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A preclinical study: correlation between PD-L1 PET imaging and the prediction of therapy efficacy of MC38 tumor with 68 Ga-labeled PD-L1 targeted nanobody.
- Source :
-
Aging [Aging (Albany NY)] 2021 Apr 27; Vol. 13 (9), pp. 13006-13022. Date of Electronic Publication: 2021 Apr 27. - Publication Year :
- 2021
-
Abstract
- Although immunotherapy has achieved great clinical success in clinical outcomes, especially the anti-PD-1 or anti-PD-L1 antibodies, not all patients respond to anti-PD-1 immunotherapy. It is urgently required for a clinical diagnosis to develop non-invasive imaging meditated strategy for assessing the expression level of PD-L1 in tumors. In this work, a <superscript>68</superscript> Ga-labeled single-domain antibody tracer, <superscript>68</superscript> Ga-NOTA-Nb109, was designed for specific and noninvasive imaging of PD-L1 expression in an MC38 tumor-bearing mouse model. Comprehensive studies including Positron Emission Tomography (PET), biodistribution, blocking studies, immunohistochemistry, and immunotherapy, have been performed in differences PD-L1 expression tumor-bearing models. These results revealed that <superscript>68</superscript> Ga-NOTA-Nb109 specifically accumulated in the MC38-hPD-L1 tumor. The content of this nanobody in MC38 hPD-L1 tumor and MC38 Mixed tumor was 8.2 ± 1.3, 7.3 ± 1.2, 3.7 ± 1.5, 2.3 ± 1.2%ID/g and 7.5 ± 1.4, 3.6 ± 1.7, 1.7 ± 0.6, 1.2 ± 0.5%ID/g at 0.5, 1, 1.5, 2 hours post-injection, respectively. <superscript>68</superscript> Ga-NOTA-Nb109 has the potential to further noninvasive PET imaging and therapy effectiveness assessments based on the PD-L1 status in tumors. To explore the possible synergistic effects of immunotherapy combined with chemotherapy, MC38 xenografts with different sensitivity to PD-L1 blockade were established. In addition, we found that PD-1 blockade also had efficacy on the PD-L1 knockout tumors. RT-PCR and immunofluorescence analysis were used to detect the expression of PD-L1. It was observed that both mouse and human PD-L1 expressed among three types of MC38 tumors. These results suggest that PD-L1 on tumor cells affect the efficacy, but it on host myeloid cells might be essential for checkpoint blockade. Moreover, anti-PD-1 treatment activates tumor-reactive CD103 <superscript>+</superscript> CD39 <superscript>+</superscript> CD8+T cells (TILs) in tumor microenvironment.
- Subjects :
- Animals
Antineoplastic Combined Chemotherapy Protocols therapeutic use
B7-H1 Antigen antagonists & inhibitors
B7-H1 Antigen genetics
B7-H1 Antigen metabolism
Cell Line, Tumor transplantation
Disease Models, Animal
Drug Resistance, Neoplasm drug effects
Drug Resistance, Neoplasm immunology
Drug Screening Assays, Antitumor
Female
Gallium Radioisotopes administration & dosage
Gallium Radioisotopes pharmacology
Gallium Radioisotopes therapeutic use
Gene Knockout Techniques
Humans
Mice
Mice, Transgenic
Neoplasms diagnosis
Neoplasms immunology
Positron-Emission Tomography methods
Prognosis
Programmed Cell Death 1 Receptor antagonists & inhibitors
Programmed Cell Death 1 Receptor genetics
Programmed Cell Death 1 Receptor metabolism
Single-Chain Antibodies therapeutic use
Tissue Distribution
Tumor Microenvironment drug effects
Tumor Microenvironment immunology
Antineoplastic Combined Chemotherapy Protocols pharmacology
B7-H1 Antigen analysis
Molecular Imaging methods
Neoplasms drug therapy
Single-Chain Antibodies pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1945-4589
- Volume :
- 13
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Aging
- Publication Type :
- Academic Journal
- Accession number :
- 33910164
- Full Text :
- https://doi.org/10.18632/aging.202981