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Killing capacity analysis of tumor-infiltrating cytotoxic lymphocytes and impact on lymph node metastasis in differentiated papillary carcinoma of thyroid with the BRAF V600E mutation.
Liu, Xiaogang; Liu, Honggang; Wang, Lu; Han, Yubing; Kong, Linghong; Zhang, Xinpeng.
Affiliation
  • Liu X; Department of Pathology, Beijing Tongren Hospital, Beijing Key Laboratory of Head and Neck Molecular Diagnostic Pathology, Capital Medical University, Beijing, 100730, China.
  • Liu H; Department of Pathology, Beijing Chuiyangliu Hospital, Beijing, 100022, China.
  • Wang L; Department of Pathology, Beijing Tongren Hospital, Beijing Key Laboratory of Head and Neck Molecular Diagnostic Pathology, Capital Medical University, Beijing, 100730, China. liuhonggang@ccmu.edu.cn.
  • Han Y; Department of Pathology, Beijing Chuiyangliu Hospital, Beijing, 100022, China.
  • Kong L; Department of Pathology, Beijing Chuiyangliu Hospital, Beijing, 100022, China.
  • Zhang X; Department of Pathology, Beijing Chuiyangliu Hospital, Beijing, 100022, China.
Diagn Pathol ; 19(1): 29, 2024 Feb 10.
Article in En | MEDLINE | ID: mdl-38341587
ABSTRACT

BACKGROUND:

Cytotoxic lymphocytes (CLs) express potent toxins, including perforin (P) and granzyme-B (G), which brings about target cell death. The purpose of this study was to evaluate the killing capacity of tumor-infiltrating CLs by means of P and G analysis, and explore the association with lymph node metastasis in papillary carcinoma of thyroid (PTC) without Hashimoto's thyroiditis (HT).

METHODS:

Infiltration of lymphocytes in PTC was observed in frozen sections. Both fresh tumor tissues and paracancerous tissues with lymphocyte infiltration were collected and prepared into a single cell suspension. Flow cytometry was used to detect the percentages of CD3+P+, CD3+G+, CD8+P+, and CD8+G+ T lymphocytes (TLs) and CD16-CD56+P+ and CD16-CD56+G+ natural killer (NK) cells. Finally, we investigated differential expression of P and G in NK cells and cytotoxic T lymphocytes (CTLs) in paired tumor tissues (group T, n = 44) and paracancerous tissues (group N, n = 44) from patients with PTC with the BRAF V600E mutation. Furthermore, patients were divided into two groups according to whether cervical central lymph node metastasis (CCLNM) existed group A (with lymph node metastases, n = 27) and group B (with nonlymph node metastases, n = 17). Patients were also divided into three groups according to the total number of positive CCLNM group B, group C (with low-level lymph node metastases, less than 5, n = 17) and group D (with high-level lymph node metastases, no less than 5, n = 10).

RESULTS:

The percentage of CD3+P+ CTLs was significantly higher in group N than in group T (P < 0.05). The percentage of CD8+G+ CTLs was significantly higher in group T than in group N (P < 0.05). The percentages of CD3+G+, CD16-CD56+P+and CD16-CD56+G+ NK cells showed no significant difference in either group T or group N (P > 0.05). The percentages of CD3+P+ CTLs in group A and group C were significantly higher in the paracancerous tissue than in the tumor tissue (P < 0.05). The percentages of CD8+G+ CTLs in group A and group C were significantly higher in the tumor tissues than in the paracancerous tissues (P < 0.05). The percentage of CD16-CD56+G+ NK cells in group D was significantly higher in the tumor tissues than in the paracancerous tissues (P < 0.05).

CONCLUSIONS:

The killing capacity of infiltrating CLs in PTC differed between tumor tissues and paracancerous tissues. In cases with CCLNM, higher expression of CD16-CD56+G+ NK cells in tumor tissues may be associated with a high risk of lymph node metastasis.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thyroid Neoplasms / Proto-Oncogene Proteins B-raf Limits: Humans Language: En Journal: Diagn Pathol / Diagn. pathol / Diagnostic pathology (Online) Journal subject: PATOLOGIA Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thyroid Neoplasms / Proto-Oncogene Proteins B-raf Limits: Humans Language: En Journal: Diagn Pathol / Diagn. pathol / Diagnostic pathology (Online) Journal subject: PATOLOGIA Year: 2024 Document type: Article Affiliation country: Country of publication: