PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 34144673-0 2021 Cisplatin-based chemoradiation decreases telomerase-specific CD4 TH1 response but increases immune suppressive cells in peripheral blood. Cisplatin 0-9 CD4 molecule Homo sapiens 61-64 19020751-8 2008 Two CDDP-resistant pancreatic cancer cell line SUIT-2 variants, SUIT-2-CD3 and SUIT-2-CD4, were established by continuously administering 10 nM CDDP to SUIT-2 cell lines for 3 and 4 months, respectively. Cisplatin 4-8 CD4 molecule Homo sapiens 79-89 35526096-8 2022 The immune profiling analysis of peripheral blood reveals an increased abundance of LAG-3hiPD-1hi memory CD4+T cell subset in relapsed cholangiocarcinoma patients after gemcitabine plus cisplatin therapy, which are more responsive to ABL501. Cisplatin 186-195 CD4 molecule Homo sapiens 105-108 35433455-14 2022 CellMinor analysis showed that the CD4 mRNA expression level dramatically climbed with increased sensitivity of tumor cells to NAC drugs such as cyclophosphamide, cisplatin, and carboplatin (p"s < 0.05). Cisplatin 163-172 CD4 molecule Homo sapiens 35-38 32878426-10 2021 The density of tumor margin-infiltrating FoxP3- CD4+ helper T cells may be associated with clinical outcomes in BTC patients treated with gemcitabine plus cisplatin. Cisplatin 155-164 CD4 molecule Homo sapiens 48-51 30952714-10 2019 Furthermore, anti-PD-L1 alone and in combination with cisplatin, but not cisplatin alone, induced interferon-gamma-producing CD4+ T-cells. Cisplatin 54-63 CD4 molecule Homo sapiens 125-128 32957741-0 2020 Anti-Telomerase CD4+ Th1 Immunity and Monocytic-Myeloid-Derived-Suppressor Cells Are Associated with Long-Term Efficacy Achieved by Docetaxel, Cisplatin, and 5-Fluorouracil (DCF) in Advanced Anal Squamous Cell Carcinoma: Translational Study of Epitopes-HPV01 and 02 Trials. Cisplatin 143-152 CD4 molecule Homo sapiens 16-19 28251947-0 2017 [Cisplatin-induced apoptotic endonuclease EndoG inhibits telomerase activity and causes malignant transformation of human CD4+ T lymphocytes]. Cisplatin 1-10 CD4 molecule Homo sapiens 122-125 28251947-5 2017 The aim of this study was to determine the ability of a DNA-damaging compound, cisplatin, to induce EndoG and its influence on alternative splicing of hTERT and telomerase activity in human CD4+ T lymphocytes. Cisplatin 79-88 CD4 molecule Homo sapiens 190-193 25531529-8 2014 Treatment with cisplatin, CpG and PADRE also enhanced the generation of PADRE-specific CD4+ T cells and E7-specific CD8+ T cells and decreased the number of MDSCs in tumor loci. Cisplatin 15-24 CD4 molecule Homo sapiens 87-90 25659373-1 2015 OBJECTIVE: To investigate the effect of gemcitabine plus cisplatin chemotherapy on the percentage of CD4(+)CD25(+)FOXP3(+) and CD8(+)CD28(-) regulatory T cells (Tregs) in the peripheral blood of patients with nonsmall-cell lung cancer (NSCLC). Cisplatin 57-66 CD4 molecule Homo sapiens 101-104 25659373-7 2015 Percentages of CD4(+)CD25(+)FOXP3(+) and CD8(+)CD28(-) Tregs were significantly reduced following gemcitabine plus cisplatin chemotherapy. Cisplatin 115-124 CD4 molecule Homo sapiens 15-18 21822560-8 2012 CONCLUSION: Neoadjuvant chemotherapy utilizing 5-fluorouracil and cisplatin in esophageal squamous cell carcinoma is useful to induce CD4 and CD8 T lymphocytes in the tumor microenvironment and to maintain HLA class I expression levels in combination with its direct cytotoxic effects. Cisplatin 66-75 CD4 molecule Homo sapiens 134-137 23600838-5 2013 Surprisingly, when the functional consequence of chemotherapy-treated CD14(+) monocytes and their capacity to activate CD4(+) T responders cells were investigated, cisplatin-treated monocytes gave rise to increased T cell proliferation. Cisplatin 164-173 CD4 molecule Homo sapiens 119-122 21949094-6 2011 In contrast, administration of recombinant IL-33 (rIL-33) exacerbated cisplatin-induced AKI, measured by an increase in CD4 T cell infiltration, serum creatinine, ATN, and apoptosis; this did not occur in CD4-deficient mice, suggesting that CD4 T cells mediate the injurious effect of IL-33. Cisplatin 70-79 CD4 molecule Homo sapiens 120-123 21949094-6 2011 In contrast, administration of recombinant IL-33 (rIL-33) exacerbated cisplatin-induced AKI, measured by an increase in CD4 T cell infiltration, serum creatinine, ATN, and apoptosis; this did not occur in CD4-deficient mice, suggesting that CD4 T cells mediate the injurious effect of IL-33. Cisplatin 70-79 CD4 molecule Homo sapiens 205-208