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A case of common variable immune deficiency with lung disease–not just bronchiectasis

Publication: LymphoSign Journal
30 August 2021

Abstract

Introduction: Common Variable Immune Deficiency (CVID) is the most prevalent form of severe antibody deficiency in children and adults. Most patients suffer recurrent, mainly sinopulmonary, infections. Despite adequate IVIG replacement therapy, chronic lung disease continues to be a main cause of morbidity and mortality. The term granulomatous-lymphocytic interstitial lung disease (GLILD) is frequently used to describe interstitial lung disease associated with immune dysregulation in primary antibody deficiency, such as CVID.
Aim: To describe the case of a 10-year-old male with CVID who developed GLILD and his response to treatment with Rituximab.
Discussion: Our patient is a young male with CVID and no genetic diagnosis, whose lung functions and general condition continued to deteriorate despite adequate intravenous immunoglobulin replacement therapy and mycophenolate mofetil treatment. After the diagnosis of GLILD, we initiated treatment with a 4-dose weekly course of Rituximab with prompt resolution of his interstitial disease. Although GLILD is a well described condition that accompanies CVID as a manifestation of immune dysregulation, it is still under recognized, especially in the pediatric population. Among experts, there is little uniformity when it comes to diagnostic and treatment approaches. Recent studies showed improved outcomes when using combination therapy with Rituximab, such as in our patient.
Statement of Novelty: We shed light on GLILD, an important condition that accompanies CVID, and demonstrate an excellent response to the steroid sparing agent Rituximab. This is a crucial aspect when considering therapeutic choices for the pediatric population.

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Information & Authors

Information

Published In

cover image LymphoSign Journal
LymphoSign Journal
Volume 8Number 3September 2021
Pages: 81 - 85

History

Received: 22 August 2021
Accepted: 30 August 2021
Accepted manuscript online: 30 August 2021

Authors

Affiliations

Sharon Polakow Farkash [email protected]
Allergy and Immunology Unit, Schneider Children’s Medical Center of Israel, Felsenstein Medical Research Center, Kipper Institute of Immunology, Petach Tikva, Israel
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
The Jeffrey Modell Foundation Israeli Network for Primary Immunodeficiency, 780 Third Avenue, New York, NY 10017, USA
Shai Ehrlich
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
The Department of Day Care Hospitalization, Schneider Children’s Medical Center, Tel Aviv University
Guy Steuer
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
Pulmonary Institute and Heart Institute, Schneider Children’s Medical Center of Israel, Petach Tikva, Israel
Joanne Yacobovich
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
Department of Pediatric Hematology-Oncology, Schneider Children’s Medical Center of Israel, Petach Tikva, Israel
Nir Diamant
Allergy and Immunology Unit, Schneider Children’s Medical Center of Israel, Felsenstein Medical Research Center, Kipper Institute of Immunology, Petach Tikva, Israel
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
The Jeffrey Modell Foundation Israeli Network for Primary Immunodeficiency, 780 Third Avenue, New York, NY 10017, USA
Nufar Marcus
Allergy and Immunology Unit, Schneider Children’s Medical Center of Israel, Felsenstein Medical Research Center, Kipper Institute of Immunology, Petach Tikva, Israel
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
The Jeffrey Modell Foundation Israeli Network for Primary Immunodeficiency, 780 Third Avenue, New York, NY 10017, USA

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