31.08.2013 Views

Experimental infection and protection against ... - TI Pharma

Experimental infection and protection against ... - TI Pharma

Experimental infection and protection against ... - TI Pharma

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

10 Chapter 1<br />

generally milder disease that is rarely fatal, but, in the case of vivax <strong>and</strong> ovale<br />

malaria, that may remain in a dormant form for years.<br />

Malaria control receives high priority from the international community, which<br />

has been established in the United Nation's Millennium Development Goal 6<br />

aiming at the reduction of the incidence of malaria <strong>and</strong> other major diseases by<br />

2015. Malaria control is also central to Millennium Development Goal 4,<br />

targeting a two-third reduction in the mortality rate among children under the<br />

age of five [5].<br />

Current control strategies are based on early diagnosis <strong>and</strong> treatment of malaria<br />

<strong>infection</strong>s combined with preventive measures aimed at mosquito control. The<br />

development of widespread resistance to the anti-malarial drugs chloroquine<br />

<strong>and</strong> sulfadoxine-pyrimethamine has re-directed treatment strategies to<br />

artemisinine-based combination therapies, such as artemether plus<br />

lumefantrine, artesunate plus amodiaquine, artesunate plus mefloquine or<br />

artesunate plus sulfadoxine-pyrimethamine, which are now the WHOrecommended<br />

treatment regimens. Unfortunately, Pf resistance has been<br />

observed to many of the currently used antimalarial drugs (amodiaquine,<br />

chloroquine, mefloquine, quinine <strong>and</strong> sulfadoxine-pyrimethamine) <strong>and</strong>, more<br />

recently, also to artemisinine derivatives [6]. To date, there are no new<br />

medicines in advanced stages of development to replace the artimisinins [7].<br />

Vector control is the primary intervention for reducing malaria transmission at<br />

the community level. When universal vector control coverage is achieved by<br />

impregnating bednets <strong>and</strong> spraying indoor surfaces of houses with insecticides,<br />

transmission can be reduced to close to zero. However, the increasing resistance<br />

of mosquitoes to insecticides including dichlorodiphenyltrichloroethane (DDT)<br />

<strong>and</strong> pyrethroids, particularly in Africa, poses challenges to current prevention<br />

policies [8].<br />

The current control strategies permitted the interruption of malaria<br />

transmission in low transmission countries, particularly in those with a robust<br />

institutional infrastructure <strong>and</strong> well-functioning health systems, <strong>and</strong> in those<br />

neighbouring malaria-free areas [8]. However, the lack of new effective antimalarial<br />

drugs <strong>and</strong> insecticides places malaria control <strong>and</strong> elimination efforts at<br />

considerable risk. In order to reach the ultimate goal of malaria eradication,<br />

much greater gains could be achieved with currently available tools, including<br />

elimination from a number of countries <strong>and</strong> regions, but even with maximal<br />

effort we will fall short of elimination in many areas <strong>and</strong> of global eradication

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!