New formulation of a recombinant anthrax vaccine stabilised with structurally modified plant viruses
Anthrax is a disease caused by Bacillus anthracis . The most promising approach to the development of anthrax vaccine is use of the anthrax protective antigen (PA). At the same time, recombinant PA is a very unstable protein. Previously, the authors have designed a stable modified recombinant anthra...
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Published in: | Frontiers in microbiology Vol. 13; p. 1003969 |
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Main Authors: | , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Frontiers Media S.A
09-09-2022
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Subjects: | |
Online Access: | Get full text |
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Summary: | Anthrax is a disease caused by
Bacillus anthracis
. The most promising approach to the development of anthrax vaccine is use of the anthrax protective antigen (PA). At the same time, recombinant PA is a very unstable protein. Previously, the authors have designed a stable modified recombinant anthrax protective antigen with inactivated proteolytic sites and substituted deamidation sites (rPA83m). As a second approach to recombinant PA stabilisation, plant virus spherical particles (SPs) were used as a stabiliser. The combination of these two approaches was shown to be the most effective. Here, the authors report the results of a detailed study of the stability, immunogenicity and protectiveness of rPA83m + SPs compositions. These compositions were shown to be stable, provided high anti-rPA83m antibody titres in guinea pigs and were able to protect them from a fully virulent 81/1
Bacillus anthracis
strain. Given these facts, the formulation of rPA83m + SPs compositions is considered to be a prospective anthrax vaccine candidate. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Piyush Baindara, University of Missouri, United States Reviewed by: Richa Dwivedi, University of Pittsburgh, United States; Zeeshan Ahmad, Wayne State University, United States; Jagpreet Singh Nanda, Cedars Sinai Medical Center, United States These authors have contributed equally to this work and share first authorship This article was submitted to Infectious Agents and Disease, a section of the journal Frontiers in Microbiology |
ISSN: | 1664-302X 1664-302X |
DOI: | 10.3389/fmicb.2022.1003969 |