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A Novel Recombinant Fcγ Receptor-Targeted Survivin Combines with Chemotherapy for Efficient Cancer Treatment. | LitMetric

AI Article Synopsis

  • - FLIPr, an Fcγ receptor antagonist, enhances immune responses by guiding a survivin-FLIPr fusion protein to FcγRs, which is vital since survivin is over-expressed in various cancers.
  • - The study shows that the rSur-FLIPr fusion protein effectively binds to FcγRs and is taken up by dendritic cells, stimulating survivin-specific immune responses that help suppress tumor growth through TAP-mediated and CD8-dependent pathways.
  • - Notably, preexisting anti-FLIPr antibodies do not hinder the immune response and when combined with chemotherapy, rSur-FLIPr shows significant benefits, indicating its potential as an effective cancer therapy.

Article Abstract

Formyl peptide receptor-like 1 inhibitor (FLIPr), an Fcγ receptor (FcγR) antagonist, can be used as a carrier to guide antigen-FLIPr fusion protein to FcγR then enhances antigen-specific immune responses. Survivin, a tumor-associated antigen, is over-expressed in various types of human cancer. In this study, we demonstrate that recombinant survivin-FLIPr fusion protein (rSur-FLIPr) binds to FcγRs, and efficient uptake by dendritic cells in vivo. In addition, rSur-FLIPr alone stimulates survivin-specific immune responses, which effectively suppresses the tumor growth. The antitumor immunities are through TAP-mediated and CD8-dependent pathways. Furthermore, preexisting anti-FLIPr antibody does not abolish antitumor responses induced by rSur-FLIPr immunization. These results suggest that FLIPr is an effective antigen delivery vector and can be repeatedly used. Combination of chemotherapy with rSur-FLIPr treatment reveals a great benefit to tumor-bearing mice. Altogether, these findings suggest that rSur-FLIPr is a potential candidate for efficient cancer therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301409PMC
http://dx.doi.org/10.3390/biomedicines9070806DOI Listing

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