Team:Evry/HumanPractice

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<h1> Human Practice overview</h1>
<h1> Human Practice overview</h1>
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  <header>New since European Jamboree</header>
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  <p>
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    After the European Jamboree, we decided to go further in our reflexion and to continue our Human Practices.   
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      <ul><li> We launched an international version of our survey to obtain and analyze responses from all over the world. We obtained more than 185 answers, 156 only from the UK !</li>
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<li> We made a simplified version of our <a href="https://2013.igem.org/Team:Evry/vf" target="_blank">wiki in French</a>  for French patients and associations.</li>
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      <li>We completed our safety reflexion by imagining various systems that could be used to improve the safety of our treatment.  </li>
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      <li>We wrote an economic report on cost and benefit of our treatment.</li>
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      <li>We had interviews with french health agency and pharmaceutical industries</li>
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      </ul>
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  </p>
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<h3>Society</h3>
<h3>Society</h3>
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<p>In the health field, ethics usually appears in the last phases of development of the treatment. Patients are seldom associated in the research process. Inspired by the dynamics of “expert patients”, the team choose to involve the patients' associations since the beginning of the project. That is why we consulted a scientist – Gaël Nicolas – but also a clinician who knows the patients very well – Pierre Brissot – and the presidents of patients' associations (see <a href="https://2013.igem.org/Team:Evry/HumanPractice/Expert_consultation">Phase 1</a>). After that, and with the presidents help, we did a large patient survey. We analysed the final results (see <a href="https://2013.igem.org/Team:Evry/HumanPractice/Patients_perceptions">Phase 2</a>), but the intermediate results helped us perfecting our treatment strategy. This led directly to the design of the pill (see <a href="https://2013.igem.org/Team:Evry/Pill_design">Pill design</a>).
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<p>In the health field, ethics usually appears in the last phases of development of the treatment. Patients are seldom associated in the research process. Inspired by the dynamics of “expert patients”, the team choosed to involve the patients' associations at the beginning of the project. This is why we consulted a scientist – Gaël Nicolas – but also a clinician who knows patients very well – Pierre Brissot – and the presidents of patients' associations (see <a href="https://2013.igem.org/Team:Evry/HumanPractice/Expert_consultation">Phase 1</a>). After that, and with the presidents help, we launched a large patient survey. 270 French patients answered, and 185 patients answered the international survey. We analysed the final results (see <a href="https://2013.igem.org/Team:Evry/HumanPractice/Patients_perceptions">Phase 2</a>), but the intermediate results helped us perfecting our treatment strategy. This led directly to the design of the pill (see <a href="https://2013.igem.org/Team:Evry/Pill_design">Pill design</a>).
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<br/>In return, we made our work the most accessible to them that it was possible: our wiki exists in French and is known by the associations, they can benefit from both our survey and our scientific work. To conclude this deep cooperation, we organized a scientific seminar. It was a privileged moment where patients, presidents of patients' associations, scientists and clinicians could discuss; it was also the moment to submit our project to them and hear their remarks (see <a href="https://2013.igem.org/Team:Evry/Seminar">Phase 3</a>).</p>
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<br/>In return, we made our work accessible to a wide audience: our wiki exists in <a href="https://2013.igem.org/Team:Evry/vf" target="_blank">French</a> and is known by the associations, they can benefit from both our survey and our scientific work. To conclude this deep cooperation, we organized a scientific seminar. It was a privileged moment where patients, presidents of patients' associations, scientists and clinicians could discuss; it was also the moment to present them our project and to hear their remarks (see <a href="https://2013.igem.org/Team:Evry/Seminar">Phase 3</a>).<br/>
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After the European Jamboree, we added the estimated costs and profitability of the treatment (see <a href="https://2013.igem.org/Team:Evry/Economy">Phase 6</a>).
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<h3>Philosophy</h3>
<h3>Philosophy</h3>
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<h3>Overview's Conclusion</h3>
<h3>Overview's Conclusion</h3>
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<p>We built the human practice as a collective cross-disciplinary thought, aiming to have the largest view on the context of our project. <b>We accomplished a strong cooperation with hemochromatosis patients' associations, and a serious and unusual philosophical experience, without ignoring the other aspects such as safety.</b> We could conclude that our project's ambition is to lead the human practice toward being as essential to synthetic biology as the scientific domains.</p>
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<p>We built the human practice as a collective cross-disciplinary thought, aiming to have the largest view on the context of our project. <em>We accomplished a strong cooperation with hemochromatosis patients' associations, and a serious and unusual philosophical experience, without ignoring the other aspects such as safety or economy.</em> Our project's ambition is to lead the human practice towards being as essential to synthetic biology as the scientific domains are.</p>
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<h2>Phase 1: Consultation of experts</h2>
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<p>Since the start we have felt the need to build this project with specialists of hæmochromatosis including both patients and scientists. The first ones were important to insert our project in the reality of a disease that none of us really knew. Furthermore they are the first concerned: we had to do our best to get them interested in our project and to make our project understandable by them.<br>
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Dr Gaël Nicolas was our main help on the scientific aspect of hæmochromatosis.</p>
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<a href='https://2013.igem.org/Team:Evry/HumanPractice/Expert_consultation' target='_blank'>Consultation of experts</a>
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<h2>Phase 2: Patients' perceptions</h2>
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<p>Because having some patients' opinions was interesting but not sufficient we decided to conduct a study as important as possible. We drew up a survey that was spread by associations of hæmochromatotics.<br>
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This survey is still going on.</p>
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<a href='https://2013.igem.org/Team:Evry/HumanPractice/Patients_perceptions' target='_blank'>Patients' perceptions</a>
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<h2>Phase 3: Meeting and discussion</h2>
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<p>At this point of our work we thought it proper to organise a seminar about the general question of hæmochromatosis and the particular approach of our treatment. This seminar will be a privileged moment to bring all the persons we have worked with together. Two round tables are planed in order to discuss further the questions raised by our project and our treatment.</p>
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<a href='https://2013.igem.org/Team:Evry/Seminar' target='_blank'>Meeting and discussion</a>
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<h2>Phase 4: Science and technique in iGEM culture</h2>
 
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<p>This last phase is a bit different. In fact it is not properly the last phase: this part is an experience of embedded philosophy conducted throughout the project. As such this phase reflects more what I, a philosopher and a bioethician, observe than what the team would have thought about by itself. Nevertheless the team takes actively part in this reflection.<br>
 
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This reflection started with the idea that synthetic biology was usually perceive as a science, but seldom as a technique, though everyone is always talking about engineering and functions and aims. The modified bacteria as a precise thing to do.</p>
 
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<a href='https://2013.igem.org/Team:Evry/Philosophy' target='_blank'>Philosophy</a>
 
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<h2>Phase 5: Safety and responsibility</h2>
 
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<p>Very quickly we were confronted by the safety of treatment: even before fulfilling our aim of chelating iron in the duodenum we had to think about all the scenarios involved by such a treatment. The entire team worked together in order to build a consequence tree. This tree tries to be exhaustive: it is only then that we can determine the more probable scenarios by biologic reflexion and modelling.<br>
 
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This consequence tree is a way to be assured that our treatment is not only safe for the patient but responsible too. We can not afford to have a synthbio-medicine that would endanger other people or the environment.</p>
 
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<a href='https://2013.igem.org/Team:Evry/Safety' target='_blank'>Safety and Responsability</a>
 

Latest revision as of 02:00, 29 October 2013

Iron coli project

Human Practice overview

New since European Jamboree

After the European Jamboree, we decided to go further in our reflexion and to continue our Human Practices.

  • We launched an international version of our survey to obtain and analyze responses from all over the world. We obtained more than 185 answers, 156 only from the UK !
  • We made a simplified version of our wiki in French for French patients and associations.
  • We completed our safety reflexion by imagining various systems that could be used to improve the safety of our treatment.
  • We wrote an economic report on cost and benefit of our treatment.
  • We had interviews with french health agency and pharmaceutical industries

Society

In the health field, ethics usually appears in the last phases of development of the treatment. Patients are seldom associated in the research process. Inspired by the dynamics of “expert patients”, the team choosed to involve the patients' associations at the beginning of the project. This is why we consulted a scientist – Gaël Nicolas – but also a clinician who knows patients very well – Pierre Brissot – and the presidents of patients' associations (see Phase 1). After that, and with the presidents help, we launched a large patient survey. 270 French patients answered, and 185 patients answered the international survey. We analysed the final results (see Phase 2), but the intermediate results helped us perfecting our treatment strategy. This led directly to the design of the pill (see Pill design).
In return, we made our work accessible to a wide audience: our wiki exists in French and is known by the associations, they can benefit from both our survey and our scientific work. To conclude this deep cooperation, we organized a scientific seminar. It was a privileged moment where patients, presidents of patients' associations, scientists and clinicians could discuss; it was also the moment to present them our project and to hear their remarks (see Phase 3).
After the European Jamboree, we added the estimated costs and profitability of the treatment (see Phase 6).

Philosophy

In parallel, and to complete the team's reflection, we conducted an experience of embedded philosophy throughout the project. We chose to collectively think about the specificities of synthetic biology as a technique. It seemed important to us, because we were not only trying to know things (it is not lonely science) but we were also trying to do something with our knowledge (we enter technique). And as everybody knows: “a great power implies great responsibilities.”
The originality of our approach was to confront what philosophers may think and what the members of the team may think. A philosophical essay was written to arouse the debate, and we chose to present the reactions of the team members on the same level as the philosophers' quotations. The concept was to update philosophy directly in the lab. As most of the philosophical discussions, we chose to let it open so you can enter a living debate (see Phase 4).

Safety

The scientific responsibility of the team concerning the project was not neglected: very quickly we were confronted with the safety of the treatment. Thus, even before fulfilling our aim of chelating iron in the duodenum, we had to think about all the scenarios involved by such a treatment. The entire team worked together in order to build a consequence tree. This tree tries to be exhaustive: it is only then that we can determine the more probable scenarios by reflexion and modelling. This consequence tree is a way to be assured that our treatment is not only safe for the patient but responsible too. We can not afford to have a synthbio-medicine that would endanger other people or the environment. The consequence tree is a very simple, quick and efficient method to measure the risks of our genetically engineered machine, and to envisage the possible solutions to these risks (see Phase 5).

Overview's Conclusion

We built the human practice as a collective cross-disciplinary thought, aiming to have the largest view on the context of our project. We accomplished a strong cooperation with hemochromatosis patients' associations, and a serious and unusual philosophical experience, without ignoring the other aspects such as safety or economy. Our project's ambition is to lead the human practice towards being as essential to synthetic biology as the scientific domains are.