| Literature DB >> 27158940 |
Tomohide Tsukahara1, Makoto Emori2, Kenji Murata1,2, Emi Mizushima1,2, Yuji Shibayama1,2, Terufumi Kubo1, Takayuki Kanaseki1, Yoshihiko Hirohashi1, Toshihiko Yamashita2, Noriyuki Sato1, Toshihiko Torigoe1.
Abstract
INTRODUCTION: The use of immunotherapeutic challenges for sarcoma has a long history. Despite the existence of objective responses, immunotherapy has been overshadowed by the results of chemotherapy, especially for osteosarcoma. However, the prognosis for non-responders to chemotherapy is still poor and immunotherapy is now focused on again. AREAS COVERED: We reviewed the following types of clinical trials of immunotherapy for sarcoma: (i) vaccination with autologous tumor cells, (ii) vaccination with peptides derived from tumor-associated antigens, (iii) adoptive cell transfer using engineered T cells expressing T cell receptor directed at NY-ESO-1 and (iv) immune checkpoint inhibitors targeting CTLA-4 and PD1/PDL1. EXPERT OPINION: The immunogenicity of sarcoma might be lower than that of melanoma. Patients with small lesions who have not received any chemotherapy are good candidates for peptide-based immunotherapy. Combining peptide vaccination and immune checkpoint inhibitors is an attractive option, and long-lived memory T cells are attracting attention. Memory T stem cells defined by CD95+ are long-lived and have the capacity for self-renewal and multidifferentiation. We also identified a novel memory T cell population, young memory T cells defined by CD73+CXCR3+. Regulation of such memory T stem cells will be useful for peptide vaccination and adoptive cell transfer.Entities:
Keywords: Osteosarcoma; immune checkpoint inhibitor; memory T stem cell; peptide vaccination; synovial sarcoma
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Year: 2016 PMID: 27158940 DOI: 10.1080/14712598.2016.1188075
Source DB: PubMed Journal: Expert Opin Biol Ther ISSN: 1471-2598 Impact factor: 4.388