A single-tube, EuroClonality-inspired, TRG ...
Type de document :
Article dans une revue scientifique
PMID :
URL permanente :
Titre :
A single-tube, EuroClonality-inspired, TRG clonality multiplex PCR aids management of patients with enteropathic diseases, including from formaldehyde-fixed, paraffin-embedded tissues.
Auteur(s) :
Derrieux, Coralie [Auteur]
Institut Necker Enfants-Malades [INEM - UM 111 (UMR 8253 / U1151)]
Trinquand, Amelie [Auteur]
Institut Necker Enfants-Malades [INEM - UM 111 (UMR 8253 / U1151)]
Bruneau, Julie [Auteur]
Université Paris Descartes, Sorbonne Paris Cité
Verkarre, Virginie [Auteur]
Université Sorbonne Paris Cité [USPC]
Lhermitte, Ludovic [Auteur]
Institut Necker Enfants-Malades [INEM - UM 111 (UMR 8253 / U1151)]
Alcantara, Marion [Auteur]
Institut Necker Enfants-Malades [INEM - UM 111 (UMR 8253 / U1151)]
Villarese, Patrick [Auteur]
Institut Necker Enfants-Malades [INEM - UM 111 (UMR 8253 / U1151)]
Meresse, Bertrand [Auteur]
Lille Inflammation Research International Center - U 995 [LIRIC]
Sibon, David [Auteur]
Institut Necker Enfants-Malades [INEM - UM 111 (UMR 8253 / U1151)]
Hermine, Olivier [Auteur]
Imagine - Institut des maladies génétiques (IHU) [Imagine - U1163]
Brousse, Nicole [Auteur]
Université Paris Descartes - Faculté de Médecine [UPD5 Médecine]
Molina, Thierry [Auteur]
Université Sorbonne Paris Cité [USPC]
Cellier, Christophe [Auteur]
Université Paris Descartes - Paris 5 [UPD5]
Cerf-Bensussan, Nadine [Auteur]
Imagine - Institut des maladies génétiques (IHU) [Imagine - U1163]
Malamut, Georgia [Auteur]
Université Paris Descartes - Paris 5 [UPD5]
Macintyre, Elizabeth [Auteur]
Institut Necker Enfants-Malades [INEM - UM 111 (UMR 8253 / U1151)]
Institut Necker Enfants-Malades [INEM - UM 111 (UMR 8253 / U1151)]
Trinquand, Amelie [Auteur]
Institut Necker Enfants-Malades [INEM - UM 111 (UMR 8253 / U1151)]
Bruneau, Julie [Auteur]
Université Paris Descartes, Sorbonne Paris Cité
Verkarre, Virginie [Auteur]
Université Sorbonne Paris Cité [USPC]
Lhermitte, Ludovic [Auteur]
Institut Necker Enfants-Malades [INEM - UM 111 (UMR 8253 / U1151)]
Alcantara, Marion [Auteur]
Institut Necker Enfants-Malades [INEM - UM 111 (UMR 8253 / U1151)]
Villarese, Patrick [Auteur]
Institut Necker Enfants-Malades [INEM - UM 111 (UMR 8253 / U1151)]
Meresse, Bertrand [Auteur]
Lille Inflammation Research International Center - U 995 [LIRIC]
Sibon, David [Auteur]
Institut Necker Enfants-Malades [INEM - UM 111 (UMR 8253 / U1151)]
Hermine, Olivier [Auteur]
Imagine - Institut des maladies génétiques (IHU) [Imagine - U1163]
Brousse, Nicole [Auteur]
Université Paris Descartes - Faculté de Médecine [UPD5 Médecine]
Molina, Thierry [Auteur]
Université Sorbonne Paris Cité [USPC]
Cellier, Christophe [Auteur]
Université Paris Descartes - Paris 5 [UPD5]
Cerf-Bensussan, Nadine [Auteur]
Imagine - Institut des maladies génétiques (IHU) [Imagine - U1163]
Malamut, Georgia [Auteur]
Université Paris Descartes - Paris 5 [UPD5]
Macintyre, Elizabeth [Auteur]
Institut Necker Enfants-Malades [INEM - UM 111 (UMR 8253 / U1151)]
Titre de la revue :
The Journal of molecular diagnostics : JMD
Nom court de la revue :
J Mol Diagn
Numéro :
21
Pagination :
111-122
Date de publication :
2019-01
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
Celiac disease is a chronic inflammation of the small intestine with villous atrophy that can become refractory to a gluten-free diet. Two categories of refractory celiac disease can be distinguished by the phenotype ...
Lire la suite >Celiac disease is a chronic inflammation of the small intestine with villous atrophy that can become refractory to a gluten-free diet. Two categories of refractory celiac disease can be distinguished by the phenotype of intraepithelial lymphocytes and the status of TRG genes. Their distinction is important because 30% to 50% of type II but only 0% to 14% of type I evolve to an aggressive enteropathy-associated T-cell lymphoma and therefore require intensive treatment. Currently, differential diagnosis integrates immunohistochemistry, immunophenotyping, and TRG clonality analyses, but each has limitations. A single-tube multiplex TRG PCR (ECN) was prospectively compared to an in-house two-tube TRG PCR (N2T) in 73 samples, including 67 cryopreserved intestine tissues. Thirteen formalin-fixed, paraffin-embedded (FFPE) samples were also analyzed retrospectively. The ECN PCR had comparable efficiency to detect major clonal rearrangements in highly infiltrated tissues from T-cell lymphoproliferative disorders and type II refractory celiac disease and to detect the persistence of minor clones in type II refractory celiac disease follow-up samples. The ECN PCR abolished the risk of amplification of false-positive weak clonal rearrangements in cryopreserved specimens and allowed improved detection of clonal rearrangements in DNA from FFPE samples. The ECN PCR allows robust assessment of cryopreserved and FFPE digestive tissues at diagnosis and follow-up of enteropathies with villous atrophy, thus guiding therapeutic management.Lire moins >
Lire la suite >Celiac disease is a chronic inflammation of the small intestine with villous atrophy that can become refractory to a gluten-free diet. Two categories of refractory celiac disease can be distinguished by the phenotype of intraepithelial lymphocytes and the status of TRG genes. Their distinction is important because 30% to 50% of type II but only 0% to 14% of type I evolve to an aggressive enteropathy-associated T-cell lymphoma and therefore require intensive treatment. Currently, differential diagnosis integrates immunohistochemistry, immunophenotyping, and TRG clonality analyses, but each has limitations. A single-tube multiplex TRG PCR (ECN) was prospectively compared to an in-house two-tube TRG PCR (N2T) in 73 samples, including 67 cryopreserved intestine tissues. Thirteen formalin-fixed, paraffin-embedded (FFPE) samples were also analyzed retrospectively. The ECN PCR had comparable efficiency to detect major clonal rearrangements in highly infiltrated tissues from T-cell lymphoproliferative disorders and type II refractory celiac disease and to detect the persistence of minor clones in type II refractory celiac disease follow-up samples. The ECN PCR abolished the risk of amplification of false-positive weak clonal rearrangements in cryopreserved specimens and allowed improved detection of clonal rearrangements in DNA from FFPE samples. The ECN PCR allows robust assessment of cryopreserved and FFPE digestive tissues at diagnosis and follow-up of enteropathies with villous atrophy, thus guiding therapeutic management.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Inserm
Université de Lille
CHU Lille
Université de Lille
CHU Lille
Équipe(s) de recherche :
Inflammatory digestive disease : pathophysiology and therapeutic targets developement
Date de dépôt :
2019-03-01T14:07:57Z
2024-03-05T12:49:43Z
2024-03-05T12:49:43Z