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Dissolving Microneedle Delivery of a Prophylactic HPV Vaccine

Sayoni RayDepartment of NanoEngineering  and  Center for Nano-ImmunoEngineering, University of California-San Diego, La Jolla, California 92039, United StatesDavid M. WirthDepartment of NanoEngineering, University of California-San Diego, La Jolla, California 92039, United StatesOscar A. Ortega‐RiveraDepartment of NanoEngineering  and  Center for Nano-ImmunoEngineering, University of California-San Diego, La Jolla, California 92039, United StatesNicole F. SteinmetzDepartment of NanoEngineering,  Center for Nano-ImmunoEngineering,  Institute for Materials Discovery and Design,  Department of Bioengineering,  Department of Radiology  and  Moores Cancer Center, University of California-San Diego, La Jolla, California 92039, United StatesJonathan K. PokorskiDepartment of NanoEngineering,  Center for Nano-ImmunoEngineering  and  Institute for Materials Discovery and Design, University of California-San Diego, La Jolla, California 92039, United States
2022en
ABI

Annotatsiya

Prophylactic vaccines capable of preventing human papillomavirus (HPV) infections are still inaccessible to a vast majority of the global population due to their high cost and challenges related to multiple administrations performed in a medical setting. In an effort to improve distribution and administration, we have developed dissolvable microneedles loaded with a thermally stable HPV vaccine candidate consisting of Qβ virus-like particles (VLPs) displaying a highly conserved epitope from the L2 protein of HPV (Qβ-HPV). Polymeric microneedle delivery of Qβ-HPV produces similar amounts of anti-HPV16 L2 IgG antibodies compared to traditional subcutaneous injection while delivering a much smaller amount of intradermal dose. However, a dose sparing effect was found. Furthermore, immunization yielded neutralizing antibody responses in a HPV pseudovirus assay. The vaccine candidate was confirmed to be stable at room temperature after storage for several months, potentially mitigating many of the challenges associated with cold-chain distribution. The ease of self-administration and minimal invasiveness of such microneedle patch vaccines may enable wide-scale distribution of the HPV vaccine and lead to higher patient compliance. The Qβ VLP and its delivery technology is a plug-and-play system that could serve as a universal platform with a broad range of applications. Qβ VLPs may be stockpiled for conjugation to a wide range of epitopes, which are then packaged and delivered directly to the patient via noninvasive microneedle patches. Such a system paves the way for rapid distribution and self-administration of vaccines.

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