Team:Slovenia/Conclusions

From 2008.igem.org

(Difference between revisions)

Latest revision as of 04:02, 30 October 2008


The problem Modern vaccines Immune response Flagellin Motivation Engineered flagellin vaccine Antigen-TLR fusion vaccine Engineered flagellin vaccine Antigen-TLR fusion vaccine "Real-life" results Biobricks Methods Safety References Notebook Acknowledgements Sponsors

Conclusions Achievements We have demonstrated the power of modular building blocks approach of synthetic biology (IMMUNOBRICKS) for the rational design of vaccines We have designed a new type of vaccine against H. pylori based on the chimeric flagellin that combines activation of innate and adaptive immunity within the same molecule Chimeric flagellins were produced in bacteria, purified and characterized Engineered H. pylori flagellins activate TLR5 as opposed to the native H. pylori flagellin Three different implementations of chimeric flagellin vaccines were prepared Chimeric flagellin is localized at the bacterial surface DNA construct based on chimeric flagellin causes transactivation of TLR5 on neighboring cells (demonstration of the feasibility of introduction of DNA into the epithelial cells to activate the underlying dendritic cells) Antigen-TLR fusions are functional and their localization can be modulated by the selection of transmembrane segment Various DNA vaccine constructs have been successfully introduced by electroporation intramuscularly or subcutanelously and expression of the fusion protein in the target tissue in vivo was demonstrated Two chimeric recombinant protein vaccines showed an intense IgG antibody response in mice and immunized sera also reacted with live and heat-killed H. pylori implying that they recognize epitopes of H. pylori. What remains to be done? Complete the animal studies: demonstrate the prophilactic efficiency of our vaccines to prevent colonization, and therapeutic value to eradicate existing infection as well as evaluate effects of vaccinations on histology of gastric mucosa…… Demonstrate the efficiency of bacterial implementation of flagellin-like vaccine on lyophilized bacterial ghosts (more safe and stable vaccine), particularly for oral and mucosal vaccination – prospects for application in third world countries Analyze different combinations of antigen-TLRs to obtain optimal immune stimulation (TLR synergy) Repeat all experiments with many controls, in comparison to currently used adjuvants etc ... ... ars longa, vita brevis Prospects Functional vaccine against H. pylori would be definitely welcome The approach with chimeric flagellins could be used against other flagellated bacteria whose flagellin does not activate innate immune system (Bartonella, Campylobacter, Borellia...) Could vaccines based on antigen-TLR fusions be used as tumor vaccines as well?

@@ Line 78: / Line 78: @@
 		<a href="https://2008.igem.org/Team:Slovenia/Background/The_problem" target="_self">The problem</a>
 		<a href="https://2008.igem.org/Team:Slovenia/Background/Modern_vaccines" target="_self">Modern vaccines</a>
+<a href="https://2008.igem.org/Team:Slovenia/Background/Immune_response" target="_self">Immune response</a>
+<a href="https://2008.igem.org/Team:Slovenia/Background/Flagellin" target="_self">Flagellin</a>
 		</div>
 	</li>
@@ Line 94: / Line 96: @@
 		<a href="https://2008.igem.org/Team:Slovenia/Results/Antigen-TLR_fusion_vaccine" target="_self">Antigen-TLR fusion vaccine</a>
 		<a href="https://2008.igem.org/Team:Slovenia/Results/Real-life_results" target="_self">"Real-life" results</a>
+<a href="https://2008.igem.org/Team:Slovenia/Results/Biobricks" target="_self">Biobricks</a>
 		</div>
 	</li>
@@ Line 104: / Line 107: @@
 		<a href="https://2008.igem.org/Team:Slovenia/Notebook/Methods" target="_self">Methods</a>
 		<a href="https://2008.igem.org/Team:Slovenia/Notebook/Safety" target="_self">Safety</a>
-		<a href="https://2008.igem.org/Team:Slovenia/Notebook/Timeline" target="_self">Timeline</a>
 		<a href="https://2008.igem.org/Team:Slovenia/Notebook/References" target="_self">References</a>
-                <a href="https://2008.igem.org/Team:Slovenia/Results/Biobricks" target="_self">Biobricks</a>
                  <a href="https://2008.igem.org/Team:Slovenia/Notebook/Notebook" target="_self">Notebook</a>
 		</div>
@@ Line 160: / Line 161: @@
 -->
 <html><center>
-<font size="-1" color="#C73E4A"><i><b>Conclusions</b></i></font>
+<font size="6" color="#C73E4A"><i>Conclusions</i></font>
 </center></html>
 ----
+<html>
+<strong><font size="4">Achievements <font size="2"><br /></strong>
+<div style="text-align:justify">
+<ul>
+  <li>We have demonstrated <b>the power of modular building blocks approach of synthetic biology (IMMUNOBRICKS)</b> for the rational design of vaccines</li>
+  <li>We have designed a new type of vaccine against <i>H. pylori</i> based on the chimeric flagellin that <b>combines activation of innate and adaptive immunity within the same molecule</b>
+      <ul>
+        <li>Chimeric flagellins were produced in bacteria, purified and characterized</li>
+        <li>Engineered <i>H. pylori</i> flagellins activate TLR5 as opposed to the native <i>H. pylori</i> flagellin</li>
+        <li>Three different implementations of chimeric flagellin vaccines were prepared</li>
+        <li>Chimeric flagellin is localized at the bacterial surface</li>
+        <li>DNA construct based on chimeric flagellin causes transactivation of TLR5 on neighboring cells (demonstration of the <b>feasibility of introduction of DNA into the epithelial cells to activate the underlying dendritic cells)</b></li>
+      </ul>
+    </li>
+    <li>Antigen-TLR fusions are functional and their localization can be modulated by the selection of transmembrane segment</li>
+<li>Various DNA vaccine constructs have been successfully introduced by electroporation intramuscularly or subcutanelously and expression of the fusion protein in the target tissue <i>in vivo</i> was demonstrated</li>
+<li>Two chimeric recombinant protein vaccines showed <b>an intense IgG antibody response in mice</b> and <b>immunized sera also reacted with live and heat-killed <i>H. pylori</i></b> implying that they recognize epitopes of <i>H. pylori</i>.</li>
+</ul>
+<br /><br />
+<strong><font size="4">What remains to be done?<font size="2"><br /></strong>
+<ul>
+   <li>Complete the animal studies: demonstrate the prophilactic efficiency of our vaccines to prevent colonization, and therapeutic value to eradicate existing infection as well as evaluate effects of vaccinations on histology of gastric mucosa……</li>
+   <li>Demonstrate the efficiency of bacterial implementation of flagellin-like vaccine on lyophilized bacterial ghosts (more safe and stable vaccine), particularly for oral and mucosal vaccination – prospects for application in third world countries</li>
+   <li>Analyze different combinations of antigen-TLRs to obtain optimal immune stimulation (TLR synergy)</li>
+<li>Repeat all experiments with many controls, in comparison to currently used adjuvants etc</li>
+<li>... ... ars longa, vita brevis</li>
+</ul><br /><br />
+<strong><font size="4">Prospects<font size="2"><br /></strong>
+<ul>
-<html>
+<li>Functional vaccine against <i>H. pylori</i> would be definitely welcome</li>
+<li>The approach with chimeric flagellins could be used against other flagellated bacteria whose flagellin does not activate innate immune system (<i>Bartonella, Campylobacter, Borellia</i>...)</li>
+<li>Could vaccines based on antigen-TLR fusions be used as tumor vaccines as well?</li>
+</ul>
+</div>
 </p>
 </td>