Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1973 Mar 31;137(4):1031–1041. doi: 10.1084/jem.137.4.1031

GLUCOCORTICOID SUPPRESSION OF MACROPHAGE MIGRATION INHIBITORY FACTOR

James E Balow 1, Alan S Rosenthal 1
PMCID: PMC2139222  PMID: 4693151

Abstract

The ability of hydrocortisone to modify antigen-mediated inhibition of macrophage migration, an in vitro correlate of cellular immunity in the guinea pig, was investigated. Only the glucocorticoids, hydrocortisone and dexamethasone, significantly blocked migration inhibitory factor (MIF) activity in pharmacologic concentrations. Hydrocortisone had no effect on antigen "processing" by macrophages, nor on the ability of antigen-stimulated peritoneal exudate lymphocytes to produce MIF. Rather, hydrocortisone antagonized directly the inhibitory effect of MIF on the macrophage.

Full Text

The Full Text of this article is available as a PDF (637.6 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Barnet K., Pekárek J., Johanovský J. Demonstration of specific induction of erythrocytes phagocytosis by macrophates from normal, non-sensitized rabbits by a factor released from lymph node cells of immunized rabbits. Experientia. 1968 Sep 15;24(9):948–949. doi: 10.1007/BF02138675. [DOI] [PubMed] [Google Scholar]
  2. Bennett B., Bloom B. R. Reactions in vivo and in vitro produced by a soluble substance associated with delayed-type hypersensitivity. Proc Natl Acad Sci U S A. 1968 Mar;59(3):756–762. doi: 10.1073/pnas.59.3.756. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bloom B. R. In vitro approaches to the mechanism of cell-mediated immune reactions. Adv Immunol. 1971;13:101–208. doi: 10.1016/s0065-2776(08)60184-4. [DOI] [PubMed] [Google Scholar]
  4. Casey W. J., McCall C. E. Suppression of the cellular interactions of delayed hypersensitivity by corticosteroid. Immunology. 1971 Aug;21(2):225–231. [PMC free article] [PubMed] [Google Scholar]
  5. Claman H. N. Corticosteroids and lymphoid cells. N Engl J Med. 1972 Aug 24;287(8):388–397. doi: 10.1056/NEJM197208242870806. [DOI] [PubMed] [Google Scholar]
  6. Claman H. N., Moorhead J. W., Benner W. H. Corticosteroids and lymphoid cells in vitro. I. Hydrocortisone lysis of human, guinea pig, and mouse thymus cells. J Lab Clin Med. 1971 Oct;78(4):499–507. [PubMed] [Google Scholar]
  7. Cline M. J., Swett V. C. The interaction of human monocytes and lymphocytes. J Exp Med. 1968 Dec 1;128(6):1309–1325. doi: 10.1084/jem.128.6.1309. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cohen J. J. Thymus-derived lymphocytes sequestered in the bone marrow of hydrocortisone-treated mice. J Immunol. 1972 Mar;108(3):841–844. [PubMed] [Google Scholar]
  9. DAVID J. R., LAWRENCE H. S., THOMAS L. DELAYED HYPERSENSITIVITY IN VITRO. 3. THE SPECIFICITY OF HAPTEN-PROTEIN CONJUGATES IN THE INHIBITION OF CELL MIGRATION. J Immunol. 1964 Aug;93:279–282. [PubMed] [Google Scholar]
  10. David J. R. Delayed hypersensitivity in vitro: its mediation by cell-free substances formed by lymphoid cell-antigen interaction. Proc Natl Acad Sci U S A. 1966 Jul;56(1):72–77. doi: 10.1073/pnas.56.1.72. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Havemann K., Horvat M., Sodomann C. P., Bürger S. Protease activity as a possible mechanism of migration inhibitory factor. Eur J Immunol. 1972 Feb;2(1):97–99. doi: 10.1002/eji.1830020118. [DOI] [PubMed] [Google Scholar]
  12. ISHIDATE M., METCALF D. THE PATTERN OF LYMPHOPOIESIS IN THE MOUSE THYMUS AFTER CORTISONE ADMINISTRATION OR ADRENALECTOMY. Aust J Exp Biol Med Sci. 1963 Dec;41:637–649. doi: 10.1038/icb.1963.53. [DOI] [PubMed] [Google Scholar]
  13. Leu R. W., Eddleston A. L., Hadden J. W., Good R. A. Mechanism of action of migration inhibitory factor (MIF). I. Evidence for a receptor for MIF present on the peritoneal macrophage but not on the alveolar macrophage. J Exp Med. 1972 Sep 1;136(3):589–603. doi: 10.1084/jem.136.3.589. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Makinodan T., Santos G. W., Quinn R. P. Immunosuppressive drugs. Pharmacol Rev. 1970 Jun;22(2):189–247. [PubMed] [Google Scholar]
  15. Makman M. H., Dvorkin B., White A. Influence of cortisol on the utilization of precursors of nucleic acids and protein by lymphoid cells in vitro. J Biol Chem. 1968 Apr 10;243(7):1485–1497. [PubMed] [Google Scholar]
  16. Mooney J. J., Waksman B. H. Activation of normal rabbit macrophage monolayers by supernatants of antigen-stimulated lymphocytes. J Immunol. 1970 Nov;105(5):1138–1145. [PubMed] [Google Scholar]
  17. Munck A., Wira C., Young D. A., Mosher K. M., Hallahan C., Bell P. A. Glucocorticoid-receptor complexes and the earliest steps in the action of glucocorticoids on thymus cells. J Steroid Biochem. 1972 Apr;3(3):567–578. doi: 10.1016/0022-4731(72)90103-3. [DOI] [PubMed] [Google Scholar]
  18. NOWELL P. C. Inhibition of human leukocyte mitosis by prednisolone in vitro. Cancer Res. 1961 Dec;21:1518–1521. [PubMed] [Google Scholar]
  19. Nathan C. F., Karnovsky M. L., David J. R. Alterations of macrophage functions by mediators from lymphocytes. J Exp Med. 1971 Jun 1;133(6):1356–1376. doi: 10.1084/jem.133.6.1356. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. North R. J. The action of cortisone acetate on cell-mediated immunity to infection. Suppression of host cell proliferation and alteration of cellular composition of infective foci. J Exp Med. 1971 Dec 1;134(6):1485–1500. doi: 10.1084/jem.134.6.1485. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Pick E., Turk J. L. The biological activities of soluble lymphocyte products. Clin Exp Immunol. 1972 Jan;10(1):1–23. [PMC free article] [PubMed] [Google Scholar]
  22. REBUCK J. W., MELLINGER R. C. Interruption by topical cortisone of leukocytic cycles in acute inflammation in man. Ann N Y Acad Sci. 1953 Jul 17;56(4):715–732. doi: 10.1111/j.1749-6632.1953.tb27394.x. [DOI] [PubMed] [Google Scholar]
  23. Roos D., Loos J. A. Changes in the carbohydrate metabolism of mitogenically stimulated human peripheral lymphocytes. I. Stimulation by phytohaemagglutinin. Biochim Biophys Acta. 1970 Dec 29;222(3):565–582. doi: 10.1016/0304-4165(70)90182-0. [DOI] [PubMed] [Google Scholar]
  24. Rosenstreich D. L., Blake J. T., Rosenthal A. S. The peritoneal exudate lymphocyte. I. Differences in antigen responsiveness between peritoneal exudate and lymph node lymphocytes from immunized guinea pigs. J Exp Med. 1971 Nov 1;134(5):1170–1186. doi: 10.1084/jem.134.5.1170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Rosenthal A. S., Davie J. M., Rosenstreich D. L., Blake J. T. Depletion of antibody-forming cells and their precursors from complex lymphoid cell populations. J Immunol. 1972 Jan;108(1):279–281. [PubMed] [Google Scholar]
  26. Schechter G. P. McFarland W,+MACFARLAND W: Interaction of lymphocytes and a radioresistant cell in PPD-stimulated human leukocyte cultures. J Immunol. 1970 Sep;105(3):661–669. [PubMed] [Google Scholar]
  27. Seeger R. C., Oppenheim J. J. Synergistic interaction of macrophages and lymphocytes in antigen-induced transformation of lymphocytes. J Exp Med. 1970 Jul 1;132(1):44–65. doi: 10.1084/jem.132.1.44. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Spitler L., Huber H., Fudenberg H. H. Inhibition of capillary migration by antigen-antibody complexes. J Immunol. 1969 Feb;102(2):404–411. [PubMed] [Google Scholar]
  29. Unanue E. R. The regulatory role of macrophages in antigenic stimulation. Adv Immunol. 1972;15:95–165. doi: 10.1016/s0065-2776(08)60684-7. [DOI] [PubMed] [Google Scholar]
  30. Ward P. A. The chemosuppression of chemotaxis. J Exp Med. 1966 Aug 1;124(2):209–226. doi: 10.1084/jem.124.2.209. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Wiener E., Marmary Y., Curelaru Z. The in vitro effect of hydrocortisone on the uptake and intracellular digestion of particulate matter by macrophages in culture. Lab Invest. 1972 Feb;26(2):220–226. [PubMed] [Google Scholar]
  32. Williams T. W., Granger G. A. Lymphocyte in vitro cytotoxicity: correlation of derepression with release of lymphotoxin from human lymphocytes. J Immunol. 1969 Aug;103(2):170–178. [PubMed] [Google Scholar]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES