Persistence of chronic inflammation after regular blood transfusion therapy in sickle cell anemia

Author:

Dembélé Abdoul Karim123,Hermand Patricia13ORCID,Missud Florence4,Lesprit Emmanuelle5,Holvoet Laurent4,Brousse Valentine134,Ithier Ghislaine4,Odievre Marie-Helene136,Benkerrou Malika47,Le Van Kim Caroline13ORCID,Koehl Berengere134

Affiliation:

1. 1UMR_S1134, BIGR, Inserm, Université de Paris, Paris, France

2. 2Centre de Recherche et de Lutte Contre la Drépanocytose, Bamako, Mali

3. 3Laboratoire d’Excellence du Globule Rouge, Imagine Institute, Paris, France

4. 4Sickle Cell Disease Center, Hematology Unit, Robert Debré Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France

5. 5Etablissement Français du Sang, Paris, France

6. 6Sickle Cell Disease Center, General Pediatric Unit, Trousseau Hospital, AP-HP, Paris, France

7. 7UMR_S1123, ECEVE, Inserm, Université de Paris, Paris, France

Publisher

American Society of Hematology

Subject

Hematology

Reference20 articles.

1. Mortality in sickle cell disease. Life expectancy and risk factors for early death;Platt;N Engl J Med,1994

2. Silent cerebral infarcts in sickle cell anemia: a risk factor analysis;Kinney;Pediatrics,1999

3. Cerebrovascular accidents in sickle cell disease: rates and risk factors;Ohene-Frempong;Blood,1998

4. Inflammatory potential of neutrophils detected in sickle cell disease;Lum;Am J Hematol,2004

5. Relationship between the clinical manifestations of sickle cell disease and the expression of adhesion molecules on white blood cells;Okpala;Eur J Haematol,2002

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