DIFFERENTIAL REGULATION OF CYTOKINE PRODUCTION IN LIPOPOLYSACCHARIDE TOLERANCE IN MICE

We investigated the pattern of down-regulation of cytokine production in endotoxin (lipopolysaccharide [LPS]) tolerance. A 4-day treatment w ith LPS (35 mug per mouse) was followed by a challenge on day 6 with o ne more injection of LPS. Circulating tumor necrosis factor (TNF) and interleukin-6 (IL-6) could not be induced (>99% inhibition) by LPS in LPS-tolerant mice; colony-stimulating factor (CSF) was also down-regul ated by more than 95%, whereas interferon (IFN) and IL-1 syntheses wer e only partially inhibited. To study the mechanism of cytokine down-re gulation in tolerance, we attempted to reverse the tolerant state by p retreatment with phorbol 12-myristate 13-acetate (PMA) (4 mug per mous e) 10 min before the LPS challenge. PMA completely restored IL-6 produ ction and partially that of CSF. PMA had no effect on IFN production a nd inhibited the induction of IL-1. TNF production was also not restor ed by PMA. To investigate the role of endogenously produced cytokines in the development of LPS tolerance, we administered IL-6, TNF, or IL- 1alpha, using the same treatment schedule as that for LPS. Whereas IL- 6 had no effect, IL-1alpha or TNF induced partial tolerance to LPS in terms of inhibition of LPS-stimulated TNF and IL-6 production. However , a full LPS-tolerant state could not be induced by administration of recombinant cytokines, suggesting the existence of additional mechanis ms, such as a loss of LPS receptors or changes in release of soluble b inding proteins.