<p>(A) Bacilli burdens in lungs of mice after 60 days of infection treated during one month with HMGB1 blocking antibodies (black bars) or isotype chiken antibodies as a control (white bars). (B) Pulmonary bacilli loads of BALB/c mice after 60 days of infection with <i>M</i>. <i>tuberculosis</i> strain H37Rv treated during one month with recombinant human HMGB1 (grey bars) or human albumin as a control (white bars) (6 mice per group). (C) Quantitative expression of mRNA of cytokines determined by real-time PCR in lungs from mice after 60 days of infection and treated with HMGB1 blocking antibodies administered each other day during one month and control non-treated animals. (D) Cytokines transcription during late disease in mice treated wit...
<p>Lung (A) or spleen (B) bacterial burdens of C57BL/6 mice infected with <i>M</i>. <i>tuberculosis<...
<p><b>Copyright information:</b></p><p>Taken from "Improve protective efficacy of a TB DNA-HSP65 vac...
<p>Evaluation of the protective capacity of BCG in mice treated with anti-CD25 mAb, and challenged w...
<p>(A) Groups of infected BALB/c mice with <i>M</i>.<i>tuberculosis</i> strain H37Rv were treated wi...
<p>(A) Groups of infected BALB/c mice with <i>M</i>.<i>tuberculosis</i> strain H37Rv were treated wi...
<p>Quantitative expression of mRNA for the indicated cytokines was determined by real-time PCR in lu...
Background: The high mobility group box 1 (HMGB1) is the prototype of alarmin protein released by st...
The high mobility group box 1 (HMGB1) is the prototype of alarmin protein released by stressed or dy...
A) Groups of five C57 mice were intradermally vaccinated with 105 CFU of BCG (BCG), heat-killed BCG ...
SummaryIntroductionThe role of damage-associated molecular pattern HMGB1 signalling in a murine BALB...
<p>Ninety days after immunization, three mice from each group (control, BCG and rBCG-CMX) were chall...
Background The high mobility group box 1 (HMGB1) is the prototype of alarmin protein released by str...
<p>(A) Lung section from a mouse after one day of infection, there is strong HMGB1 immunostaining in...
<p>B6 mice were infected with ∼100 CFU <i>M.tuberculosis</i> via the aerosol route and treated with ...
<p>Pulmonary mycobacterial load (CFUs/lung) and cellular infiltrate (% pneumonic areas) were quantif...
<p>Lung (A) or spleen (B) bacterial burdens of C57BL/6 mice infected with <i>M</i>. <i>tuberculosis<...
<p><b>Copyright information:</b></p><p>Taken from "Improve protective efficacy of a TB DNA-HSP65 vac...
<p>Evaluation of the protective capacity of BCG in mice treated with anti-CD25 mAb, and challenged w...
<p>(A) Groups of infected BALB/c mice with <i>M</i>.<i>tuberculosis</i> strain H37Rv were treated wi...
<p>(A) Groups of infected BALB/c mice with <i>M</i>.<i>tuberculosis</i> strain H37Rv were treated wi...
<p>Quantitative expression of mRNA for the indicated cytokines was determined by real-time PCR in lu...
Background: The high mobility group box 1 (HMGB1) is the prototype of alarmin protein released by st...
The high mobility group box 1 (HMGB1) is the prototype of alarmin protein released by stressed or dy...
A) Groups of five C57 mice were intradermally vaccinated with 105 CFU of BCG (BCG), heat-killed BCG ...
SummaryIntroductionThe role of damage-associated molecular pattern HMGB1 signalling in a murine BALB...
<p>Ninety days after immunization, three mice from each group (control, BCG and rBCG-CMX) were chall...
Background The high mobility group box 1 (HMGB1) is the prototype of alarmin protein released by str...
<p>(A) Lung section from a mouse after one day of infection, there is strong HMGB1 immunostaining in...
<p>B6 mice were infected with ∼100 CFU <i>M.tuberculosis</i> via the aerosol route and treated with ...
<p>Pulmonary mycobacterial load (CFUs/lung) and cellular infiltrate (% pneumonic areas) were quantif...
<p>Lung (A) or spleen (B) bacterial burdens of C57BL/6 mice infected with <i>M</i>. <i>tuberculosis<...
<p><b>Copyright information:</b></p><p>Taken from "Improve protective efficacy of a TB DNA-HSP65 vac...
<p>Evaluation of the protective capacity of BCG in mice treated with anti-CD25 mAb, and challenged w...