srinivasa Reddy Kurapati, Rajendra K, Pavithra Lu, Bowen Lim, Jing Ming Yu, Boyue Zheng, Junnian Song, Siyuan Neeli, Praveen Sobhani, Navid Chai, Dafei |
AuthorAffiliation | 7 School of Chemistry, Indian Institute of Science Education and Research Thiruvananthapuram , Thiruvananthapuram , India 8 Department of Microbiology and Immunology, University of Texas Medical Branch , Galveston, TX , United States 3 Center of Clinical Oncology, Affiliated Hospital of Xuzhou Medical University , Xuzhou, Jiangsu , China 4 Department of Medicine, Baylor College of Medicine , Houston, TX , United States 5 Department of Environmental Science, Policy, and Management, University of California at Berkeley , Berkeley, CA , United States 2 Jiangsu Center for the Collaboration and Innovation of Cancer Biotherapy, Cancer Institute, Xuzhou Medical University , Xuzhou, Jiangsu , China 1 Cancer Institute, Xuzhou Medical University , Xuzhou, Jiangsu , China 6 Department of Neuroscience, Baylor College of Medicine , Houston, TX , United States |
AuthorAffiliation_xml | – name: 8 Department of Microbiology and Immunology, University of Texas Medical Branch , Galveston, TX , United States – name: 5 Department of Environmental Science, Policy, and Management, University of California at Berkeley , Berkeley, CA , United States – name: 3 Center of Clinical Oncology, Affiliated Hospital of Xuzhou Medical University , Xuzhou, Jiangsu , China – name: 2 Jiangsu Center for the Collaboration and Innovation of Cancer Biotherapy, Cancer Institute, Xuzhou Medical University , Xuzhou, Jiangsu , China – name: 4 Department of Medicine, Baylor College of Medicine , Houston, TX , United States – name: 7 School of Chemistry, Indian Institute of Science Education and Research Thiruvananthapuram , Thiruvananthapuram , India – name: 1 Cancer Institute, Xuzhou Medical University , Xuzhou, Jiangsu , China – name: 6 Department of Neuroscience, Baylor College of Medicine , Houston, TX , United States |
Author_xml | – sequence: 1 givenname: Bowen surname: Lu fullname: Lu, Bowen – sequence: 2 givenname: Jing Ming surname: Lim fullname: Lim, Jing Ming – sequence: 3 givenname: Boyue surname: Yu fullname: Yu, Boyue – sequence: 4 givenname: Siyuan surname: Song fullname: Song, Siyuan – sequence: 5 givenname: Praveen surname: Neeli fullname: Neeli, Praveen – sequence: 6 givenname: Navid surname: Sobhani fullname: Sobhani, Navid – sequence: 7 givenname: Pavithra surname: K fullname: K, Pavithra – sequence: 8 givenname: Srinivasa Reddy surname: Bonam fullname: Bonam, Srinivasa Reddy – sequence: 9 givenname: Rajendra surname: Kurapati fullname: Kurapati, Rajendra – sequence: 10 givenname: Junnian surname: Zheng fullname: Zheng, Junnian – sequence: 11 givenname: Dafei surname: Chai fullname: Chai, Dafei |
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Copyright | Copyright © 2024 Lu, Lim, Yu, Song, Neeli, Sobhani, K, Bonam, Kurapati, Zheng and Chai. Copyright © 2024 Lu, Lim, Yu, Song, Neeli, Sobhani, K, Bonam, Kurapati, Zheng and Chai 2024 Lu, Lim, Yu, Song, Neeli, Sobhani, K, Bonam, Kurapati, Zheng and Chai |
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SubjectTerms | Animals delivery system DNA vaccines Drug Delivery Systems Humans Immunology Models, Animal nanoparticles non-viral vectors Vaccines, DNA viral vectors |
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Title | The next-generation DNA vaccine platforms and delivery systems: advances, challenges and prospects |
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