The American journal of pathology · 1992
Application of a multiprobe RNase protection assay and junctional sequences to define V beta gene diversity in Sezary syndrome.
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Kono D H, Baccala R, Balderas R S, Kovac S J, Heald P W, Edelson R L, Theofilopoulos A N
Аннотация
Nineteen patients with mycosis fungoides/Sezary syndrome (MF/SZ), a malignancy of the mature helper T-cell phenotype (CD4+TCR alpha beta+), were screened for clonotypic V beta expansions in peripheral blood with a multiprobe RNase protection assay. A different predominant V beta gene was identified in 9 of 14 patients with high peripheral blood CD4/CD8 ratios, whereas 4 of these patients showed T-cell expansions expressing V beta genes other than those included in the assay. In contrast, five patients with few, if any, malignant cells in the circulation had V beta expression levels similar to that in normal peripheral blood. A unique V-D-J sequence was found for each highly expressed V beta gene, thereby documenting monoclonality of the expanded T-cell populations. Polymerase chain reaction (PCR) primers specific for the D-J beta junction accurately identified the corresponding malignant clonotype in peripheral blood. The diverse TCR V beta gene usage found in these MF/SZ patients suggests that T-cell receptor (TCR) specificity has no bearing on this disease.
Предметные рубрики MeSH
AdultAgedAged, 80 and overBase SequenceCloning, MolecularFemaleGene Expression Regulation, NeoplasticGenetic TechniquesGenetic VariationHumansMaleMiddle AgedMolecular Sequence DataMycosis FungoidesOligonucleotide ProbesPolymerase Chain ReactionReceptors, Antigen, T-CellRibonucleasesSezary SyndromeSkin Neoplasms