TY - JOUR
T1 - The Basis of Oncoimmunology
AU - Palucka, A. Karolina
AU - Coussens, Lisa M.
N1 - Funding Information:
The authors thank members of the Palucka and Coussens laboratories for critical insight and discussions; Amanda Lund and Jeffrey Nolz for critical feedback; Anna Lisa Lucido for help with editing the manuscript; and all authors contributing to studies discussed herein but not mentioned due to space consideration. A.K.P. thanks Jacques Banchereau, a long-time collaborator. The authors acknowledge support from the NIH/NCI and Susan B. Komen Foundation (A.K.P. and L.M.C.), Baylor Research Foundation (A.K.P.), DOD BCRP Era of Hope Scholar Expansion Award, Breast Cancer Research Foundation, a Stand Up To Cancer–Lustgarten Foundation Pancreatic Cancer Convergence Dream Team Translational Research Grant (SU2C-AACR-DT14-14), and Brenden-Colson Center for Pancreatic Care (to L.M.C.).
Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/3/10
Y1 - 2016/3/10
N2 - Cancer heterogeneity, a hallmark enabling clonal survival and therapy resistance, is shaped by active immune responses. Antigen-specific T cells can control cancer, as revealed clinically by immunotherapeutics such as adoptive T-cell transfer and checkpoint blockade. The host immune system is thus a powerful tool that, if better harnessed, could significantly enhance the efficacy of cytotoxic therapy and improve outcomes for cancer sufferers. To realize this vision, however, a number of research frontiers must be tackled. These include developing strategies for neutralizing tumor-promoting inflammation, broadening T-cell repertoires (via vaccination), and elucidating the mechanisms by which immune cells organize tumor microenvironments to regulate T-cell activity. Such efforts will pave the way for identifying new targets for combination therapies that overcome resistance to current treatments and promote long-term cancer control.
AB - Cancer heterogeneity, a hallmark enabling clonal survival and therapy resistance, is shaped by active immune responses. Antigen-specific T cells can control cancer, as revealed clinically by immunotherapeutics such as adoptive T-cell transfer and checkpoint blockade. The host immune system is thus a powerful tool that, if better harnessed, could significantly enhance the efficacy of cytotoxic therapy and improve outcomes for cancer sufferers. To realize this vision, however, a number of research frontiers must be tackled. These include developing strategies for neutralizing tumor-promoting inflammation, broadening T-cell repertoires (via vaccination), and elucidating the mechanisms by which immune cells organize tumor microenvironments to regulate T-cell activity. Such efforts will pave the way for identifying new targets for combination therapies that overcome resistance to current treatments and promote long-term cancer control.
UR - http://www.scopus.com/inward/record.url?scp=84960422665&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84960422665&partnerID=8YFLogxK
U2 - 10.1016/j.cell.2016.01.049
DO - 10.1016/j.cell.2016.01.049
M3 - Review article
C2 - 26967289
AN - SCOPUS:84960422665
SN - 0092-8674
VL - 164
SP - 1233
EP - 1247
JO - Cell
JF - Cell
IS - 6
ER -