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  1. General Info
  2. Effects Info
  3. Reference
Drug Interaction Details
01. General Information
Pair Name Vitamin C, Anti-PD-1 antibody
Phytochemical Name Vitamin C (PubChem CID: 54670067 )
Anticancer drug Name Anti-PD-1 antibody (PubChem CID: / )
Structure of
Phytochemical
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2D MOL 3D MOL
Structure of
Anticancer Drug
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2D MOL 3D MOL
02. Combinatorial Therapeutic Effect(s)
Synergistic Effect
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Enhancing Drug Efficacy
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Combination Pair ID: 534
Pair Name Vitamin C, Anti-PD-1 antibody
Disease Info [ICD-11: 2B33.5] Lymphoma Investigative
Biological Phenomena Inhibition-->Anti-PD1 checkpoint
Gene Regulation Up-regulation Expression GZMB hsa3002
Up-regulation Expression IL12B hsa3593
In Vitro Model A20 Reticulum cell sarcoma Mus musculus (Mouse) CVCL_1940
SU-DHL-6 Diffuse large B-cell lymphoma germinal center B-cell type Homo sapiens (Human) CVCL_2206
OCI-Ly1 Diffuse large B-cell lymphoma Homo sapiens (Human) CVCL_1879
OCI-Ly7 Diffuse large B-cell lymphoma germinal center B-cell type Homo sapiens (Human) CVCL_1881
OCI-Ly3 Diffuse large B-cell lymphoma activated B-cell type Homo sapiens (Human) CVCL_8800
In Vivo Model 40 BALB/c mice received a subcutaneous (s.c.) right flank injection of 5×10⁶ A20 tumor cells in phosphate-buffered saline (PBS) and were randomly assigned to 4 groups of 10 mice: vehicle, anti-PD1 (α-PD1), AA, and AA+α-PD1.
Result This study shows that AA treatment 1) increases immunogenicity of lymphoma cells; 2) enhances intratumoral infiltration of CD8+ T cells and macrophages; and 3) synergizes with anti-PD1 checkpoint inhibition in a syngeneic lymphoma mouse model via marked activation of cytotoxic cells (cytotoxic T cells and NK cells) and antigen presenting cells. The data provide a compelling rationale for testing combinations of high-dose AA and anti-PD1 agents in patients with aggressive B cell lymphoma and in preclinical models of other malignancies.
03. Reference
No. Title Href
1 High-dose ascorbic acid synergizes with anti-PD1 in a lymphoma mouse model. Proc Natl Acad Sci U S A. 2020 Jan 21;117(3):1666-1677. doi: 10.1073/pnas.1908158117. Click
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