Expression of HLA-DR antigens in nasopharyngeal carcinoma: An immunohistological analysis of the tumour cells and infiltrating lymphocytes
✍ Scribed by J. Alero Thomas; Virginia Iliescu; Dorothy H. Crawford; Ridha Ellouz; Mohamed Cammoun; Guy De-Thé
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- French
- Weight
- 818 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0020-7136
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✦ Synopsis
Abstract
A panel of conventional and monoclonal antibodies was used to examine the immunohistological characteristics of malignant epithelial cells and infiltrating lymphocytes in frozen sections of nasopharyngeal carcinoma (NPC) biopsies from 10 Tunisian patients. Three main categories of cells were identified. (1) Tumour cells which were positive for Epstein‐Barr nuclear antigen, HLA‐ABC and keratin determinants. In most samples, the tumour cells also expressed variable amounts of HLA‐DR antigens. The presence of HLA‐DR antigens has not been previously reported in NPC and may be a contributory factor in effecting the transfer of Epstein‐Barr virus to the epithelial cells. (2) Infiltrating lymphocytes which were mainly composed of T inducer (T4^+^) and T suppressor/cytotoxic (T8^+^) cells although one sample contained predominantly immature T cells expressing the HTA‐1^+^ cortical thymocyte phenotype. Few B cells or natural killer cells were demonstrated. (3) Large HTA‐1^+^ dendritic cells which were invariably present within the tumour masses. These were morphologically and phenotypically similar to antigen presenting Langerhans cells which are usually located in the skin but also found in other epithelial sites. These cells may be a residual population from the normal nasopharynx or represent part of a specific immunological response to the presence of Epstein‐Barr virus in the epithelial cells.
📜 SIMILAR VOLUMES
Epstein-Barr Virus (EBV) is associated with two malignant diseases, African Burkitt's Lymphoma (BL) and Undifferentiated Nasopharyngeal Carcinoma (UNPC). North Africa is a geographical area with a high incidence of NPC. Our purpose in this study was to explore cell-mediated immunity of peripheral bl