| Literature DB >> 28854371 |
Tadepally Lakshmikanth1, Axel Olin1, Yang Chen1, Jaromir Mikes1, Erik Fredlund2, Mats Remberger3, Brigitta Omazic4, Petter Brodin5.
Abstract
Human immune systems are variable, and immune responses are often unpredictable. Systems-level analyses offer increased power to sort patients on the basis of coordinated changes across immune cells and proteins. Allogeneic stem cell transplantation is a well-established form of immunotherapy whereby a donor immune system induces a graft-versus-leukemia response. This fails when the donor immune system regenerates improperly, leaving the patient susceptible to infections and leukemia relapse. We present a systems-level analysis by mass cytometry and serum profiling in 26 patients sampled 1, 2, 3, 6, and 12 months after transplantation. Using a combination of machine learning and topological data analyses, we show that global immune signatures associated with clinical outcome can be revealed, even when patients are few and heterogeneous. This high-resolution systems immune monitoring approach holds the potential for improving the development and evaluation of immunotherapies in the future.Entities:
Keywords: ASCT; CyTOF; bone marrow transplantation; immune system reconstitution; immunotherapy; leukemia; mass cytometry; stem cell transplantation; systems immunology; tumor immunology
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Year: 2017 PMID: 28854371 DOI: 10.1016/j.celrep.2017.08.021
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423