How to End Malaria Once and for All | Abdoulaye Diabaté | TED

(Mosquitoes buzzing)

Mosquitoes.

I don't know about you,

but I don't have a good relationship with them.

(Laughter)

A friend of mine said one day,

if you think that you are too small to make a big difference,

you've never spent a night with mosquitoes in a room.

(Laughter)

But ...

I don't have any mosquitoes in my pocket to release tonight,

so it's going to be fine.

So let's start.

As unbelievable as it may sound, malaria is as old as humankind.

And malaria once was a public health issue all over the world.

But then it has been successfully tackled in the US and Europe.

And yet, decades later,

malaria still kills millions of people

in Africa

and in Asia.

Why?

I'm Abdoulaye Diabaté, a medical entomologist

from l'Institut de Recherche en Science de la Santé.

I'm here today,

flying all the way from Burkina Faso,

to tell you that we might be closer than ever

to eliminate malaria in Africa.

(Applause)

Thank you.

Malaria is tightly linked to poverty.

But then you have no idea of how expensive it is to be poor.

There are 200 million cases worldwide

that end up sadly every year with about 600,000 deaths.

And this is not a random collection of statistics on a piece of paper.

Behind each of these 600,000 deaths,

there is a personal, tragic story, sometimes behind closed doors.

Most of these deaths happen in Africa.

Children and pregnant women bear the highest burden.

And I'm a fortunate childhood malaria survivor.

When I was a kid, I used to think that my dad was a superhero.

I could see him leaving the house every morning at six,

riding his bicycle to the farm, working very hard all day long.

We did not have much for living.

But who said you need more to be happy?

But when happiness hangs by a thread,

it doesn't take much to turn your life around.

My certainty in my dad got deeply shaken the day I got struck down by malaria.

I was three or four years old.

As we used to say in my country,

kids may not understand the complexity of suffering,

but pain has no age.

And gosh, I was in pain.

I can still clearly see myself

laying down there on the bed with high fever and suffering.

I could not eat anything.

Throwing up all the time.

Will I survive? Will I not?

The psychological trauma my parents were going through

was unbearable.

But against all odds, I survived.

But can we say today that we are done with malaria

because Diabaté survived and made it all the way down to Vancouver?

If I say yes, no one can blame me.

But it’s a lie, because many children are still dying of malaria.

The real question then is:

Why have we not been able to defeat it so far?

Well because malaria is a complex parasitic disease

that plays on three grounds.

Plasmodium, the pathogen;

anopheles, the vector;

and human, the victim.

Each of these elements is very complex on its own,

and the interactions make it even more complex

to devise interventions that are really effective.

But of course we are trying.

Currently, there are two vaccines to immunize people,

but the heavy logistics to deliver this vaccine

may not allow us to reach their full potential.

Bed nets and first-hand treatment

are both threatened by insecticide and drug resistance,

meaning that our best interventions have started to fail.

And there is a general consensus today that without additional new tools,

we may never cross the last mile of malaria elimination.

And this is exactly where I come in.

My colleagues and I at Target Malaria,

and are working on something called gene drive:

a way to control mosquito population and halt malaria transmission.

So what is gene drive?

It's a natural molecular mechanism

that augments the frequency of a certain gene in the population

beyond the normal Mendelian inheritance.

So what does it mean?

If you take any gene,

in natural circumstances,

it has only a 50 percent chance of being transmitted to the next generation.

Meaning that if the parents have 100 babies, like in mosquitoes,

only 50 of them will get the gene and the other 50 will not.

But not all genes behave this way in nature.

Some genes have found a very clever way to bypass this law,

and can augment their own prospect to up to 90 percent.

Such genes are said to drive, and so the name "gene drive."

Our most promising strain affects female fertility

by targeting a gene called doublesex.

This gene is responsible for the sex determination in mosquitoes,

and so disrupting the doublesex gene

may affect the sexual development for adult mosquitoes

and their reproduction.

Now

it may sound counterintuitive to affect female fertility

and spread a gene of interest in mosquito population at the same time.

But it's working.

And let me show you how.

We target a specific region of the gene called doublesex

that affects only females.

Males bearing this modified gene are not affected at all.

Females with just one copy of the altered gene are fully fertile.

However, females bearing two copies

of the modified gene

cannot lay eggs,

fail to bite

and also have the physical characteristics of both male and female.

It's called a suppression strategy.

Once these mosquitoes are released in the field,

they're going to spread the gene of interest to the wild population,

and this is going to reduce dramatically their reproductive capacity.

Fewer mosquitoes means less malaria transmission

until it stops.

Mathematical models predict

that releasing such mosquitoes in the field

is going to stop malaria transmission in just 20 generations.

That means in two years.

And the technology is sustainable,

cost-effective and easy to deploy,

as the released mosquitoes will do the job themselves

by finding the last hiding pocket of wild mosquitoes to convert.

Fantastic.

The only problem,

gene drive has never been tested anywhere in Africa.

And while the technology brings a lot of hope,

it also carries its share of fear and skepticism.

The pathway from the bench to the field

is not straightforward and is full of pitfalls.

Maybe the mosquitoes in the field

will develop resistance to the spread of the transgene.

Or maybe two countries don't agree,

but released mosquitoes do not respect the human borders.

Or also, maybe there are risks to the environment.

And finally, the community that we are working with

need to feel comfortable about this technology

and give us the green light to operate.

And so for such,

Target Malaria has adopted an incremental approach, step by step,

whereby we will start releasing first non-gene-drive mosquitoes,

meaning that the gene of interest here cannot self-propagate

and will just go extinct in a few generations.

The gene drive, the exposure of this gene to the environment

is incrementally augmented

in a way that we start first with small cages

and big indoor cages in Europe,

and then these mosquitoes are sent to Burkina Faso,

where they are tested in a contained facility first,

and subsequently in a big indoor small cage field release.

Now the gene drive mosquitoes are going to be tested in an open field

only after this preliminary step

and the potential risks have been looked at very carefully.

And also additional research questions have been developed

to address these risks, if any.

Now the question, how far are we from releasing gene drive?

Four to five years.

But let me tell you this.

Gene drive mosquitoes are already in the lab,

and releasing them in the field

is not going to take us more than 30 minutes.

But we need five years to get ready for these 30 minutes.

And why is that?

The answer is simple.

Because we need to engage the community

and get the social license to operate.

And so if there is one thing that you cannot afford the luxury to miss,

it's the stakeholder engagement.

I cannot just pop up in a village with a bucket of mosquitoes

on the assumption that I'm a scientist working for the public good.

It will not take anyone a PhD to understand

if we are respectful of their values or not.

We need to engage the community

and then co-develop the technology with them.

And so for that,

we've built our engagement strategy on the pyramidal structure,

starting with the villages where we operate

all the way to the top with the government officials.

The engagement is done step-by-step.

It’s done in an inclusive way

and also is done in full transparency.

Ladies and gentlemen,

there is one more thing that needs to be done

before gene drive can be released in the field in Africa.

That is capacity building.

Gene drive holds a lot of promises,

but it will not take us anywhere

if we Africans aren’t enabled to run it on our own.

Sadly,

the technical platform in Africa is really very poor,

and this has to be solved before we can really beat malaria.

And so for that, we've set up in Burkina Faso

a World Bank-funded center of excellence on vector-borne diseases, like malaria.

And also with additional funds from the Gates Foundation,

we are building a critical mass of next generation scientists

all over the continent

to fill the knowledge gap and the know-how gap as well.

In April 1969, a child was born in a remote village of Burkina Faso.

Like any other child of the world,

he had dreams and expectations.

Sadly, however, as he came to learn,

the place where you are born in on this planet

very often affects your perspective on life,

and may even set the path you need to walk through into your future.

That shouldn't be the case.

We are all citizens of the world.

Our dreams and aspirations should not be constrained

by the place where we are born.

And this is the reason why I became a scientist.

To offer endless possibility to any child anywhere on this continent,

so that they can see the future with hope.

But there is no hope if you are cut short with malaria.

But Target Malaria is here to fix that.

A world free of malaria is our vision.

And I will say, yes, we can.

Thank you for your attention.

(Applause)