Fig. 6.
Fig. 6. Assessment of telomere length in CD45RA+ and CD45RO+ EBV-specific CD8+ T cells. / CD8+, CD45RA+ and CD8+, CD45RO+ T cells were first isolated by magnetic bead depletion from PBMCs of healthy persons who recovered from AIM. These cells were then stained with EBV lytic epitope-specific tetramers coupled to Cy5 and the PNA telomeric probe coupled to FITC as described in “Materials and methods.” We gated on tetramer-positive populations, and the telomeric staining (median fluorescence intensity) of total CD8+CD45RA+, lytic epitope-specific CD8+ T cells that express CD45RA+ (Tet RA) or CD45RO+ (Tet RO) in 5 different persons who had recovered from AIM were investigated. Each person is represented by one symbol, and the telomere staining of the 3 different subsets for that subject is shown. The significance of the results was determined by the Student t test.

Assessment of telomere length in CD45RA+ and CD45RO+ EBV-specific CD8+ T cells.

CD8+, CD45RA+ and CD8+, CD45RO+ T cells were first isolated by magnetic bead depletion from PBMCs of healthy persons who recovered from AIM. These cells were then stained with EBV lytic epitope-specific tetramers coupled to Cy5 and the PNA telomeric probe coupled to FITC as described in “Materials and methods.” We gated on tetramer-positive populations, and the telomeric staining (median fluorescence intensity) of total CD8+CD45RA+, lytic epitope-specific CD8+ T cells that express CD45RA+ (Tet RA) or CD45RO+ (Tet RO) in 5 different persons who had recovered from AIM were investigated. Each person is represented by one symbol, and the telomere staining of the 3 different subsets for that subject is shown. The significance of the results was determined by the Student t test.

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