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PMID: 3498787 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Resistance of cloned cytotoxic T lymphocytes to cell-mediated cytotoxicity.

The Journal of experimental medicine ·Vol. 166 ·No. 4 ·1987-10-01 ·Pages 1070-83

Blakely A, Gorman K, Ostergaard H, Svoboda K, Liu CC, Young JD, Clark WR

Abstract

Cloned CTLs show an unusually high resistance to lysis by effector CTLs. Several cloned CTL lines in our laboratories are absolutely refractory to lysis by other cloned CTLs, either (a) directly, (b) in the presence of lectin, or (c) by PMA-induced CTLs. They can be lysed to some extent by primary CTL, although they are less than 5% as sensitive as target cells normally used to assay primary CTL lytic activity. Lysis of cloned CTLs by primary CTL effector cells is not enhanced by the presence of lectin, and cloned T cells are also highly resistant to lysis by primary lymphokine-activated killer cells. Cloned CTLs are highly resistant to lysis by isolated CTL granules that contain the membranolytic pore-forming protein (PFP or perforin), while non-CTL targets are highly susceptible to granule-mediated killing, indicating that cloned CTLs resist lysis not only at the intact effector cell level but also when soluble effector proteins are used. This resistance mechanism may explain how CTLs kill but spare themselves from being killed during the cytolytic event.

MeSH Terms
Animals Antibody-Dependent Cell Cytotoxicity Cell Survival Clone Cells/immunology Ethers/pharmacology H-2 Antigens/analysis Ionomycin Mice Mice, Inbred C57BL Mice, Inbred CBA T-Lymphocytes, Cytotoxic/immunology Tetradecanoylphorbol Acetate/pharmacology
Chemicals
Ethers H-2 Antigens Ionomycin Tetradecanoylphorbol Acetate
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Blakely A
Department of Biology, University of California, Los Angeles 90024.
Gorman K
Ostergaard H
Svoboda K
Liu C C
Young J D
Clark W R
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1987-10-01
Pages
1070-83
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2188734
Subset
IM
Grants
NIAID NIH HHS · AI-14747 · United States
NCI NIH HHS · CA-09120 · United States
NIGMS NIH HHS · GM-07185 · United States
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