The Intracellular Intensity of CD3 on Aberrant Intraepithelial Lymphocytes Is a Prognostic Factor of the Progression to Overt Lymphoma in Refractory Celiac Disease Type II (Pre-Enteropathy-Associated T Cell Lymphoma).


Journal

Digestive diseases (Basel, Switzerland)
ISSN: 1421-9875
Titre abrégé: Dig Dis
Pays: Switzerland
ID NLM: 8701186

Informations de publication

Date de publication:
2020
Historique:
received: 04 03 2019
accepted: 31 01 2020
pubmed: 6 2 2020
medline: 26 11 2020
entrez: 5 2 2020
Statut: ppublish

Résumé

Refractory celiac disease type II (RCD-II) is a very rare yet severe complication of celiac disease (CD) with a 50% rate of progression to Enteropathy-associated T-cell lymphoma (EATL). Timely diagnosis and treatment of RCD-II is of the essence and requires the identification of a population of frequently clonal, phenotypically aberrant intraepithelial lymphocytes (IELs). Flow Cytometry of intestinal IELs is the recommended method to identify the aberrant surface CD3-negative (sCD3-) intracytoplasmic CD3-positive (icCD3ε+) IELs, and a proportion of >20% is diagnostic of RCD-II. There is substantial heterogeneity in the clinical course of RCD-II, and insufficient information on prognostic factors. To establish flow cytometric predictors of the clinical evolution of RCD-II, to help guide treatment approaches. Retrospective single-center study of clinical and immunological features of 6 RCD-II patients and a control group, both identified from a 2,000-patient cohort over 16 years. IEL subset frequencies and the intensity of staining for surface (s) and intracytoplasmic (ic) CD3ε+ on IEL subsets were quantified and correlated with the clinical outcome. Unexpectedly, the frequency of aberrant sCD3- icCD3ε+ cells at diagnosis did not correlate with histological or clinical affection. However, a higher intensity of icCD3ε+ staining in the aberrant IELs relative to expression on normal IELs correlated with monoclonality and with worse clinical outcomes. The ratio of icCD3ε+ on aberrant IELs vs. normal IELs appears to be a useful indicator of prognosis at the time of diagnosis, and may represent a novel tool in the follow-up of RCD-II patients after therapy.

Sections du résumé

BACKGROUND BACKGROUND
Refractory celiac disease type II (RCD-II) is a very rare yet severe complication of celiac disease (CD) with a 50% rate of progression to Enteropathy-associated T-cell lymphoma (EATL). Timely diagnosis and treatment of RCD-II is of the essence and requires the identification of a population of frequently clonal, phenotypically aberrant intraepithelial lymphocytes (IELs). Flow Cytometry of intestinal IELs is the recommended method to identify the aberrant surface CD3-negative (sCD3-) intracytoplasmic CD3-positive (icCD3ε+) IELs, and a proportion of >20% is diagnostic of RCD-II. There is substantial heterogeneity in the clinical course of RCD-II, and insufficient information on prognostic factors.
AIM OBJECTIVE
To establish flow cytometric predictors of the clinical evolution of RCD-II, to help guide treatment approaches.
PATIENTS AND METHODS METHODS
Retrospective single-center study of clinical and immunological features of 6 RCD-II patients and a control group, both identified from a 2,000-patient cohort over 16 years. IEL subset frequencies and the intensity of staining for surface (s) and intracytoplasmic (ic) CD3ε+ on IEL subsets were quantified and correlated with the clinical outcome.
RESULTS RESULTS
Unexpectedly, the frequency of aberrant sCD3- icCD3ε+ cells at diagnosis did not correlate with histological or clinical affection. However, a higher intensity of icCD3ε+ staining in the aberrant IELs relative to expression on normal IELs correlated with monoclonality and with worse clinical outcomes.
CONCLUSION CONCLUSIONS
The ratio of icCD3ε+ on aberrant IELs vs. normal IELs appears to be a useful indicator of prognosis at the time of diagnosis, and may represent a novel tool in the follow-up of RCD-II patients after therapy.

Identifiants

pubmed: 32015237
pii: 000506305
doi: 10.1159/000506305
doi:

Substances chimiques

Biomarkers 0
CD3 Complex 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

490-499

Informations de copyright

© 2020 S. Karger AG, Basel.

Auteurs

Carlota García-Hoz (C)

Department of Immunology, Hospital Universitario Ramón y Cajal, Madrid, Spain.

Laura Crespo (L)

Department of Gastroenterology, Hospital Universitario Ramón y Cajal, Madrid, Spain.

Natalia Lopez (N)

Department of Gastroenterology, Hospital Clínico de san Carlos, Madrid, Spain.

Ana De Andrés (A)

Department of Immunology, Hospital Universitario Ramón y Cajal, Madrid, Spain.

Raquel Ríos León (R)

Department of Gastroenterology, Hospital Universitario Ramón y Cajal, Madrid, Spain.

Almudena Santón (A)

Department of Pathological Anatomy, Hospital Universitario Ramón y Cajal, Madrid, Spain.

Maria Garriga (M)

Department of Endocrinology and Nutrition, Hospital Universitario Ramón y Cajal, Madrid, Spain.

Eric Butz (E)

Provention Bio, Oldwick, New Jersey, USA.

Francisco León (F)

Provention Bio, Oldwick, New Jersey, USA.

Garbiñe Roy Ariño (G)

Department of Immunology, Hospital Universitario Ramón y Cajal, Madrid, Spain, groy.hrc@salud.madrid.org.

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Classifications MeSH