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  1. Article ; Online: Immunogenicity of poxvirus-based vaccines against Nipah virus.

    Medina-Magües, Emily S / Lopera-Madrid, Jaime / Lo, Michael K / Spiropoulou, Christina F / Montgomery, Joel M / Medina-Magües, Lex G / Salas-Quinchucua, Cristhian / Jiménez-Mora, Angela P / Osorio, Jorge E

    Scientific reports

    2023  Volume 13, Issue 1, Page(s) 11384

    Abstract: ... vaccinia Ankara (MVA) and raccoon pox (RCN) viral vectors expressing the NiV fusion (F) and glycoprotein (G ...

    Abstract Nipah virus (NiV), an emerging zoonotic pathogen in Southeast Asia, is transmitted from Pteropus species of fruit bats to a wide range of species, including humans, pigs, horses, dogs, and cats. NiV has killed millions of animals and caused highly fatal human outbreaks since no vaccine is commercially available. This study characterized the immunogenicity and safety of poxvirus-based Nipah vaccines that can be used in humans and species responsible for NiV transmission. Mice were vaccinated with modified vaccinia Ankara (MVA) and raccoon pox (RCN) viral vectors expressing the NiV fusion (F) and glycoprotein (G) proteins subcutaneously (SC) and intranasally (IN). Importantly, both vaccines did not induce significant weight loss or clinical signs of disease while generating high circulating neutralizing antibodies and lung-specific IgG and IgA responses. The MVA vaccine saw high phenotypic expression of effector and tissue resident memory CD8ɑ
    MeSH term(s) Animals ; Humans ; Cats ; Mice ; Dogs ; Swine ; Horses ; Nipah Virus ; Viral Vaccines ; Poxviridae ; Vaccinia virus/genetics ; Genetic Vectors/genetics ; Antibodies, Viral
    Chemical Substances Viral Vaccines ; Antibodies, Viral
    Language English
    Publishing date 2023-07-14
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-023-38010-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Immunogenicity and protective activity of mRNA vaccine candidates against yellow fever virus in animal models.

    Medina-Magües, Lex G / Mühe, Janine / Jasny, Edith / Medina-Magües, Emily S / Roth, Nicole / Lopera-Madrid, Jaime / Salas-Quinchucua, Cristhian / Knuese, Cole / Petsch, Benjamin / Osorio, Jorge E

    NPJ vaccines

    2023  Volume 8, Issue 1, Page(s) 31

    Abstract: Despite the success of the widely used attenuated yellow fever (YF) vaccine, its global supply remains a substantial barrier to implementing vaccination campaigns in endemic regions and combating emerging epidemics. In A129 mice and rhesus macaques, we ... ...

    Abstract Despite the success of the widely used attenuated yellow fever (YF) vaccine, its global supply remains a substantial barrier to implementing vaccination campaigns in endemic regions and combating emerging epidemics. In A129 mice and rhesus macaques, we evaluated the immunogenicity and protective activity of messenger RNA (mRNA) vaccine candidates encapsulated in lipid nanoparticles, expressing the pre-membrane and envelope proteins or the non-structural protein 1 of YF virus. Vaccine constructs induced humoral and cell-mediated immune responses in mice, resulting in protection against lethal YF virus infection after passive administration of serum or splenocytes from vaccinated mice. Vaccination of macaques induced sustained high humoral and cellular immune responses for at least 5 months after the second dose. Our data demonstrate that these mRNA vaccine candidates can be considered an attractive addition to the licensed YF vaccine supply based on the induction of functional antibodies correlating with protection and T-cell responses; they could alleviate the limited supply of current YF vaccines, mitigating future YF epidemics.
    Language English
    Publishing date 2023-03-04
    Publishing country England
    Document type Journal Article
    ISSN 2059-0105
    ISSN (online) 2059-0105
    DOI 10.1038/s41541-023-00629-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Impact of Molecular Modifications on the Immunogenicity and Efficacy of Recombinant Raccoon Poxvirus-Vectored Rabies Vaccine Candidates in Mice.

    Malavé, Carly M / Lopera-Madrid, Jaime / Medina-Magües, Lex G / Rocke, Tonie E / Osorio, Jorge E

    Vaccines

    2021  Volume 9, Issue 12

    Abstract: Rabies is an ancient disease that is responsible for approximately 59,000 human deaths annually. Bats ( ... ...

    Abstract Rabies is an ancient disease that is responsible for approximately 59,000 human deaths annually. Bats (Order
    Language English
    Publishing date 2021-12-04
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2703319-3
    ISSN 2076-393X
    ISSN 2076-393X
    DOI 10.3390/vaccines9121436
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Optimization in the expression of ASFV proteins for the development of subunit vaccines using poxviruses as delivery vectors.

    Lopera-Madrid, Jaime / Medina-Magües, Lex G / Gladue, Douglas P / Borca, Manuel V / Osorio, Jorge E

    Scientific reports

    2021  Volume 11, Issue 1, Page(s) 23476

    Abstract: African swine fever virus (ASFV) causes a highly contagious hemorrhagic disease that affects domestic pig and Eurasian wild boar populations. To date, no safe and efficacious treatment or vaccine against ASF is available. Nevertheless, there are several ... ...

    Abstract African swine fever virus (ASFV) causes a highly contagious hemorrhagic disease that affects domestic pig and Eurasian wild boar populations. To date, no safe and efficacious treatment or vaccine against ASF is available. Nevertheless, there are several reports of protection elicited by experimental vaccines based on live attenuated ASFV and some levels of protection and reduced viremia in other approaches such as DNA, adenovirus, baculovirus, and vaccinia-based vaccines. Current ASF subunit vaccine research focuses mainly on delivering protective antigens and antigen discovery within the ASFV genome. However, due to the complex nature of ASFV, expression vectors need to be optimized to improve their immunogenicity. Therefore, in the present study, we constructed several recombinant MVA vectors to evaluate the efficiency of different promoters and secretory signal sequences in the expression and immunogenicity of the p30 protein from ASFV. Overall, the natural poxvirus PrMVA13.5L promoter induced high levels of both p30 mRNA and specific anti-p30 antibodies in mice. In contrast, the synthetic PrS5E promoter and the S E/L promoter linked to a secretory signal showed lower mRNA levels and antibodies. These findings indicate that promoter selection may be as crucial as the antigen used to develop ASFV subunit vaccines using MVA as the delivery vector.
    MeSH term(s) African Swine Fever/virology ; African Swine Fever Virus/genetics ; Animals ; Antibodies, Viral/genetics ; Baculoviridae/genetics ; Cell Line ; Chlorocebus aethiops ; Female ; Mice ; Mice, Inbred BALB C ; Poxviridae/genetics ; Promoter Regions, Genetic/genetics ; Swine ; Vaccines, Attenuated/genetics ; Vaccines, Subunit/genetics ; Vero Cells ; Viral Proteins/genetics ; Viral Vaccines/genetics ; Virus Replication/genetics
    Chemical Substances Antibodies, Viral ; Vaccines, Attenuated ; Vaccines, Subunit ; Viral Proteins ; Viral Vaccines
    Language English
    Publishing date 2021-12-06
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-021-02949-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Immunogenicity of poxvirus-based vaccines against Nipah virus

    Emily S. Medina-Magües / Jaime Lopera-Madrid / Michael K. Lo / Christina F. Spiropoulou / Joel M. Montgomery / Lex G. Medina-Magües / Cristhian Salas-Quinchucua / Angela P. Jiménez-Mora / Jorge E. Osorio

    Scientific Reports, Vol 13, Iss 1, Pp 1-

    2023  Volume 15

    Abstract: ... vaccinia Ankara (MVA) and raccoon pox (RCN) viral vectors expressing the NiV fusion (F) and glycoprotein (G ...

    Abstract Abstract Nipah virus (NiV), an emerging zoonotic pathogen in Southeast Asia, is transmitted from Pteropus species of fruit bats to a wide range of species, including humans, pigs, horses, dogs, and cats. NiV has killed millions of animals and caused highly fatal human outbreaks since no vaccine is commercially available. This study characterized the immunogenicity and safety of poxvirus-based Nipah vaccines that can be used in humans and species responsible for NiV transmission. Mice were vaccinated with modified vaccinia Ankara (MVA) and raccoon pox (RCN) viral vectors expressing the NiV fusion (F) and glycoprotein (G) proteins subcutaneously (SC) and intranasally (IN). Importantly, both vaccines did not induce significant weight loss or clinical signs of disease while generating high circulating neutralizing antibodies and lung-specific IgG and IgA responses. The MVA vaccine saw high phenotypic expression of effector and tissue resident memory CD8ɑ+ T cells in lungs and splenocytes along with the expression of central memory CD8ɑ+ T cells in lungs. The RCN vaccine generated effector memory (SC) and tissue resident (IN) CD8ɑ+ T cells in splenocytes and tissue resident (IN) CD8ɑ+ T cells in lung cells. These findings support MVA-FG and RCN-FG viral vectors as promising vaccine candidates to protect humans, domestic animals, and wildlife from fatal disease outcomes and to reduce the global threat of NiV.
    Keywords Medicine ; R ; Science ; Q
    Subject code 630
    Language English
    Publishing date 2023-07-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article: mRNA Vaccine Protects against Zika Virus.

    Medina-Magües, Lex G / Gergen, Janina / Jasny, Edith / Petsch, Benjamin / Lopera-Madrid, Jaime / Medina-Magües, Emily S / Salas-Quinchucua, Cristhian / Osorio, Jorge E

    Vaccines

    2021  Volume 9, Issue 12

    Abstract: Zika virus (ZIKV), a mosquito-borne flavivirus, has recently triggered global concern due to severe health complications. In 2015, a large ZIKV outbreak occurred in the Americas and established a link between ZIKV and microcephaly in newborn babies, ... ...

    Abstract Zika virus (ZIKV), a mosquito-borne flavivirus, has recently triggered global concern due to severe health complications. In 2015, a large ZIKV outbreak occurred in the Americas and established a link between ZIKV and microcephaly in newborn babies, spontaneous abortion, persistent viremia, and Guillain-Barré syndrome. While antivirals are being developed and prevention strategies focus on vector control, a safe and effective Zika vaccine remains unavailable. Messenger RNA (mRNA) vaccine technology has arisen as a flexible, simplified, and fast vaccine production platform. Here, we report on an mRNA vaccine candidate that encodes the pre-membrane and envelope (prM-E) glycoproteins of ZIKV strain Brazil SPH2015 and is encapsulated in lipid nanoparticles (LNPs). Our ZIKV prM-E mRNA-LNP vaccine candidate induced antibody responses that protected in AG129 mice deficient in interferon (IFN) alpha/beta/gamma (IFN-α/β/γ) receptors. Notably, a single administration of ZIKV prM-E mRNA-LNP protected against a lethal dose of ZIKV, while a two-dose strategy induced strong protective immunity. E-specific double-positive IFN-γ and TNF-α T-cells were induced in BALB/c mice after immunizations with a two-dose strategy. With the success of mRNA vaccine technology in facing the coronavirus (COVID-19) pandemic, our data support the development of prM-E RNActive
    Language English
    Publishing date 2021-12-10
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2703319-3
    ISSN 2076-393X
    ISSN 2076-393X
    DOI 10.3390/vaccines9121464
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: mRNA Vaccine Protects against Zika Virus

    Lex G. Medina-Magües / Janina Gergen / Edith Jasny / Benjamin Petsch / Jaime Lopera-Madrid / Emily S. Medina-Magües / Cristhian Salas-Quinchucua / Jorge E. Osorio

    Vaccines, Vol 9, Iss 1464, p

    2021  Volume 1464

    Abstract: Zika virus (ZIKV), a mosquito-borne flavivirus, has recently triggered global concern due to severe health complications. In 2015, a large ZIKV outbreak occurred in the Americas and established a link between ZIKV and microcephaly in newborn babies, ... ...

    Abstract Zika virus (ZIKV), a mosquito-borne flavivirus, has recently triggered global concern due to severe health complications. In 2015, a large ZIKV outbreak occurred in the Americas and established a link between ZIKV and microcephaly in newborn babies, spontaneous abortion, persistent viremia, and Guillain–Barré syndrome. While antivirals are being developed and prevention strategies focus on vector control, a safe and effective Zika vaccine remains unavailable. Messenger RNA (mRNA) vaccine technology has arisen as a flexible, simplified, and fast vaccine production platform. Here, we report on an mRNA vaccine candidate that encodes the pre-membrane and envelope (prM–E) glycoproteins of ZIKV strain Brazil SPH2015 and is encapsulated in lipid nanoparticles (LNPs). Our ZIKV prM–E mRNA-LNP vaccine candidate induced antibody responses that protected in AG129 mice deficient in interferon (IFN) alpha/beta/gamma (IFN-α/β/γ) receptors. Notably, a single administration of ZIKV prM–E mRNA-LNP protected against a lethal dose of ZIKV, while a two-dose strategy induced strong protective immunity. E-specific double-positive IFN-γ and TNF-α T-cells were induced in BALB/c mice after immunizations with a two-dose strategy. With the success of mRNA vaccine technology in facing the coronavirus (COVID-19) pandemic, our data support the development of prM–E RNActive ® as a promising mRNA vaccine against Zika to counter future epidemics.
    Keywords AG129 ; challenge ; flavivirus ; lipid nanoparticles ; mice ; mRNA vaccines ; Medicine ; R
    Language English
    Publishing date 2021-12-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article ; Online: Optimization in the expression of ASFV proteins for the development of subunit vaccines using poxviruses as delivery vectors

    Jaime Lopera-Madrid / Lex G. Medina-Magües / Douglas P. Gladue / Manuel V. Borca / Jorge E. Osorio

    Scientific Reports, Vol 11, Iss 1, Pp 1-

    2021  Volume 12

    Abstract: Abstract African swine fever virus (ASFV) causes a highly contagious hemorrhagic disease that affects domestic pig and Eurasian wild boar populations. To date, no safe and efficacious treatment or vaccine against ASF is available. Nevertheless, there are ...

    Abstract Abstract African swine fever virus (ASFV) causes a highly contagious hemorrhagic disease that affects domestic pig and Eurasian wild boar populations. To date, no safe and efficacious treatment or vaccine against ASF is available. Nevertheless, there are several reports of protection elicited by experimental vaccines based on live attenuated ASFV and some levels of protection and reduced viremia in other approaches such as DNA, adenovirus, baculovirus, and vaccinia-based vaccines. Current ASF subunit vaccine research focuses mainly on delivering protective antigens and antigen discovery within the ASFV genome. However, due to the complex nature of ASFV, expression vectors need to be optimized to improve their immunogenicity. Therefore, in the present study, we constructed several recombinant MVA vectors to evaluate the efficiency of different promoters and secretory signal sequences in the expression and immunogenicity of the p30 protein from ASFV. Overall, the natural poxvirus PrMVA13.5L promoter induced high levels of both p30 mRNA and specific anti-p30 antibodies in mice. In contrast, the synthetic PrS5E promoter and the S E/L promoter linked to a secretory signal showed lower mRNA levels and antibodies. These findings indicate that promoter selection may be as crucial as the antigen used to develop ASFV subunit vaccines using MVA as the delivery vector.
    Keywords Medicine ; R ; Science ; Q
    Subject code 570
    Language English
    Publishing date 2021-12-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article ; Online: Impact of Molecular Modifications on the Immunogenicity and Efficacy of Recombinant Raccoon Poxvirus-Vectored Rabies Vaccine Candidates in Mice

    Carly M. Malavé / Jaime Lopera-Madrid / Lex G. Medina-Magües / Tonie E. Rocke / Jorge E. Osorio

    Vaccines, Vol 9, Iss 1436, p

    2021  Volume 1436

    Abstract: Rabies is an ancient disease that is responsible for approximately 59,000 human deaths annually. Bats (Order Chiroptera ) are thought to be the original hosts of rabies virus (RABV) and currently account for most rabies cases in wildlife in the Americas. ...

    Abstract Rabies is an ancient disease that is responsible for approximately 59,000 human deaths annually. Bats (Order Chiroptera ) are thought to be the original hosts of rabies virus (RABV) and currently account for most rabies cases in wildlife in the Americas. Vaccination is being used to manage rabies in other wildlife reservoirs like fox and raccoon, but no rabies vaccine is available for bats. We previously developed a recombinant raccoonpox virus (RCN) vaccine candidate expressing a mosaic glycoprotein (MoG) gene that protected mice and big brown bats when challenged with RABV. In this study, we developed two new recombinant RCN candidates expressing MoG (RCN-tPA-MoG and RCN-SS-TD-MoG) with the aim of improving RCN-MoG. We assessed and compared in vitro expression, in vivo immunogenicity, and protective efficacy in vaccinated mice challenged intracerebrally with RABV. All three candidates induced significant humoral immune responses, and inoculation with RCN-tPA-MoG or RCN-MoG significantly increased survival after RABV challenge. These results demonstrate the importance of considering molecular elements in the design of vaccines, and that vaccination with either RCN-tPA-MoG or RCN-MoG confers adequate protection from rabies infection, and either may be a sufficient vaccine candidate for bats in future work.
    Keywords rabies ; rabies virus ; RABV ; raccoon poxvirus ; recombinant ; vaccine ; Medicine ; R
    Subject code 570
    Language English
    Publishing date 2021-12-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article ; Online: Clinical Presentation and Serologic Response during a Rabies Epizootic in Captive Common Vampire Bats

    Cárdenas-Canales, Elsa M / Gigante, Crystal M / Greenberg, Lauren / Velasco-Villa, Andres / Ellison, James A / Satheshkumar, Panayampalli S / Medina-Magües, Lex G / Griesser, Richard / Falendysz, Elizabeth / Amezcua, Ignacio / Osorio, Jorge E / Rocke, Tonie E

    Tropical medicine and infectious disease

    2020  Volume 5, Issue 1

    Abstract: We report mortality events in a group of 123 common vampire bats ( ...

    Abstract We report mortality events in a group of 123 common vampire bats (
    Language English
    Publishing date 2020-03-01
    Publishing country Switzerland
    Document type Case Reports
    ISSN 2414-6366
    ISSN (online) 2414-6366
    DOI 10.3390/tropicalmed5010034
    Database MEDical Literature Analysis and Retrieval System OnLINE

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