Browsing by Author Ma, Chun

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Issue DateTitleAuthor(s)Citation
2015Addition of varicella zoster virus-specific T cells to cytomegalovirus, Epstein-Barr virus and adenovirus tri-specific T cells as adoptive immunotherapy in patients undergoing allogeneic hematopoietic stem cell transplantationBlyth, Emily; Brown, Rebecca; Burgess, Jane; Clancy, Leighton; Deo, Shivashni Swasthika; Gottlieb, David; Ma, Chun; Micklethwaite, Kenneth; Simms, Renee; Western Clinical School: Westmead Institute for Medical Res; School of Public Health: Public Health; Western Clinical School: Westmead Institute for Medical Res; Western Clinical School: Medicine (Westmead); Western Clinical School: Westmead Institute for Medical Res; Western Clinical School: Westmead Institute for Medical Res; Western Clinical School: Westmead Institute for Medical Res; Western Clinical School: Medicine (Westmead); Western Clinical School: Westmead Institute for Medical ResAddition of varicella zoster virus-specific T cells to cytomegalovirus, Epstein-Barr virus and adenovirus tri-specific T cells as adoptive immunotherapy in patients undergoing allogeneic hematopoietic stem cell transplantation, Cytotherapy, vol.17, 10, 2015,pp 1406-1420
2013Cytomegalovirus-specific cytotoxic T lymphocytes can be efficiently expanded from granulocyte colony-stimulating factor-mobilized hemopoietic progenitor cell products ex vivo and safely transferred to stem cell transplantation recipients to facilitate immune reconstitutionBlyth, Emily; Burgess, Jane; Clancy, Leighton; Gottlieb, David; Ma, Chun; Micklethwaite, Kenneth; Shaw, Peter; Simms, Renee; Antonenas, Vicky; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Medicine (Westmead); Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Medicine (Westmead); Children's Hospital Westmead: Paediatrics & Child Health; Western Clinical School: Westmead Millennium InstituteCytomegalovirus-specific cytotoxic T lymphocytes can be efficiently expanded from granulocyte colony-stimulating factor-mobilized hemopoietic progenitor cell products ex vivo and safely transferred to stem cell transplantation recipients to facilitate immune reconstitution, Biology of Blood and Marrow Transplantation, vol.19, 5, 2013,pp 725-734
2013Donor-derived CMV specific T-cells reduce the requirement for CMV-directed pharmacotherapy after allogeneic stem cell transplantationBlyth, Emily; Burgess, Jane; Byth Wilson, Karen; Clancy, Leighton; Gaundar (nee Deo), Shivashni; Gottlieb, David; Ma, Chun; Micklethwaite, Kenneth; Shaw, Peter; Simms, Renee; Dubosq, Ming Celine; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium Institute; School of Public Health: NH&MRC Clinical Trials Centre; Western Clinical School: Medicine (Westmead); Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Medicine (Westmead); Children's Hospital Westmead: Paediatrics & Child Health; Western Clinical School: Westmead Millennium InstituteDonor-derived CMV specific T-cells reduce the requirement for CMV-directed pharmacotherapy after allogeneic stem cell transplantation, Blood, vol.121, 18, 2013,pp 3745-3758
2014Factors determining pbsc mobilization efficiency and nonmobilization following ICE with or without rituximab (R-ICE) salvage therapy for refractory or relapsed lymphoma prior to autologous transplantationBai, Lijun; Greenwood, Matthew; Kerridge, Ian; Ma, Chun; Ward, Christopher; Xia, Wei; Reid, C.; Wong, Kelly; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; School of Public Health: Ctr for Values Ethics & Law in Med; Western Clinical School: Westmead Millennium Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling InstituteFactors determining pbsc mobilization efficiency and nonmobilization following ICE with or without rituximab (R-ICE) salvage therapy for refractory or relapsed lymphoma prior to autologous transplantation, Journal of Clinical Apheresis, vol.29, 6, 2014,pp 322-330
2012In vitro generation of influenza-specific polyfunctional CD4 + T cells suitable for adoptive immunotherapyBlyth, Emily; Clancy, Leighton; Gaundar (nee Deo), Shivashni; Gottlieb, David; Ma, Chun; Simms, Renee; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Medicine (Westmead); Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium InstituteIn vitro generation of influenza-specific polyfunctional CD4 + T cells suitable for adoptive immunotherapy, Cytotherapy, vol.14, 2, 2012,pp 182-193
2017Long-term control of recurrent or refractory viral infections after allogeneic HSCT with third-party virus-specific T cellsBishop, David; Blyth, Emily; Brown, Rebecca; Burgess, Jane; Clancy, Leighton; Dubosq, Ming-Celine; Gottlieb, David; Kliman, David; Ma, Chun; Micklethwaite, Kenneth; Simms, Renee; Sutrave, Gaurav; Withers, Barbara Phyllis; Fraser, Chris; Shaw, Peter; Yong, Agnes; Westmead Clinical School: Medicine; Westmead Clinical School: Westmead Institute for Medical Res; School of Public Health: Public Health; Westmead Clinical School: Westmead Institute for Medical Res; Westmead Clinical School: Medicine; Westmead Clinical School: Medicine; Westmead Clinical School: Westmead Institute for Medical Res; Northern Clinical School: Kolling Institute; Westmead Clinical School: Westmead Institute for Medical Res; Westmead Clinical School: Medicine; Westmead Clinical School: Westmead Institute for Medical Res; Westmead Clinical School: Westmead Institute for Medical Res; Westmead Clinical School: MedicineLong-term control of recurrent or refractory viral infections after allogeneic HSCT with third-party virus-specific T cells, Blood Advances, vol.1, 24, 2017,pp 2193-2205