Skip to main content
The Journal of Clinical Investigation logoLink to The Journal of Clinical Investigation
. 1973 Oct;52(10):2629–2640. doi: 10.1172/JCI107455

Effects of Corticosteroids on Immunity in Man I. DECREASED SERUM IgG CONCENTRATION CAUSED BY 3 OR 5 DAYS OF HIGH DOSES OF METHYLPREDNISOLONE

William T Butler 1,2, Roger D Rossen 1,2
PMCID: PMC302523  PMID: 4729056

Abstract

To study the effects of methylprednisolone on immune mechanisms in the absence of other immunosuppressive agents or immunologically mediated diseases, we gave 17 normal adult male volunteers 96 mg of methylprednisolone daily for 3-5 days and compared results with 12 untreated controls who were studied simultaneously, 86% of treated volunteers had significant decreases in the concentrations of serum IgG. 2-4 wk after methylprednisolone, the treated volunteers had a mean decrease in IgG of 22% compared with a decrease of only 1% in untreated controls. Likewise, significant decreases in IgA concentration occurred in 43% of treated volunteers, whereas significant decreases in IgM occurred in only 14%. The lowest immunoglobulin levels occurred during the 2nd wk after a 3 day course of methylprednisolone and during the 3rd wk after a 5 day course of drug. Slightly decreased plasma concentration of [125I]IgG was seen in six of seven volunteers who received a 5 day course but in only one of four who received a 3 day course of drug. However, an increase in the rate of plasma clearance of IgG occurred only during the treatment period itself. During the period when the serum concentration of IgG was falling, the specific activity of IgG in the serum was relatively higher in treated men than in controls indicating decreased entry of newly synthesized IgG into the circulation. These findings suggest that a short course of methylprednisolone treatment causes a pronounced and sustained decrease in serum IgG due to increased catabolism during drug administration and to decreased synthesis during and for a variable time after drug administration.

Full text

PDF
2629

Selected References

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

  1. BILLINGHAM R. E., KROHN P. L., MEDAWAR P. B. Effect of cortisone on survival of skin homografts in rabbits. Br Med J. 1951 May 26;1(4716):1157–1163. doi: 10.1136/bmj.1.4716.1157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Baum J., Ziff M. Decreased 19S antibody response to bacterial antigens in systemic lupus erythematosus. J Clin Invest. 1969 Apr;48(4):758–767. doi: 10.1172/JCI106033. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Butler W. T., Rossen R. D., Reisberg M. A., Mazow J. B., Trentin J. J., Judd K. P. Antibody formation to equine anti-lymphocytic globulin (ALG) in man: effect on absorption, distribution and effectiveness of the ALG. J Immunol. 1971 Jan;106(1):1–10. [PubMed] [Google Scholar]
  4. Butler W. T., Rossen R. D., Waldmann T. A. The mechanism of appearance of immunoglobulin A in nasal secretions in man. J Clin Invest. 1967 Dec;46(12):1883–1893. doi: 10.1172/JCI105678. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Elliott E. V., Wallis V., Davies A. J. Origin of PHA-responsive cells in the mouse thymus after treatment of the animal with hydrocortisone. Nat New Biol. 1971 Nov 17;234(46):77–78. doi: 10.1038/newbio234077a0. [DOI] [PubMed] [Google Scholar]
  6. FISCHEL E. E., STOERK H. C., BJØRNEBOE M. Failure of cortisone to affect rate of disappearance of antibody protein. Proc Soc Exp Biol Med. 1951 May;77(1):111–114. doi: 10.3181/00379727-77-18695. [DOI] [PubMed] [Google Scholar]
  7. GERMUTH F. G., Jr, OYAMA J., OTTINGER B. The mechanism of action of 17-hydroxy-11-dehydrocorticosterone (compound E) and of the adrenocorticotropic hormone in experimental hypersensitivity in rabbits. J Exp Med. 1951 Aug;94(2):139–170. doi: 10.1084/jem.94.2.139. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Gabrielsen A. E., Good R. A. Chemical suppression of adaptive immunity. Adv Immunol. 1967;6:91–229. doi: 10.1016/s0065-2776(08)60522-2. [DOI] [PubMed] [Google Scholar]
  9. Griggs R. C., Condemi J. J., Vaughan J. H. Effect of therapeutic dosages of prednisone on human immunoglobulin G metabolism. J Allergy Clin Immunol. 1972 May;49(5):267–273. doi: 10.1016/0091-6749(72)90094-2. [DOI] [PubMed] [Google Scholar]
  10. HELMKAMP R. W., GOODLAND R. L., BALE W. F., SPAR I. L., MUTSCHLER L. E. High specific activity iodination of gamma-globulin with iodine-131 monochloride. Cancer Res. 1960 Nov;20:1495–1500. [PubMed] [Google Scholar]
  11. JAGER B. V., BROWN H., NICKERSON M. Alterations in plasma proteins, plasma volume, and volume of packed red cells in patients receiving ACTH or cortisone. J Lab Clin Med. 1951 Mar;37(3):431–443. [PubMed] [Google Scholar]
  12. Levine M. A., Claman H. N. Bone marrow and spleen: dissociation of immunologic properties by cortisone. Science. 1970 Mar 13;167(3924):1515–1517. doi: 10.1126/science.167.3924.1515. [DOI] [PubMed] [Google Scholar]
  13. Levy A. L., Waldmann T. A. The effect of hydrocortisone on immunoglobulin metabolism. J Clin Invest. 1970 Sep;49(9):1679–1684. doi: 10.1172/JCI106385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. MIRICK G. S. The effects of ACTH and cortisone on antibodies in human beings. Bull Johns Hopkins Hosp. 1951 Apr;88(4):332–351. [PubMed] [Google Scholar]
  15. MORGAN J. A. The influence for cortisone on the survival of homografts of skin in the rabbit. Surgery. 1951 Sep;30(3):506–515. [PubMed] [Google Scholar]
  16. North R. J. The action of cortisone acetate on cell-mediated immunity to infection: histogenesis of the lymphoid cell response and selective elimination of committed lymphocytes. Cell Immunol. 1972 Mar;3(3):501–515. doi: 10.1016/0008-8749(72)90255-9. [DOI] [PubMed] [Google Scholar]
  17. ROTHSCHILD M. A., BAUMAN A., YALOW R. S., BERSON S. A. The effect of large doses of desiccated thyroid on the distribution and metabolism of albumin-I 131 in euthyroid subjects. J Clin Invest. 1957 Mar;36(3):422–428. doi: 10.1172/JCI103438. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Rosenau W., Baxter J. D., Rousseau G. G., Tomkins G. M. Mechanism of resistance to steroids: glucocorticoid receptor defect in lymphoma cells. Nat New Biol. 1972 May 3;237(70):20–24. doi: 10.1038/newbio237020a0. [DOI] [PubMed] [Google Scholar]
  19. SPRAGUE R. G., POWER M. H. Observations on the physiologic effects of cortisone and ACTH in man. Arch Intern Med (Chic) 1950 Feb;85(2):199–258. doi: 10.1001/archinte.1950.00230080003001. [DOI] [PubMed] [Google Scholar]
  20. Segal S., Cohen I. R., Feldman M. Thymus-derived lymphocytes: humoral and cellular reactions distinguished by hydrocortisone. Science. 1972 Mar 10;175(4026):1126–1128. doi: 10.1126/science.175.4026.1126. [DOI] [PubMed] [Google Scholar]
  21. Waldmann T. A., Strober W. Metabolism of immunoglobulins. Prog Allergy. 1969;13:1–110. doi: 10.1159/000385919. [DOI] [PubMed] [Google Scholar]
  22. Wollheim F. A. Inverse effect on the serum levels of gamma-G- and gamma-M-globulins after prednisone treatment of lupoid hepatitis. Clin Exp Immunol. 1967 Jul;2(4):497–500. [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Clinical Investigation are provided here courtesy of American Society for Clinical Investigation

RESOURCES