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Increased Mortality and Impaired Clonal Deletion After Staphylococcal Enterotoxin B Injection in Old Mice: Relation to Cytokines and Nitric Oxide Production
Author(s) -
KUSCHNAROFF L. M.,
GOEBELS J.,
VALCKX D.,
HEREMANS H.,
MATTHYS P.,
WAER M.
Publication year - 1997
Publication title -
scandinavian journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.934
H-Index - 88
eISSN - 1365-3083
pISSN - 0300-9475
DOI - 10.1046/j.1365-3083.1997.d01-153.x
Subject(s) - immunology , superantigen , nitric oxide , interferon gamma , enterotoxin , microbiology and biotechnology , tumor necrosis factor alpha , biology , nitric oxide synthase , cytokine , endocrinology , t cell , immune system , gene , biochemistry , escherichia coli
In the present study peripheral T cell tolerance and the occurrence of shock were evaluated in young and old mice after injection of Staphylococcal enterotoxin B (SEB). In young mice SEB immunization leads to tolerance based on deletion and anergy of SEB‐reactive Vβ8 + T cells. With aging, mice developed resistance to SEB‐induced deletion of Vβ8 + T cells as well as a high sensitivity to toxic shock. Compared to young mice, older mice injected with SEB showed increased serum levels of interferon‐γ (IFN‐γ), interleukin‐2 (IL‐2) and IL‐4. These results were confirmed by reverse transcription‐polymerase chain reaction (RT‐PCR), as splenic mRNA levels taken 2 h after SEB injection showed higher values of IL‐2, IL‐4, and IFN‐γ in old mice. In contrast, mRNA levels for FasL and tumour necrosis factor‐α (TNF‐α) were lower. No difference in IL‐10 mRNA was found. Compared to young mice, old mice showed a high, but statistically not significantly different ( P = 0.20), production of nitric oxide (NO). Blocking of IFN‐γ with antibodies or reducing IFN‐γ by depletion of natural killer (NK) cells resulted, respectively, in a complete or partial protection against mortality in aged mice. Suppressing the NO production by the NO synthase inhibitor N‐nitro‐L‐arginine methylester (L‐NAME) increased the mortality in both young and old mice, and abrogated clonal deletion in the surviving young mice. In conclusion, in young mice NO production is a key factor in the protection against mortality and the development of clonal deletion after SEB injection. The higher mortality seen in older mice is mainly related to the elevated production of IFN‐γ and occurs despite a sufficient production of NO. The decreased clonal deletion of old mice may be related to their decreased expression of Fas ligand or TNF‐α after SEB injection.