Zobrazeno 1 - 10
of 243
pro vyhledávání: '"William J Burlingham"'
Publikováno v:
Frontiers in Immunology, Vol 7 (2016)
Cell based therapies have been studied extensively in the context of transplantation tolerance induction. The most successful protocols have relied on transfusion of bone marrow prior to the transplantation of a renal allograft. However, it is not cl
Externí odkaz:
https://doaj.org/article/8cc54f6796ab49bbb6376cd41dd0e130
Autor:
Miranda P Dierselhuis, Ewa Jankowska-Gan, Els Blokland, Jos Pool, William J Burlingham, Astrid G S van Halteren, Els Goulmy
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e91274 (2014)
Sex difference is an established risk factor for hematopoietic stem cell transplantation (HSCT)-related complications like graft versus host disease (GVHD). CD8pos cytotoxic T cells specific for Y chromosome-encoded minor Histocompatibility antigens
Externí odkaz:
https://doaj.org/article/014d146200644273897296edba74785e
Autor:
Melissa R Keller, Lynn D Haynes, Ewa Jankowska-Gan, Jeremy A Sullivan, Vrushali V Agashe, Scott R Burlingham, William J Burlingham
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e79601 (2013)
IL-17-dependent cellular immune responses to the α1 chain of collagen type V are associated with development of bronchiolitis obliterans syndrome after lung transplantation, and with idiopathic pulmonary fibrosis and coronary artery disease, primary
Externí odkaz:
https://doaj.org/article/897a43cab5a3419ab3128aef1ce463f0
Autor:
Jennifer L Lockridge, Xiuxu Chen, Ying Zhou, Deepika Rajesh, Drew A Roenneburg, Subramanya Hegde, Sarah Gerdts, Tan-Yun Cheng, Regan J Anderson, Gavin F Painter, D Branch Moody, William J Burlingham, Jenny E Gumperz
Publikováno v:
PLoS ONE, Vol 6, Iss 6, p e21701 (2011)
CD1 molecules are glycoproteins that present lipids and glycolipids for recognition by T cells. CD1-dependent immune activation has been implicated in a wide range of immune responses, however, our understanding of the role of this pathway in human d
Externí odkaz:
https://doaj.org/article/c32569081ef64fd7a9252970b7d1d093
Autor:
William J. Burlingham, PhD, Ewa Jankowska-Gan, MS, John H. Fechner, MS, Christopher J. Little, MD, Jianxin Wang, PhD, Seungpyo Hong, PhD, Miraf Molla, BS, Jeremy A. Sullivan, PhD, David P. Foley, MD
Publikováno v:
Transplantation Direct, Vol 9, Iss 6, p e1475 (2023)
Background. Here we test the hypothesis that, like CD81-associated “latent” IL35, the transforming growth factor (TGF)β:latency-associated peptide (LAP)/glycoprotein A repetitions predominant (GARP) complex was also tethered to small extracellul
Externí odkaz:
https://doaj.org/article/55c62bbd8b1e4c159f6be1fe92b81bef
Autor:
William J. Burlingham
Publikováno v:
Haematologica, Vol 104, Iss 2 (2019)
Externí odkaz:
https://doaj.org/article/6b71bc8c5b8e491e8ca8551b9c28f937
Autor:
William J. Burlingham, Bret M Verhoven, Sarah E. Panzer, Lei Shi, Robert R. Redfield, Weixiong Zhong, Xiang Ding, Shannon R. Reese, Arjang Djamali, Nancy A. Wilson, Loren C. Denlinger
Publikováno v:
Kidney360
Background: Extracellular adenosine triphosphate (ATP) binds to purinergic receptors and promotes inflammatory responses. We tested whether oxidized ATP (oATP), P2X7 receptor antagonist can attenuate acute kidney allograft rejection. Methods: Brown N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b949f1f39da915625de3636af4578f59
https://doi.org/10.34067/kid.0000692019
https://doi.org/10.34067/kid.0000692019
Autor:
Jeremy A. Sullivan, William J. Burlingham, Seungpyo Hong, Qianxia Zhang, Ewa Jankowska-Gan, Ying Zhou, Andrea L. Szymczak-Workman, Creg J. Workman, Yusuke Tomita, William Bracamonte-Baran, Weixiong Zhong, Kristy Meyer, Ashita Nair, Deepali V. Sawant, Diego A Lema, Dario A. A. Vignali, Matt P. Arvedson
Publikováno v:
Cell Reports, Vol 30, Iss 4, Pp 1039-1051.e5 (2020)
Summary: Interleukin-35 (IL-35) is an immunosuppressive cytokine composed of Epstein-Barr-virus-induced protein 3 (Ebi3) and IL-12α chain (p35) subunits, yet the forms that IL-35 assume and its role in peripheral tolerance remain elusive. We induce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83089e27591cb4e5eb9f7b73c0b07a78
http://www.sciencedirect.com/science/article/pii/S2211124719317462
http://www.sciencedirect.com/science/article/pii/S2211124719317462
Autor:
Yolanda Ponstein, Luis A. Fernandez, Juan S. Danobeitia, Peter J. Chlebeck, Erzsebet Polyak, Jose R. Torrealba, Casi L. Blanton, Yücel Yankol, Megan L. Springer, Michael J. Eerhart, Jeremy A. Sullivan, Saverio Capuano, Jose A. Reyes, Jennifer Coonen, Myron A. Pozniak, Laura J. Zitur, Anthony M. D'Alessandro, Weixiong Zhong, Edwin Van Amersfoort, William J. Burlingham, Cees van Kooten
Publikováno v:
Transplantation
Transplantation, 106(1), 60-71. LIPPINCOTT WILLIAMS & WILKINS
Transplantation, 106(1), 60-71. LIPPINCOTT WILLIAMS & WILKINS
Background: Complement activation in kidney transplantation is implicated in the pathogenesis of delayed graft function (DGF). This study evaluated the therapeutic efficacy of high-dose recombinant human C1 esterase inhibitor (rhC1INH) to prevent DGF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeeda53f63c1477d0615d8ab46b90c68
https://pubmed.ncbi.nlm.nih.gov/34905763
https://pubmed.ncbi.nlm.nih.gov/34905763
Autor:
Diego A. Lema, Ewa Jankowska-Gan, Ashita Nair, Sami B. Kanaan, Christopher J. Little, David P. Foley, Afsar Raza Naqvi, Jianxin Wang, Seungpyo Hong, J. Lee Nelson, David Al-Adra, William J. Burlingham, Jeremy A. Sullivan
Publikováno v:
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons. 22(5)
Exposure to non-inherited maternal antigens (NIMA) during the fetal period induces lifelong split tolerance to grafts expressing these allo-antigens. In adult mice, the production of extracellular vesicles (EVs) from maternal microchimeric cells caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65073b17ef81b499727af95114a73a0d
https://pubmed.ncbi.nlm.nih.gov/35143105
https://pubmed.ncbi.nlm.nih.gov/35143105