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Feline Immunodeficiency Virus Infection Is Characterized by B7<sup>+</sup>CTLA4<sup>+</sup>T Cell Apoptosis
52
Citations
52
References
2002
Year
Cd4+ CellsImmunodeficienciesImmunologyImmune RegulationImmunologic MechanismAntigen ProcessingCd4 T Cell ResponsesImmune SystemT Cell ApoptosisFeline Immunodeficiency VirusAllergyAutoimmune DiseaseVirologyAutoimmunityT Cell ImmunityChronic Viral InfectionHivAntiviral ResponseVirus-host InteractionCellular Immune ResponseMedicineViral Immunity
The B7.1 and B7.2 costimulatory molecules on antigen-presenting cells provide second signals for regulating T cell immune responses via CD28 and cytotoxic T lymphocyte antigen 4 (CTLA4) on T cells. CD28 signals cell proliferation, whereas CTLA4 signals for anergy or apoptosis, terminating the immune response. Because T cell apoptosis and immunodeficiency is a characteristic of feline immunodeficiency virus (FIV)-infected cats, it is possible that negative T cell signaling via B7 and CTLA4 may be favored in these cats. Flow cytometry revealed high percentages of CD8+ and CD4+ cells expressing B7.1, B7.2, and CTLA4 in lymph nodes of FIV-positive cats and a large fraction of CTLA4+ T cells coexpressing B7.1 and B7.2. Three-color analysis with anti-B7.1, anti-B7.2, or anti-CTLA4 and TUNEL (terminal deoxynucleotidyl transferase nick-end-labeling) analysis revealed that apoptosis was a characteristic of B7.1+ B7.2+ CTLA4+ T cells. These data support the hypothesis that lymph node apoptosis and immune deterioration in FIV-infected cats results from chronic B7.1- and/or B7.2-CTLA4-mediated T-T interactions.
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1999 | 971 | |
1985 | 781 | |
1993 | 558 | |
1997 | 495 | |
B-cell surface antigen B7 provides a costimulatory signal that induces T cells to proliferate and secrete interleukin 2. Claude Gimmi, Gordon J. Freeman, JG Gribben, Proceedings of the National Academy of Sciences Adaptive Immune SystemCellular ImmunologyImmunologyImmunologic MechanismCd4 T Cell Responses | 1991 | 440 |
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