Team:Paris Bettencourt/Human Practice/TB France

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TB in France

While looking at TB facts and thinking on how could synthetic biology be useful to deal with TB, we asked Christopher Dye, Director of Health Information in the Office of HIV/AIDS, Tuberculosis, Malaria and Neglected Tropical Diseases at the World Health Organization (WHO) , that very question. Here are some elements of his answers :
« Differently, depending on where you are – you have to do the local research on this »

« Yes very interdisciplinary – try to see problems from the viewpoint of others »

Therefore we followed his advice and tried to investigate locally (in France) and to meet different actors (Medical Personnal, Patients, Political and social actors). Why France? First, it was the easiest to meet people and to get reports. Secondly, it is very interesting, to look at TB in a country, where people thing TB is completely controlled and see what are the new problems linked with TB.

Contents

I) General overview of Tuberculosis in France : epidemiological, medical and political perspectives


A) Epidemiological view of TB in France in the last ten years.


1) A very slow decrease of the incidence rate


TB was a huge problem at the beginning of the century but with emergence of antibiotics and vaccines, it was thought that the disease would be eradicated by the end of the 20th century. Even if the TB incidence rate has been going down, this sinking rate has been less important than what could be expected. People living in precarious situations, migrants, immuno depressed people (especially HIV patient) still suffer from TB and keep the number of TB case per year from going too low. Therefore in France, 4991 cases of Tuberculosis were diagnosed in 2011.

<img src="PB_TBF_IncidencerateTBfrance.png" width="350px" height="200px"/>

Plotted from dta from INVS)

2) Some departments and class of people are more affected than others

TB does not affect French Territory the same way. On 22 regions, Ile de France (Paris region) represents 1768 cases (more than 1/3rd). This epidemiological différence can be explained by the different demographic profile of the French Regions. Il de France is by far the most urbanized and dense region of France. Promiscuity being a very important in the transmission of TB, it is logical to see those kind of differences.

<img src="PB_TBF_IncidencerateiDF.png" width="350px" height="200px"/>


Population groups are also affected differently. Infant and young people are qui protected. This is mainly due to a very strong vaccination policy that will be explained a bit later. The most affected age group is adults under 60. Indeed, this corresponds to migrants and a lot of HIV patients.

Number of cases of TB-disease according to group age in 2011 in France (Data from INVS)

<tbody> </tbody>

Age

0-20

20-40

40-60

60-80

+80

Number of cases

435

1777

1338

680

499

3) The problem of the rise of MDR forms

The most interesting factor is the apparition of Multi-drug resistance TB (MDR TB)in the last years. Even if the incidence rate has decreased, the number of MDR TB has risen and is expected to continue to rise. Those forms comes mainly from foreign patients arriving in France mainly from the former Soviet Union and South Africa. This aspect will be developed a bit later



<img src="PB_TBF_MDRforms.png" width="350px" height="200px"/>

B) A patient arrives in a French hospital, what happens ?


1) General medical description of TB


The infection with Mycobacterium tuberculosis doesn’t necessary evolve in a disease. Most of the time, the infection is controlled by the immune system (even if the pathogen remains latent somewhere).

When the tuberculose remains latent (no symptoms), it will not be treated except for very specific cases (immunodeficient patient, people that will receive a transplant …)

When patient becomes symptomatic (long lasting cough, spitting, fiever, loss of wheigh, night sweats…), TB-disease becomes contagious ( droplets produced when coughing or sneezing).

During the tuberculosis-disease we have 3 kinds of bacilli’s populations:

• extracellular bacilli = 95% of bacilli, active, fast multiplication, responsible of contamination and symptoms.

• intra-cellullar quiescent bacilli, in macrophages, slow multiplication.

• extracellular bacilli in the caseous and some other extra-pulmonary locations, latent, responsible of the risk of relapse, very slow multiplication.

The tubercle bacillus is known as an intracellular pathogen. However it is the extracellular population that clinicians aim to eliminate.

When a TB case is diagnosed in France it has to be reported to the ARS (Agence Régionale de la Santé), French Regional Agency of Health.


2) Diagnostical tools


When a patient expresses symptoms or corresponds to categories of when TB latent has to be treated, different diagnostic tests are run to dertermine if those sympthoms are caused by a Mycobacterium or not.

The first test is to get an inoculum by having the patient spit or by getting this with a tube near the lungs. The sample is then analyzed under the microscope. The unit that is looked at is the number of “bar” in the sample, meaning the number of bacteria resembling M. Tuberculosis. If the test is negative, it is done at least three times to be sure.

Samples are then culture and a PCR is ran to confirm the strain and to check the most common resistance. It takes approximatively a week to get the results. No treatment is given before getting those results, the worst fear being of selecting resistant forms.

Finally there is a third test that is not used by every hospital because it can be difficult to interpret : the intra Dermo Reaction. Basically, a droplet of liquid containing TB antigenes is put on the skin of the arm of the patient. If the patient has ever been exposed to a mycobacterium in his life,an inflammatory reaction happens. This test is difficult to analyze because it does not give the type of Mycobacterium the patient has been exposed to nor if the patient is still infected with Mycobacterium nor the stage of the TB.

Of course, in extreme cases of pulmonary TB, a lung radio can reveal some elements called “cavern” which directly confirm the TB-disease.

<img src="PB_TBF_Caverns.png" width="350px" height="200px"/>


3) Treatment


The treatment consists of 4 first-line drugs in combination during 2 months: isoniazid, rifampicine, ethambutol and pyrazinamide. Within the first 2 months of appropriate chemotherapy, the vast majority of bacilli have been killed. It allows clinicians to virtually eliminate the risk of transmission and the selection of drug-resistant mutants. The patient need to follow the treatment during 4 other months (bitherapy: isoniazid, rifampicin).

<img src="PB_TBF_TreatmentTB.png" width="350px" height="200px"/>

4) Pharmacological caracteristics of antituberculosis drugs

Isoniazid: The most active drug for the treatment of tuberculosis.

The mechanism of action is the Inhibition of synthesis of mycolic acids, which are main components of mycobacterial cell wall. As a result of the activity, tubercle bacilli lose their features of acid-resistance, water-resistance and proliferating ability, leading to death.Due to its mechanism of action, it is bactericidal against actively growing tubercle bacilli. For resting tubercle bacilli it is bacteriostatic. It is active both on intracellular and extracellular Mycobacteria. Good distribution, it can also penetrate inside the macrophages. It main problem are hepatotoxicity (20% of patients) and neurotoxicity.The metabolism is hepatic including by acetylation (interindividual pharmacogenetic variability). It is eliminated by the kidney.

Rifampicine: The most colored drug for the treatment of tuberculosis.

It Inhibits the transcription by binding to the subunit β of bacterian RNA-polymérase.

(Funny fact: Occidental people don’t like it because they can’t wear lenses, it indeed color their urine and tears in orange… Whereas African people like it because they can “see” the effect)Bactericidal against intra and extra cellular Mycobacteria. Very good drug diffusion (pulmonary, meningeal, bones, ganglionary…). However, enzymatic induction of cytochrome P 450 result in a modification of other drugs metabolism (drug-drug interaction).

Ethambutol

Mycobacteria catch ethambutol when they are in exponantial growth phase. Ethambutol inhibits acid mycolic or arabinose incorporation into the cell wall.Bacteriostatic for extra-cellular bacilli. Good tissular diffusion. Renal elimination. The most common serious adverse effect is optic neuritis, causing loss of visual acuity and red-green color-blindness, but are reversible.

Pyrazinamid

It Inhibits FAS (Fatty acids synthase), binds to the ribosomal protein S1 (RpsA) and inhibits trans-translation. This may explain the ability of the drug to kill dormant mycobacteria.Bactericidal for intra-cellular bacilli. Good diffusion inside the macrophages. Hepatic metabolism. Renal elimination.

5) Drug resistant form of TB

A multidrug-resistant tuberculosis (MDR TB) is a tuberculosis resistant to isoniazid and rifampicine

An extensively drug-resistant tuberculosis (XDR TB) is an MDR TB + a resistance to a second line drug treatment (fluoroquinolone and aminosids (kanamycine/amikacine/capreomycine). Mortality rate : 35%.

One of the main concern of the clinicans is the appearance of those resistances. The main cause of apparition of resistances in a patient in France, is the patient’s lack of observance. In order to improve observance, some pills combining 3 drugs (rifampicine/isoniazide/pyrazinamide) have been developped.

The treatment is accompanied by an educational monitoring. The patient is thouroughly explained the importance of observing the treatment as well as the best conditions to avoid contagion of their closed ones. This monitoring is mainly handled by the CLAT (Centre de Luttre Anti Tuberculeuse), Fight Against Tuberculosis Center.

In the end, for regular TB, the outcome is extremely good (almost 100% people cured).


c) Public policies put in place to deal with TB


1) The fight against tuberculosis : a multiplicity of actors


As everything in French public policy systems, missions to fight tuberculosis are divided between several institutions and types of administrations. In a few words, French policy system has three main types of structures :

- The government represented by the ministries and what is called “services déconcentrés”, services that are responsible at a departmental and regional level of the application of the government policies

- The local powers or “collectivités territoriales” : from the city, to the department or regions, those administration are run by people elected locally and are responsible of making the specific interest of a defined territories known and put in place

- Public or semi-public institutions : Might they be firms like the “SNCF” which is responsible for the train or research institutions or monitoring administrations, they are quite independent but under the general direction of ministry and have one or several specific missions.

In order to see clearly who does what, here is a synthetic table which underlines who deals with what in the general monitoring of TB.

<tbody> </tbody>

Institutions

Missions

Level of public involvement

Ministry of Health

Definition of the general plan to fight against TB (attribution of financial means, vaccination policies, coordination…)

Government

HCSP (High Council For Public Health)

- Evaluation of the policy

- Consultative administration to advise the ministry

ARS (Regional Agency of Health)

Gather the declaration of diagnosed TB case (using a software call BK4)

Regional Representation of the Ministry

DDASS (Direction of social and health Affairs

Coordinates investigations after declaration of Tuberculosis.

Responsible of implementing regionally the policies developed by the Ministry

Departmental Representation of the Ministry

INVS (National Institute of Health Monitoring)

Responsible for the epidemiological Monitoring

Expertise for the Ministry, under the tutorship of the Ministry

CLAT (Fight Against Tuberculosis Center)

- Investigate the environment of diagnosed patients

- Organize detection, free medical consultations and prevention actions

- Coordinate and animate the local policy against TB

Local or departmental administration (= local powers)

Hospitals

Diagnostic – Treatment – Monitoring of patients

Immediate Declaration to the CLAT and the DDASS of diagnosed case

First meeting with the CLAT and the patient

Declaration of the outcome of each diagnosed patient

Liberal Doctors

Diagnostic – Treatment – Monitoring of patients

Immediate Declaration to the CLAT and the DDASS of diagnosed case

Declaration of the outcome of each diagnosed patient



2) The French “Plan de lutte anti Tuberculeuse 2007-2009 “ aka plan for the fight against TB.


This national plan was created in 2006 after TB was put in the 100 highest priorities for health policy par the French Parliament. It’s goal is to improve the fight against TB.

Its implementation revolves around six main axis. has 6 axis :

- to ensure an early diagnosis and an adapted treatment for all TB disease cases

- To improve the detection of TB

- TO optimize the vaccinale strategy of TB

- to maintain resistance to antibiotics to a low level

- to improve the epidemiological monitoring and the knowledge about determinants of TB

- to improve the coordination of the fight against TB



This plan mainly changed 2 things. : the vaccination policy and the delegation to local powers (CLAT) the main concrete actions.

Until 2007, vaccination was mandatory for every child. The vaccination coverage was higher than 90%. Due to a lack of efficiency of the vaccine (BCG) and the idea that TB was almost eradicated, the vaccination stopped being mandatory. Today, it is highly recommended, especially when the children start going to school. However, this led to a drastic reduction of vaccinated children (only 59% today). Vaccination is still mandatory for all medical personnal. A lot of pediatrician think this was a huge mistake and keep on vaccinating all the children they see. However, the evaluation of this policy by the HCSP (High Council for public health) lead to the conclusion that no strong problem has been reported until nowand that therefore this policy should be maintained.

The second main change was the delegation of power to the CLAT. The CLAT located in every department coordinates medical centers, leads teams of investigators, organize detection activities … The efficacity of the active detection has been questioned. Indeed, out of more than 1000 detection done, only a few cases (less than 5) have been reported in the last year. Moreover the evaluation of the HCSP has concluded, more means should be given to CLAT which perform most of the action and don’t benefit from enough fundings.

II)Tuberculosis,a social disease: the “migrants" problem in French fight against Tuberculosis


<img src="PB_TBF_Tbcasebyorigin.png" width="350px" height="200px"/>

<img src="PB_TBF_Tbcasebytreatmenthistory.png" width="350px" height="200px"/>

<img src="PB_TBF_TboutcomeMDR.png" width="350px" height="200px"/>

<img src="PB_TBF_Treatmentoutcome2001_2010.png" width="350px" height="200px"/>

III)Tuberculosis,a therapeutic impass?




Centre for Research and Interdisciplinarity (CRI)
Faculty of Medicine Cochin Port-Royal, South wing, 2nd floor
Paris Descartes University
24, rue du Faubourg Saint Jacques
75014 Paris, France
+33 1 44 41 25 22/25
team2013@igem-paris.org
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