TABLE 6.
T-cell line | Results obtained in the presence of:
|
|||||
---|---|---|---|---|---|---|
MIM
|
HKM
|
rAg85B
|
||||
SI | IFN-γ level | SI | IFN-γ level | SI | IFN-γ level | |
N-85B.149 | 5.0 | <5 | 2.0 | 71 | 2.0 | <5 |
T-85B.149 | 3.2 | 40 | 2.0 | 223 | 2.1 | 92 |
N-85B.159 | 1.0 | 62 | ND | ND | 3.8 | 240 |
T-85B.159 | 2.0 | 190 | ND | ND | 4.6 | 641 |
N-85B.173 | ND | 43 | ND | 61 | ND | <5 |
T-85B.173 | ND | 864 | ND | 3,106 | ND | 336 |
N-85B.186 | 10.0 | <5 | 10.7 | <5 | 4.5 | 12 |
T-85B.186 | 6.8 | <5 | 10.4 | 31 | 15 | 107 |
N-85B.187 | 10.7 | 5 | 3.6 | <5 | 6.6 | <5 |
T-85B.187 | 3.8 | 594 | 1.5 | 260 | 2.7 | 734 |
N-85B.191 | 4.2 | <5 | 2.3 | <5 | 2.4 | <5 |
T-85B.191 | 3.3 | 50 | 2.3 | 36 | 2.3 | 48 |
Resting cells from rAg85B-specific T-cell lines were stimulated in vitro with MIM (20:1) or HKM (15 μg/ml)- or rAg85B (10 μg/ml)-pulsed normal macrophages for 3 days. Supernatants were harvested and tested for the IFN-γ concentration (picograms per milliliter) by an ELISA. Proliferation was assessed by measuring 3H-thymidine incorporation. ND, not determined. T-cell lines designated with “N” were generated by immunization of normal PBMC with rAg85B. T-cell lines designated with “T” were generated by immunization of normal PBMC with rAg85B plus IL-12 (1 ng/ml).