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PMID: 8758890 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

CD95-induced apoptosis of lymphocytes in an immune privileged site induces immunological tolerance.

Immunity ·Vol. 5 ·No. 1 ·1996-07-00 ·Pages 7-16

Griffith TS, Yu X, Herndon JM, Green DR, Ferguson TA

Abstract

We examined the relationship between cell death and tolerance induction following antigen injection into the anterior chamber of the eye. Our data show that when inflammatory cells undergo apoptosis following infection with HSV-1, tolerance to the virus was observed. In contrast, when cell death was absent due to defects in Fas or FasL, immune tolerance was not observed. Further studies revealed that cell death and tolerance required that the lymphoid cells be Fas+ and the eye be FasL+. Additionally, we show that while Fas/FasL-mediated apoptosis occurred in the eye, it was apoptotic cell death that was critical for tolerance induction. Our results further demonstrate immune privilege is not a passive process involving physical barriers, but is an active process that employs an important natural mechanism to induce cell death and immune tolerance.

MeSH Terms
Animals Apoptosis/genetics,immunology Bone Marrow Transplantation/immunology Eye/immunology Fas Ligand Protein Herpesvirus 1, Human/immunology Immune Tolerance/drug effects,genetics Ligands Lymphocytes/immunology Membrane Glycoproteins/deficiency,genetics Mice Mice, Inbred C57BL Mice, Mutant Strains Mice, Transgenic Radiation Chimera/immunology fas Receptor/genetics,pharmacology
Chemicals
FASLG protein, human Fas Ligand Protein Fasl protein, mouse Ligands Membrane Glycoproteins fas Receptor
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Griffith T S
Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Yu X
Herndon J M
Green D R
Ferguson T A
Article Info
Journal
Immunity
Abbr.
Immunity
ISSN
1074-7613
Published
1996-07-00
Pages
7-16
Language
English
Region
United States
NLM ID
9432918
Subset
IM
Grants
NEI NIH HHS · EY06374 · United States
NEI NIH HHS · EY06765 · United States
NIGMS NIH HHS · GM52735 · United States
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