Cao Ye, Wu Qian, Lian Shixian, Deng Li
Department of General Surgery, The Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Front Oncol. 2022 Mar 2;12:827596. doi: 10.3389/fonc.2022.827596. eCollection 2022.
Tumor-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.
We 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) 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.
The mean densities of tumor-infiltrating CD4, CD8, CD56 immune cells were 620.2, 261.2, and 0.2 cells/mm, respectively, in HIV-infected colorectal tumors compared with 698.6, 243, and 14 cells/mm in non-HIV-infected tumors. PD-1 expression was 227 cells/mm in HIV-infected tumors and 365.2 cells/mm in non-HIV-infected tumors. Besides, PD-L1 expression was 108.5 cells/mm in HIV-infected tumors and 126.8 cells/mm 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.
HIV-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.
肿瘤浸润淋巴细胞(TILs)以及程序性细胞死亡蛋白1(PD-1)/程序性死亡配体1(PD-L1)的表达对抗肿瘤免疫至关重要。然而,在HIV感染的结直肠癌(CRC)中其状态仍未明确,这限制了免疫疗法在HIV感染的CRC患者中的应用。
我们于2015年至2020年在上海公共卫生临床中心检查了27例HIV感染的CRC患者和120例非HIV感染的CRC患者。在匹配倾向得分后,还比较了两组中的13对配对患者。使用多重免疫荧光分析检测PD-1/PD-L1以及肿瘤浸润的CD4、CD8和CD56免疫细胞的表达。计算阳性染色的细胞密度(细胞/mm)并在HIV感染组和非HIV感染组之间进行比较。此外,比较了这两组中免疫细胞上PD-1与肿瘤细胞上PD-L1的共表达情况。
HIV感染的结直肠肿瘤中肿瘤浸润的CD4、CD8、CD56免疫细胞的平均密度分别为620.2、261.2和0.2细胞/mm,而非HIV感染的肿瘤中分别为698.6、243和14细胞/mm。HIV感染的肿瘤中PD-1表达为227细胞/mm,非HIV感染的肿瘤中为365.2细胞/mm。此外,HIV感染的肿瘤中PD-L1表达为108.5细胞/mm,非HIV感染的肿瘤中为126.