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Stefania Giannelli

Explore the profile of Stefania Giannelli including associated specialties, affiliations and a list of published articles. Areas
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Articles 24
Citations 1280
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Recent Articles
1.
Calabria A, Spinozzi G, Cesana D, Buscaroli E, Benedicenti F, Pais G, et al.
Nature . 2024 Oct; 636(8041):162-171. PMID: 39442556
Haematopoietic stem cell (HSC) gene therapy (GT) may provide lifelong reconstitution of the haematopoietic system with gene-corrected cells. However, the effects of underlying genetic diseases, replication stress and ageing on...
2.
Barzaghi F, Visconti C, Pipitone G, Bondesan S, Molli G, Giannelli S, et al.
J Infect Dis . 2024 Jul; 231(1):e206-e212. PMID: 38976510
Patients with severe West Nile virus and SARS-CoV-2 infections deserve accurate diagnosis of underlying diseases, determining possible anti-interferon autoantibody production, since they must receive antiviral and immunological therapies to enhance...
3.
Cesana D, Cicalese M, Calabria A, Merli P, Caruso R, Volpin M, et al.
Nat Commun . 2024 Apr; 15(1):3662. PMID: 38688902
Hematopoietic stem cell gene therapy (GT) using a γ-retroviral vector (γ-RV) is an effective treatment for Severe Combined Immunodeficiency due to Adenosine Deaminase deficiency. Here, we describe a case of...
4.
Quaranta P, Basso-Ricci L, Hernandez R, Pacini G, Naldini M, Barcella M, et al.
Blood . 2024 Mar; 143(19):1937-1952. PMID: 38446574
In physiological conditions, few circulating hematopoietic stem/progenitor cells (cHSPCs) are present in the peripheral blood, but their contribution to human hematopoiesis remain unsolved. By integrating advanced immunophenotyping, single-cell transcriptional and...
5.
Migliavacca M, Barzaghi F, Fossati C, Rancoita P, Gabaldo M, Dionisio F, et al.
Nat Med . 2024 Feb; 30(2):488-497. PMID: 38355973
Adenosine deaminase (ADA) deficiency leads to severe combined immunodeficiency (SCID). Previous clinical trials showed that autologous CD34 cell gene therapy (GT) following busulfan reduced-intensity conditioning is a promising therapeutic approach...
6.
Fratini E, Migliavacca M, Barzaghi F, Fossati C, Giannelli S, Monti I, et al.
Front Immunol . 2023 Jul; 14:1187959. PMID: 37435083
Hemophagocytic inflammatory syndrome (HIS) is a rare form of secondary hemophagocytic lymphohistiocytosis caused by an impaired equilibrium between natural killer and cytotoxic T-cell activity, evolving in hypercytokinemia and multiorgan failure....
7.
Scala S, Ferrua F, Basso-Ricci L, Dionisio F, Omrani M, Quaranta P, et al.
Nat Commun . 2023 May; 14(1):3068. PMID: 37244942
Mobilized peripheral blood is increasingly used instead of bone marrow as a source of autologous hematopoietic stem/progenitor cells for ex vivo gene therapy. Here, we present an unplanned exploratory analysis...
8.
Migliavacca M, Basso Ricci L, Farinelli G, Calbi V, Tucci F, Barzaghi F, et al.
J Clin Immunol . 2022 Aug; 42(8):1742-1747. PMID: 35945378
X-linked chronic granulomatous disease is a rare disease caused by mutations in the CYBB gene. While more extensive knowledge is available on genetics, pathogenesis, and possible therapeutic options, mitochondrial activity...
9.
Cenciarelli S, Calbi V, Barzaghi F, Bernardo M, Oltolini C, Migliavacca M, et al.
Front Immunol . 2020 Dec; 11:603428. PMID: 33329599
In this work we present the case of SARS-CoV-2 infection in a 1.5-year-old boy affected by severe Wiskott-Aldrich Syndrome with previous history of autoinflammatory disease, occurring 5 months after treatment...
10.
Ferrua F, Cicalese M, Galimberti S, Giannelli S, Dionisio F, Barzaghi F, et al.
Lancet Haematol . 2019 Apr; 6(5):e239-e253. PMID: 30981783
Background: Wiskott-Aldrich syndrome is a rare, life-threatening, X-linked primary immunodeficiency characterised by microthrombocytopenia, infections, eczema, autoimmunity, and malignant disease. Lentiviral vector-mediated haemopoietic stem/progenitor cell (HSPC) gene therapy is a potentially...