TY - JOUR
T1 - Videos of Sipuleucel-T Programmed T Cells Lysing Cells That Express Prostate Cancer Target Antigens
AU - Kibel, Adam S.
AU - Inman, Brant A.
AU - Pachynski, Russell K.
AU - Vu, Tuyen
AU - Sheikh, Nadeem A.
AU - Petrylak, Daniel P.
N1 - Publisher Copyright:
© 2021 The Author(s). Published by Oxford University Press.
PY - 2022/2/1
Y1 - 2022/2/1
N2 - Sipuleucel-T, an autologous cellular immunotherapy, was approved to treat metastatic castration-resistant prostate cancer in 2010 in the United States. Treatment with sipuleucel-T primes the immune system to target prostate acid phosphatase, which is expressed by prostate cancer cells, potentially leading to lysis of cancer cells. Expanding on previously reported indirect evidence of cell killing with sipuleucel-T treatment, we sought to provide direct evidence of cell lysis through visualization. We used advanced video technology and available samples of peripheral blood mononuclear cells from subjects enrolled in the STAMP trial (NCT01487863). Isolated CD8+ T cells were used as effector cells and cocultured with autologous monocytes pulsed with control or target antigens. Differentially stained effector and target cells were then video recorded during coculture. Here, we present video recordings and analyses of T cells from sipuleucel-T-treated subjects showing-for the first time-direct lysis of cells that express prostate cancer target antigens, prostate acid phosphatase, or prostate-specific antigen.
AB - Sipuleucel-T, an autologous cellular immunotherapy, was approved to treat metastatic castration-resistant prostate cancer in 2010 in the United States. Treatment with sipuleucel-T primes the immune system to target prostate acid phosphatase, which is expressed by prostate cancer cells, potentially leading to lysis of cancer cells. Expanding on previously reported indirect evidence of cell killing with sipuleucel-T treatment, we sought to provide direct evidence of cell lysis through visualization. We used advanced video technology and available samples of peripheral blood mononuclear cells from subjects enrolled in the STAMP trial (NCT01487863). Isolated CD8+ T cells were used as effector cells and cocultured with autologous monocytes pulsed with control or target antigens. Differentially stained effector and target cells were then video recorded during coculture. Here, we present video recordings and analyses of T cells from sipuleucel-T-treated subjects showing-for the first time-direct lysis of cells that express prostate cancer target antigens, prostate acid phosphatase, or prostate-specific antigen.
UR - http://www.scopus.com/inward/record.url?scp=85124432894&partnerID=8YFLogxK
U2 - 10.1093/jnci/djab025
DO - 10.1093/jnci/djab025
M3 - Article
C2 - 33630063
AN - SCOPUS:85124432894
SN - 0027-8874
VL - 114
SP - 310
EP - 313
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
IS - 2
ER -