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Marie-Cécile Michallet

Researcher at French Institute of Health and Medical Research

Publications -  74
Citations -  2556

Marie-Cécile Michallet is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Transplantation & Bone marrow. The author has an hindex of 26, co-authored 67 publications receiving 2418 citations.

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Staphylococcus aureus Panton-Valentine leukocidin directly targets mitochondria and induces Bax-independent apoptosis of human neutrophils

TL;DR: Panton-Valentine leukocidin, which belongs to the pore-forming toxin family, could act at the mitochondrion level by creating pores in the mitochondrial outer membrane and was detected in lung sections of patients with necrotizing pneumonia, suggesting that PVL induces apoptosis in vivo and thereby is directly involved in the pathophysiology of necrotized pneumonia.
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Allogeneic bone marrow transplantation for acute myeloid leukemia in first remission: a randomized trial of a busulfan-Cytoxan versus Cytoxan-total body irradiation as preparative regimen: a report from the Group d'Etudes de la Greffe de Moelle Osseuse.

TL;DR: The present limitation of busulfan use in this setting is demonstrated, possibly due to probable individual variations in biodisponibility, and besides the anti-leukemic effect of preparative regimens, the progress accomplished in BMT management is pointed out.
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Consolidation treatment of adult acute lymphoblastic leukemia: a prospective, randomized trial comparing allogeneic versus autologous bone marrow transplantation and testing the impact of recombinant interleukin-2 after autologous bone marrow transplantation. BGMT Group

TL;DR: It is concluded that, in ALL, early allogeneic BMT after the BFM induction regimen is an effective consolidation treatment and that IL-2 does not decrease the high relapse rate observed after autologous BMT.
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Functional antibodies to leukocyte adhesion molecules in antithymocyte globulins.

TL;DR: Results show that ATG may interfere with leukocyte responses to chemotactic signals but mostly inhibit the expression of integrins required for firm cellular adhesion, and may contribute to decreasing graft cellular infiltration during acute rejection and possibly after postischemic reperfusion.