by hilzoy
Wonderful news from the New England Journal of Medicine (1, 2), summarized by FP Passport:
Results of the latest malaria vaccine trials will be published today in The New England Journal of Medicine, and from the looks of it, the news is good--fantastic, in fact. "We are closer than every before to having a malaria vaccine for use by children in Africa, says Christian Lucq, director of the PATH Malaria Vaccine Initiative.
First, some background: The new trials use a vaccine candidate known as RTSS, the most clinically advanced malaria vaccine in development. The two tests took place in Kenya and Tanzania, and included 340 and 894 children, respectively. After vaccination, children were visited in their homes to follow up on their health and most importantly, their contraction (or not) of malaria.
Here are some highlights from the results:
* Unlike previous trials, these studies administered the malaria vaccine in conjunction with the normal WHO schedule of vaccines like polio, MMR, and others. There was no interference on either side. That matters because if a malaria vaccine is every to be administered, it is likely to be administered in tandem with others.
* In infants of 8, 12, and 16 weeks, the vaccine reduced malaria infections by 65%.
* In children aged five to 17 months, the incidence of clinical malaria was reduced by 53%.
The results today set the stage for more Phase 3 trials--the last needed before lisencing of the vaccine. Future trials will continue to test safety, efficacy, and the possibility of a "booster" shot lengthening the already lengthy 18-month protection observed. 16,000 children will be involved in 11 sites found in 7 countries."
According to the CDC, malaria is the fourth leading cause of death among children under five. It kills at least a million people a year, and sickens hundreds of times that number. Besides the horrific burden of disease, death, and misery that malaria places on large chunks of the world, it also puts a serious economic burden on those countries where it's endemic -- which are, as it happens, often the countries that can least afford it.
So a malaria vaccine that's 50-65% effective would be a wonderful, wonderful thing.
Woo hoo!
Ahem.
What I mean to say is:
Hey, spiffy, that's great news! Go humanity!
Posted by: Anthony Damiani | December 09, 2008 at 04:39 AM
Yay!
Posted by: Jesurgislac | December 09, 2008 at 05:34 AM
This is amazing. So good to see this work is still being done, and that it's so close to being put into use.
Posted by: mattH | December 09, 2008 at 10:51 AM
Awesome news.
Posted by: nous | December 09, 2008 at 12:41 PM
It's worth pointing out that the effectiveness rate of a vaccine actually understates its impact. After all, diseases like malaria rely upon a host population to spread. Reduce that host population, and you can reduce the rate of infection - not just in those who have been vaccinated and in whom the vaccination has proven preventative, but for the population at large.
Take, for example, another recently-introduced early childhood vaccine. The pneumococcal conjugate vaccine was targeted at children under the age of two. After two years of widespread administration, rates of infection of the targeted strains dropped by 78% among children under two. But here's the really good news: "Among children younger than five years, there was a 59 percent decline in rates of invasive disease. Even adult populations showed reduced rates of invasive disease, with 32 percent fewer cases in persons 20 to 39 years, 8 percent less disease in those 40 to 64 years, and an 18 percent reduction in invasive infection among persons 65 years or older."
There are two take-away points from that case study. The first is that vaccines like this can act very rapidly - the authors concluded that it was having a dramatic effect within the first year. The second is that an early-childhood vaccine can have a dramatic impact on the population at large, as well. So much the better.
Posted by: Cynic | December 09, 2008 at 12:48 PM
That is excellent news. Thanks for giving me the heads up on this.
Posted by: Feddie | December 09, 2008 at 01:27 PM
After all, diseases like malaria rely upon a host population to spread. Reduce that host population, and you can reduce the rate of infection - not just in those who have been vaccinated and in whom the vaccination has proven preventative, but for the population at large.
It's actually even better than this. There's a fairly strong relationship between how widespread a disease-causing organism is and how nasty it can afford to be to its host. Cutting the number of malaria infections in half will, according to virulence theory, create a strong selection pressure for "weaker" malarial infections in those that acquire it despite vaccination.
Widespread vaccination attacks disease on three fronts: fewer people are infected, there are fewer reserves of disease, and the pathogen is "encouraged" to be nicer to those it does infect. This is incredibly good news.
Posted by: Robert M. | December 09, 2008 at 02:20 PM
This is great news, but it is worth pausing to note that world does not need to wait for the development of an effective vaccine to substantially reduce morbidity and mortality from malaria in Africa. Heck, the basic provision of mosquito nets has been proven time and again to be an evidence-based intervention.
What this does suggest is not that we should not spend money on developing vaccines, but that due attention to the social determinants of health on a global scale ought to be a top priority. For much more on this, of course, see the work of, among many others, Amartya Sen and Paul Farmer.
Posted by: Daniel S. Goldberg | December 09, 2008 at 03:05 PM
Robert M.,
Thanks for bringing up the virulence point. It's (good) news to me.
Posted by: Bernard Yomtov | December 10, 2008 at 01:59 PM