Your browser doesn't support javascript.
loading
The Basics of Artificial Antigen Presenting Cells in T Cell-Based Cancer Immunotherapies.
Neal, Lillian R; Bailey, Stefanie R; Wyatt, Megan M; Bowers, Jacob S; Majchrzak, Kinga; Nelson, Michelle H; Haupt, Carl; Paulos, Chrystal M; Varela, Juan C.
Affiliation
  • Neal LR; Department of Microbiology & Immunology, Medical University of South Carolina, Charleston, SC 29425.
  • Bailey SR; Department of Dermatological Surgery and Dermatology, Medical University of South Carolina, Charleston, SC 29425.
  • Wyatt MM; Department of Surgery, Medical University of South Carolina, Charleston, SC 29425.
  • Bowers JS; Department of Hematology and Oncology, Medical University of South Carolina, Charleston, 29425.
  • Majchrzak K; Department of Microbiology & Immunology, Medical University of South Carolina, Charleston, SC 29425.
  • Nelson MH; Department of Dermatological Surgery and Dermatology, Medical University of South Carolina, Charleston, SC 29425.
  • Haupt C; Department of Surgery, Medical University of South Carolina, Charleston, SC 29425.
  • Paulos CM; Department of Microbiology & Immunology, Medical University of South Carolina, Charleston, SC 29425.
  • Varela JC; Department of Dermatological Surgery and Dermatology, Medical University of South Carolina, Charleston, SC 29425.
J Immunol Res Ther ; 2(1): 68-79, 2017.
Article in En | MEDLINE | ID: mdl-28825053
Adoptive T cell transfer (ACT) can mediate objective responses in patients with advanced malignancies. There have been major advances in this field, including the optimization of the ex vivo generation of tumor-reactive lymphocytes to ample numbers for effective ACT therapy via the use of natural and artificial antigen presenting cells (APCs). Herein we review the basic properties of APCs and how they have been manufactured through the years to augment vaccine and T cell-based cancer therapies. We then discuss how these novel APCs impact the function and memory properties of T cells. Finally, we propose new ways to synthesize aAPCs to augment the therapeutic effectiveness of antitumor T cells for ACT therapy.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Immunol Res Ther Year: 2017 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Immunol Res Ther Year: 2017 Document type: Article Country of publication: United States