Passage of immunomodulators across the blood-brain barrier.

The question is considered of how and where cytokines, such as interleukin 1 (IL-1), that are released into the circulation during the host defense response, reach and interact with the central nervous system to produce fever or act as neuroimmunomodulators. Evidence is presented suggesting a role for a brain circumventricular organ (CVO) in this respect. Several interactions between a specific CVO, the organum vasculosum laminae terminalis (OVLT) and endogenous pyrogen (EP) in the production of fever are reviewed. A more general hypothesis is developed on a role for the brain CVOs in monitoring the blood concentrations of several proteins and complex polypeptides such as the circulating endocrines that are regulated via the autonomic nervous system. A proposed connection between the release of prostaglandin E (PGE) at the blood-brain interface in response to infection and the ability of the brain to maintain an immunoprivileged status in the face of exposure of its CVOs to foreign antigens is discussed.

[1]  C. Blatteis Neuromodulative actions of cytokines. , 1990, The Yale journal of biology and medicine.

[2]  S. G. Shimada,et al.  Enhancement of the febrile responses of rats to endogenous pyrogen occurs within the OVLT region. , 1989, Journal of applied physiology.

[3]  S. G. Shimada,et al.  Immunoadjuvants enhance the febrile responses of rats to endogenous pyrogen. , 1989, Journal of applied physiology.

[4]  J. Stitt Evidence for the involvement of the organum vasculosum laminae terminalis in the febrile response of rabbits and rats. , 1985, The Journal of physiology.

[5]  J. Stitt,et al.  Differences in endogenous pyrogen fevers induced by iv and icv routes in rabbits. , 1985, Journal of applied physiology.

[6]  J. Ninnemann Prostaglandins and immunity. , 1984, Immunology today.

[7]  C. Blatteis,et al.  Suppression of fever after lesions of the anteroventral third ventricle in guinea pigs , 1983, Brain Research Bulletin.

[8]  R. Whisler,et al.  Inhibition of human B lymphocyte colony responses by endogenous synthesized hydrogen peroxide and prostaglandins. , 1982, Cellular immunology.

[9]  John,et al.  Demonstration and characterization of Ia-positive dendritic cells in the interstitial connective tissues of rat heart and other tissues, but not brain , 1981, The Journal of experimental medicine.

[10]  L. Lichtenstein,et al.  The role of agonists that activate adenylate cyclase in the control of cAMP metabolism and enzyme release by human polymorphonuclear leukocytes. , 1980, Journal of immunology.

[11]  R. Messner,et al.  Suppression of human T-cell mitogenesis by prostaglandin. Existence of a prostaglandin-producing suppressor cell , 1977, The Journal of experimental medicine.

[12]  M. A. Bray,et al.  Control of lymphokine secretion by prostaglandins , 1976, Nature.

[13]  R. L. Holmes Brain—Endocrine Interaction. II. The Ventricular System in Neuroendocrine Mechanisms , 1976 .

[14]  D. Ramsay,et al.  Some central mechanisms of thirst in the dog. , 1975, The Journal of physiology.

[15]  A. Routtenberg,et al.  Subfornical Organ: Site of Drinking Elicitation by Angiotensin II , 1973, Science.

[16]  L. Lichtenstein,et al.  The immediate allergic response: in vitro action of cyclic AMP-active and other drugs on the two stages of histamine release. , 1971, Journal of immunology.

[17]  M. Droller Prostaglandins and Expression of Lymphocyte Cytotoxicity , 1985 .

[18]  S. Kunkel,et al.  Effects of Prostaglandins on In Vivo Immune and Inflammatory Reactions , 1985 .

[19]  R. Hellon,et al.  Mechanisms of fever. , 1982, Pharmacology & therapeutics.

[20]  A. Weindl,et al.  Relation of neuropeptides to mammalian circumventricular organs. , 1981, Advances in biochemical psychopharmacology.

[21]  A. Globerson,et al.  The effect of various prostaglandins on plasma membrane receptors and function of mouse macrophages. , 1979, Advances in experimental medicine and biology.