Fig. 9.
Fig. 9. Expression of the CD8αα homodimer, CD57, and perforin on CD8dull subsets. (Left panels) Shown are the percentages of cells in either the CD8dullCD4+, CD8dullCD4−, or the CD8bright subsets that express CD8αα homodimers or CD57. Subjects had been treated for HD 3 to 25 years before analysis. Four had elevated levels (<19/μL) of the CD8dullCD4+ cells; three had elevated levels (<61/μL) of the CD8dullCD4−cells; two of these subjects had elevated levels of both subsets. The gray box indicates the median and interquartile range for the expression of CD57 on CD8bright cells in a group of 19 healthy controls. The gray bars below and above this box are the 10th and 90th percentiles of the distribution. (Right panels). T cells from two healthy individuals who have enough CD4+CD8dull (top plots) or CD4−CD8dull (bottom) were stained for intracellular perforin in addition to the immunophenotyping stains. The CD8dull populations exhibit a high degree of perforin, including the CD57− cells within the CD4−CD8dull population. These data suggest that the CD8dull cells may have cytotoxic function in the body. The perforin expressing (CD57+) CD4+ T cells in the CD8− fraction were entirely negative for CD8, ie, they are not contaminating cells from the CD8dull fraction and represent yet another phenotypically distinct subset of cells.

Expression of the CD8αα homodimer, CD57, and perforin on CD8dull subsets. (Left panels) Shown are the percentages of cells in either the CD8dullCD4+, CD8dullCD4, or the CD8bright subsets that express CD8αα homodimers or CD57. Subjects had been treated for HD 3 to 25 years before analysis. Four had elevated levels (<19/μL) of the CD8dullCD4+ cells; three had elevated levels (<61/μL) of the CD8dullCD4cells; two of these subjects had elevated levels of both subsets. The gray box indicates the median and interquartile range for the expression of CD57 on CD8bright cells in a group of 19 healthy controls. The gray bars below and above this box are the 10th and 90th percentiles of the distribution. (Right panels). T cells from two healthy individuals who have enough CD4+CD8dull (top plots) or CD4CD8dull (bottom) were stained for intracellular perforin in addition to the immunophenotyping stains. The CD8dull populations exhibit a high degree of perforin, including the CD57 cells within the CD4CD8dull population. These data suggest that the CD8dull cells may have cytotoxic function in the body. The perforin expressing (CD57+) CD4+ T cells in the CD8 fraction were entirely negative for CD8, ie, they are not contaminating cells from the CD8dull fraction and represent yet another phenotypically distinct subset of cells.

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