Q
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.
Papers
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Journal ArticleDOI
Variable chimerism, graft-versus-host disease, and tolerance after different kinds of cell and whole organ transplantation from Lewis to brown Norway rats.
Noriko Murase,Thomas E. Starzl,Minoru Tanabe,Shigeru Fujisaki,H. Miyazawa,Qing Ye,Conor P. Delaney,John J. Fung,Anthony J. Demetris +8 more
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
Yuanyuan Yang,Huan Liu,Haiyue Zhang,Qing Ye,Jianyi Wang,Boyu Yang,Leilei Mao,Wen Zhu,Rehana K. Leak,Bo Xiao,Binfeng Lu,Jun Chen,Xiaoming Hu +12 more
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
Anthony J. Demetris,Noriko Murase,Qing Ye,Flávio Henrique Ferreira Galvão,C. Richert,Reda S. Saad,Si M. Pham,R. J. Duquesnoy,Adriana Zeevi,John J. Fung,T. E. Starzl +10 more
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.