TY - JOUR
T1 - Trial Watch
T2 - Peptide-based anticancer vaccines
AU - Pol, Jonathan
AU - Bloy, Norma
AU - Buqué, Aitziber
AU - Eggermont, Alexander
AU - Cremer, Isabelle
AU - Sautès-Fridman, Catherine
AU - Galon, Jérôme
AU - Tartour, Eric
AU - Zitvogel, Laurence
AU - Kroemer, Guido
AU - Galluzzi, Lorenzo
N1 - Publisher Copyright:
© 2015 Taylor & Francis Group, LLC.
PY - 2015/1/1
Y1 - 2015/1/1
N2 - Malignant cells express antigens that can be harnessed to elicit anticancer immune responses. One approach to achieve such goal consists in the administration of tumor-associated antigens (TAAs) or peptides thereof as recombinant proteins in the presence of adequate adjuvants. Throughout the past decade, peptide vaccines have been shown to mediate antineoplastic effects in various murine tumor models, especially when administered in the context of potent immunostimulatory regimens. In spite of multiple limitations, first of all the fact that anticancer vaccines are often employed as therapeutic (rather than prophylactic) agents, this immunotherapeutic paradigm has been intensively investigated in clinical scenarios, with promising results. Currently, both experimentalists and clinicians are focusing their efforts on the identification of so-called tumor rejection antigens, i.e., TAAs that can elicit an immune response leading to disease eradication, as well as to combinatorial immunostimulatory interventions with superior adjuvant activity in patients. Here, we summarize the latest advances in the development of peptide vaccines for cancer therapy.
AB - Malignant cells express antigens that can be harnessed to elicit anticancer immune responses. One approach to achieve such goal consists in the administration of tumor-associated antigens (TAAs) or peptides thereof as recombinant proteins in the presence of adequate adjuvants. Throughout the past decade, peptide vaccines have been shown to mediate antineoplastic effects in various murine tumor models, especially when administered in the context of potent immunostimulatory regimens. In spite of multiple limitations, first of all the fact that anticancer vaccines are often employed as therapeutic (rather than prophylactic) agents, this immunotherapeutic paradigm has been intensively investigated in clinical scenarios, with promising results. Currently, both experimentalists and clinicians are focusing their efforts on the identification of so-called tumor rejection antigens, i.e., TAAs that can elicit an immune response leading to disease eradication, as well as to combinatorial immunostimulatory interventions with superior adjuvant activity in patients. Here, we summarize the latest advances in the development of peptide vaccines for cancer therapy.
KW - Carbohydrate-mimetic peptides
KW - Immune checkpoint blockers
KW - Immunostimulatory cytokines
KW - Survivin
KW - Synthetic long peptides
KW - WT1
UR - http://www.scopus.com/inward/record.url?scp=84954328791&partnerID=8YFLogxK
U2 - 10.4161/2162402X.2014.974411
DO - 10.4161/2162402X.2014.974411
M3 - Article
AN - SCOPUS:84954328791
SN - 2162-4011
VL - 4
JO - OncoImmunology
JF - OncoImmunology
IS - 4
ER -