% of Suppression a-TGFb (ug/ml) Tr/Tresp 1:1 1:4

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% of Suppression a-TGFb (ug/ml) 0 5 10 Tr/Tresp 1:1 1:4 0 5 10 Tr/Tresp 1:1 1:4 Figure S1: anti-TGFb cannot block the suppression function of CD8+ NKT-like cells. Freshly isolated C57BL/6 CD4+CD25- responder T cells were cultured in 96-well plates with anti-CD3 (1.5 ug/ml), irradiated splenic APCs (2000 rads), and different concentration of suppressive CD8+ NKT-like cells with or without indicated anti-TGFb antibody (5, 10 ug/ml) for 72 h. The cultures were pulsed with 0.5 Ci/ well [3H]thymidine for the last 16 h of 72h culture and the level of proliferation was assessed by the [3H]thymidine incorporation by scintillation counting after cell harvesting. The suppression effects value was then calculated according to the formula: % of suppression= (CPM value Tresp only -CPM value Tresp+Treg)/ CPM value Tresp only. Supplementary Fig. 1. anti-TGFb can not block the suppression function of CD8+ NKT cells. Freshly isolated C57BL/6 CD4+CD25- responder T cells were cultured in 96-well plates with anti-CD3 (1.5 ug/ml), irradiated splenic APCs (2000 rads), and different concentration of suppressive CD8+ NKT cells with or without indicated anti-TGFb antibody (5, 10 ug/ml) for 72 h. The cultures were pulsed with 0.5 Ci/ well [3H]thymidine for the last 16 h of 72h culture and the level of proliferation was assessed by the [3H]thymidine incorporation by scintillation counting after cell harvesting. The suppression effects value was then calculated according to the formula: % of suppression= (CPM value Tresp only -CPM value Tresp+Treg)/ CPM value Tresp only.

% of 7-AAD positive INFg (ng/ml) 0 10 50 Figure S2: INF-g restores the viability of in vitro cultured CD8+ NKT-like cells from INF-g-/- mouse. INF-g (10, 50ng/ml) was added to the CD8+ T cell culture (7th day culture) and cells were further kept in culture for 24h. At the end of the culture, cells were harvested and cell viability was determined by the positivity for 7-AAD staining measured by flow cytometry. Supplementary Fig. 2. INFg restore the viability of in vitro cultured CD8+ T cells from INFg -/- mouse. INFg (10, 50ng/ml) was added to the CD8+ NKT cell culture (7th day culture) and cells were continuely cultured for additionally 24h. At the end of the culture, cells were harvested and cells viability was determined by the positivity for 7-AAD staining measured by flow cytometry.