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A novel Chimpanzee serotype-based adenoviral vector as delivery tool for cancer vaccines
The use of adenovirus (Ad) as vaccine vectors is hindered by pre-existing immunity to human Ads in most of the human population. In order to overcome this limitation, uncommon alternative Ad serotypes need to be utilized. In this study, an E1–E3 deleted recombinant Ad based on the chimpanzee serotyp...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115565/ https://www.ncbi.nlm.nih.gov/pubmed/19162112 http://dx.doi.org/10.1016/j.vaccine.2008.12.051 |
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author | Peruzzi, Daniela Dharmapuri, Sridhar Cirillo, Agostino Bruni, Bruno Ercole Nicosia, Alfredo Cortese, Riccardo Colloca, Stefano Ciliberto, Gennaro La Monica, Nicola Aurisicchio, Luigi |
author_facet | Peruzzi, Daniela Dharmapuri, Sridhar Cirillo, Agostino Bruni, Bruno Ercole Nicosia, Alfredo Cortese, Riccardo Colloca, Stefano Ciliberto, Gennaro La Monica, Nicola Aurisicchio, Luigi |
author_sort | Peruzzi, Daniela |
collection | PubMed |
description | The use of adenovirus (Ad) as vaccine vectors is hindered by pre-existing immunity to human Ads in most of the human population. In order to overcome this limitation, uncommon alternative Ad serotypes need to be utilized. In this study, an E1–E3 deleted recombinant Ad based on the chimpanzee serotype 3 (ChAd3) was engineered to express human carcinoembryonic antigen (CEA) protein or rat neu extracellular/transmembrane domains (ECD.TM). ChAd3 vectors were tested in CEA transgenic (CEA.Tg) and BALB/NeuT mice, which show immunologic tolerance to these antigens. ChAd3 is capable of inducing an immune response comparable to that of hAd5 serotype-based vectors, thus breaking tolerance to tumor associated antigens (TAAs) and achieving anti-tumor effects. Of importance is that ChAd3 can overcome hAd5 pre-existing immunity and work in conjunction with DNA electroporation (DNA-EP) and other Ad vaccines based on common human serotypes. |
format | Online Article Text |
id | pubmed-7115565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71155652020-04-02 A novel Chimpanzee serotype-based adenoviral vector as delivery tool for cancer vaccines Peruzzi, Daniela Dharmapuri, Sridhar Cirillo, Agostino Bruni, Bruno Ercole Nicosia, Alfredo Cortese, Riccardo Colloca, Stefano Ciliberto, Gennaro La Monica, Nicola Aurisicchio, Luigi Vaccine Article The use of adenovirus (Ad) as vaccine vectors is hindered by pre-existing immunity to human Ads in most of the human population. In order to overcome this limitation, uncommon alternative Ad serotypes need to be utilized. In this study, an E1–E3 deleted recombinant Ad based on the chimpanzee serotype 3 (ChAd3) was engineered to express human carcinoembryonic antigen (CEA) protein or rat neu extracellular/transmembrane domains (ECD.TM). ChAd3 vectors were tested in CEA transgenic (CEA.Tg) and BALB/NeuT mice, which show immunologic tolerance to these antigens. ChAd3 is capable of inducing an immune response comparable to that of hAd5 serotype-based vectors, thus breaking tolerance to tumor associated antigens (TAAs) and achieving anti-tumor effects. Of importance is that ChAd3 can overcome hAd5 pre-existing immunity and work in conjunction with DNA electroporation (DNA-EP) and other Ad vaccines based on common human serotypes. Elsevier Ltd. 2009-02-25 2009-01-20 /pmc/articles/PMC7115565/ /pubmed/19162112 http://dx.doi.org/10.1016/j.vaccine.2008.12.051 Text en Copyright © 2009 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Peruzzi, Daniela Dharmapuri, Sridhar Cirillo, Agostino Bruni, Bruno Ercole Nicosia, Alfredo Cortese, Riccardo Colloca, Stefano Ciliberto, Gennaro La Monica, Nicola Aurisicchio, Luigi A novel Chimpanzee serotype-based adenoviral vector as delivery tool for cancer vaccines |
title | A novel Chimpanzee serotype-based adenoviral vector as delivery tool for cancer vaccines |
title_full | A novel Chimpanzee serotype-based adenoviral vector as delivery tool for cancer vaccines |
title_fullStr | A novel Chimpanzee serotype-based adenoviral vector as delivery tool for cancer vaccines |
title_full_unstemmed | A novel Chimpanzee serotype-based adenoviral vector as delivery tool for cancer vaccines |
title_short | A novel Chimpanzee serotype-based adenoviral vector as delivery tool for cancer vaccines |
title_sort | novel chimpanzee serotype-based adenoviral vector as delivery tool for cancer vaccines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115565/ https://www.ncbi.nlm.nih.gov/pubmed/19162112 http://dx.doi.org/10.1016/j.vaccine.2008.12.051 |
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