التفاصيل البيبلوغرافية
العنوان: |
Recombinant Costimulatory Fusion Proteins as Functional Immunomodulators Enhance Antitumor Activity in Murine B16F10 Melanoma |
المؤلفون: |
Huaman Cai, Wenfang Wang, Zhibing Lin, Yan Zhang, Bing Wu, Yuhua Wan, Rongxiu Li |
المصدر: |
Vaccines; Volume 8; Issue 2; Pages: 223 |
بيانات النشر: |
Multidisciplinary Digital Publishing Institute |
سنة النشر: |
2020 |
المجموعة: |
MDPI Open Access Publishing |
مصطلحات موضوعية: |
cancer immunotherapy, OX40L, 4-1BBL, immunomodulator, tumor microenvironment |
الوصف: |
Blocking inhibitory signaling and engaging stimulatory signaling have emerged as important therapeutic modalities for cancer immunotherapy. This study aimed to investigate immunomodulatory features of three recombinant costimulatory ligand proteins in a mouse model, which are extracellular domains of OX40-ligand (OX40L), 4-1BB-ligand (4-1BBL), or two domains in tandem, fused with the transmembrane domain of diphtheria toxin (DTT), named DTT-COS1, DTT-COS2, and DTT-COS12, respectively. In vitro study showed that DTT-COS1 and DTT-COS12 had immunological activity increasing the ratio of CD8/CD4 T cells. Treatments with DTT-COS1 and DTT-COS12 dramatically generated immune protection against the B16F10 tumor challenge in both prophylactic and therapeutic efficacy. Furthermore, regarding tumor microenvironment (TME) immunomodulation, DTT-COS1 treatment increased the proportion of CD4+ effector T cells (Teff) and decreased the expression of a suppressive cytokine. Meanwhile, DTT-COS12 reduced regulatory T cells (Treg) and improved the level of stimulatory cytokines. In addition, endogenous antibodies against OX40L/4-1BBL were generated, which may help with antitumor responses. Unexpectedly, DTT-COS2 lacked antitumor effects in vitro and in vivo. Importantly, serum analysis of liver-function associated factors and pro-inflammatory cytokines demonstrated that treatments were safe formulations in mice without signs of systemic toxicity. Remarkably, DTT-COS1 and DTT-COS12 are functional immunomodulators for mouse B16F10 melanoma, creating practical preclinical value in cancer immunotherapy. |
نوع الوثيقة: |
text |
وصف الملف: |
application/pdf |
اللغة: |
English |
Relation: |
Cancer Vaccines and Immunotherapy; https://dx.doi.org/10.3390/vaccines8020223 |
DOI: |
10.3390/vaccines8020223 |
الاتاحة: |
https://doi.org/10.3390/vaccines8020223 |
Rights: |
https://creativecommons.org/licenses/by/4.0/ |
رقم الانضمام: |
edsbas.8AE0DD42 |
قاعدة البيانات: |
BASE |