We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.
To send content items to your account,
please confirm that you agree to abide by our usage policies.
If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account.
Find out more about sending content to .
To send content items to your Kindle, first ensure no-reply@cambridge.org
is added to your Approved Personal Document E-mail List under your Personal Document Settings
on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part
of your Kindle email address below.
Find out more about sending to your Kindle.
Note you can select to send to either the @free.kindle.com or @kindle.com variations.
‘@free.kindle.com’ emails are free but can only be sent to your device when it is connected to wi-fi.
‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
By
A. Dessein, Immunology and Genetics of Parasitic Diseases, INSERM, U. 399, Marseille, France,
B. Bucheton, Immunology and Genetics of Parasitic Diseases, INSERM, U. 399, Marseille, France,
L. Argiro, Immunology and Genetics of Parasitic Diseases, INSERM, U. 399, Marseille, France,
N. M. A. Elwali, Institute of Nuclear Medicine and Molecular Biology, University of Gezira, Wad Medani, Sudan,
V. Rodrigues, Laboratory of Immunology, University of Medicine, Triangulo Miniero, Uberaba, Brazil,
C. Chevillard, Immunology and Genetics of Parasitic Diseases, INSERM, U. 399, Marseille, France,
S. Marquet, Immunology and Genetics of Parasitic Diseases, INSERM, U. 399, Marseille, France,
H. Dessein, Immunology and Genetics of Parasitic Diseases, INSERM, U. 399, Marseille, France,
S. H. El-Safi, Institute for Tropical Medicine, PO Box 1304, Khartoum, Sudan,
L. Abel, Laboratory of Human Genetics of Infectious Diseases, INSERM, U. 550, Paris, France
SUSCEPTIBILITY TO SEVERE DISEASE DURING AN OUTBREAK OF VISCERAL LEISHMANIASIS IN A SUDANESE VILLAGE
Visceral leishmaniasis (VL) is caused by protozoan parasites of the Leishmania genus that are transmitted to humans by infected sandflies (Figure 10.1a). Parasites rapidly invade host phagocytes and multiply inside phagolysosomes. Clinical disease is primarily due to the uncontrolled multiplication of the parasite in many organs including the spleen and the liver; clinical symptoms include recurrent fever, considerable splenomegaly, hepatomegaly, and adenopathy (1). Death is certain if the patient is left untreated. Violent outbreaks of VL have occurred in regions of eastern Africa (2) (Kenya, Sudan) and in India (Bihar). VL is endemic in South America and in the Mediterranean basin. VL is caused by three Leishmania species: Leishmania donovani, L. chagasi/infantum, and L. archibaldi (L. donovani being the most pathogenic) (3). To identify the principal risk factors in VL, we carried out a five-year longitudinal study on 1,600 subjects from a village located on the Sudanese–Ethiopian border. The study was initiated in 1995 when the number of VL cases had just begun to rise in the village (4). Within five years, 28% of the population had been affected by VL. Most of these VL patients were treated and cured. Unfortunately, a small percentage either failed to respond to treatment or were not treated because of the difficulties involved in reaching them during the rainy season.
Recommend this
Email your librarian or administrator to recommend adding this to your organisation's collection.