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Modulation of murine T and B cell reactivity after short-term cadmium exposure in vivo
This study assessed early effects of short-term Cd exposure on T and B cell responsiveness. Spleen cells from mice injected s.c. with a daily dosage of 1 mg, 0.33 mg, or 0.11 mg Cd (as CdCl2) per kg body weight for 5 days were examined for their potential to generate alloreactive T cells in a mixed...
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Published in: | Archives of toxicology 1988-08, Vol.62 (1), p.22-28 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | This study assessed early effects of short-term Cd exposure on T and B cell responsiveness. Spleen cells from mice injected s.c. with a daily dosage of 1 mg, 0.33 mg, or 0.11 mg Cd (as CdCl2) per kg body weight for 5 days were examined for their potential to generate alloreactive T cells in a mixed lymphocyte reaction (MLR) and for mitogen reactivity to concanavalin A (Con A) in vitro. Spleen cells from the same mice were also assayed for the total number of IgM- and IgG-secreting B cells. Whereas alloreactivity was reduced, mitogen response to Con A was not different from controls or was even enhanced. The decrease in allogeneic MLR was dependent on the injected Cd dosage. No difference in susceptibility to Cd-induced effects was observed among the mouse strains tested, i.e. BALB/c, DBA/2, C57BL/6, and C3H/He. Co-cultivation of spleen cells, obtained from Cd-treated mice that exhibited deficient T cell reactivity, with splenic responder cells from untreated mice resulted in dose-dependent suppression of the normal MLR. These results indicate that the harmful effects of Cd on the immune system include the inhibition of antigen-specific T cell responses by the activation of an antigen non-specific suppressor system. In contrast to the suppressed allogeneic MLR, the same spleen cell populations showed augmented numbers of IgM- and IgG-antibody producing cells. |
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ISSN: | 0340-5761 1432-0738 |
DOI: | 10.1007/BF00316252 |