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Co-infection of Two genetic diseases makes them susceptible to malaria

out discrete, if complex, biological mechanisms at work in naturally acquired immunity.

For several years Williams' research has probed how certain genetic factors provide Africans with a degree of natural protection against malaria. A key focus of his work has been the underlying effects of the sickle cell trait, which became relatively common in humans as an evolutionary, protective genetic response to thousands of years of exposure to malaria.

Individuals with sickle cell trait inherit one normal hemoglobin gene from one parent and a sickle hemoglobin gene from another. (They don't have sickle disease, which occurs when someone inherits two copies of the sickle gene, one from each parent.) Studies have shown that when children with the sickle trait are exposed to malaria, they suffer far fewer parasites and are 90 percent less likely to be hospitalized by a malaria infection than those without the trait. The protective effect increases with age.

Meanwhile, Williams said researchers have long known that a genetic variation known as alpha thalassemia--which is common in sub-Saharan Africa but, unlike beta thalassemia, is not associated with major health problems--also helps people fight malaria. While not offering as much protection as the sickle trait, Williams said children with the thalassemia trait are less likely to die from a malaria infection because it prevents severe anemia, which can complicate other malaria-induced conditions.

The degree to which the interaction between the traits dilutes their protective effect depends on the type of alpha thalassemia gene involved. (There are two sub-varieties.) But Williams said when the sickle trait exists alongside the type found routinely in malaria endemic regions of Africa, "all the good work of these genes is lost and you end up with the same degree of risk as someone who has neither trait."

Williams said the finding does not affect treatment decisions
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