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A pilot study of peripheral blood BDCA-1 (CD1c) positive dendritic cells pulsed with NY-ESO-1 ISCOMATRIX™ adjuvant.
Davis, Ian D; Quirk, Juliet; Morris, Leone; Seddon, Lauren; Tai, Tsin Yee; Whitty, Genevieve; Cavicchiolo, Tina; Ebert, Lisa; Jackson, Heather; Browning, Judy; MacGregor, Duncan; Wittke, Frederick; Winkels, Gregor; Alex, Regina; Miloradovic, Lena; Maraskovsky, Eugene; Chen, Weisan; Cebon, Jonathan.
Afiliação
  • Davis ID; Ludwig Institute for Cancer Research, Victoria, Australia.
  • Quirk J; Austin Health, Department of Medical Oncology, Victoria, Australia.
  • Morris L; Monash University Eastern Health Clinical School, Level 2, 5 Arnold St, Box Hill, Victoria 3128, Australia.
  • Seddon L; Eastern Health, Victoria, Australia.
  • Tai TY; Ludwig Institute for Cancer Research, Victoria, Australia.
  • Whitty G; Ludwig Institute for Cancer Research, Victoria, Australia.
  • Cavicchiolo T; Ludwig Institute for Cancer Research, Victoria, Australia.
  • Ebert L; Ludwig Institute for Cancer Research, Victoria, Australia.
  • Jackson H; Ludwig Institute for Cancer Research, Victoria, Australia.
  • Browning J; Ludwig Institute for Cancer Research, Victoria, Australia.
  • MacGregor D; Ludwig Institute for Cancer Research, Victoria, Australia.
  • Wittke F; Ludwig Institute for Cancer Research, Victoria, Australia.
  • Winkels G; Austin Health, Department of Anatomical Pathology, Victoria, Australia.
  • Alex R; Austin Health, Department of Anatomical Pathology, Victoria, Australia.
  • Miloradovic L; Miltenyi Biotec, Germany.
  • Maraskovsky E; Miltenyi Biotec, Germany.
  • Chen W; Miltenyi Biotec, Germany.
  • Cebon J; CSL Limited, Melbourne, Australia.
Immunotherapy ; 9(3): 249-259, 2017 03.
Article em En | MEDLINE | ID: mdl-28183192
AIM: Pilot clinical trial of NY-ESO-1 (ESO) protein in ISCOMATRIX™ adjuvant pulsed onto peripheral blood dendritic cells (PBDC), to ascertain feasibility, evaluate toxicity and assess induction of ESO-specific immune responses. PATIENTS & METHODS: Eligible participants had resected cancers expressing ESO or LAGE-1 and were at high risk of relapse. PBDC were produced using CliniMACS®plus, with initial depletion of CD1c+ B cells followed by positive selection of CD1c+ PBDC. Patients received three intradermal vaccinations of ESO/IMX-pulsed PBDC at 4-week intervals. RESULTS: The process was feasible and safe. No vaccine-induced immune responses were detected. Assays of immunomodulatory cells did not correlate with outcomes. One patient had a long lasting complete remission. CONCLUSION: This method was feasible and safe but was minimally immunogenic.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Células Sanguíneas / Células Dendríticas / Carcinoma Basocelular / Linfócitos T / Vacinas Anticâncer / Imunoterapia Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Células Sanguíneas / Células Dendríticas / Carcinoma Basocelular / Linfócitos T / Vacinas Anticâncer / Imunoterapia Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article