| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-119 |
Sentence |
denotes |
A long, naturally presented immunodominant epitope from NY-ESO-1 tumor antigen: implications for cancer vaccine design. |
| T1 |
0-119 |
Sentence |
denotes |
A long, naturally presented immunodominant epitope from NY-ESO-1 tumor antigen: implications for cancer vaccine design. |
| TextSentencer_T2 |
120-184 |
Sentence |
denotes |
The tumor antigen NY-ESO-1 is a promising cancer vaccine target. |
| T2 |
120-184 |
Sentence |
denotes |
The tumor antigen NY-ESO-1 is a promising cancer vaccine target. |
| TextSentencer_T3 |
185-341 |
Sentence |
denotes |
We describe here a novel HLA-B7-restricted NY-ESO-1 epitope, encompassing amino acids 60-72 (APRGPHGGAASGL), which is naturally presented by melanoma cells. |
| T3 |
185-341 |
Sentence |
denotes |
We describe here a novel HLA-B7-restricted NY-ESO-1 epitope, encompassing amino acids 60-72 (APRGPHGGAASGL), which is naturally presented by melanoma cells. |
| TextSentencer_T4 |
342-426 |
Sentence |
denotes |
The tumor epitope bound to HLA-B7 by bulging outward from the peptide-binding cleft. |
| T4 |
342-426 |
Sentence |
denotes |
The tumor epitope bound to HLA-B7 by bulging outward from the peptide-binding cleft. |
| TextSentencer_T5 |
427-648 |
Sentence |
denotes |
This bulged epitope was not an impediment to T-cell recognition, however, because four of six HLA-B7(+) melanoma patients vaccinated with NY-ESO-1 ISCOMATRIX vaccine generated a potent T-cell response to this determinant. |
| T5 |
427-648 |
Sentence |
denotes |
This bulged epitope was not an impediment to T-cell recognition, however, because four of six HLA-B7(+) melanoma patients vaccinated with NY-ESO-1 ISCOMATRIX vaccine generated a potent T-cell response to this determinant. |
| TextSentencer_T6 |
649-872 |
Sentence |
denotes |
Moreover, the response to this epitope was immunodominant in three of these patients and, unlike the T-cell responses to bulged HLA class I viral epitopes, the responding T cells possessed a remarkably broad TCR repertoire. |
| T6 |
649-872 |
Sentence |
denotes |
Moreover, the response to this epitope was immunodominant in three of these patients and, unlike the T-cell responses to bulged HLA class I viral epitopes, the responding T cells possessed a remarkably broad TCR repertoire. |
| TextSentencer_T7 |
873-1162 |
Sentence |
denotes |
Interestingly, HLA-B7(+) melanoma patients who did not receive the NY-ESO-1 ISCOMATRIX vaccine rarely generated a spontaneous T-cell response to this cryptic epitope, suggesting a lack of priming of such T cells in the natural anti-NY-ESO-1 response, which may be corrected by vaccination. |
| T7 |
873-1162 |
Sentence |
denotes |
Interestingly, HLA-B7(+) melanoma patients who did not receive the NY-ESO-1 ISCOMATRIX vaccine rarely generated a spontaneous T-cell response to this cryptic epitope, suggesting a lack of priming of such T cells in the natural anti-NY-ESO-1 response, which may be corrected by vaccination. |
| TextSentencer_T8 |
1163-1289 |
Sentence |
denotes |
Together, our results reveal several surprising aspects of antitumor immunity and have implications for cancer vaccine design. |
| T8 |
1163-1289 |
Sentence |
denotes |
Together, our results reveal several surprising aspects of antitumor immunity and have implications for cancer vaccine design. |