| Sign In to gain access to subscriptions and/or personal tools. |
Characterization of T-cell population in children with prolonged fetal exposure to dexamethasone for anti-Ro/SS-A antibodies associated congenital heart blockRheumatology and Clinical Immunology, Spedali Civili of Brescia, Brescia, Italy, airo{at}bresciareumatologia.it
Rheumatology and Clinical Immunology, Spedali Civili of Brescia, Brescia, Italy
Department of Rheumatology, Niguarda Hospital, Milan, Italy
Laboratory Diagnostics, Spedali Civili of Brescia, Brescia, Italy
Rheumatology and Clinical Immunology, Spedali Civili of Brescia, Brescia, Italy
Rheumatology and Clinical Immunology, Spedali Civili of Brescia, Brescia, Italy
Rheumatology and Clinical Immunology, Spedali Civili of Brescia, Brescia, Italy
Department of Pediatrics, Niguarda Hospital, Milan, Italy
Department of Neonatology, Spedali Civili of Brescia, Brescia, Italy
Laboratory Diagnostics, Spedali Civili of Brescia, Brescia, Italy
Rheumatology and Clinical Immunology, Spedali Civili of Brescia, Brescia, Italy
Laboratory Diagnostics, Spedali Civili of Brescia, Brescia, Italy
The objectives of the study were to characterize the production, function and survival of T lymphocytes of children with prolonged fetal exposure to dexamethasone for anti-Ro/SS-A antibodies associated congenital complete heart block. The analysis of thymic function, studied by measuring the level of T-cell receptor excision circles, was performed by real time PCR, the composition of T-cell subpopulation was evaluated by flow cytometry and the T-cell diversity was assayed by heteroduplex analysis. T-cell competence was gauged at two functional levels by determining the proliferation and the number of T-cell divisions and by measuring In conclusion, the analysis of the T-cell compartment in children with prolonged intrauterine exposure to high dose dexamethasone did not disclose any relevant abnormality, except a restriction of T-cell receptor diversity in some patients.
Key Words: congenital complete heart block dexamethasone T lymphocytes TRECs
Lupus, Vol. 15, No. 9,
553-561 (2006) This article has been cited by other articles:
|
|||||||||||||||||||||||||||
-interferon production after mitogenic stimulation. We observed that the thymic output, distribution of T-cell subsets, thymidine incorporation, number of T-cell divisions, and 
