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NCERT Exemplar · Q23

Q.A person with sickle cell anemia is

(a) more prone to malaria
(b) more prone to typhoid
(c) less prone to malaria
(d) less prone to typhoid
Madhya Pradesh MpbseMCQ· 1mImportance★★★★★
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A person with sickle cell anemia, specifically those carrying one copy of the sickle cell gene (sickle cell trait), is less prone to malaria because their altered red blood cells hinder the malaria parasite's life cycle.

To understand why a person with sickle cell anemia might be less prone to malaria, we first need to grasp what each condition entails and how they interact at a cellular level. This is a fascinating example of how a genetic condition, while detrimental in its full form, can offer a protective advantage in a heterozygous state against another widespread disease.

Sickle cell anemia is a genetic blood disorder caused by a mutation in the gene responsible for producing hemoglobin, the protein in red blood cells that carries oxygen. This mutation leads to the production of an abnormal type of hemoglobin, often referred to as hemoglobin S (HbS). Under conditions of low oxygen, or even sometimes under normal conditions, red blood cells containing HbS become rigid, sticky, and take on a characteristic crescent or "sickle" shape, rather than their usual flexible, biconcave disc form. These sickled cells can block small blood vessels, leading to pain, organ damage, and are also prematurely destroyed, causing anemia.

Malaria, on the other hand, is a life-threatening parasitic disease caused by Plasmodium parasites, primarily Plasmodium falciparum in severe cases. It is transmitted to humans through the bites of infected female Anopheles mosquitoes. Once inside the human body, the parasites travel to the liver, mature, and then infect red blood cells. Within the red blood cells, the parasites multiply rapidly, eventually causing the cells to burst, releasing more parasites that infect other red blood cells. This cycle of infection and rupture of red blood cells leads to the characteristic symptoms of malaria, including fever, chills, and anemia.

The intriguing connection between sickle cell anemia and malaria lies in how the altered red blood cells of individuals with the sickle cell trait affect the Plasmodium parasite. People who inherit one copy of the sickle cell gene (heterozygotes) have what is known as sickle cell trait. They typically do not experience the severe symptoms of sickle cell anemia, as they also produce normal hemoglobin. However, their red blood cells contain a mix of normal and abnormal hemoglobin.

When the Plasmodium parasite infects these red blood cells, the presence of hemoglobin S causes the infected cells to sickle more readily. There are several proposed mechanisms for why this provides protection:

  • Premature Destruction of Infected Cells: The sickled red blood cells are recognized and destroyed by the body's immune system more quickly than normal red blood cells. This means that the parasites, which are multiplying inside these cells, are eliminated from the bloodstream before they can complete their life cycle and reach high numbers. …

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