Table 2.

Expression of bcl-2 and bcl-xL in clonal Th2 cells

CellsAgent addedBcl-xLBcl-2
024 h024 h
CD4+CD45RO+(controls) — 83 021 ± 6427 71 524 ± 4752 64 986 ± 5483 58 933 ± 4982 
CD3CD4+ (patient 2) — 85 432 ± 5561 — 26 048 ± 6843* — 
CD3CD4+ (patient 1) — 96 953 ± 11704 58 644 ± 10128 29 839 ± 5290* 19 973 ± 2213 
 +IFN-α (104IU/mL) — 62 563 ± 13723 — 19 911 ± 2555 
 +IL-2 (100 IU/mL) — 66 238 ± 22834 — 23 647 ± 3371 
CellsAgent addedBcl-xLBcl-2
024 h024 h
CD4+CD45RO+(controls) — 83 021 ± 6427 71 524 ± 4752 64 986 ± 5483 58 933 ± 4982 
CD3CD4+ (patient 2) — 85 432 ± 5561 — 26 048 ± 6843* — 
CD3CD4+ (patient 1) — 96 953 ± 11704 58 644 ± 10128 29 839 ± 5290* 19 973 ± 2213 
 +IFN-α (104IU/mL) — 62 563 ± 13723 — 19 911 ± 2555 
 +IL-2 (100 IU/mL) — 66 238 ± 22834 — 23 647 ± 3371 

Intracytoplasmic bcl-xL and bcl-2 staining was performed on purified CD3+CD4+CD45RO+ cells from healthy individuals (n = 6) and CD3CD4+ from hypereosinophilic patients (for each patient 6 determinations were performed). For patient 1, bcl-xL and bcl-2 levels were compared with those obtained after 24 hours of incubation in the absence or presence of IFN-α (104 IU/mL) or IL-2 (100 IU/mL). Results shown are the mean ± SD of bcl-xL and bcl-2 staining within live FSChigh/SSClow cells expressed in MESF.

*

P < .05 as compared with CD4+CD45RO+ cells from healthy individuals.

P < .05 as compared with bcl-2 expression obtained in absence of IL-2 (ANOVA test).

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