Combined immunodeficiency with marginal zone lymphoma due to a novel homozygous mutation in IL-21R gene and successful treatment with hematopoietic stem cell transplantation-Reference-Cited by-同舟云学术

Combined immunodeficiency with marginal zone lymphoma due to a novel homozygous mutation in IL-21R gene and successful treatment with hematopoietic stem cell transplantation

Published:2021-05-08 Issue:8 Volume:38 Page:745-752
ISSN:0888-0018
Container-title:Pediatric Hematology and Oncology
language:en
Short-container-title:Pediatric Hematology and Oncology

Author:

Edeer Karaca Neslihan¹,Özek Gülcihan²,Ataseven Eda²,Tökmeci Nazan¹,Şenol Handan Duman¹,Kıran Ezgi³,Aykut Ayça⁴,Durmaz Asude⁴,Aksu Güzide¹,Aksoylar Serap²,Aydoğdu Sema³,Çetingül Nazan²,Kütükçüler Necil¹

Affiliation:

1. Faculty of Medicine, Department of Pediatric Immunology and Allergy, Ege University, İzmir, Turkey;

2. Faculty of Medicine, Department of Pediatric Hematology and Oncology, Ege University, İzmir, Turkey;

3. Faculty of Medicine, Department of Pediatric Gastroenterology Gastroenterology, Hepatology and Nutrition, Ege University, İzmir, Turkey;

4. Faculty of Medicine, Department of Medical Genetics, Ege University, İzmir, Turkey

Publisher

Informa UK Limited

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/08880018.2021.1924326

Reference16 articles.

1. The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies

2. Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndrome

3. IL-21 Induces Differentiation of Human Naive and Memory B Cells into Antibody-Secreting Plasma Cells

4. IL-21 Limits NK Cell Responses and Promotes Antigen-Specific T Cell Activation

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