2010
DOI: 10.4161/hv.6.4.10172
|View full text |Cite
|
Sign up to set email alerts
|

Tuberculosis vaccine development :The development of a novel (preclinical) DNA vaccine

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
29
0

Year Published

2010
2010
2022
2022

Publication Types

Select...
7
3

Relationship

1
9

Authors

Journals

citations
Cited by 23 publications
(30 citation statements)
references
References 78 publications
1
29
0
Order By: Relevance
“…15 Aeras-402 DNA (DNA that expressed 85A, 85B and TB10.4) vaccine using adenovirus vector is intended for use as a boosting vaccine in BCG-primed individuals. 16 Several vaccines use a prime-boost strategy to enhance the immune responses. 17 In Japan and other countries, the BCG vaccine is inoculated into human infants (0-6 months after birth).…”
Section: Discussionmentioning
confidence: 99%
“…15 Aeras-402 DNA (DNA that expressed 85A, 85B and TB10.4) vaccine using adenovirus vector is intended for use as a boosting vaccine in BCG-primed individuals. 16 Several vaccines use a prime-boost strategy to enhance the immune responses. 17 In Japan and other countries, the BCG vaccine is inoculated into human infants (0-6 months after birth).…”
Section: Discussionmentioning
confidence: 99%
“…This approach was used successfully against Mycobacterium tuberculosis [106], Yersinia pestis [107,108], HIV [3,109], cytomegalovirus [110], and tumors [111]. The coadministration of plasmids encoding IL-12 and IL-15 in macaques increased the specific CD8 + T cell memory populations and their ability to produce cytokines [112].…”
Section: Adjuvantsmentioning
confidence: 99%
“…Besides, it is generally believed that novel TB vaccines will be tested in the context of the widely used BCG and perhaps different kinds of vaccines are needed for the eradication of TB (Mitsuyama & McMurray, 2007;Sander & McShane, 2007). As a result, enhancement of TB DNA vaccine efficacy has become the active field of current research (Okada & Kita, 2010). In this context, Baldwin et al have shown that inclusion of the secretion signal peptide from tissue plasminogen activator (tPA) into a DNA vaccine construct resulted in stronger immune responses to Ag85A, and provided sustained protection upon M. tuberculosis challenge in mice, as compared to the DNA vaccine construct based on the parent plasmid lacking tPA (Baldwin et al, 1999).…”
Section: Cloning Expression and Immunogenicity Of Rd Genes In Dna Vamentioning
confidence: 99%