دورية أكاديمية

A model for preservation of thymocyte-depleted thymus

التفاصيل البيبلوغرافية
العنوان: A model for preservation of thymocyte-depleted thymus
المؤلفون: A.S. Dias, N.R. Damaceno-Rodrigues, T.M. Gimenez, P.M. Oliveira, M.C. Zerbini, M. Carneiro-Sampaio, V. Odone Filho, M.B. Jatene, D.M. Vasconcelos, V. Rocha, E.M. Novak
المصدر: Brazilian Journal of Medical and Biological Research, Vol 56 (2023)
بيانات النشر: Associação Brasileira de Divulgação Científica, 2023.
سنة النشر: 2023
المجموعة: LCC:Medicine (General)
LCC:Biology (General)
مصطلحات موضوعية: Thymus tissue, Depletion, Cryopreservation, DiGeorge syndrome, Medicine (General), R5-920, Biology (General), QH301-705.5
الوصف: DiGeorge syndrome is a disorder caused by a microdeletion on the long arm of chromosome 22. Approximately 1% of patients diagnosed with DiGeorge syndrome may have an absence of a functional thymus, which characterizes the complete form of the syndrome. These patients require urgent treatment to reconstitute T cell immunity. Thymus transplantation is a promising investigational procedure for reconstitution of thymic function in infants with congenital athymia. Here, we demonstrate a possible optimization of the preparation of thymus slices for transplantation through prior depletion of thymocytes and leukocyte cell lineages followed by cryopreservation with cryoprotective media (5% dextran FP 40, 5% Me2SO, and 5% FBS) while preserving tissue architecture. Thymus fragments were stored in liquid nitrogen at -196°C for 30 days or one year. The tissue architecture of the fragments was preserved, including the distinction between medullary thymic epithelial cells (TECs), cortical TECs, and Hassall bodies. Moreover, depleted thymus fragments cryopreserved for one year were recolonized by intrathymic injections of 3×106 thymocytes per mL, demonstrating the capability of these fragments to support T cell development. Thus, this technique opens up the possibility of freezing and storing large volumes of thymus tissue for immediate transplantation into patients with DiGeorge syndrome or atypical (Omenn-like) phenotype.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1414-431X
1414-431x
Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2023000100654&lng=en&tlng=en; http://www.scielo.br/pdf/bjmbr/v56/1414-431X-bjmbr-56-e12647.pdf; https://doaj.org/toc/1414-431X
DOI: 10.1590/1414-431x2023e12647
URL الوصول: https://doaj.org/article/14ceb14f44e54c68a0776c8c8802bc0c
رقم الأكسشن: edsdoj.14ceb14f44e54c68a0776c8c8802bc0c
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:1414431X
1414431x
DOI:10.1590/1414-431x2023e12647