Fig. 2. Flow cytometric Vβ repertoire analysis using Vβ mAb mixtures in mature T-cell proliferation patients. / (A) In healthy controls, 60% to 65% of CD3+ cells are recognized in double immunofluorescence stainings with 6 different Vβ mAbs mixtures in combination with CD3-PerCP.10 (B) Using comparable stainings in T-CLL patient 98-086, 99% of CD3+ cells are recognized by Vβ mAbs mix 1, whereas all other 5 mixes only recognize less than 1% of all CD3+cells. This indicates the presence of a large, presumably clonal CD3+ T-cell population with single Vβ expression. (C) Double immunofluorescence stainings with the 6 Vβ mAbs mixtures resulted in less than 5% CD3+/Vβ+ cells in T-CLL patient 98-002, suggesting the presence of a large, presumably clonal CD3+ T-cell population with single Vβ expression not recognized by any of the Vβ mAbs in the current panel.
Fig. 2.

Flow cytometric Vβ repertoire analysis using Vβ mAb mixtures in mature T-cell proliferation patients.

(A) In healthy controls, 60% to 65% of CD3+ cells are recognized in double immunofluorescence stainings with 6 different Vβ mAbs mixtures in combination with CD3-PerCP.10 (B) Using comparable stainings in T-CLL patient 98-086, 99% of CD3+ cells are recognized by Vβ mAbs mix 1, whereas all other 5 mixes only recognize less than 1% of all CD3+cells. This indicates the presence of a large, presumably clonal CD3+ T-cell population with single Vβ expression. (C) Double immunofluorescence stainings with the 6 Vβ mAbs mixtures resulted in less than 5% CD3+/Vβ+ cells in T-CLL patient 98-002, suggesting the presence of a large, presumably clonal CD3+ T-cell population with single Vβ expression not recognized by any of the Vβ mAbs in the current panel.

or Create an Account

Close Modal
Close Modal