書誌事項
- 公開日
- 1996-03
- 権利情報
-
- http://www.springer.com/tdm
- DOI
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- 10.1038/nm0396-317
- 公開者
- Springer Science and Business Media LLC
この論文をさがす
説明
The Fas ligand (FasL), a member of the tumor necrosis factor family, induces apoptosis in Fas-bearing cells. The membrane-bound human FasL was found to be converted to a soluble form (sFasL) by the action of a matrix metalloproteinase-like enzyme. Two neutralizing monoclonal anti-human FasL antibodies were identified, and an enzyme-linked immunosorbent assay (ELISA) for sFasL in human sera was established. Sera from healthy persons did not contain a detectable level of sFasL, whereas those from patients with large granular lymphocytic (LGL) leukemia and natural killer (NK) cell lymphoma did. These malignant cells constitutively expressed FasL, whereas peripheral NK cells from healthy persons expressed FasL only on activation. These results suggested that the systemic tissue damage seen in most patients with LGL leukemia and NK-type lymphoma is due to sFasL produced by these malignant cells. Neutralizing anti-FasL antibodies or matrix metalloproteinase inhibitors may be of use in modulating such tissue damage.
収録刊行物
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- Nature Medicine
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Nature Medicine 2 (3), 317-322, 1996-03
Springer Science and Business Media LLC
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キーワード
- Fas Ligand Protein
- Leukemia, T-Cell
- Lymphoma
- T-Lymphocytes
- Molecular Sequence Data
- Enzyme-Linked Immunosorbent Assay
- In Vitro Techniques
- Ligands
- Lymphocyte Activation
- Mice
- Transformation, Genetic
- Neutralization Tests
- Animals
- Humans
- DNA Primers
- Membrane Glycoproteins
- Base Sequence
- Antibodies, Monoclonal
- Metalloendopeptidases
- Killer Cells, Natural
- Solubility
詳細情報 詳細情報について
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- CRID
- 1364233268503096192
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- NII論文ID
- 80008840374
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- ISSN
- 1546170X
- 10788956
- https://id.crossref.org/issn/13403443
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- PubMed
- 8612231
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- データソース種別
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- Crossref
- CiNii Articles
- OpenAIRE

