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Advancements in DNA vaccine vectors, non-mechanical delivery methods, and molecular adjuvants to increase immunogenicity

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TLDR
Advances in DNA vaccine vector design, the inclusion of genetically engineered cytokine adjuvants, and novel non-mechanical delivery methods show promise for increasing the immunogenicity of DNA vaccines.
Abstract
A major advantage of DNA vaccination is the ability to induce both humoral and cellular immune responses. DNA vaccines are currently used in veterinary medicine, but have not achieved widespread acceptance for use in humans due to their low immunogenicity in early clinical studies. However, recent clinical data have re-established the value of DNA vaccines, particularly in priming high-level antigen-specific antibody responses. Several approaches have been investigated for improving DNA vaccine efficacy, including advancements in DNA vaccine vector design, the inclusion of genetically engineered cytokine adjuvants, and novel non-mechanical delivery methods. These strategies have shown promise, resulting in augmented adaptive immune responses in not only mice, but also in large animal models. Here, we review advancements in each of these areas that show promise for increasing the immunogenicity of DNA vaccines.

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mRNA vaccines — a new era in vaccinology

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DNA Vaccines-How Far From Clinical Use?

TL;DR: Improvements in DNA vaccine design include the use of APC-specific promotors for transcriptional targeting, the arrangement of multiple antigen sequences, the co-delivery of molecular adjuvants to prevent tolerance induction, and strategies to circumvent potential inhibitory effects of the vector backbone.
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TL;DR: This review summarizes the most important developments in mRNA vaccines from the past few years and discusses the challenges and future directions for the field.
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COVID-19 vaccines: The status and perspectives in delivery points of view.

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Cancer DNA vaccines: current preclinical and clinical developments and future perspectives.

TL;DR: The strategies that are being developed to overcome the limitations in cancer DNA vaccination are investigated, revisiting the rationale for different combinations of therapy and the different possibilities in antigen choice.
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