Cargando…

Outcome of BCG Vaccination in ADA-SCID Patients: A 12-Patient Series

Vaccination with Bacillus Calmette–Guérin (BCG) can be harmful to patients with combined primary immunodeficiencies. We report the outcome of BCG vaccination in a series of twelve patients affected by adenosine deaminase deficiency (ADA-SCID). BCG vaccination resulted in a very high incidence of com...

Descripción completa

Detalles Bibliográficos
Autores principales:	Canarutto, Daniele, Oltolini, Chiara, Barzaghi, Federica, Calbi, Valeria, Migliavacca, Maddalena, Tucci, Francesca, Gallo, Vera, Consiglieri, Giulia, Ferrua, Francesca, Recupero, Salvatore, Cervi, Maria Celia, Al-Mousa, Hamoud, Pituch-Noworolska, Anna, Tassan Din, Chiara, Scarpellini, Paolo, Silvani, Paolo, Fossati, Claudia, Casiraghi, Miriam, Cirillo, Daniela Maria, Castagna, Antonella, Bernardo, Maria Ester, Aiuti, Alessandro, Cicalese, Maria Pia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10376767/ https://www.ncbi.nlm.nih.gov/pubmed/37509449 http://dx.doi.org/10.3390/biomedicines11071809

Ejemplares similares

Hemophagocytic inflammatory syndrome in ADA-SCID: report of two cases and literature review
por: Fratini, Elena Sophia, et al.
Publicado: (2023)

Third cranial nerve palsy in an 88-year-old man after SARS-CoV-2 mRNA vaccination: change of injection site and type of vaccine resulted in an uneventful second dose with humoral immune response
por: Cicalese, Maria Pia, et al.
Publicado: (2022)

Peripheral blood stem and progenitor cell collection in pediatric candidates for ex vivo gene therapy: a 10-year series
por: Canarutto, Daniele, et al.
Publicado: (2021)

Emapalumab treatment in an ADA-SCID patient with refractory hemophagocytic lymphohistiocytosis- related graft failure and disseminated bacillus Calmette-Guérin infection
por: Tucci, Francesca, et al.
Publicado: (2020)

Bone marrow harvesting from paediatric patients undergoing haematopoietic stem cell gene therapy
por: Tucci, Francesca, et al.
Publicado: (2019)

A Case of Two Adult Brothers with Wiskott-Aldrich Syndrome, One Treated with Gene Therapy and One with HLA-Identical Hematopoietic Stem Cell Transplantation
por: Consiglieri, Giulia, et al.
Publicado: (2021)

Successful Treatment With Ledipasvir/Sofosbuvir in an Infant With Severe Combined Immunodeficiency Caused by Adenosine Deaminase Deficiency With HCV Allowed Gene Therapy with Strimvelis
por: Tucci, Francesca, et al.
Publicado: (2018)

Wiskott–Aldrich syndrome: Oral findings and microbiota in children and review of the literature
por: Lucchese, Alessandra, et al.
Publicado: (2022)

Mild SARS-CoV-2 Infection After Gene Therapy in a Child With Wiskott-Aldrich Syndrome: A Case Report
por: Cenciarelli, Sabina, et al.
Publicado: (2020)

Use of Defibrotide to help prevent post-transplant endothelial injury in a genetically predisposed infant with metachromatic leukodystrophy undergoing hematopoietic stem cell gene therapy
por: Calbi, Valeria, et al.
Publicado: (2018)

First Occurrence of Plasmablastic Lymphoma in Adenosine Deaminase-Deficient Severe Combined Immunodeficiency Disease Patient and Review of the Literature
por: Migliavacca, Maddalena, et al.
Publicado: (2018)

Alterations in the brain adenosine metabolism cause behavioral and neurological impairment in ADA-deficient mice and patients
por: Sauer, Aisha V., et al.
Publicado: (2017)

Lentiviral haemopoietic stem/progenitor cell gene therapy for treatment of Wiskott-Aldrich syndrome: interim results of a non-randomised, open-label, phase 1/2 clinical study
por: Ferrua, Francesca, et al.
Publicado: (2019)

Pioglitazone as a novel therapeutic approach in chronic granulomatous disease
por: Migliavacca, Maddalena, et al.
Publicado: (2016)

A Novel Assay in Whole Blood Demonstrates Restoration of Mitochondrial Activity in Phagocytes After Successful HSCT in Hyperinflamed X-Linked Chronic Granulomatous Disease
por: Migliavacca, Maddalena, et al.
Publicado: (2022)

Case Report: Consistent disease manifestations with a staggered time course in two identical twins affected by adenosine deaminase 2 deficiency
por: Barzaghi, Federica, et al.
Publicado: (2022)

Urogenital Abnormalities in Adenosine Deaminase Deficiency
por: Pajno, Roberta, et al.
Publicado: (2020)

ALPS-Like Phenotype Caused by ADA2 Deficiency Rescued by Allogeneic Hematopoietic Stem Cell Transplantation
por: Barzaghi, Federica, et al.
Publicado: (2019)

Lentiviral haematopoietic stem-cell gene therapy for early-onset metachromatic leukodystrophy: long-term results from a non-randomised, open-label, phase 1/2 trial and expanded access
por: Fumagalli, Francesca, et al.
Publicado: (2022)

Gene Therapy for Adenosine Deaminase Deficiency: A Comprehensive Evaluation of Short- and Medium-Term Safety
por: Cicalese, Maria Pia, et al.
Publicado: (2018)

P1392: INTERIM ANALYSIS OF FIRST IN HUMAN PHASE I-II CLINICAL TRIAL OF EX-VIVO GENE THERAPY FOR HURLER SYNDROME: AN UPDATE AT 3 YEAR FOLLOW-UP
por: Tucci, Francesca, et al.
Publicado: (2023)

A novel genomic inversion in Wiskott-Aldrich–associated autoinflammation
por: Brigida, Immacolata, et al.
Publicado: (2016)

2408. Is Shorter Antibiotic Treatment Feasible in Patients with Cardiac Implantable Electronic Devices (CIED) Infections? Impact of Treatment Duration on 6-Month Recurrence and Mortality
por: Ponta, Giacomo, et al.
Publicado: (2023)

Gene therapy for lysosomal storage disorders: recent advances for metachromatic leukodystrophy and mucopolysaccaridosis I
por: Penati, Rachele, et al.
Publicado: (2017)

Gene therapy in rare diseases: the benefits and challenges of developing a patient-centric registry for Strimvelis in ADA-SCID
por: Stirnadel-Farrant, Heide, et al.
Publicado: (2018)

NK cells in SARS-CoV-2 infection
por: Pituch-Noworolska, Anna Marta
Publicado: (2022)

Gene therapy for ADA‐SCID, the first marketing approval of an ex vivo gene therapy in Europe: paving the road for the next generation of advanced therapy medicinal products
por: Aiuti, Alessandro, et al.
Publicado: (2017)

Breakthrough Invasive Fungal Infections in Allogeneic Hematopoietic Stem Cell Transplantation
por: Liberatore, Carmine, et al.
Publicado: (2021)

Lentiviral gene therapy corrects platelet phenotype and function in patients with Wiskott-Aldrich syndrome
por: Sereni, Lucia, et al.
Publicado: (2019)

Coronavirus Disease 2019 in Recipient of Allogeneic Hematopoietic Stem Cell Transplantation: Life-threating Features Within the Early Post-engraftment Phase
por: Oltolini, Chiara, et al.
Publicado: (2020)

SARS-CoV-2 and thyroid diseases
por: Staruszkiewicz, Małgorzata, et al.
Publicado: (2023)

Long-term efficacy of etanercept in ADA2 deficiency
por: Caorsi, Roberta, et al.
Publicado: (2014)

1559. Hematopoietic Cell Transplantation with Post-transplant Cyclophosphamide: Impact of Donor Type on Pre-engraftment Blood-Stream Infections
por: Oltolini, Chiara, et al.
Publicado: (2018)

Occurrence of autoantibodies for gastrointestinal autoimmune diseases in children with common variable immune deficiency and selected IgA deficiency
por: Pituch-Noworolska, Anna, et al.
Publicado: (2013)

Frailty as a predictor of mortality in COVID-19 patients receiving CPAP for respiratory insufficiency
por: Damanti, Sarah, et al.
Publicado: (2022)

Monogenic polyarteritis: the lesson of ADA2 deficiency
por: Caorsi, Roberta, et al.
Publicado: (2016)

S250: UNVEILING THE BIOLOGICAL ROLE OF PERIPHERAL BLOOD HUMAN CIRCULATING HEMATOPOIETIC STEM AND PROGENITOR CELLS
por: Quaranta, Pamela, et al.
Publicado: (2023)

Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies
por: Cifaldi, Cristina, et al.
Publicado: (2019)

Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies
por: Cifaldi, Cristina, et al.
Publicado: (2019)

Ada Lovelace
por: Jeapes, Ben, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_2onl9q5i04utdgfq4atcg42dkr