<p>The mice received three times of inoculation with the protein vaccine candidates in DDA/Poly(I:C)/Gelatin. The vaccinated mice were challenged with virulent <i>M. tuberculosis</i> 10 weeks after the final vaccination. Six weeks after challenge with virulent <i>M. tuberculosis</i>, the animals were sacrificed, and the numbers of CFU of <i>M. tuberculosis</i> in the lungs (A) and spleens (B) were determined. Results are presented as mean ± SD, <i>n</i> = 4 or 7. <i>p</i> < 0.05 <i>vs</i>. PBS. ** <i>p</i> < 0.05 vs. PBS, EAMM and MH.</p
DNA vaccine may be a promising tool for controlling tuberculosis development. However, vaccines enco...
Immune response and protective efficacy for the combination of four tuberculosis DNA vaccines were e...
<p>The figure depicts (A) the bacillary load in lungs and spleen of mice (n = 4) at 4 weeks post-inf...
<p>Mice were primed with BCG and boosted by EAMM/AMM two times at the 12th and 14th week. Ten weeks ...
<p>Mice were immunized subcutaneously with two different doses (10 μg and 2 μg) of LT69 formulated i...
To search for more effective tuberculosis (TB) subunit vaccines, antigens expressed in different gro...
<p>Mice vaccinated with different plasmids and boosted with Esat-6/3e peptides for two times were in...
<p>Mice were infected 12 weeks after primary immunization and euthanized at 2, 4 and 10 weeks post-i...
Background. Studies of different vaccine constructs have demonstrated variable efficacy against Myco...
In this study we have evaluated the vaccine potential of a Mycobacterium tuberculosis antigen of the...
The prophylactic capacity of the RUTI® vaccine, based on fragmented cells of Mycobacterium tuberculo...
<p>In this study we have evaluated the vaccine potential of a Mycobacterium tuberculosis antig...
<p>C57BL/6 mice were immunised three times at two-weekly intervals with PLGA particles (n = 6) or DD...
<p>Lung (A) or spleen (B) bacterial burdens of C57BL/6 mice infected with <i>M</i>. <i>tuberculosis<...
Protein subunit vaccines present a compelling new area of research for control of tuberculosis (TB)....
DNA vaccine may be a promising tool for controlling tuberculosis development. However, vaccines enco...
Immune response and protective efficacy for the combination of four tuberculosis DNA vaccines were e...
<p>The figure depicts (A) the bacillary load in lungs and spleen of mice (n = 4) at 4 weeks post-inf...
<p>Mice were primed with BCG and boosted by EAMM/AMM two times at the 12th and 14th week. Ten weeks ...
<p>Mice were immunized subcutaneously with two different doses (10 μg and 2 μg) of LT69 formulated i...
To search for more effective tuberculosis (TB) subunit vaccines, antigens expressed in different gro...
<p>Mice vaccinated with different plasmids and boosted with Esat-6/3e peptides for two times were in...
<p>Mice were infected 12 weeks after primary immunization and euthanized at 2, 4 and 10 weeks post-i...
Background. Studies of different vaccine constructs have demonstrated variable efficacy against Myco...
In this study we have evaluated the vaccine potential of a Mycobacterium tuberculosis antigen of the...
The prophylactic capacity of the RUTI® vaccine, based on fragmented cells of Mycobacterium tuberculo...
<p>In this study we have evaluated the vaccine potential of a Mycobacterium tuberculosis antig...
<p>C57BL/6 mice were immunised three times at two-weekly intervals with PLGA particles (n = 6) or DD...
<p>Lung (A) or spleen (B) bacterial burdens of C57BL/6 mice infected with <i>M</i>. <i>tuberculosis<...
Protein subunit vaccines present a compelling new area of research for control of tuberculosis (TB)....
DNA vaccine may be a promising tool for controlling tuberculosis development. However, vaccines enco...
Immune response and protective efficacy for the combination of four tuberculosis DNA vaccines were e...
<p>The figure depicts (A) the bacillary load in lungs and spleen of mice (n = 4) at 4 weeks post-inf...