Structure and regulation of the Blast-2/CD23 antigen in epithelial cells from nasopharyngeal carcinoma
Autor: | Hiro Wakasugi, Gilbert M. Lenoir, Germain Rousselet, Thomas Tursz, Christine Scamps, Jean-Michel Guillon, Marc Billaud, Philippe Busson |
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Předmět: |
Oncology
medicine.medical_specialty Immunology Tumor cells Receptors Fc Biology Epithelium Virus Pathogenesis Interferon-gamma Mice Lymphocytes Tumor-Infiltrating Antigen Antigens CD In vivo hemic and lymphatic diseases Internal medicine otorhinolaryngologic diseases medicine Animals Humans Immunology and Allergy RNA Messenger Receptors IgE Tumor-infiltrating lymphocytes Carcinoma CD23 Antibodies Monoclonal Nasopharyngeal Neoplasms hemic and immune systems General Medicine medicine.disease Recombinant Proteins Antigens Differentiation B-Lymphocyte stomatognathic diseases Nasopharyngeal carcinoma Cancer research Interleukin-4 |
Zdroj: | Scopus-Elsevier Europe PubMed Central |
Popis: | Undifferentiated nasopharyngeal carcinoma (NPC) is tightly associated with the Epstein-Barr virus (EBV) and very heavily infiltrated with T lymphocytes. We demonstrated recently that NPC epithelial cells produce immuno-regulatory molecules, including the Blast-2/CD23 antigen, which is induced in B lymphocytes upon infection by EBV. We demonstrate here that CD23 expression is a non-constant but highly specific feature of epithelial cells from NPC. The C15 and C17 NPC tumor cells express mainly the b form of CD23, which is known to be non-lineage-specific and IL-4-inducible. C17 cells were found also to weakly express the a form of CD23, which has been described as B cell-specific. In addition, several factors potentially released in vivo by tumor infiltrating lymphocytes (TILs) are able to regulate CD23 expression in NPC cells. In particular, we found that IL-4 was a potent inducer of CD23 expression in C15 cells, as shown at both the protein and the mRNA levels. These results, together with the already reported expression of class II MHC antigens and the release of IL-1 by NPC cells, suggest that the interactions between TILs and malignant cells are a key factor in NPC pathogenesis and development. |
Databáze: | OpenAIRE |
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