Development of an attenuated smallpox vaccine candidate: The KVAC103 strain.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
23 08 2021
Historique:
received: 19 10 2020
revised: 14 05 2021
accepted: 22 06 2021
pubmed: 3 8 2021
medline: 16 9 2021
entrez: 2 8 2021
Statut: ppublish

Résumé

Smallpox, a disease caused by the variola virus, is one of the most dangerous diseases and had killed numerous people before it was eradicated in 1980. However, smallpox has emerged as the most threatening bio-terrorism agent; as the first- and second-generation smallpox vaccines have been controversial and have caused severe adverse reactions, new demands for safe smallpox vaccines have been raised and some attenuated smallpox vaccines have been developed. We have developed a cell culture-based highly attenuated third-generation smallpox vaccine candidate KVAC103 strain by 103 serial passages of the Lancy-Vaxina strain derived from the Lister in Vero cells. Several clones were selected, taking into consideration their shape, size, and growth rate in mammalian cells. The clones were then inoculated intracerebrally in suckling mice to test for neurovirulence by observing survival. Protective immune responses in adult mice were examined by measuring the levels of neutralization antibodies and IFN-γ expression. Among several clones, clone 7 was considered the best alternative candidate because there was no mortality in suckling mice against a lethal challenge. In addition, enhanced neutralizing antibodies and T-cell mediated IFN-γ production were observed in clone 7-immunized mice. Clone 7 was named "KVAC103" and was used for the skin toxicity test and full-genome analysis. KVAC103-inoculated rabbits showed reduced skin lesions compared to those inoculated with the Lister strain, Lancy-Vaxina. A whole genome analysis of KVAC103 revealed two major deleted regions that might contribute to the reduced virulence of KVAC103 compared to the Lister strain. Phylogenetic inference supported the close relationship with the Lister strain. Collectively, our data demonstrate that KVAC103 holds promise for use as a third-generation smallpox vaccine strain due to its enhanced safety and efficacy.

Identifiants

pubmed: 34334254
pii: S0264-410X(21)00810-0
doi: 10.1016/j.vaccine.2021.06.060
pii:
doi:

Substances chimiques

Antibodies, Viral 0
Smallpox Vaccine 0
Vaccines, Attenuated 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5214-5223

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Heeji Lim (H)

Center for Vaccine Research, National Institute of Infectious Diseases, National Institute of Health, CheongJu, Chungbuk 28159, Republic of Korea.

Hyun Ju In (HJ)

Center for Vaccine Research, National Institute of Infectious Diseases, National Institute of Health, CheongJu, Chungbuk 28159, Republic of Korea.

You-Jin Kim (YJ)

Center for Vaccine Research, National Institute of Infectious Diseases, National Institute of Health, CheongJu, Chungbuk 28159, Republic of Korea.

Sundong Jang (S)

College of Pharmacy, Chungbuk National University, CheongJu, Chungbuk 28160, Republic of Korea.

Yun Ha Lee (YH)

Center for Vaccine Research, National Institute of Infectious Diseases, National Institute of Health, CheongJu, Chungbuk 28159, Republic of Korea.

Su Hwan Kim (SH)

Center for Vaccine Research, National Institute of Infectious Diseases, National Institute of Health, CheongJu, Chungbuk 28159, Republic of Korea.

Sun Hwa Lee (SH)

Department of Laboratory Medicine, KU Medicine, Seoul 02841, Republic of Korea.

Jun Hyuk Park (JH)

Department of Laboratory Medicine Chungcheongnam-do Institute of Health and Environment Research, Hongseong 32254, Republic of Korea.

Hyo Jin Yang (HJ)

Korea Disease Control and Prevention Agency, CheongJu, Chungbuk 28159, Republic of Korea.

Jung-Sik Yoo (JS)

Center for Infectious Disease Research, National Institute of Infectious Diseases, National Institute of Health, CheongJu, Chungbuk 28159, Republic of Korea.

Sang-Won Lee (SW)

Korea Disease Control and Prevention Agency, CheongJu, Chungbuk 28159, Republic of Korea.

Mi Young Kim (MY)

Center for Vaccine Research, National Institute of Infectious Diseases, National Institute of Health, CheongJu, Chungbuk 28159, Republic of Korea.

Gyung Tae Chung (GT)

Center for Vaccine Research, National Institute of Infectious Diseases, National Institute of Health, CheongJu, Chungbuk 28159, Republic of Korea.

Sang Gu Yeo (SG)

Division of Infectious Diseases, Sejong Institute of Health and Environment Research, Sejong City 30015, Republic of Korea. Electronic address: sg10003@gmail.com.

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Classifications MeSH