Experimental infection and protection against ... - TI Pharma
Experimental infection and protection against ... - TI Pharma
Experimental infection and protection against ... - TI Pharma
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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