TY - JOUR
T1 - Cancer vaccine formulation dictates synergy with CTLA-4 and PD-L1 checkpoint blockade therapy
AU - Hailemichael, Yared
AU - Woods, Amber
AU - Fu, Tihui
AU - He, Qiuming
AU - Nielsen, Michael C.
AU - Hasan, Farah
AU - Roszik, Jason
AU - Xiao, Zhilan
AU - Vianden, Christina
AU - Khong, Hiep
AU - Singh, Manisha
AU - Sharma, Meenu
AU - Faak, Faisal
AU - Moore, Derek
AU - Dai, Zhimin
AU - Anthony, Scott M.
AU - Schluns, Kimberly S.
AU - Sharma, Padmanee
AU - Engelhard, Victor H.
AU - Overwijk, Willem W.
N1 - Funding Information:
The work was supported by the University of Texas MD Anderson Cancer Center Specialized Program of Research Excellence in Melanoma Career Development Award (P50 CA093459) to YH, and a Cancer Prevention and Research Institute of Texas (CPRIT) grant (RP140522) to WWO.
Publisher Copyright:
© 2018 American Society for Clinical Investigation. All rights reserved.
PY - 2018/4/2
Y1 - 2018/4/2
N2 - Anticancer vaccination is a promising approach to increase the efficacy of cytotoxic T lymphocyte-associated protein 4 (CTLA-4) and programmed death ligand 1 (PD-L1) checkpoint blockade therapies. However, the landmark FDA registration trial for anti-CTLA-4 therapy (ipilimumab) revealed a complete lack of benefit of adding vaccination with gp100 peptide formulated in incomplete Freund's adjuvant (IFA). Here, using a mouse model of melanoma, we found that gp100 vaccination induced gp100-specific effector T cells (Teffs), which dominantly forced trafficking of anti-CTLA-4-induced, non-gp100-specific Teffs away from the tumor, reducing tumor control. The inflamed vaccination site subsequently also sequestered and destroyed anti-CTLA-4-induced Teffs with specificities for tumor antigens other than gp100, reducing the antitumor efficacy of anti-CTLA-4 therapy. Mechanistically, Teffs at the vaccination site recruited inflammatory monocytes, which in turn attracted additional Teffs in a vicious cycle mediated by IFN-γ, CXCR3, ICAM-1, and CCL2, dependent on IFA formulation. In contrast, nonpersistent vaccine formulations based on dendritic cells, viral vectors, or water-soluble peptides potently synergized with checkpoint blockade of both CTLA-4 and PD-L1 and induced complete tumor regression, including in settings of primary resistance to dual checkpoint blockade. We conclude that cancer vaccine formulation can dominantly determine synergy, or lack thereof, with CTLA-4 and PD-L1 checkpoint blockade therapy for cancer.
AB - Anticancer vaccination is a promising approach to increase the efficacy of cytotoxic T lymphocyte-associated protein 4 (CTLA-4) and programmed death ligand 1 (PD-L1) checkpoint blockade therapies. However, the landmark FDA registration trial for anti-CTLA-4 therapy (ipilimumab) revealed a complete lack of benefit of adding vaccination with gp100 peptide formulated in incomplete Freund's adjuvant (IFA). Here, using a mouse model of melanoma, we found that gp100 vaccination induced gp100-specific effector T cells (Teffs), which dominantly forced trafficking of anti-CTLA-4-induced, non-gp100-specific Teffs away from the tumor, reducing tumor control. The inflamed vaccination site subsequently also sequestered and destroyed anti-CTLA-4-induced Teffs with specificities for tumor antigens other than gp100, reducing the antitumor efficacy of anti-CTLA-4 therapy. Mechanistically, Teffs at the vaccination site recruited inflammatory monocytes, which in turn attracted additional Teffs in a vicious cycle mediated by IFN-γ, CXCR3, ICAM-1, and CCL2, dependent on IFA formulation. In contrast, nonpersistent vaccine formulations based on dendritic cells, viral vectors, or water-soluble peptides potently synergized with checkpoint blockade of both CTLA-4 and PD-L1 and induced complete tumor regression, including in settings of primary resistance to dual checkpoint blockade. We conclude that cancer vaccine formulation can dominantly determine synergy, or lack thereof, with CTLA-4 and PD-L1 checkpoint blockade therapy for cancer.
UR - http://www.scopus.com/inward/record.url?scp=85045052518&partnerID=8YFLogxK
U2 - 10.1172/JCI93303
DO - 10.1172/JCI93303
M3 - Article
C2 - 29480817
AN - SCOPUS:85045052518
SN - 0021-9738
VL - 128
SP - 1338
EP - 1354
JO - Journal of Clinical Investigation
JF - Journal of Clinical Investigation
IS - 4
ER -