4.6 Article

Lymphocytes Infiltration and Expression of PD-1 and PD-L1 in Colorectal Cancer Between HIV-Infected and Non-HIV-Infected Patients: A Propensity Score Matched Cohort Study

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FRONTIERS IN ONCOLOGY
卷 12, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2022.827596

关键词

HIV; colorectal cancer; tumor-infiltrating lymphocytes; PD-1; PD-L1; multiplex immuno-fluorescent analysis

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  1. clinical research program of Shanghai Public Health Clinical Center [KY-GW-2021-20]

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Tumor-infiltrating lymphocytes (TILs) and programmed cell death 1 (PD-1)/programmed death ligand-1 (PD-L1) expression were examined in HIV-infected colorectal cancer (CRC) patients. The study found that HIV-infected CRC patients had similar TILs and similar PD-1 expression on TILs and PD-L1 expression on tumors compared to non-HIV-infected patients. These results suggest that HIV-infected CRC patients can be included in future immunotherapy trials.
BackgroundTumor-infiltrating lymphocytes (TILs) and expression of programmed cell death 1 (PD-1)/programmed death ligand-1 (PD-L1) are crucial for antitumor immunity. However, the status remains undetermined in HIV-infected colorectal cancer (CRC), limiting the use of immunotherapy in HIV-infected CRC patients. MethodsWe examined 27 HIV-infected patients and 120 non-HIV-infected patients with CRC from 2015-2020 at Shanghai Public Health Clinical Center. After matching the propensity score, 13 paired patients in the two groups were also compared. The expression of PD-1/PD-L1 as well as tumor-infiltrating CD4, CD8, and CD56 immune cells was examined using multiplex immunofluorescent analysis. The cell density for positive staining was calculated (cells/mm(2)) and compared between HIV-infected and non-HIV-infected groups. In addition, the co-expression of PD-1 on immune cells and PD-L1 on tumor cells was compared in these two groups. ResultsThe mean densities of tumor-infiltrating CD4, CD8, CD56 immune cells were 620.2, 261.2, and 0.2 cells/mm(2), respectively, in HIV-infected colorectal tumors compared with 698.6, 243, and 14 cells/mm(2) in non-HIV-infected tumors. PD-1 expression was 227 cells/mm(2) in HIV-infected tumors and 365.2 cells/mm(2) in non-HIV-infected tumors. Besides, PD-L1 expression was 108.5 cells/mm(2) in HIV-infected tumors and 126.8 cells/mm(2) in non-HIV-infected tumors, and no significant difference was found between the two groups. Similarly, there were no significant differences in the expression of PD-1 on TILs and PD-L1 on tumor cells. ConclusionHIV-infected CRC patients had similar tumor-infiltrating lymphocytes (CD4 and CD8 T cells) compared to non-HIV-infected controls and substantially similar PD-1 expression on TILs and PD-L1 expression on tumors. These results support the inclusion of HIV-infected CRC patients in future immunotherapy trials.

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