• NORIA OTHMAN RAFFALLA Department of Pathology, Faculty of Medicine, University of Omar Al-Mukhtar, Al Bayda, Libya.
  • SUZAN MOHAMED FAROUK HELAL Department of Pathology, Faculty of Medicine, University of Alexandria, Alexandria Governorate, Egypt.
  • AMANY ABD EL-BARY ABD EL-LATIF Department of Pathology, Faculty of Medicine, University of Alexandria, Alexandria Governorate, Egypt.
  • RASHA OMAR ELSAKA Department of Clinical Oncology and Nuclear Medicine, Faculty of Medicine, University of Alexandria, Alexandria Governorate, Egypt.


Objective: This study aimed to evaluate the immunohistochemical expression of forkhead boxP3 (Foxp3), CD8, CD68, and CD21 in stroma between tumor cells of colorectal cancer (CRC) patients and examines the relationship between these variables and clinicopathological parameter and patients’ prognosis.

Methods: In this work, 50 cases of colorectal carcinomas were included and immunohistochemical evaluation of Foxp3, CD8, CD68, and CD21 in tumor tissue samples.

Results: Tumor-infiltrating lymphocytes (TILs) including cytotoxic T cells and regulatory T cells as well as tumor-associated macrophages and follicular dendritic cells (FDCs) were studied in the stroma of the tumor using immunostaining technique for CD8, Foxp3, CD68, and CD21, respectively. Cases were followed up. CD8-positive cytotoxic T cells, Foxp3-positive regulatory T cells, and CD21 positive-FDCs were significantly more pronounced in early tumors and those with longer overall survival. On the other hand, CD68 positive macrophages were more encountered in late stage and metastatic tumors as well as tumors with shorter overall survival, but these results not reached the level of significance.

Conclusion: We concluded that (TILs) and FDCs are conferring better prognosis in CRCs, they may act synergistically in stimulating a protective immune response in the tumor microenvironment that hinders tumor progression, while the role of tumor-associated macrophages in CRCs is still controversial and needs further studies.

Keywords: Colorectal cancer, Lymphocyte subsets, Tumor-associated macrophage, Tertiary lymphoid structure, Survival


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