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Acute Chest Syndrome Is Strongly Associated Parvo Virus B19 Seroconversion in Patients with Hemoglobin SC Disease
- Source :
- Blood. 104:1664-1664
- Publication Year :
- 2004
- Publisher :
- American Society of Hematology, 2004.
-
Abstract
- Parvovirus B19 replicates principally in human erythrocyte precursors resulting in temporary cessation of erythropoiesis. In patients with sickle hemoglobinopathies, parvovirus B19 infection has been associated with acute chest syndrome and may lead to transient aplastic crisis. Evidence of prior infection with parvovirus B19 is found in 50 to 60% of adults. Infection appears to be followed by lifelong immunity. The objectives of the Study of Seroprevalence and Incidence of Parvovirus B19Infection in Children with Sickle Hemoglobinopathies are to determine the prevalence of parvovirus B19 antibodies in children less than 16 years old; determine the rate of parvovirus B19 seroconversion; and determine whether parvovirus B19 seroconversion is associated with the occurrence of aplastic crisis or acute chest syndrome. Between April 2000 and June 2002 a total of 1039 children from eight Comprehensive Sickle Cell Centers (CSCC) were enrolled in the study and 898 had at least one follow up visit. Participants ranged in age from These data show a clear causal relation between parvovirus B19 seroconversions and acute chest syndrome in subjects with hemoglobin SC disease and confirm the previously known association aplastic crisis.
- Subjects :
- Pediatrics
medicine.medical_specialty
biology
Hemoglobin SC Disease
Parvovirus
business.industry
viruses
Incidence (epidemiology)
Immunology
virus diseases
Cell Biology
Hematology
biology.organism_classification
medicine.disease
Biochemistry
Acute chest syndrome
Sickle cell anemia
Virus
Medicine
Seroprevalence
Seroconversion
business
Subjects
Details
- ISSN :
- 15280020 and 00064971
- Volume :
- 104
- Database :
- OpenAIRE
- Journal :
- Blood
- Accession number :
- edsair.doi...........046f43c3cd60720632501af99c4e7eb6
- Full Text :
- https://doi.org/10.1182/blood.v104.11.1664.1664