Id |
Subject |
Object |
Predicate |
Lexical cue |
S1 |
0-100 |
Sentence |
denotes |
The tumour associated cell surface antigen A6H is costimulatory for human CD4+ but not CD8+ T cells. |
S2 |
101-284 |
Sentence |
denotes |
The A6H monoclonal antibody (mAb) recognizes a 120,000-140,000 MW antigen that is expressed at similar densities on 85-90% of human CD4+ and CD8+ T cells and on renal cell carcinomas. |
S3 |
285-373 |
Sentence |
denotes |
The binding of the A6H mAb induced a costimulatory signal in anti-CD3 activated T cells. |
S4 |
374-495 |
Sentence |
denotes |
In the present report, we show that A6H costimulated cell proliferation and cytokine production in purified CD4+ T cells. |
S5 |
496-558 |
Sentence |
denotes |
Unexpectedly, the CD8+ T-cell subpopulation failed to respond. |
S6 |
559-783 |
Sentence |
denotes |
CD4+ T cells costimulated with the A6H mAb upregulated CD80, CD86, CD71, interleukin-2 (IL-2)R alpha, IL-2R beta and IL-2R gamma, while no corresponding up-regulation of these cell surface molecules was seen in CD8+ T cells. |
S7 |
784-1090 |
Sentence |
denotes |
In order to investigate the nature of the A6H mAb costimulus at the transcriptional level we have examined induction of the transcription factors OCT-1, AP-1 and NF-kappa B which are known to be transcriptional regulators of several cytokine and cytokine receptor genes, including the IL-2 and IL-2R genes. |
S8 |
1091-1340 |
Sentence |
denotes |
Co-ligation of the A6H antigen and the CD3 complex induced expression of the transcription factor AP-1 in CD4+ T cells, whereas no increase in NF-kappa B and octamer-binding (Oct) proteins was seen compared to T cells stimulated with anti-CD3 alone. |
S9 |
1341-1417 |
Sentence |
denotes |
Furthermore, no induction of AP-1 was seen in A6H costimulated CD8+ T cells. |
S10 |
1418-1553 |
Sentence |
denotes |
These results suggests that both proximal steps in CD8+ T-cell activation as well as the later phases are unresponsive to A6H ligation. |
S11 |
1554-1714 |
Sentence |
denotes |
Molecular differences of the A6H molecule or distinct regulation of the A6H transduced AP-1 activation pathway may exist in CD4+ and CD8+ T cell subpopulations. |