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Vol. 288, Issue 3, 1174-1184, March 1999
the
Disulfide Dimer of N-acetylcysteine
Is a Potent
Modulator of Contact Sensitivity/Delayed Type Hypersensitivity
Reactions in Rodents1
Department of Pharmacology, Astra Draco AB, Lund, Sweden
Oral N-acetyl-L-cysteine
(NAC) is used clinically for treatment of chronic obstructive pulmonary
disease. NAC is easily oxidized to its disulfide. We show here
that N,N'-diacetyl-L-cystine
(DiNAC) is a potent modulator of contact sensitivity
(CS)/delayed type hypersensitivity (DTH) reactions in rodents. Oral
treatment of BALB/c mice with 0.003 to 30 µmol/kg DiNAC leads to
enhancement of a CS reaction to oxazolone; DiNAC is 100 to 1000 times more potent than NAC in this respect, indicating that it
does not act as a prodrug of NAC. Structure-activity studies suggest
that a stereochemically-defined disulfide element is needed for
activity. The DiNAC-induced enhancement of the CS reaction is
counteracted by simultaneous NAC-treatment; in contrast, the CS
reaction is even more enhanced in animals treated with DiNAC
together with the glutathione-depleting agent buthionine
sulfoximine. These data suggest that DiNAC acts via redox
processes. Immunohistochemically, ear specimens from
oxazolone-sensitized and -challenged BALB/c mice treated with DiNAC
display increased numbers of CD8+ cells. DiNAC treatment
augments the CS reaction also when fluorescein isothiocyanate is used as a sensitizer in BALB/c mice; this is a
purported TH2 type of response. However, when
dinitrofluorobenzene is used as a sensitizer, inducing a purported TH1
type of response, DiNAC treatment reduces the reaction.
Treatment with DiNAC also reduces a DTH footpad-swelling reaction to
methylated BSA. Collectively, these data indicate that DiNAC in vivo
acts as a potent and effective immunomodulator that can either enhance
or reduce the CS or DTH response depending on the experimental conditions.
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