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Qing Ye

Researcher at University of Pittsburgh

Publications -  84
Citations -  2785

Qing Ye is an academic researcher from University of Pittsburgh. The author has contributed to research in topics: Transplantation & Bone marrow. The author has an hindex of 28, co-authored 79 publications receiving 2442 citations. Previous affiliations of Qing Ye include Carnegie Mellon University & Veterans Health Administration.

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Variable chimerism, graft-versus-host disease, and tolerance after different kinds of cell and whole organ transplantation from Lewis to brown Norway rats.

TL;DR: Both the GVHD propensity and tolerogenicity in these experiments were closely associated with recipient tissue chimerism 30 and 100 days after the experiments began, and these observations provide guidelines that should be considered in devising leukocyte augmentation protocols for human whole organ recipients.
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In situ labeling of immune cells with iron oxide particles: An approach to detect organ rejection by cellular MRI

TL;DR: A noninvasive approach using MRI to detect graft rejection after solid organ transplantation and the feasibility of imaging individual macrophages in vivo by MRI in a rodent heterotopic working-heart transplantation model using a more sensitive contrast agent, the micrometer-sized paramagnetic iron oxide particle, is presented.
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ST2/IL-33-Dependent Microglial Response Limits Acute Ischemic Brain Injury

TL;DR: It is demonstrated here that ST2 deficiency shifted microglia/macrophages toward a M1-like phenotype, thereby expanding brain infarcts and exacerbating long-term behavioral deficits after stroke, and shed new light on the IL-33/ST2 axis as an immune regulatory mechanism that serves as a natural brake on the progression of ischemic brain injury.
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19F MRI detection of acute allograft rejection with in vivo perfluorocarbon labeling of immune cells.

TL;DR: With no background signal, 19F MRI/magnetic resonance spectroscopy can provide unambiguous detection of fluorine labeled cells, and may be a useful technique for detecting and quantifying rejection grade in patients.
Journal Article

Analysis of chronic rejection and obliterative arteriopathy : Possible contributions of donor antigen-presenting cells and lymphatic disruption

TL;DR: It is not unreasonable to raise the testable hypothesis that direct presentation of alloantigen by donor antigen-presenting cells is required for long-term, chronic-rejection-free allograft acceptance, and chronic intermittent lymphatic disruption is implicated as a possible mechanism for the association between chronic interstitial allografted inflammation and the development of obliterative arteriopathy.