Team:Goettingen/project overview/therapeutics

From 2014.igem.org

(Difference between revisions)
m
m
 
(49 intermediate revisions not shown)
Line 1: Line 1:
{{:Team:Goettingen/header}}
{{:Team:Goettingen/header}}
-
 
+
{{:Team:Goettingen/projectLP}}
<html>
<html>
<body>
<body>
Line 9: Line 9:
<!-- main part of the subpage -->
<!-- main part of the subpage -->
<div id="subpage">     
<div id="subpage">     
-
<!-- left column-->
 
-
<div class="proLP">
 
-
        <h3>Project</h3>
 
-
        <ul>
+
<!-- right column-->
-
        <li>Background
+
<div class="proRP" id="rpart1">
-
              <ul>
+
-
              <li><a href="https://2014.igem.org/Team:Goettingen/project_overview"><b>The global burden of fungal infections</b></a></li>
+
-
              <li><a href="https://2014.igem.org/Team:Goettingen/project_overview/fungal_infections">Fungal infections</a></li>
+
-
              <li><a href="https://2014.igem.org/Team:Goettingen/project_overview/current_tools">Current diagnostic tools</a></li>
+
-
              </ul>
+
-
        </li>
+
-
        <li><a href="https://2014.igem.org/Team:Goettingen/project_overview/project">Our project!</a></li>
+
-
        <li><a href="https://2014.igem.org/Team:Goettingen/project_overview/perspectives">Further perspectives</a>
+
-
                <ul>
+
-
                <li><a href="https://2014.igem.org/Team:Goettingen/project_overview/diganosis">Diagnosis</a></li>
+
-
                <li><a href="https://2014.igem.org/Team:Goettingen/project_overview/therapeutics">Therapeutics</a></li>
+
-
                </ul>
+
-
        </li>
+
          
          
 +
<div id="goenext"><a id="prev"><img id="pButton"></a> 14/15 <a id="next"><img id="nButton"></a></div>
 +
<br />
 +
          <br /><br />
 +
      <h1>Therapeutic Applications</h1><br />   
-
       
+
<h2>Fungal Infections and  the branches of the immune system that deal with them</h2><br />
-
<li><a href="https://2014.igem.org/Team:Goettingen/project_overview/project_drylab">Dry lab</a></li>
+
<p>
-
<li><a href="https://2014.igem.org/Team:Goettingen/project_overview/project_wetlab">Wet lab</a></li>
+
The peptides we developed have significant applications from a clinical standpoint. It has been observed in that individuals suffering from deficiencies in antibody and complement mediated cytotoxicity are less vulnerable to fungal infections than the ones suffering from phagocytic defects. Moreover studies have shown that neutrophils are pivotal in fending off fungal infections.  This is further supported by the fact that many cases of fungal infections were following a period of neutropenia (low neutrophil count in blood).</p> <br />
-
<li><a href="https://2014.igem.org/Team:Goettingen/project_overview/project_gallery">Gallery</a></li>
+
<p>Two vital principles can be gathered from the aforementioned information:</p> <br />  
-
        <li><a href="https://2014.igem.org/Team:Goettingen/project_overview/project_biobrick">BioBrick</a></li>
+
<ul>
-
        </ul>
+
<li>- Phagocytes (especially neutrophils) play a very important role in the resolution (clearance) of the fungal infection.</li> <br />
 +
<li>- Antibodies and the complement system are not that effective against fungal pathogens due to the surface of these pathogens being unfriendly to binding.</li><br />
-
        </div>
+
<p>As such, the modulation of these branches of the immune system should aid in the resolution of the disease.  It's important to mention that since most patients suffering from invasive mycoses are immuno-compromised and that there are different types of immunodeficiencies. Depending upon which branch is dysfunctional, an appropriate strategy of immunomodulation can be adopted.</p> <br />
-
<!-- end of left column-->
+
-
<!-- right column-->
 
-
<div class="proRP" id="rpart1">
 
-
<div id="goenext"><a href="https://2014.igem.org/Team:Goettingen/project_overview/diganosis"><img src='https://static.igem.org/mediawiki/2014/3/32/Goettingen2014-previous.png' width='50px'></a> 7/11</div><br />
 
-
      <h1 >Further perspectives</h1>
 
-
      <h2 id="global_burden">Therapeutics</h2>      <br />   
 
-
<p>Our peptides can also be attached to an antimycotic or opsonizing moiety and act as a therapeutic tool. Again, if the specificity of the peptides is high enough at the species level, it can help to reduce the toxicity issues related to broad-spectrum antimycotics. Regarding opsonizing moieties (such as immune tags or complement ligands), they may help the weakened immune system to attack the fungal cells. An interesting option to explore would be to attach the constant region of human IgG3 immunoglobulins, which can elicit the response of macrophages and neutophils antibody-dependent cell-mediated cytotoxicity and complement-mediated cytotoxicity.</p><br />
+
<h2>Modifications to the peptide so that it  can emulate an antibody's stimulatory function</h2><br />
 +
<p>
 +
The novelty in our peptides is that it CAN bind to the fungal surface and it can be further modified using the Fc(constant) region of the IgG1 or IgG3 antibody subtype (IgG2a in mice). This region is important as it is recognized by the effector cells (neutrophils and macrophages) of the immune system and thereafter, leads to the death of the target cell. This way, not only can it bind to fungal pathogens but can also “draw attention” towards itself from the immune system. In addition to this, the constant region can also activate the compliment cascade via the "classical" pathway. Essentially, this set-up functions as a modified antibody with an added bonus of greater affinity. </p> <br />
-
<p>It's important to mention that because most patients suffering from invasive mycoses are immunocompromised patients, the eventual application of peptides as therapeutic tools has to be concomitant with immunostimulant therapy, preferably by activating the celular response.</p><br />
 
 +
 +
<h2>Enhancement of immune response in immunodeficient individuals</h2><br />
 +
<p>
 +
As for the stimulation of the immune system in case of individuals with immunodeficiencies, the use of adjuvants (immune response enhancers) to augment the response is one strategy. In addition to this, natural immuno-modulatory molecules called cytokines (such as Interleukin-1 and Interferon-gamma) to stimulate the appropriate branches of the immune system can be employed as well. </p>
 +
 +
 +
<br />
 +
<h2>Homing the anti-fungal drug to the site of infection</h2><br />
 +
<p>Anti-mycotics have such as Amphotericin B are fluconazole have been used extensively to treat fungal infections. While they’ve been effective, they are more toxic to the human body than antibiotics that kill bacteria. This is due to the fact that bacteria are more dissimilar to humans than fungi are. As a result, it’s relatively simpler to find targets for antibiotics than anti-mycotics. Simply put, the more we humans have in common with a pathogen, the greater is the difficulty in coming up with a drug that harms only one (in other words, there is a need for selective toxicity).</p>
 +
<br />
 +
<p>Thus, yet another potential application of the novel peptides we developed is that they can act as “guides” to these molecules thereby reducing side-effects due to the drug in question.</p>
 +
<br />
 +
<hr>
 +
<h2>References</h2>
 +
<br /><br />
 +
<ul>
 +
<li>
 +
1. Raghavan M, Bjorkman P (1996). "Fc receptors and their interactions with immunoglobulins". Annu Rev Cell Dev Biol 12: 181–220.
 +
<br /><br /></li>
 +
<li>
 +
2. Swanson J, Hoppe A (2004). "The coordination of signaling during Fc receptor-mediated phagocytosis", J Leukoc Biol 76 (6): 1093–103. doi:10.1189/jlb.0804439
 +
<br /><br /></li>
 +
<li>
 +
3. Pan L, Pei P (2003). "Signaling transduction by IgG receptors". Chin Med J (Engl) 116 (4): 487–94.
 +
<br /><br /></li>
 +
<li>
 +
4.  Mueller-Loebnitz C, Ostermann H, Franzke A,Loeffler J, Uharek L, Topp M, and  Einsel H: Immunological Aspects of Candida and Aspergillus Systemic Fungal Infections: Interdisciplinary Perspectives on Infectious Diseases, Volume 2013 (2013), Article ID 102934
 +
<br /><br /></li>
 +
</p>
 +
 +
</center>
Line 84: Line 99:
}(document, 'script', 'facebook-jssdk'));</script>
}(document, 'script', 'facebook-jssdk'));</script>
<br /><br />
<br /><br />
 +
       
 +
 +
<div id="goenext"><a id="prev"><img id="pButton"></a> 14/15 <a id="next"><img id="nButton"></a></div>
 +
<br />
<div class="fb-like" data-layout="standard" data-action="like" data-show-faces="true" data-share="true"></div>
<div class="fb-like" data-layout="standard" data-action="like" data-show-faces="true" data-share="true"></div>
<script>
<script>
Line 94: Line 113:
</div>
</div>
-
<script>var url1 = "https://2014.igem.org/Team:Goettingen/project_overview";
+
 
-
var url2="https://2014.igem.org/Team:Goettingen/project_overview/fungal_infections";
+
 
-
var url3="https://2014.igem.org/Team:Goettingen/project_overview/current_tools";
+
 
-
var url4="https://2014.igem.org/Team:Goettingen/project_overview/project";
+
-
var url5="https://2014.igem.org/Team:Goettingen/project_overview/perspectives";
+
-
var url6="https://2014.igem.org/Team:Goettingen/project_overview/diganosis";
+
-
var url7="https://2014.igem.org/Team:Goettingen/project_overview/therapeutics";</script>
+
<script>$(document).keydown(function(e) {
<script>$(document).keydown(function(e) {
     switch(e.which) {
     switch(e.which) {
         case 37: // left
         case 37: // left
-
window.location = url6;
+
window.location = url13;
         break;
         break;
      
      
Line 110: Line 125:
         case 39: // right
         case 39: // right
console.log("right");
console.log("right");
 +
window.location = url15;
         break;
         break;
Line 119: Line 135:
     e.preventDefault(); // prevent the default action (scroll / move caret)
     e.preventDefault(); // prevent the default action (scroll / move caret)
});</script>
});</script>
 +
<script>
 +
$( "[id=next]" ).attr("href", url15);
 +
$( "[id=prev]" ).attr("href", url13);
 +
$( "[id=nButton]" ).attr("src", nextButton).attr("width", "40");
 +
$( "[id=pButton]" ).attr("src", prevButton).attr("width", "40");
 +
</script>
 +
</body>
</body>
</html>
</html>

Latest revision as of 11:42, 2 October 2014

14/15



Therapeutic Applications


Fungal Infections and the branches of the immune system that deal with them


The peptides we developed have significant applications from a clinical standpoint. It has been observed in that individuals suffering from deficiencies in antibody and complement mediated cytotoxicity are less vulnerable to fungal infections than the ones suffering from phagocytic defects. Moreover studies have shown that neutrophils are pivotal in fending off fungal infections. This is further supported by the fact that many cases of fungal infections were following a period of neutropenia (low neutrophil count in blood).


Two vital principles can be gathered from the aforementioned information:


  • - Phagocytes (especially neutrophils) play a very important role in the resolution (clearance) of the fungal infection.

  • - Antibodies and the complement system are not that effective against fungal pathogens due to the surface of these pathogens being unfriendly to binding.

  • As such, the modulation of these branches of the immune system should aid in the resolution of the disease. It's important to mention that since most patients suffering from invasive mycoses are immuno-compromised and that there are different types of immunodeficiencies. Depending upon which branch is dysfunctional, an appropriate strategy of immunomodulation can be adopted.


    Modifications to the peptide so that it can emulate an antibody's stimulatory function


    The novelty in our peptides is that it CAN bind to the fungal surface and it can be further modified using the Fc(constant) region of the IgG1 or IgG3 antibody subtype (IgG2a in mice). This region is important as it is recognized by the effector cells (neutrophils and macrophages) of the immune system and thereafter, leads to the death of the target cell. This way, not only can it bind to fungal pathogens but can also “draw attention” towards itself from the immune system. In addition to this, the constant region can also activate the compliment cascade via the "classical" pathway. Essentially, this set-up functions as a modified antibody with an added bonus of greater affinity.


    Enhancement of immune response in immunodeficient individuals


    As for the stimulation of the immune system in case of individuals with immunodeficiencies, the use of adjuvants (immune response enhancers) to augment the response is one strategy. In addition to this, natural immuno-modulatory molecules called cytokines (such as Interleukin-1 and Interferon-gamma) to stimulate the appropriate branches of the immune system can be employed as well.


    Homing the anti-fungal drug to the site of infection


    Anti-mycotics have such as Amphotericin B are fluconazole have been used extensively to treat fungal infections. While they’ve been effective, they are more toxic to the human body than antibiotics that kill bacteria. This is due to the fact that bacteria are more dissimilar to humans than fungi are. As a result, it’s relatively simpler to find targets for antibiotics than anti-mycotics. Simply put, the more we humans have in common with a pathogen, the greater is the difficulty in coming up with a drug that harms only one (in other words, there is a need for selective toxicity).


    Thus, yet another potential application of the novel peptides we developed is that they can act as “guides” to these molecules thereby reducing side-effects due to the drug in question.



    References



    • 1. Raghavan M, Bjorkman P (1996). "Fc receptors and their interactions with immunoglobulins". Annu Rev Cell Dev Biol 12: 181–220.

    • 2. Swanson J, Hoppe A (2004). "The coordination of signaling during Fc receptor-mediated phagocytosis", J Leukoc Biol 76 (6): 1093–103. doi:10.1189/jlb.0804439

    • 3. Pan L, Pei P (2003). "Signaling transduction by IgG receptors". Chin Med J (Engl) 116 (4): 487–94.

    • 4. Mueller-Loebnitz C, Ostermann H, Franzke A,Loeffler J, Uharek L, Topp M, and Einsel H: Immunological Aspects of Candida and Aspergillus Systemic Fungal Infections: Interdisciplinary Perspectives on Infectious Diseases, Volume 2013 (2013), Article ID 102934



    • 14/15