TY - JOUR
T1 - Intrathymic adeno-associated virus gene transfer rapidly restores thymic function and long-term persistence of gene-corrected T cells
AU - Pouzolles, Marie
AU - Machado, Alice
AU - Guilbaud, Mickaël
AU - Irla, Magali
AU - Gailhac, Sarah
AU - Barennes, Pierre
AU - Cesana, Daniela
AU - Calabria, Andrea
AU - Benedicenti, Fabrizio
AU - Sergé, Arnauld
AU - Raman, Indu
AU - Li, Quan Zhen
AU - Montini, Eugenio
AU - Klatzmann, David
AU - Adjali, Oumeya
AU - Taylor, Naomi
AU - Zimmermann, Valérie S.
N1 - Funding Information:
M.P. was supported by a PhD fellowship from the LABEX EpiGenMed and the FRM. M.I. and O.A. are supported by INSERM, N.T. was supported by INSERM and the National Institutes of Health, and V.S.Z. is supported by CNRS. This work was funded by the AFM, grant R01AI059349 from the National Institute of Allergy and Infectious Diseases, and the ANR, ARC, FRM, INCA, and ERC-Advanced TRiPoD (#322856 to D.K.).
Publisher Copyright:
© 2019 American Academy of Allergy, Asthma & Immunology
PY - 2020/2
Y1 - 2020/2
N2 - Background: Patients with T-cell immunodeficiencies are generally treated with allogeneic hematopoietic stem cell transplantation, but alternatives are needed for patients without matched donors. An innovative intrathymic gene therapy approach that directly targets the thymus might improve outcomes. Objective: We sought to determine the efficacy of intrathymic adeno-associated virus (AAV) serotypes to transduce thymocyte subsets and correct the T-cell immunodeficiency in a zeta-associated protein of 70 kDa (ZAP-70)–deficient murine model. Methods: AAV serotypes were injected intrathymically into wild-type mice, and gene transfer efficiency was monitored. ZAP-70−/− mice were intrathymically injected with an AAV8 vector harboring the ZAP70 gene. Thymus structure, immunophenotyping, T-cell receptor clonotypes, T-cell function, immune responses to transgenes and autoantibodies, vector copy number, and integration were evaluated. Results: AAV8, AAV9, and AAV10 serotypes all transduced thymocyte subsets after in situ gene transfer, with transduction of up to 5% of cells. Intrathymic injection of an AAV8–ZAP-70 vector into ZAP-70−/− mice resulted in a rapid thymocyte differentiation associated with the development of a thymic medulla. Strikingly, medullary thymic epithelial cells expressing the autoimmune regulator were detected within 10 days of gene transfer, correlating with the presence of functional effector and regulatory T-cell subsets with diverse T-cell receptor clonotypes in the periphery. Although thymocyte reconstitution was transient, gene-corrected peripheral T cells harboring approximately 1 AAV genome per cell persisted for more than 40 weeks, and AAV vector integration was detected. Conclusions: Intrathymic AAV-transduced progenitors promote a rapid restoration of the thymic architecture, with a single wave of thymopoiesis generating long-term peripheral T-cell function.
AB - Background: Patients with T-cell immunodeficiencies are generally treated with allogeneic hematopoietic stem cell transplantation, but alternatives are needed for patients without matched donors. An innovative intrathymic gene therapy approach that directly targets the thymus might improve outcomes. Objective: We sought to determine the efficacy of intrathymic adeno-associated virus (AAV) serotypes to transduce thymocyte subsets and correct the T-cell immunodeficiency in a zeta-associated protein of 70 kDa (ZAP-70)–deficient murine model. Methods: AAV serotypes were injected intrathymically into wild-type mice, and gene transfer efficiency was monitored. ZAP-70−/− mice were intrathymically injected with an AAV8 vector harboring the ZAP70 gene. Thymus structure, immunophenotyping, T-cell receptor clonotypes, T-cell function, immune responses to transgenes and autoantibodies, vector copy number, and integration were evaluated. Results: AAV8, AAV9, and AAV10 serotypes all transduced thymocyte subsets after in situ gene transfer, with transduction of up to 5% of cells. Intrathymic injection of an AAV8–ZAP-70 vector into ZAP-70−/− mice resulted in a rapid thymocyte differentiation associated with the development of a thymic medulla. Strikingly, medullary thymic epithelial cells expressing the autoimmune regulator were detected within 10 days of gene transfer, correlating with the presence of functional effector and regulatory T-cell subsets with diverse T-cell receptor clonotypes in the periphery. Although thymocyte reconstitution was transient, gene-corrected peripheral T cells harboring approximately 1 AAV genome per cell persisted for more than 40 weeks, and AAV vector integration was detected. Conclusions: Intrathymic AAV-transduced progenitors promote a rapid restoration of the thymic architecture, with a single wave of thymopoiesis generating long-term peripheral T-cell function.
KW - Severe combined immunodeficiency
KW - T-cell reconstitution
KW - gene therapy
KW - humoral immunity
KW - intrathymic gene transfer
KW - medulla formation
KW - thymus
KW - zeta-associated protein of 70kDa
UR - http://www.scopus.com/inward/record.url?scp=85072798596&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85072798596&partnerID=8YFLogxK
U2 - 10.1016/j.jaci.2019.08.029
DO - 10.1016/j.jaci.2019.08.029
M3 - Article
C2 - 31513879
AN - SCOPUS:85072798596
SN - 0091-6749
VL - 145
SP - 679-697.e5
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 2
ER -