2019
DOI: 10.1016/j.vaccine.2019.08.077
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Intranasal nanoemulsion-adjuvanted HSV-2 subunit vaccine is effective as a prophylactic and therapeutic vaccine using the guinea pig model of genital herpes

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Cited by 27 publications
(15 citation statements)
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“…Despite setbacks over three decades [ 77 , 85 , 90 , 91 , 92 ], optimism is grounded on progress in basic science and results of vaccine candidates currently in phase I and/or II trials [ 29 , 35 , 93 ]. Optimism is also grounded on several lines of evidence suggesting vaccine feasibility [ 35 ], including improved understanding of HSV immunology [ 35 , 40 , 94 , 95 ], growing knowledge of the optimal combination of antigens and adjuvants that could lead to vaccine protection [ 77 , 85 , 93 , 95 , 96 , 97 , 98 , 99 , 100 , 101 ], success and availability of both prophylactic and therapeutic vaccines against varicella zoster virus (VZV) [ 35 , 102 , 103 ], which is a closely related alpha-herpes virus, success and availability of animal herpes vaccines such as the bovine herpesvirus-1 [ 104 ] and the suid herpesvirus-1 (pseudorabies virus) [ 35 , 105 ], demonstration that intramuscular vaccination can induce genital mucosal immunity [ 35 ], as is the case for HPV vaccination [ 106 ], and the partial protection in the Herpvac trial against HSV-1 infection and genital disease [ 35 , 85 ] given the strong homology between HSV-1 and HSV-2 viruses [ 17 , 82 ].…”
Section: Discussionmentioning
confidence: 99%
“…Despite setbacks over three decades [ 77 , 85 , 90 , 91 , 92 ], optimism is grounded on progress in basic science and results of vaccine candidates currently in phase I and/or II trials [ 29 , 35 , 93 ]. Optimism is also grounded on several lines of evidence suggesting vaccine feasibility [ 35 ], including improved understanding of HSV immunology [ 35 , 40 , 94 , 95 ], growing knowledge of the optimal combination of antigens and adjuvants that could lead to vaccine protection [ 77 , 85 , 93 , 95 , 96 , 97 , 98 , 99 , 100 , 101 ], success and availability of both prophylactic and therapeutic vaccines against varicella zoster virus (VZV) [ 35 , 102 , 103 ], which is a closely related alpha-herpes virus, success and availability of animal herpes vaccines such as the bovine herpesvirus-1 [ 104 ] and the suid herpesvirus-1 (pseudorabies virus) [ 35 , 105 ], demonstration that intramuscular vaccination can induce genital mucosal immunity [ 35 ], as is the case for HPV vaccination [ 106 ], and the partial protection in the Herpvac trial against HSV-1 infection and genital disease [ 35 , 85 ] given the strong homology between HSV-1 and HSV-2 viruses [ 17 , 82 ].…”
Section: Discussionmentioning
confidence: 99%
“…There was a higher level of neutralizing antibodies compared to the single-surface glycoprotein candidate vaccine when both were injected into the guinea pig model. Furthermore, there was a significant reduction in the ability of the challenge of HSV-2 establishing latent infection in the dorsal root ganglia of the vaccinated guinea pigs [ 153 ].…”
Section: Hsv Vaccination and Immunotherapiesmentioning
confidence: 99%
“…Apart from antiviral drug delivery, the NE system was effectively utilized as an immunization vehicle to deliver/present the inactivated viral proteins to the host immune system. NE was prepared by emulsification of soybean oil, Tween 80, cetylpyridinium chloride, ethanol, and water and used to develop intranasal vaccine containing HSV-2 surface glycoproteins gD2 and gB2 (NE01-gD2/gB2) [ 86 ]. The guinea pigs were immunized either intranasally or intramuscularly with NE01-gD2/gB2 at 63, 42, and 21 days before viral treatment.…”
Section: Role Of Eo-mes and -Nes In Viral Vaccine Deliverymentioning
confidence: 99%
“…Furthermore, only 1 in 12 NE01-gD2/gB2-intranasally vaccinated animals was detected with the latent virus at dorsal root ganglia. In the therapeutic study, a significant reduction in the recurrent lesions in the guinea pigs immunized with NE01-gD2/gB2 (intranasal) was observed [ 86 ]. In the same NE01 system plant-derived recombinant influenza H5 (rH5) antigen was incorporated to produce a novel intranasal influenza vaccine.…”
Section: Role Of Eo-mes and -Nes In Viral Vaccine Deliverymentioning
confidence: 99%