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Daniela Montagna

Researcher at University of Pavia

Publications -  118
Citations -  7060

Daniela Montagna is an academic researcher from University of Pavia. The author has contributed to research in topics: Cytotoxic T cell & Leukemia. The author has an hindex of 33, co-authored 108 publications receiving 5589 citations. Previous affiliations of Daniela Montagna include Novartis.

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Journal ArticleDOI

Autoantibodies against type I IFNs in patients with life-threatening COVID-19.

Paul Bastard, +140 more
- 23 Oct 2020 - 
TL;DR: A means by which individuals at highest risk of life-threatening COVID-19 can be identified is identified, and the hypothesis that neutralizing auto-Abs against type I IFNs may underlie critical CO VID-19 is tested.
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Interaction of human mesenchymal stem cells with cells involved in alloantigen-specific immune response favors the differentiation of CD4+ T-cell subsets expressing a regulatory/suppressive phenotype

TL;DR: The results strongly suggest that MSC-mediated inhibition of alloantigen-induced DC1 differentiation and preferential activation of CD4+ CD25+ T-cell subsets with presumed regulatory activity represent important mechanisms contributing to the immunosuppressive activity of MSC.
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Anti-leukemia activity of alloreactive NK cells in KIR ligand-mismatched haploidentical HSCT for pediatric patients: evaluation of the functional role of activating KIR and redefinition of inhibitory KIR specificity

TL;DR: It is shown that, in most transplantation patients, variable proportions of donor-derived alloreactive natural killer cells displaying anti-leukemia activity were generated and maintained even late after transplantation, and this may have important clinical implications for the selection of optimal donors for haplo-HSCT.
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Infusion of autologous Epstein-Barr virus (EBV)–specific cytotoxic T cells for prevention of EBV-related lymphoproliferative disorder in solid organ transplant recipients with evidence of active virus replication

TL;DR: The data suggest that the infusion of autologous EBV-specific CTLs obtained from peripheral blood mononuclear cells recovered at the time of viral reactivation is able to augment virus-specific immune response and to reduce viral load in organ transplant recipients.