Diagnostic value of peripheral blood immune profiling in colorectal cancer

• Published in: Annals of surgical treatment and research Vol. 94; no. 6; pp. 312 - 321
• Main Authors: Choi, Joungbum, Maeng, Hyung Gun, Lee, Su Jin, Kim, Young Joo, Kim, Da Woon, Lee, Ha Na, Namgung, Ji Hyeon, Oh, Hyun-Mee, Kim, Tae Joo, Jeong, Ji Eun, Park, Sang Jean, Choi, Yong Man, Kang, Yong Won, Yoon, Seo Gue, Lee, Jong Kyun
• Format: Journal Article
• Language: English
• Published: Korea (South) 대한외과학회 01.06.2018; The Korean Surgical Society
• Subjects: Original; 일반외과학; Flow cytometry; Early diagnosis of cancer; Colorectal neoplasms; Blood cells
• ISSN: 2288-6575; 2288-6796
• DOI: 10.4174/astr.2018.94.6.312

Little is known about the clinical value of peripheral blood immune profiling. Here, we aimed to identify colorectal cancer (CRC)-related peripheral blood immune cells and develop liquid biopsy-based immune profiling models for CRC diagnosis. Peripheral blood from 131 preoperative patients with CRC and 174 healthy controls was analyzed by flow cytometry and automated hematology. CRC-related immune factors were identified by comparing the mean values of immune cell percentages and counts. Subsequently, CRC diagnostic algorithms were constructed using binary logistic regression. Significant differences were observed in percentages and counts of white blood cells, lymphocytes, neutrophils, regulatory T cells, and myeloid-derived suppressor cells (MDSCs) of patients and controls. The neutrophil/lymphocyte and Th1/Th2 ratios were also significantly different. Likewise, the percentages and counts of peripheral blood programed death 1, cytotoxic T lymphocyte antigen 4, B-and T-lymphocyte attenuator, and lymphocyte activation gene-3 were higher in patients with CRC. The binary logistic regression model included 12 variables, age, CD3 %, NK%, CD4 CD279 %, CD4 CD25 %, CD4 CD152 %, CD3 CD366 %, CD3 CD272 %, CD3 CD223 %, CD158b CD314 CD3 CD56 %, Th2%, and MDSCs cells/µL, for the prediction of cancer. Results of retrospective and prospective evaluation of the area under the curve, sensitivity, and specificity were 0.980 and 0.940, 91.53% and 85.80%, and 93.50% and 86.20%, respectively. Peripheral blood immune profiling may be valuable in evaluating the immunity of CRC patients. Our liquid biopsy-based immune diagnostic method and its algorithms may serve as a novel tool for CRC diagnosis. Future largescale studies are needed for better characterization of its diagnostic value and potential for clinical application.