Tumor-associated macrophages and CD3-ζ expression of tumor-infiltrating lymphocytes in human esophageal squamous-cell carcinoma


Address correspondence to: Shuren Zhang, Department of Immunology, Cancer Institute & Cancer Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, 17 Pan Jia Yuan Nan Li, Chao Yang District, Beijing 100021, China. Email: biotherapy@caca.sina.net


SUMMARY.  The clinical significance of tumor-associated macrophages (TAMs) and CD3-ζ chain expression of tumor-infiltrating lymphocytes (TILs), and their correlation in human esophageal squamous cell carcinoma (SCC) are not very clear. Serial histological slides from 137 esophageal SCC patients who had undergone tumor resection were immunohistochemically studied with anti-CD68, anti-CD3-ζ and anti-CD3-ɛ antibodies. TAMs infiltration (expressed as macrophage index, MI) and CD3-ζ expression (judged by Z/E = CD3-ζ+ cells/CD3-ɛ+ cells ratio) in different tissue compartments were observed. We found that the total tumor tissue region had significantly higher macrophage density and lower CD3-ζ expression (mean ± SD: MInormal: 225.3 ± 85.9; Z/Etotal: 0.52 ± 0.25; n = 137) relative to adjacent histologically normal esophageal squamous epithelium (MInormal: 60.5 ± 31.7, P < 0.001; Z/Enormal: 0.79 ± 0.35, P = 0.001; n = 70). Significantly higher MIstroma (P = 0.006) and lower Z/Etotal (P = 0.016) were detected in patients with lymph node metastasis than in those without. Patients with high MItotal and MIcancer but low Z/Etotal had poorer surgical outcomes. Univariate analysis of MItotal and multivariate analysis of MItotal with specific clinico-pathological parameters demonstrated MItotal to be an independent prognostic factor for survival in esophageal SCC patients (Cox proportional hazard model, P = 0.029 and P = 0.031, respectively).