| Literature DB >> 30254128 |
Immacolata Brigida1, Matteo Zoccolillo1,2, Maria Pia Cicalese1,3,4, Laurène Pfajfer5,6,7,8,9, Federica Barzaghi3,2, Serena Scala1, Carmen Oleaga-Quintas10,11, Jesus A Álvarez-Álvarez12,13, Lucia Sereni1, Stefania Giannelli1, Claudia Sartirana1, Francesca Dionisio1, Luca Pavesi14, Marta Benavides-Nieto15,16, Luca Basso-Ricci1, Paola Capasso1, Benedetta Mazzi17, Jeremie Rosain10,11,18, Nufar Marcus19, Yu Nee Lee20, Raz Somech20, Massimo Degano21, Giuseppe Raiola22, Roberta Caorsi23, Paolo Picco23, Marcela Moncada Velez12, Joelle Khourieh10,11, Andrés Augusto Arias12,24, Aziz Bousfiha25, Thomas Issekutz26, Andrew Issekutz26, Bertrand Boisson10,11,27, Kerry Dobbs28, Anna Villa1,29, Angelo Lombardo1,4, Benedicte Neven15, Despina Moshous15,16, Jean-Laurent Casanova10,11,15,27,30, José Luis Franco12, Luigi D Notarangelo28, Cristina Scielzo14, Stefano Volpi23,31, Loïc Dupré5,6,7,8,9, Jacinta Bustamante10,11,18,27, Marco Gattorno23,32, Alessandro Aiuti1,3,4.
Abstract
ARPC1B is a key factor for the assembly and maintenance of the ARP2/3 complex that is involved in actin branching from an existing filament. Germline biallelic mutations in ARPC1B have been recently described in 6 patients with clinical features of combined immunodeficiency (CID), whose neutrophils and platelets but not T lymphocytes were studied. We hypothesized that ARPC1B deficiency may also lead to cytoskeleton and functional defects in T cells. We have identified biallelic mutations in ARPC1B in 6 unrelated patients with early onset disease characterized by severe infections, autoimmune manifestations, and thrombocytopenia. Immunological features included T-cell lymphopenia, low numbers of naïve T cells, and hyper-immunoglobulin E. Alteration in ARPC1B protein structure led to absent/low expression by flow cytometry and confocal microscopy. This molecular defect was associated with the inability of patient-derived T cells to extend an actin-rich lamellipodia upon T-cell receptor (TCR) stimulation and to assemble an immunological synapse. ARPC1B-deficient T cells additionally displayed impaired TCR-mediated proliferation and SDF1-α-directed migration. Gene transfer of ARPC1B in patients' T cells using a lentiviral vector restored both ARPC1B expression and T-cell proliferation in vitro. In 2 of the patients, in vivo somatic reversion restored ARPC1B expression in a fraction of lymphocytes and was associated with a skewed TCR repertoire. In 1 revertant patient, memory CD8+ T cells expressing normal levels of ARPC1B displayed improved T-cell migration. Inherited ARPC1B deficiency therefore alters T-cell cytoskeletal dynamics and functions, contributing to the clinical features of CID.Entities:
Mesh:
Substances:
Year: 2018 PMID: 30254128 PMCID: PMC6265646 DOI: 10.1182/blood-2018-07-863431
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113