Expression of a C terminally truncated form of pertussis toxin S1 subunit effectively induces protection against pertussis toxin following DNA-based immunization

Kazunari Kamachi; Yoshichika Arakawa

doi:10.1128/IAI.72.7.4293-4296.2004

Expression of a C terminally truncated form of pertussis toxin S1 subunit effectively induces protection against pertussis toxin following DNA-based immunization

Kazunari Kamachi, Yoshichika Arakawa

Research output: Contribution to journal › Article › peer-review

10 Citations (Scopus)

Abstract

Four plasmids encoding different C terminally and N terminally truncated pertussis toxin S1 subunits of Bordetella pertussis were constructed and tested for inducibility of protection against pertussis toxin in mice after DNA-based immunization. The region encoding an N-terminal 180-amino-acid fragment of the S1 subunit had the most potent ability to induce protective immunity.

Original language	English
Pages (from-to)	4293-4296
Number of pages	4
Journal	Infection and Immunity
Volume	72
Issue number	7
DOIs	https://doi.org/10.1128/IAI.72.7.4293-4296.2004
Publication status	Published - 07-2004
Externally published	Yes

All Science Journal Classification (ASJC) codes

Parasitology
Microbiology
Immunology
Infectious Diseases

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1128/IAI.72.7.4293-4296.2004

Cite this

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abstract = "Four plasmids encoding different C terminally and N terminally truncated pertussis toxin S1 subunits of Bordetella pertussis were constructed and tested for inducibility of protection against pertussis toxin in mice after DNA-based immunization. The region encoding an N-terminal 180-amino-acid fragment of the S1 subunit had the most potent ability to induce protective immunity.",

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AB - Four plasmids encoding different C terminally and N terminally truncated pertussis toxin S1 subunits of Bordetella pertussis were constructed and tested for inducibility of protection against pertussis toxin in mice after DNA-based immunization. The region encoding an N-terminal 180-amino-acid fragment of the S1 subunit had the most potent ability to induce protective immunity.

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Expression of a C terminally truncated form of pertussis toxin S1 subunit effectively induces protection against pertussis toxin following DNA-based immunization

Abstract

All Science Journal Classification (ASJC) codes

UN SDGs

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