The Role of Toll-like Receptors in the Immune–Adrenal Crosstalk

S.R. BORNSTEIN; C.G. ZIEGLER; A.W. KRUG; W. KANCZKOWSKI; V. BESUHLI DE RETTORI; S.M. MCCANN; M. WIRTH; K. ZACHAROWSKI

ANNALS OF THE NEW YORK ACADEMY OF SCIENCES.

Año: 2006 vol. 1088 p. 307 - 318

0077-8923

Sepsis and septic shock remain major health concernsworldwide, and rapid activation of adrenal steroid release is a key event in the organism’s first line of defense during this form of severe illness. Tolllike receptors (TLRs) are critical in the early immune response upon bacterial infection, and recent data from our lab demonstrate a novel link between the innate immune system and the adrenal stress response mediated by TLRs. Glucocorticoids and TLRs regulate each other in a bidirectional way. Bacterial toxins acting through TLRs directly activate adrenocortical steroid release. TLR-2 and TLR-4 are expressed in human and mice adrenals and TLR-2 deficiency is associated with an impaired glucocorticoid response. Furthermore, TLR-2 deficiency in mice is associated with marked cellular alterations in adrenocortical tissue. TLR-2-deficient mice have an impaired adrenal corticosterone release following inflammatory stress induced by bacterial cell wall compounds. This defect appears to be associated with a decrease in systemic and intraadrenal cytokine expression. In conclusion, TLRs play a crucial role in theimmune–adrenal crosstalk. This close functional relationship needs to be considered in the treatment of inflammatory diseases requiring an intact adrenal stress response.