Asparaginyl endopeptidases (AEP) are ideal for peptide and protein labeling. Its pairing with a simple chemical reaction significantly lowers the amount of label needed for effective bioconjugation.

Conjugation of small molecules to a simple cyanine dye can lead to organelle-specific delivery.

The synthesis of proteins by solid-phase chemical ligation (SPCL) suffers from paucity of linkers that can be cleaved under mild conditions. Here, we deployed the spontaneous nickel-assisted cleavage (SNAC) tag,...

In conclusion, IL-2 and TNF-a coding adenoviruses can break tumor-associated immunotolerance and significantly increase the levels of active, tumor-reactive T-cells both in injected cutaneous lesions and in non-injected metastatic lymph nodes. Importantly, this triple modality may represent an efficient approach to achieve "CD19-like" clinical responses in the treatment of solid, metastatic cancers currently incurable by standard therapies.

Immunosuppression of established tumors is a major obstacle hindering the efficacy of anti-tumor T cells. Antagonistic mAbs targeting the PD-1/PD-L1 axis represent an effective way to decrease T cell exhaustion and/or anergy, but the efficacy of such therapies seems to be limited to specific cohorts of patients with ongoing immune responses against the tumor. Thus, we hypothesized that we could boost the efficacy of PD-L1 blockade by using an oncolytic cancer vaccine PeptiCrad, which has previously been shown to elicit potent tumor-specific T cell responses by stimulating antigen-presenting cells. First, we demonstrated that the outcome of therapy may depend on the treatment schedule as mice with high B16.OVA tumor burden were refractory to combination of PD-L1 blockade and oncolytic vaccine PeptiCrad targeting the tumor antigen OVA. In fact, mice receiving combination therapy showed only a modest increase in median survival compared to control groups. However, immunological analyses revealed that combination therapy elicited strong anti-tumor immune responses, observed both by tetramer analysis and IFN γ ELISPOT. Hence, we hypothesized that a different treatment schedule could be beneficial in the case of aggressive melanoma such as B16.OVA. In a subsequent experiment, we started the treatments earlier with an overlapping schedule, allowing the PD-L1 blockade to affect the newly primed T cells induced by PeptiCrad. With this regimen, combination treatment notably inhibited tumor growth and a significant increase in median survival of mice was observed when compared to groups receiving monotherapies. Moreover, 37.5% of combination treated mice were cured, suggesting that PeptiCrad can synergize with PD-L1 blockade. In order to eradicate the residual immunoedited tumors, we utilized the major advantage of PeptiCrad technology by treating the survivor mice with a single PeptiCRAd targeting two endogenous melanoma antigens (TRP-2 and gp100, respectively). As a result, the combination therapy was able to slow down the growth of the residual tumors, suggesting that targeting multiple cancer antigens simultaneously could be a feasible approach also in terms of immune checkpoint blockade. Further analyses on the effect of the combination therapy on antigen-specific T cell subsets and on PD-L1 expressing immune cells (such as MDSCs) are ongoing. Citation Format: Cristian Capasso, Siri Tähtinen, Federica Frascaro, Sara Carpi, Manlio Fusciello, Davide Cardella, Daniela Cropp, Karita Peltonen, Beatriz Martins, Madeleine Sjöberg, Sari Pesonen, Tuuli Ranki, Lukasz Kuryk, Erkko Ylösmäki, Vincenzo Cerullo. Boosting the efficacy of PD-L1 blockade with oncolytic vaccine for improved antitumor responses in melanoma [abstract]. In: Proceedings of the Second CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; 2016 Sept 25-28; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2016;4(11 Suppl):Abstract nr A034.