Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/13247
Title: Mechanisms of cytotoxicity used by human peripheral blood CD4+ and CD8+ T cell subsets. The role of granule exocytosis.
Authors: Smyth, Mark J;Ortaldo, J R
Affiliation: Cellular Cytotoxicity Laboratory, Austin Research Institute, Austin Hospital, Heidelberg, Victoria.
Issue Date: 15-Jul-1993
Citation: Journal of Immunology (baltimore, Md. : 1950); 151(2): 740-7
Abstract: The broad lytic properties of high buoyant density CD4+ and CD8+ T cell subsets were examined by activating these populations with anti-CD3 mAb and IL-2 for 1 to 5 days and testing their cytotoxic activity against various target cells. The effects of a variety of metabolic inhibitors and anti-TNF antibodies were examined to distinguish several different mechanisms of cytotoxicity used by CD4+ and CD8+ T cell effectors isolated from human PBL. In particular, activated CD4+ and CD8+ T cells were cytotoxic when redirected by an anti-nitrophenyl (NP)-anti-CD3 mAb heteroconjugate against NP-modified nucleated target cells (TC) and anucleated SRBC and also lysed L929 in a TNF-alpha-dependent manner. CD4+ and CD8+ T cells displayed distinct pathways of antibody-redirected lysis against NP-EL4, yet common mechanisms of SRBC redirected lysis by CD4+ and CD8+ efforts were implied by a similar pattern of sensitivity to cholera toxin, cyclosporin A (CsA), and EGTA. CsA inhibited CD4+ and CD8+ T cell redirected lysis of SRBC, but not EL4, suggesting that T cells redirectedly lyse nucleated and anucleated TC by different mechanisms. Cholera toxin, CsA, or EGTA pretreatment also significantly inhibited their release of alpha-N-benzyloxycarbonyl-L-lysine-thiobenzylester-esterase activity suggesting that degranulation of CD4+ and CD8+ effectors may be a critical step in their redirected lysis of SRBC. Overall, these findings suggested that activated human PBL CD4+ or CD8+ effectors can lyse TC by at least three distinct mechanisms: 1) a CsA-sensitive redirected lysis of SRBC that correlates with exocytosis and presumably occurs via membrane lesions; 2) a CsA-insensitive redirected lysis of NP-modified nucleated TC that does not appear to involve exocytosis and is metabolically distinct in activated CD4+ and CD8+ T cell effectors; and 3) a direct TNF-dependent lysis of TNF-sensitive TC.
Internal ID Number: 8101537
URI: http://ahro.austin.org.au/austinjspui/handle/1/13247
URL: http://www.ncbi.nlm.nih.gov/pubmed/8101537
Type: Journal Article
Subjects: Antigens, CD4.analysis
Antigens, CD8.analysis
CD4-Positive T-Lymphocytes.immunology
Cells, Cultured
Cycloheximide.pharmacology
Cytotoxicity, Immunologic
Dactinomycin.pharmacology
Exocytosis
Humans
Lymphocyte Activation
T-Lymphocyte Subsets.immunology
T-Lymphocytes, Cytotoxic.immunology
Tumor Necrosis Factor-alpha.physiology
Appears in Collections:Journal articles

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