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                <identifier>oai:data.mendeley.com/mjbgkg63m2.1</identifier>
                <datestamp>2022-02-07T14:17:06Z</datestamp>
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    <dc:creator>Castiello, Maria Carmina</dc:creator>
    <dc:title>Efficacy and safety of anti-CD45-saporin as conditioning agent for RAG deficiency</dc:title>
    <dc:publisher>San Raffaele Open Research Data Repository</dc:publisher>
    <dc:description>TITLE: Efficacy and safety of anti-CD45–saporin as conditioning agent for RAG deficiency 

Maria Carmina Castiello, Marita Bosticardo, Nicolò Sacchetti, Enrica Calzoni, Elena Fontana, Yasuhiro Yamazaki, Elena Draghici, Cristina Corsino , Ileana Bortolomai, Lucia Sereni, Hsin-Hui Yu, Paolo Uva, Rahul Palchaudhuri, David T. Scadden, Anna Villa, Luigi D. Notarangelo.

PMID: 32387109 


Background: Mutations in the recombinase-activating genes cause severe immunodeficiency, with a spectrum of phenotypes ranging from severe combined immunodeficiency to immune dysregulation. Hematopoietic stem cell transplantation is the only curative option, but a high risk of graft failure and poor immune reconstitution have been observed in the absence of myeloablation.
Objectives: Our aim was to improve multilineage engraftment; we tested nongenotoxic conditioning with anti-CD45 mAbs conjugated with saporin CD45 (CD45-SAP).
Methods: Rag1-KO and Rag1-F971L mice, which represent models of severe combined immune deficiency and combined immune deficiency with immune dysregulation, respectively, were conditioned with CD45-SAP, CD45-SAP plus 2 Gy of total body irradiation (TBI), 2 Gy of TBI, 8 Gy of TBI, or no conditioning and treated by using transplantation with lineage-negative bone marrow cells from wild-type mice. Flow cytometry and immunohistochemistry were used to assess engraftment and immune reconstitution. Antibody responses to 2,4,6-trinitrophenyl-conjugated keyhole limpet hemocyanin were measured by ELISA, and presence of autoantibody was detected by microarray.
Results: Conditioning with CD45-SAP enabled high levels of multilineage engraftment in both Rag1 mutant models, allowed overcoming of B- and T-cell differentiation blocks and thymic epithelial cell defects, and induced robust cellular and humoral immunity in the periphery.
Conclusions: Conditioning with CD45-SAP allows multilineage engraftment and robust immune reconstitution in mice with either null or hypomorphic Rag mutations while preserving thymic epithelial cell homeostasis.

</dc:description>
    <dc:subject>Immunology</dc:subject>
    <dc:subject>Transplantation</dc:subject>
    <dc:subject>Immunodeficiency</dc:subject>
    <dc:subject>Viral Infection of Hematopoietic Progenitor Cells</dc:subject>
    <dc:contributor>Bosticardo, Marita</dc:contributor>
    <dc:contributor>Villa, Anna</dc:contributor>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/mjbgkg63m2.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/mjbgkg63m2.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
    <dc:rights>http://creativecommons.org/licenses/by/4.0</dc:rights>
    <dc:relation>https://ordr.hsr.it/datasets/mjbgkg63m2</dc:relation>
    <dc:date>2022-02-07T14:17:06Z</dc:date>
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