TABLE 7.
Target | Peptide | Amt of GM-CSF produced (pg/ml/48 h) by T cells from patient in indicated expt
|
|||||
---|---|---|---|---|---|---|---|
7
|
13
|
14
|
|||||
A | B | A | B | A | B | ||
T2 cells pulsed with: | |||||||
Medium alone | 0 | 0 | 0 | 0 | 0 | 0 | |
HPV16 E7 | YMLDLQPET | 37 | 43 | 51 | 12 | 27 | 30 |
Human DNA clone 342 | YMLILHPET | 10 | 7 | 0 | 0 | 13 | 0 |
Coronavirus NS2 | TMLDIOPED | 139 | 50 | 11 | 5 | 123 | NDb |
gp100 (control) | YLEPGPVTA | 0 | 0 | 0 | 0 | 0 | 0 |
YMLDLQPET tetramer-reactive T cells from PBL from patient 7 with CIN (Table 5) or patients 13 and 14 with invasive cervical cancer (Table 6) were isolated as described in detail in Materials and Methods. The patient designation corresponds to the numbering in Tables 5 and 6. Two independent experiments (this table and Table 8) have been performed. HPV16 E7-isolated T cells recognize the nominal T-cell epitope as well as the peptide derived from the coronavirus NS2 gene product. T2 cells alone, or those pulsed with a self peptide, or a non-HPV-related (melanoma-associated peptide, i.e., gp 100) peptide, were not recognized. T cells responded with GM-CSF production but not with IFN-γ production. Due to the low number of tetramer-sorted T cells, blocking experiments using the anti-MHC-I-specific MAb W6/32 could not be performed. A and B indicate two independent experiments.
ND, not determined.