2016
DOI: 10.1080/21645515.2016.1239668
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Current prospects and future challenges for nasal vaccine delivery

Abstract: Nasal delivery offers many benefits over traditional approaches to vaccine administration. These include ease of administration without needles that reduces issues associated with needlestick injuries and disposal. Additionally, this route offers easy access to a key part of the immune system that can stimulate other mucosal sites throughout the body. Increased acceptance of nasal vaccine products in both adults and children has led to a burgeoning pipeline of nasal delivery technology. Key challenges and oppo… Show more

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Cited by 122 publications
(91 citation statements)
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“…Indeed, sterilizing immunity to influenza A virus re-infection requires local adaptive immune responses in the lung, which is optimally induced by intranasal and not intramuscular inoculation (Dutta et al, 2016;Laurie et al, 2010). While there are concerns with administering live-attenuated viral vaccines via an intranasal route, subunit-based or replication-incompetent vectored vaccines are promising for generating mucosal immunity in a safer manner, especially given advances in formulation (Yusuf and Kett, 2017).…”
Section: Discussionmentioning
confidence: 99%
“…Indeed, sterilizing immunity to influenza A virus re-infection requires local adaptive immune responses in the lung, which is optimally induced by intranasal and not intramuscular inoculation (Dutta et al, 2016;Laurie et al, 2010). While there are concerns with administering live-attenuated viral vaccines via an intranasal route, subunit-based or replication-incompetent vectored vaccines are promising for generating mucosal immunity in a safer manner, especially given advances in formulation (Yusuf and Kett, 2017).…”
Section: Discussionmentioning
confidence: 99%
“…In contrast, oral delivery is the most desirable route, especially for mass immunizations. Importantly, mucosal vaccine delivery, including oral strategies, not only generates systemic immune responses but can also trigger mucosal immunity, which prevents the initial mucosal colonization of a pathogen [7][8][9]. The challenge with oral administration is that vaccine components such as proteins, polysaccharides, and peptides are extremely labile and are degraded while passing through the stomach and gut [10].…”
Section: Introductionmentioning
confidence: 99%
“…11,12) Several veterinary vaccines against dermatomycosis, including Insol Dermatophyton, Biocan-M, and RIVAC Mikroderm, are clinically available. 17,18) Although Cn: C. neoformans; Cg: C. gattii; HK: heat-killed; ND: not determined; ∆cna1: disruptant of gene coding calcineurin A1, avirulent temperature-sensitive mutant; ∆cda1/2/3: disruptant of three genes coding chitin deacetylase, chitosan-deficient avirulent strain; ∆sgl1: disruptant of gene coding sterylglucosidase-1, avirulent strain accumulating sterylglucosides; ∆cap59, ∆cap60: disruptant of capsule synthesis-related gene, acapsular mutant; ZNF2: gene coding the transcriptional factor, zinc finger protein (the overexpression strain forms hyphae in C. neoformans, and this strain strongly induced inflammatory response in the lungs after infection); ura5: mutant of orotidine monophosphate pyrophosphorylase which is uracil auxotrophic and can proliferate in medium containing 5-fluoroorotic acid (5-FOA) (wild-type cryptococcal cells used for immunization cannot grow in the medium and thus cryptococcal cells for immunization and challenge are distinguishable on plates containing 5-FOA); Th1: CD4 + helper T cells producing IFN-γ; Th17: CD4 + helper T cells producing IL-17A; μMT mice: B-cell deficient mice; DR4 mice: humanized mice expressing human HLA-DR4 (DRB*0401) and lacking endogenous mouse MHC class II; Aβ null mice: MHC class II-deficient mice in which CD4 + T cells are absent; Protection (+/−): +=immunization improved survival rates or reduced fungal burdens after challenge. Other abbreviations are defined in the main text.…”
Section: History Of Cryptococcal Vaccinesmentioning
confidence: 99%
“…To augment pulmonary local immunity more efficiently, intranasal forms are being used in the development of experimental and clinical vaccines against pulmonary infectious diseases including influenza, tuberculosis, pertussis, and pneumococcal infection. 19) Vaccines generally induce memory B cells and antibodymediated immunity (AMI), while several cryptococcal vaccines depend on T cell-mediated immunity (CMI) including the delayed-type hypersensitivity (DTH) response in a B cellindependent manner. [20][21][22] Since C. neoformans often infects immunocompromised hosts such as AIDS patients, vaccines have also been evaluated in immunodeficient mice lacking T cells, B cells, and/or other immune cells.…”
Section: History Of Cryptococcal Vaccinesmentioning
confidence: 99%