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2777. Live-Attenuated Vaccine Against RSV Generates Robust Cellular and Humoral Immune Responses

BACKGROUND: In people over 65, there are on average 177,000 hospitalizations and 14,000 deaths because of respiratory syncytial virus (RSV) each year. Elderly patients infected with RSV can suffer serious infections leading to pneumonia and congestive heart failure. RSV vaccines have failed in the e...

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Autores principales: Mueller, Steffen, Nouen, Cyril Le, Buchholz, Ursula J, Kalkeri, Raj, Koide, Fusataka, Collins, Peter, Coleman, J Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811147/
http://dx.doi.org/10.1093/ofid/ofz360.2454
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author Mueller, Steffen
Nouen, Cyril Le
Buchholz, Ursula J
Kalkeri, Raj
Koide, Fusataka
Collins, Peter
Coleman, J Robert
author_facet Mueller, Steffen
Nouen, Cyril Le
Buchholz, Ursula J
Kalkeri, Raj
Koide, Fusataka
Collins, Peter
Coleman, J Robert
author_sort Mueller, Steffen
collection PubMed
description BACKGROUND: In people over 65, there are on average 177,000 hospitalizations and 14,000 deaths because of respiratory syncytial virus (RSV) each year. Elderly patients infected with RSV can suffer serious infections leading to pneumonia and congestive heart failure. RSV vaccines have failed in the elderly in part because they have been unable to mount a robust cellular immune response. METHODS: RSV-MinL4.0 is a live-attenuated intranasal vaccine candidate that was generated by codon pair deoptimization of the L gene followed by the addition of four stabilizing mutations found via stress passaging. Four African Green Monkeys (AGMs) per group were vaccinated with RSV-MinL4.0 or wild-type (WT) RSV at 2 × 10(6) PFU, boosted on day 28 and challenged with wild-type (WT) RSV on day 104. Oropharyngeal swabs and tracheal lavage were collected daily and every other day, respectively, to evaluate virus shedding (qPCR) and blood was drawn on days 1, 14, 21, 28, and 49 for antibody titers (PRNT(50)), and PBMC activation (IFNγ ELISPOT with whole inactivated virus). RESULTS: MinL4.0 was 2 to 3 log(10) attenuated when compared with WT RSV in AGMs. Despite the presence of antibodies on day 28, there was a “take” of the boost indicating the potential for this vaccine to be immunogenic in the elderly with pre-existing circulating antibodies (Figure 1A). MinL4.0 led to robust activation of PBMCs comparable to WT RSV (> 2,000 spots per 10(6) total cells, Figure 1B). Shedding of the vaccine and challenge viruses was minimal (data not shown). CONCLUSION: MinL4.0 led to robust activation of cellular and humoral immune responses, which are critical for induction of protective immunity in the elderly. Animals were protected from WT challenge. Preliminary data in AGMs with pre-existing antibodies to RSV indicate that circulating antibodies do not prevent vaccine “take,” critical for a vaccine targeting sero-positive elderly individuals. [Image: see text] DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-68111472019-10-29 2777. Live-Attenuated Vaccine Against RSV Generates Robust Cellular and Humoral Immune Responses Mueller, Steffen Nouen, Cyril Le Buchholz, Ursula J Kalkeri, Raj Koide, Fusataka Collins, Peter Coleman, J Robert Open Forum Infect Dis Abstracts BACKGROUND: In people over 65, there are on average 177,000 hospitalizations and 14,000 deaths because of respiratory syncytial virus (RSV) each year. Elderly patients infected with RSV can suffer serious infections leading to pneumonia and congestive heart failure. RSV vaccines have failed in the elderly in part because they have been unable to mount a robust cellular immune response. METHODS: RSV-MinL4.0 is a live-attenuated intranasal vaccine candidate that was generated by codon pair deoptimization of the L gene followed by the addition of four stabilizing mutations found via stress passaging. Four African Green Monkeys (AGMs) per group were vaccinated with RSV-MinL4.0 or wild-type (WT) RSV at 2 × 10(6) PFU, boosted on day 28 and challenged with wild-type (WT) RSV on day 104. Oropharyngeal swabs and tracheal lavage were collected daily and every other day, respectively, to evaluate virus shedding (qPCR) and blood was drawn on days 1, 14, 21, 28, and 49 for antibody titers (PRNT(50)), and PBMC activation (IFNγ ELISPOT with whole inactivated virus). RESULTS: MinL4.0 was 2 to 3 log(10) attenuated when compared with WT RSV in AGMs. Despite the presence of antibodies on day 28, there was a “take” of the boost indicating the potential for this vaccine to be immunogenic in the elderly with pre-existing circulating antibodies (Figure 1A). MinL4.0 led to robust activation of PBMCs comparable to WT RSV (> 2,000 spots per 10(6) total cells, Figure 1B). Shedding of the vaccine and challenge viruses was minimal (data not shown). CONCLUSION: MinL4.0 led to robust activation of cellular and humoral immune responses, which are critical for induction of protective immunity in the elderly. Animals were protected from WT challenge. Preliminary data in AGMs with pre-existing antibodies to RSV indicate that circulating antibodies do not prevent vaccine “take,” critical for a vaccine targeting sero-positive elderly individuals. [Image: see text] DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2019-10-23 /pmc/articles/PMC6811147/ http://dx.doi.org/10.1093/ofid/ofz360.2454 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Mueller, Steffen
Nouen, Cyril Le
Buchholz, Ursula J
Kalkeri, Raj
Koide, Fusataka
Collins, Peter
Coleman, J Robert
2777. Live-Attenuated Vaccine Against RSV Generates Robust Cellular and Humoral Immune Responses
title 2777. Live-Attenuated Vaccine Against RSV Generates Robust Cellular and Humoral Immune Responses
title_full 2777. Live-Attenuated Vaccine Against RSV Generates Robust Cellular and Humoral Immune Responses
title_fullStr 2777. Live-Attenuated Vaccine Against RSV Generates Robust Cellular and Humoral Immune Responses
title_full_unstemmed 2777. Live-Attenuated Vaccine Against RSV Generates Robust Cellular and Humoral Immune Responses
title_short 2777. Live-Attenuated Vaccine Against RSV Generates Robust Cellular and Humoral Immune Responses
title_sort 2777. live-attenuated vaccine against rsv generates robust cellular and humoral immune responses
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811147/
http://dx.doi.org/10.1093/ofid/ofz360.2454
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