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Roberto Bellucci

Researcher at Harvard University

Publications -  20
Citations -  1911

Roberto Bellucci is an academic researcher from Harvard University. The author has contributed to research in topics: Antigen & Multiple myeloma. The author has an hindex of 12, co-authored 20 publications receiving 1765 citations. Previous affiliations of Roberto Bellucci include Brigham and Women's Hospital.

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Reduced frequency of FOXP3+ CD4+CD25+ regulatory T cells in patients with chronic graft-versus-host disease.

TL;DR: It is indicated that patients with active cGVHD have reduced frequencies of Tregs but the function of these cells remains normal, and these findings support the development of new strategies to increase the number of T Regs following allogeneic hematopoietic stem cell transplantation.
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Interferon-γ-induced activation of JAK1 and JAK2 suppresses tumor cell susceptibility to NK cells through upregulation of PD-L1 expression

TL;DR: The results show that NK cell activation and secretion of IFNγ results in activation of JAK1, JAK2 and STAT1 in tumor cells, resulting in rapid up-regulation of PD-L1 expression, suggesting that JAK pathway inhibitors as well as PD-1 and PD- L1 antibodies may work synergistically with other immune therapies by preventing IFN-induced inhibition of NK cell-mediated tumor cell lysis.
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Graft-versus-tumor response in patients with multiple myeloma is associated with antibody response to BCMA, a plasma-cell membrane receptor.

TL;DR: It is demonstrated that B-cell maturation antigen (BCMA), a transmembrane receptor of the tumor necrosis factor (TNF) superfamily, is a target of donor B- cell immunity in patients with myeloma who respond to DLI.
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Complete response to donor lymphocyte infusion in multiple myeloma is associated with antibody responses to highly expressed antigens

TL;DR: It is demonstrated that the GVM response is associated with antibody responses to highly expressed myeloma-associated antigens, and an association between antibody response and time of best response after DLI is shown.