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The influence of antibody CD166 on the treatment of tumor and the immunological mechanism in mice bearing oral squamous cell carcinoma

BACKGROUND: This study aimed to investigate the influence of antibody CD166 on the inhibition of tumor and further investigate the influence on immune cells of tumor tissues in mice bearing oral squamous cell carcinoma (OSCC). METHODS: The xenograft model was established through subcutaneously injec...

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Detalles Bibliográficos
Autores principales: Yu, Binbin, Li, Rui, Zhu, Xueqin, Chi, Zhengbing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174996/
https://www.ncbi.nlm.nih.gov/pubmed/37180656
http://dx.doi.org/10.21037/tcr-22-2704
Descripción
Sumario:BACKGROUND: This study aimed to investigate the influence of antibody CD166 on the inhibition of tumor and further investigate the influence on immune cells of tumor tissues in mice bearing oral squamous cell carcinoma (OSCC). METHODS: The xenograft model was established through subcutaneously injection of mouse OSCCs cells. Ten mice were randomly divided into two groups. The treatment group was treated with antibody CD166 and the control group was injected with the same volume normal saline. Hematoxylin and eosin (H&E) was used to confirm the tissue histopathology of xenograft mice model. Flow cytometry was used to detect the proportion of CD3(+)CD8(+) T cells, CD8(+)PD-1(+) cells and CD11b(+)Gr-1(+) myeloid-derived suppressor cells (MDSCs) cells in the tumor tissues. RESULTS: After treatment with antibody CD166, the tumor volume and weight in xenograft mice model were significantly reduced. The result of flow cytometry showed that antibody CD166 showed no obvious influence on the proportion of CD3(+)CD8(+) and CD8(+)PD-1(+) T lymphocyte cells in the tumor tissues. In the antibody CD166 treatment group, the proportion of CD11b(+)Gr-1(+) MDSCs cells in tumor tissues was 1.930%±0.5317%, which was significantly lower than that of the control group, 4.940%±0.3252% (P=0.0013). CONCLUSIONS: Antibody CD166 treatment helped reduce the proportion of CD11b(+)Gr-1(+) MDSCs cells, and produced obvious therapeutic effect on the treatment of mice bearing OSCC.