Safety and Cross-Variant Immunogenicity of a Three-dose COVID-19 mRNA Vaccine Regimen in Kidney Transplant Recipients

Autor: Filippo Massa, PhD, Marion Cremoni, MD, Alexandre Gérard, MD, Hanen Grabsi, Lory Rogier, Mathilde Blois, MD, Chloé Couzin, MD, Nadia Ben Hassen, Matthieu Rouleau, PhD, Susana Barbosa, PhD, Emanuela Martinuzzi, PhD, Julien Fayada, Ghislaine Bernard, MD-PhD, Guillaume Favre, MD-PhD, Paul Hofman, MD-PhD, Vincent L.M. Esnault, MD-PhD, Cecil Czerkinsky, MD-PhD, Barbara Seitz-Polski, MD-PhD, Nicolas Glaichenhaus, PhD, Antoine Sicard, MD-PhD

Publikováno v: EBioMedicine, Vol 73, Iss , Pp 103679- (2021)

Background: The immunogenicity of a two-dose mRNA COVID-19 vaccine regimen is low in kidney transplant (KT) recipients. Here, we provide a thorough assessment of the immunogenicity of a three-dose COVID-19 vaccine regimen in this population. Methods:

Externí odkaz: https://doaj.org/article/6aec33f0dd6e4ddba8069d07e0e047f1

Coronary Artery Formation Is Driven by Localized Expression of R-spondin3

Autor: Fabio Da Silva, Ana Sofia Rocha, Fariba Jian Motamedi, Filippo Massa, Cem Basboga, Harris Morrison, Kay Dietrich Wagner, Andreas Schedl

Publikováno v: Cell Reports, Vol 20, Iss 8, Pp 1745-1754 (2017)

Coronary arteries are essential to support the heart with oxygen, and coronary heart disease is one of the leading causes of death worldwide. The coronary arteries form at highly stereotyped locations and are derived from the primitive vascular plexu

Externí odkaz: https://doaj.org/article/b5d3959c5e6d460b9214ee8e84f439d9

Arrest of WNT/β-catenin signaling enables the transition from pluripotent to differentiated germ cells in mouse ovaries

Autor: Morgane Le Rolle, Anne-Amandine Chassot, Pam Siggers, Filippo Massa, Marie-Christine Chaboissier, Bon-Kyoung Koo, Andreas Schedl, Hans Clevers, Agnès Loubat, Laurent Turchi, Andy Greenfield

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2021, 118 (30), pp.e2023376118. ⟨10.1073/pnas.2023376118⟩
Proceedings of the National Academy of Sciences of the United States of America, 2021, 118 (30), pp.e2023376118. ⟨10.1073/pnas.2023376118⟩
Proceedings of the National Academy of Sciences of the United States of America, 118(30). National Academy of Sciences

Significance In the mammalian ovary, primordial germ cells maintain a genomic program associated with pluripotency until they stop proliferating, move toward oogenesis, and enter meiosis. The molecular mechanisms that enable primordial germ cells to

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32b8b5f82de617033f1b5409e3c126ab
https://hal.archives-ouvertes.fr/hal-03357217/document

Developmental Renal Glomerular Defects at the Origin of Glomerulocystic Disease

Autor: Arianna, Fiorentino, Armelle, Christophorou, Filippo, Massa, Serge, Garbay, Magali, Chiral, Mette, Ramsing, Maria, Rasmussen, Marie-Claire, Gubler, Bettina, Bessieres, Laurence, Heidet, Evelyne, Fischer, Marco, Pontoglio

Publikováno v: Fiorentino, A, Christophorou, A, Massa, F, Garbay, S, Chiral, M, Ramsing, M, Rasmussen, M, Gubler, M-C, Bessieres, B, Heidet, L, Fischer, E & Pontoglio, M 2020, ' Developmental Renal Glomerular Defects at the Origin of Glomerulocystic Disease ', Cell Reports, vol. 33, no. 4, 108304 . https://doi.org/10.1016/j.celrep.2020.108304
Cell Reports
Cell Reports, Elsevier Inc, 2020, 33 (4), pp.108304. ⟨10.1016/j.celrep.2020.108304⟩
Cell Reports, 2020, 33 (4), pp.108304. ⟨10.1016/j.celrep.2020.108304⟩

International audience; The architecture of renal glomeruli is acquired through intricate and still poorly understood developmental steps. In our study we identify a crucial glomerular morphogenetic event in nephrogenesis that drives the remodeling/s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7267091dcb606498e51f563aadcceec7
https://findresearcher.sdu.dk:8443/ws/files/175869624/PIIS2211124720312936.pdf

Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT): SOX11 and CAKUT

Autor: Franz Schaefer, Ernie M.H.F. Bongers, Mansoureh Tabatabaei, Véronique Lefebvre, Kirsten Y. Renkema, Helen McNeill, Wout F.J. Feitz, Haroun Dhib, Herbert Schulz, Michael Wegner, Vladimir M. Kozlov, Elisabeth Sock, Filippo Massa, Yasmine Neirijnck, Albertien M. van Eerde, Nine V A M Knoers, Andreas Schedl, Antoine Reginensi

Publikováno v: Kidney International, 93, 1142-1153
Kidney International, 93, 5, pp. 1142-1153
Kidney International
Kidney International, Nature Publishing Group, 2018, 93 (5), pp.1142-1153. ⟨10.1016/j.kint.2017.11.026⟩
Kidney International, 2018, 93 (5), pp.1142-1153. ⟨10.1016/j.kint.2017.11.026⟩

International audience; Congenital abnormalities of the kidney and the urinary tract (CAKUT) belong to the most common birth defectsin human, but the molecular basis for the majority of CAKUT patients remains unknown. Here we show thatthe transcripti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d044617c724b0214f558d95b118e63d1
https://doi.org/10.1016/j.kint.2017.11.026