Inducible Nonlymphoid Expression of Fas Ligand Is Responsible for Superantigen-Induced Peripheral Deletion of T Cells
Fas (CD95) and Fas ligand (FasL) play major roles in staphylococcal enterotoxin B (SEB)–induced peripheral deletion of Vβ8 + T cells. We found that peripheral deletion was defective in radiation chimeras with nonfunctional tissue FasL, regardless of the FasL status of the bone marrow–derived cells....
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| Published in | Immunity (Cambridge, Mass.) Vol. 9; no. 5; pp. 711 - 720 |
|---|---|
| Main Authors | , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
Elsevier Inc
01.11.1998
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| Subjects | |
| Online Access | Get full text |
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| Abstract | Fas (CD95) and Fas ligand (FasL) play major roles in staphylococcal enterotoxin B (SEB)–induced peripheral deletion of Vβ8
+ T cells. We found that peripheral deletion was defective in radiation chimeras with nonfunctional tissue FasL, regardless of the FasL status of the bone marrow–derived cells. SEB induced a dramatic upregulation of FasL expression and function in nonlymphoid cells of liver and small intestine. This effect was resistant to inhibition by cyclosporin A, which also failed to inhibit peripheral deletion. In SCID animals nonlymphoid tissues did not express FasL in response to SEB unless transplanted lymphocytes were present. Thus, some immune responses induce FasL in nonlymphoid tissues, which in turn kills activated lymphocytes, leading to peripheral T cell deletion. |
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| AbstractList | Fas (CD95) and Fas ligand (FasL) play major roles in staphylococcal enterotoxin B (SEB)-induced peripheral deletion of Vbeta8+ T cells. We found that peripheral deletion was defective in radiation chimeras with non-functional tissue FasL, regardless of the FasL status of the bone marrow-derived cells. SEB induced a dramatic upregulation of FasL expression and function in nonlymphoid cells of liver and small intestine. This effect was resistant to inhibition by cyclosporin A, which also failed to inhibit peripheral deletion. In SCID animals nonlymphoid tissues did not express FasL in response to SEB unless transplanted lymphocytes were present. Thus, some immune responses induce FasL in nonlymphoid tissues, which in turn kills activated lymphocytes, leading to peripheral T cell deletion. Fas (CD95) and Fas ligand (FasL) play major roles in staphylococcal enterotoxin B (SEB)–induced peripheral deletion of Vβ8 + T cells. We found that peripheral deletion was defective in radiation chimeras with nonfunctional tissue FasL, regardless of the FasL status of the bone marrow–derived cells. SEB induced a dramatic upregulation of FasL expression and function in nonlymphoid cells of liver and small intestine. This effect was resistant to inhibition by cyclosporin A, which also failed to inhibit peripheral deletion. In SCID animals nonlymphoid tissues did not express FasL in response to SEB unless transplanted lymphocytes were present. Thus, some immune responses induce FasL in nonlymphoid tissues, which in turn kills activated lymphocytes, leading to peripheral T cell deletion. |
| Author | Lin, Tesu Nakajima, Hiroo Gao, Yakun Ferguson, Thomas A Griffith, Thomas S Green, Douglas R Bonfoco, Emanuela Brunner, Thomas Henkart, Pierre A Stuart, Patrick M |
| Author_xml | – sequence: 1 givenname: Emanuela surname: Bonfoco fullname: Bonfoco, Emanuela organization: Division of Cellular Immunology, La Jolla Institute for Allergy and Immunology, San Diego, California 92121, USA – sequence: 2 givenname: Patrick M surname: Stuart fullname: Stuart, Patrick M organization: Department of Ophthalmology, Washington University, St. Louis, Missouri 63110, USA – sequence: 3 givenname: Thomas surname: Brunner fullname: Brunner, Thomas organization: Institute for Pathology, University of Bern, 3010 Bern, Switzerland – sequence: 4 givenname: Tesu surname: Lin fullname: Lin, Tesu organization: Division of Cellular Immunology, La Jolla Institute for Allergy and Immunology, San Diego, California 92121, USA – sequence: 5 givenname: Thomas S surname: Griffith fullname: Griffith, Thomas S organization: Department of Ophthalmology, Washington University, St. Louis, Missouri 63110, USA – sequence: 6 givenname: Yakun surname: Gao fullname: Gao, Yakun organization: Department of Ophthalmology, Washington University, St. Louis, Missouri 63110, USA – sequence: 7 givenname: Hiroo surname: Nakajima fullname: Nakajima, Hiroo organization: Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA – sequence: 8 givenname: Pierre A surname: Henkart fullname: Henkart, Pierre A organization: Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA – sequence: 9 givenname: Thomas A surname: Ferguson fullname: Ferguson, Thomas A organization: Department of Ophthalmology, Washington University, St. Louis, Missouri 63110, USA – sequence: 10 givenname: Douglas R surname: Green fullname: Green, Douglas R email: dgreen5240@aol.com organization: Division of Cellular Immunology, La Jolla Institute for Allergy and Immunology, San Diego, California 92121, USA |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/9846492$$D View this record in MEDLINE/PubMed |
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| Snippet | Fas (CD95) and Fas ligand (FasL) play major roles in staphylococcal enterotoxin B (SEB)–induced peripheral deletion of Vβ8
+ T cells. We found that peripheral... Fas (CD95) and Fas ligand (FasL) play major roles in staphylococcal enterotoxin B (SEB)-induced peripheral deletion of Vbeta8+ T cells. We found that... |
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| SubjectTerms | AIDS/HIV Animals CD8-Positive T-Lymphocytes - cytology CD8-Positive T-Lymphocytes - drug effects CD8-Positive T-Lymphocytes - metabolism Cyclosporine - pharmacology Enterotoxins - pharmacology Fas Ligand Protein Immunosuppressive Agents - pharmacology In Situ Hybridization Intestine, Small - cytology Intestine, Small - metabolism Liver - cytology Liver - metabolism Lymphocyte Activation - drug effects Membrane Glycoproteins - biosynthesis Membrane Glycoproteins - immunology Mice Mice, Inbred C57BL Mice, Inbred Strains Mice, SCID Radiation Chimera - immunology Reverse Transcriptase Polymerase Chain Reaction Superantigens - immunology Superantigens - pharmacology |
| Title | Inducible Nonlymphoid Expression of Fas Ligand Is Responsible for Superantigen-Induced Peripheral Deletion of T Cells |
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