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Chronic granulomatous disease: Clinical, molecular, and therapeutic aspects
Author(s) -
Chiriaco Maria,
Salfa Irene,
Di Matteo Gigliola,
Rossi Paolo,
Finocchi Andrea
Publication year - 2016
Publication title -
pediatric allergy and immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.269
H-Index - 89
eISSN - 1399-3038
pISSN - 0905-6157
DOI - 10.1111/pai.12527
Subject(s) - chronic granulomatous disease , medicine , primary immunodeficiency , immunology , genetic enhancement , hematopoietic stem cell transplantation , disease , severe combined immunodeficiency , gene , immune system , biology , genetics
Chronic granulomatous disease ( CGD ) is a rare primary immunodeficiency caused by defects in the genes encoding any of the NADPH oxidase components responsible for the respiratory burst of phagocytic leukocytes. CGD is a genetically heterogeneous disease with an X‐linked recessive ( XR ‐ CGD ) form caused by mutations in the CYBB gene encoding the gp91 phox protein, and an autosomal recessive ( AR ‐ CGD ) form caused by mutations in the CYBA , NCF 1 , NCF 2 , or NCF 4 genes encoding p22 phox , p47 phox , p67 phox , and p40 phox , respectively. Patients suffering from this disease are susceptible to severe life‐threatening bacterial and fungal infections and excessive inflammation characterized by granuloma formation in any organ, for instance, the gastrointestinal and genitourinary tract. An early diagnosis of and the prompt treatment for these conditions are crucial for an optimal outcome of affected patients. To prevent infections, CGD patients should receive lifelong antibiotics and antifungal prophylaxis. These two measures, as well as newer more effective antimicrobials, have significantly modified the natural history of CGD , resulting in a remarkable change in overall survival, which is now around 90%, reaching well into adulthood. At present, hematopoietic stem cell transplantation ( HSCT ) is the only definitive treatment that can cure CGD and reverse organ dysfunction. Timing, donor selection, and conditioning regimens remain the key points of this therapy. In recent years, gene therapy ( GT ) for XR ‐ CGD has been proposed as an alternative to HSCT for CGD patients without a matched donor. After the failure of the first trials performed with retroviral vectors, some groups have proposed the use of regulated SIN ‐lentiviral vectors targeting gp91 phox expression in myeloid cells to increase the safety and efficacy of the GT protocols.