6533b85ffe1ef96bd12c2592
RESEARCH PRODUCT
CD1a and antitumour immune response
Giovanni ZummoGiampiero La RoccaRita AnzaloneFelicia FarinaFrancesco CappelloBucchieri Fabiosubject
Follicular dendritic cellsT-LymphocytesImmunologyAntigen presentationCD1Epithelial Cellshemic and immune systemschemical and pharmacologic phenomenaDendritic CellsCD1aBiologyAcquired immune systemNatural killer T cellAntigens CD1B-1 cellBarrett EsophagusNeoplasmsImmunologyCancer researchLymph node stromal cellHumansImmunology and AllergyAntigen-presenting celldescription
Primary immune response is based on the capacity of local professional antigen-presenting cells (whose prototype is represented by dendritic cells, DCs) to take up and present antigens to selected clones of T cells, but also to non-specific effector cells such as macrophages or natural killer cells. The four CD1 proteins, all of which share a limited homology to class I MHC proteins, are differently expressed in various cell types, of both mesenchymal and, as recently described, epithelial lineage. Regarding the role of CD1 molecules in the anti-tumour response, it has been reported that CD1+ dendritic cells are involved in the first steps of the primary immune response in a number of malignancies. Moreover, the presence of a high number of DCs in the tumoral or peritumoral area, as well as in the draining lymph nodes, has been shown to correlate with a better prognosis. A recent report on the presence of CD1a in metaplastic epithelial cells of Barrett esophagus introduced new questions about CD1a expression patterns. Moreover, the strong correlation between the lack of CD1a+ cells and the malignant evolution of the lesion may indicate a possible role of non-professional APCs in mediating and/or potentiating immune responses to tumours.
year | journal | country | edition | language |
---|---|---|---|---|
2004-03-22 | Immunology Letters |