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In vivo rapid reduction of alloantigen‐activated CD8 + mature cytotoxic T cells by inhibitors of acidification of intracellular organelles, prodigiosin 25‐C and concanamycin B
Author(s) -
Lee M.H.,
Kataoka T.,
Honjo N.,
Magae J.,
Nagai K.
Publication year - 2000
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1046/j.1365-2567.2000.00961.x
Subject(s) - cytotoxic t cell , ctl* , in vivo , perforin , biology , cd8 , intracellular , priming (agriculture) , population , in vitro , microbiology and biotechnology , immunology , immune system , biochemistry , medicine , botany , germination , environmental health
Summary Prodigiosin (PrG) 25‐C and concanamycin B (CMB) are immunosuppressants that specifically inhibit the induction of cytotoxic T cells (CTL) without affecting the function of B cells and helper T cells in vivo . Both compounds inhibit acidification of intracellular organelles and induce destruction of cytotoxic granules and degradation of perforin in vitro . Here we show that a single intraperitoneal (i.p.) injection of PrG 25‐C, and of CMB, into mice eliminates cytotoxic activity 7 days after alloantigen stimulation (when mature CTL activity has been detected in control mice), with minimal effect on the alloantigen‐specific antibody titre in serum. FK506 did not suppress the cytotoxic activity with this administration schedule. Suppression was accompanied by a decrease in the CD8 + population and in perforin expression of spleen cells induced by alloantigen stimulation. The suppression of CTL activity and decrease in CD8 + cell number was detected as early as 7 hr after the injection of compounds. These results suggest that inhibitors of acidification of intracellular organelles suppress CTL activity in vivo by reducing the number of mature CD8 + CTL.