| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
0-124 |
Sentence |
denotes |
Cellular and molecular mechanisms of IL-5 synthesis in atopic diseases: a study with allergen-specific human helper T cells. |
| T1 |
0-124 |
Sentence |
denotes |
Cellular and molecular mechanisms of IL-5 synthesis in atopic diseases: a study with allergen-specific human helper T cells. |
| T2 |
125-136 |
Sentence |
denotes |
BACKGROUND: |
| T2 |
125-136 |
Sentence |
denotes |
BACKGROUND: |
| T3 |
137-269 |
Sentence |
denotes |
Cytokines produced by helper T cells are intimately involved in chronic allergic diseases associated with eosinophilic inflammation. |
| T3 |
137-269 |
Sentence |
denotes |
Cytokines produced by helper T cells are intimately involved in chronic allergic diseases associated with eosinophilic inflammation. |
| T4 |
270-280 |
Sentence |
denotes |
OBJECTIVE: |
| T4 |
270-280 |
Sentence |
denotes |
OBJECTIVE: |
| T5 |
281-430 |
Sentence |
denotes |
We investigated the production of IL-5, a potent growth factor and chemotactic factor for eosinophils, by CD4+ T lymphocytes in patients with asthma. |
| T5 |
281-430 |
Sentence |
denotes |
We investigated the production of IL-5, a potent growth factor and chemotactic factor for eosinophils, by CD4+ T lymphocytes in patients with asthma. |
| T6 |
431-439 |
Sentence |
denotes |
METHODS: |
| T6 |
431-439 |
Sentence |
denotes |
METHODS: |
| T7 |
440-627 |
Sentence |
denotes |
Allergen-specific T cell clones and T cell hybridomas were established from the peripheral blood lymphocytes of patients with asthma, and the responses to various stimuli were determined. |
| T7 |
440-627 |
Sentence |
denotes |
Allergen-specific T cell clones and T cell hybridomas were established from the peripheral blood lymphocytes of patients with asthma, and the responses to various stimuli were determined. |
| T8 |
628-636 |
Sentence |
denotes |
RESULTS: |
| T8 |
628-636 |
Sentence |
denotes |
RESULTS: |
| T9 |
637-829 |
Sentence |
denotes |
After nonspecific stimulation, IL-5 production by CD4+ T cells from both atopic and nonatopic subjects with asthma was significantly enhanced compared with that by cells from healthy controls. |
| T9 |
637-829 |
Sentence |
denotes |
After nonspecific stimulation, IL-5 production by CD4+ T cells from both atopic and nonatopic subjects with asthma was significantly enhanced compared with that by cells from healthy controls. |
| T10 |
830-1075 |
Sentence |
denotes |
Peripheral blood mononuclear cells from atopic asthma patients both proliferated and produced IL-5 after incubation with mite allergen, suggesting that mite-specific helper T cells were involved in the eosinophilic inflammation of atopic asthma. |
| T10 |
830-1075 |
Sentence |
denotes |
Peripheral blood mononuclear cells from atopic asthma patients both proliferated and produced IL-5 after incubation with mite allergen, suggesting that mite-specific helper T cells were involved in the eosinophilic inflammation of atopic asthma. |
| T11 |
1076-1376 |
Sentence |
denotes |
A human IL-5 promoter/enhancer luciferase gene construct transfected into IL-5-producing T cell clones was clearly transcribed after stimulation, indicating that the 515 base pair IL-5 gene segment upstream of the coding region was sufficient to respond to activating signals in human helper T cells. |
| T11 |
1076-1376 |
Sentence |
denotes |
A human IL-5 promoter/enhancer luciferase gene construct transfected into IL-5-producing T cell clones was clearly transcribed after stimulation, indicating that the 515 base pair IL-5 gene segment upstream of the coding region was sufficient to respond to activating signals in human helper T cells. |
| T12 |
1377-1541 |
Sentence |
denotes |
The same gene segment was not transcribed in IL-5-nonproducing T cell clones, suggesting that human T cell IL-5 synthesis is regulated at the transcriptional level. |
| T12 |
1377-1541 |
Sentence |
denotes |
The same gene segment was not transcribed in IL-5-nonproducing T cell clones, suggesting that human T cell IL-5 synthesis is regulated at the transcriptional level. |
| T13 |
1542-1702 |
Sentence |
denotes |
Experiments with T cell hybridomas confirmed these findings and suggested that a unique transcription factor may be essential for human IL-5 gene transcription. |
| T13 |
1542-1702 |
Sentence |
denotes |
Experiments with T cell hybridomas confirmed these findings and suggested that a unique transcription factor may be essential for human IL-5 gene transcription. |
| T14 |
1703-1714 |
Sentence |
denotes |
CONCLUSION: |
| T14 |
1703-1714 |
Sentence |
denotes |
CONCLUSION: |
| T15 |
1715-1839 |
Sentence |
denotes |
Enhanced IL-5 production by helper T cells seems to cause the eosinophilic inflammation of both atopic and nonatopic asthma. |
| T15 |
1715-1839 |
Sentence |
denotes |
Enhanced IL-5 production by helper T cells seems to cause the eosinophilic inflammation of both atopic and nonatopic asthma. |
| T16 |
1840-2006 |
Sentence |
denotes |
Elucidation of IL-5-specific regulatory mechanisms may facilitate the development of novel treatments for allergic diseases associated with eosinophilic inflammation. |
| T16 |
1840-2006 |
Sentence |
denotes |
Elucidation of IL-5-specific regulatory mechanisms may facilitate the development of novel treatments for allergic diseases associated with eosinophilic inflammation. |