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Emmanuel Clave

Researcher at French Institute of Health and Medical Research

Publications -  65
Citations -  3337

Emmanuel Clave is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Hematopoietic stem cell transplantation & Transplantation. The author has an hindex of 28, co-authored 55 publications receiving 2973 citations. Previous affiliations of Emmanuel Clave include National Institutes of Health & Finnish Red Cross.

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Engraftment kinetics after nonmyeloablative allogeneic peripheral blood stem cell transplantation: full donor T-cell chimerism precedes alloimmune responses.

TL;DR: The results emphasize the importance of lineage-specific chimerism analysis to successfully manipulate engraftment after nonmyeloablative allogeneic PBSC transplantation.
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Cytotoxic T Lymphocytes Specific for a Nonpolymorphic Proteinase 3 Peptide Preferentially Inhibit Chronic Myeloid Leukemia Colony-Forming Units

TL;DR: Results show that PR1-specific allogeneic T cells preferentially inhibit leukemic CFU-GM based on overexpression of proteinase 3, and thatproteinase 3-specific CTL could be used for leukemia-specific adoptive immunotherapy.
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A broad T-cell repertoire diversity and an efficient thymic function indicate a favorable long-term immune reconstitution after cord blood stem cell transplantation.

TL;DR: Data indicate an efficient thymic regeneration pathway from CB lymphoid progenitors despite the low number of cells infused compared to bone marrow, arguing for a complete clinical immune recovery after CB transplantation.
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Successful Treatment of Metastatic Renal Cell Carcinoma With a Nonmyeloablative Allogeneic Peripheral-Blood Progenitor-Cell Transplant: Evidence for a Graft-Versus-Tumor Effect

TL;DR: The complete regression of metastatic disease, which has now been maintained for more than 1 year, is compatible with a graft-versus-tumor effect.
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T cell-depleted bone marrow transplantation and delayed T cell add- back to control acute GVHD and conserve a graft-versus-leukemia effect

TL;DR: Results indicate that the risk of acute GVHD is low following substantial T cell doses, transfused 45 days after transplant, using cyclosporine prophylaxis and a graft-versus-leukemia effect was conserved.