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Michael Papamichail

Researcher at Boston Children's Hospital

Publications -  132
Citations -  6477

Michael Papamichail is an academic researcher from Boston Children's Hospital. The author has contributed to research in topics: Cytotoxic T cell & Cancer. The author has an hindex of 38, co-authored 132 publications receiving 6082 citations.

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Interactions between human mesenchymal stem cells and natural killer cells.

TL;DR: It is demonstrated that at low NK‐to‐MSC ratios, MSCs alter the phenotype of NK cells and suppress proliferation, cytokine secretion, and cyto‐toxicity against HLA‐class I– expressing targets.
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Characterization of the optimal culture conditions for clinical scale production of human mesenchymal stem cells.

TL;DR: The optimal culture conditions for the successful isolation and expansion of human MSCs in high numbers for subsequent cellular therapeutic approaches are defined.
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Transcoronary transplantation of autologous mesenchymal stem cells and endothelial progenitors into infarcted human myocardium.

TL;DR: Investigating whether a combination of mesenchymal stem cells capable of differentiating into cardiac myocytes and endothelial progenitors that mainly promote neoangiogenesis might be able to facilitate tissue repair in myocardial scars found it feasible, safe, and may contribute to regional regeneration of myocardIAL tissue early or late following MI.
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An improved fluorescence assay for the determination of lymphocyte-mediated cytotoxicity using flow cytometry.

TL;DR: An improved flow cytometric method that is able to measure cytotoxicity, based on two fluorescent dyes, is developed and used to quantify natural killer and lymphokine-activated killer activities against human K562 and Daudi cell lines and the murine YAC-1 and L1210 cell lines respectively.
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A phase I trial of adoptive transfer of allogeneic natural killer cells in patients with advanced non-small cell lung cancer

TL;DR: In conclusion, repetitive infusions of allogeneic, in vitro activated and expanded with IL-15/HC NK cells, in combination with chemotherapy are safe and potentially clinically effective.