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. 1984 Dec 1;160(6):1672–1685. doi: 10.1084/jem.160.6.1672

Purification and characterization of a mannose-containing disaccharide obtained from human pregnancy urine. A new immunoregulatory saccharide

PMCID: PMC2187526  PMID: 6334714

Abstract

Endogenous mammalian lectin-like sugar-binding molecules have been previously described that have immunoregulatory properties. Further, the addition of defined simple saccharides to lymphocyte cultures has been shown to inhibit a variety of in vitro lymphocyte functions, presumably because these sugars are able to compete with the binding of endogenous lectins to critical membrane receptors. In this report, we describe the isolation and characterization of a D-mannose-containing disaccharide in human pregnancy urine that inhibits the proliferative response of human T lymphocytes. The inhibitory disaccharide was purified to homogeneity by sequential steps including affinity chromatography on immobilized concanavalin A and molecular sizing on Sephadex G-75 and then Fractogel 40S columns, with final purification on high-performance thin-layer chromatography. By mass spectrometry of the purified material as its permethylated derivative, the deduced structure of this compound was alpha-D-Manp 1-6-D-Man. To confirm that this disaccharide was in fact immunosuppressive, an identical disaccharide was prepared by sequential digestion of yeast cell wall polysaccharide. The urinary and yeast disaccharides had identical immunosuppressive properties. It has been previously reported that D- mannose is inhibitory for antigen-specific proliferative assays in the range of 10-50 mM. The purified alpha-D-Manp 1-6-D-Man disaccharide was inhibitory at 100-fold-lower concentrations. Further, while D-mannose inhibits T cell proliferation when added at anytime up to 24 h before harvest of a 6-d lymphocyte culture, alpha-D-Manp 1-6-D-Man disaccharide was inhibitory only if added at the initiation of culture and had no inhibitory effect if added just 24 h later. These data support the concept that simple sugar compounds can exhibit marked immunoregulatory activity in vitro. The impact of these molecules on the regulation of immune responses in vivo is unknown, as is their precise mechanism of action, but structural and chemical identification should now permit a detailed analysis of these issues.

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Selected References

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  1. Ashwell G., Morell A. G. The role of surface carbohydrates in the hepatic recognition and transport of circulating glycoproteins. Adv Enzymol Relat Areas Mol Biol. 1974;41(0):99–128. doi: 10.1002/9780470122860.ch3. [DOI] [PubMed] [Google Scholar]
  2. Cohen R. E., Zhang W., Ballou C. E. Effects of mannoprotein mutations on Saccharomyces cerevisiae core oligosaccharide structure. J Biol Chem. 1982 May 25;257(10):5730–5737. [PubMed] [Google Scholar]
  3. Fischer A., Ballet J. J., Griscelli C. Specific inhibition of in vitro Candida-induced lymphocyte proliferation by polysaccharidic antigens present in the serum of patients with chronic mucocutaneous candidiasis. J Clin Invest. 1978 Nov;62(5):1005–1013. doi: 10.1172/JCI109204. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Fleisher T. A., Greene W. C., Blaese R. M., Waldmann T. A. Soluble suppressor supernatants elaborated by concanavalin A-activated human mononuclear cells. II. Characterization of a soluble suppressor of B cell immunoglobulin production. J Immunol. 1981 Mar;126(3):1192–1197. [PubMed] [Google Scholar]
  5. Greene W. C., Fleisher T. A., Waldmann T. A. Soluble suppressor supernatants elaborated by concanavalin A-activated human mononuclear cells. I. Characterization of a soluble suppressor T cell proliferation. J Immunol. 1981 Mar;126(3):1185–1191. [PubMed] [Google Scholar]
  6. HAKOMORI S. A RAPID PERMETHYLATION OF GLYCOLIPID, AND POLYSACCHARIDE CATALYZED BY METHYLSULFINYL CARBANION IN DIMETHYL SULFOXIDE. J Biochem. 1964 Feb;55:205–208. [PubMed] [Google Scholar]
  7. Kirchner H., Blaese R. M. Pokeweed mitogen-, concanavalin A-, and phytohemagglutinin-induced development of cytotoxic effector lymphocytes. An evaluation of the mechanisms of T cell-mediated cytotoxicity. J Exp Med. 1973 Oct 1;138(4):812–824. doi: 10.1084/jem.138.4.812. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Kleinerman E. S., Louie J. S., Wahl L. M., Muchmore A. V. Pharmacology of human spontaneous monocyte-mediated cytotoxicity. I. Enhancement by salicylates and steroids. Arthritis Rheum. 1981 Jun;24(6):774–780. doi: 10.1002/art.1780240604. [DOI] [PubMed] [Google Scholar]
  9. Kleinerman E. S., Zwelling L. A., Howser D., Barlock A., Young R. C., Decker J. M., Bull J., Muchmore A. V. Defective monocyte killing in patients with malignancies and restoration of function during chemotherapy. Lancet. 1980 Nov 22;2(8204):1102–1105. doi: 10.1016/s0140-6736(80)92540-4. [DOI] [PubMed] [Google Scholar]
  10. Kleinerman E. S., Zwelling L. A., Muchmore A. V. Enhancement of naturally occurring human spontaneous monocyte-mediated cytotoxicity by cis-diamminedichloroplatinum(II). Cancer Res. 1980 Sep;40(9):3099–3102. [PubMed] [Google Scholar]
  11. Kleinerman E. S., Zwelling L. A., Schwartz R., Muchmore A. V. Effect of L-phenylalanine mustard, adriamycin, actinomycin D, and 4'-(9-acridinylamino)methanesulfon-m-anisidide on naturally occurring human spontaneous monocyte-mediated cytotoxicity. Cancer Res. 1982 May;42(5):1692–1695. [PubMed] [Google Scholar]
  12. MacDermott R. P., Kienker L. J., Bertovich M. J., Muchmore A. V. Inhibition of spontaneous but not antibody-dependent cell-mediated cytotoxicity by simple sugars: evidence that endogenous lectins may mediate spontaneous cell-mediated cytotoxicity. Immunology. 1981 Sep;44(1):143–152. [PMC free article] [PubMed] [Google Scholar]
  13. Muchmore A. V., Blaese R. M. Immunoregulatory properties of fractions from human pregnancy urine: evidence that human chorionic gonadotropin is not responsible. J Immunol. 1977 Mar;118(3):881–886. [PubMed] [Google Scholar]
  14. Muchmore A. V., Decker J. M., Blaese R. M. Spontaneous cytotoxicity by human peripheral blood monocytes: inhibition by monosaccharides and oligosaccharides. Immunobiology. 1981;158(3):191–206. doi: 10.1016/S0171-2985(81)80069-1. [DOI] [PubMed] [Google Scholar]
  15. Muchmore A. V., Decker J. M., Blaese R. M. Spontaneous cytotoxicity of human peripheral blood mononuclear cells toward red blood cell targets. II. Time-dependent loss of suppressor cell activity. J Immunol. 1977 Nov;119(5):1686–1689. [PubMed] [Google Scholar]
  16. Muchmore A. V., Decker J. M., Blaese R. M. Spontaneous cytotoxicity of human peripheral mononuclear cells toward red blood cell targets in vitro. I. characterization of the killer cell. J Immunol. 1977 Nov;119(5):1680–1685. [PubMed] [Google Scholar]
  17. Muchmore A. V., Nelson D. L., Kirchner H., Blaese R. M. A reappraisal of the effector cells mediating mitogen induced cellular cytotoxicity. Cell Immunol. 1975 Sep;19(1):78–90. doi: 10.1016/0008-8749(75)90293-2. [DOI] [PubMed] [Google Scholar]
  18. Nilsson B., Nordén N. E., Svensson S. Structural studies on the carbohydrate portion of fetuin. J Biol Chem. 1979 Jun 10;254(11):4545–4553. [PubMed] [Google Scholar]
  19. Remold H. G. Requirement for alpha-L-fucose on the macrophage membrane receptor for MIF. J Exp Med. 1973 Nov 1;138(5):1065–1076. doi: 10.1084/jem.138.5.1065. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Sando G. N., Neufeld E. F. Recognition and receptor-mediated uptake of a lysosomal enzyme, alpha-l-iduronidase, by cultured human fibroblasts. Cell. 1977 Nov;12(3):619–627. doi: 10.1016/0092-8674(77)90262-8. [DOI] [PubMed] [Google Scholar]
  21. Sharon N., Lis H. Lectins: cell-agglutinating and sugar-specific proteins. Science. 1972 Sep 15;177(4053):949–959. doi: 10.1126/science.177.4053.949. [DOI] [PubMed] [Google Scholar]
  22. Stutman O., Dien P., Wisun R. E., Lattime E. C. Natural cytotoxic cells against solid tumors in mice: blocking of cytotoxicity by D-mannose. Proc Natl Acad Sci U S A. 1980 May;77(5):2895–2898. doi: 10.1073/pnas.77.5.2895. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Tadakuma T., Kühner A. L., Rich R. R., David J. R., Pierce C. W. Biological expressions of lymphocyte activation. V. Characterization of a soluble immune response suppressor (SIRS) produced by concanavalin A-activated spleen cells. J Immunol. 1976 Jul;117(1):323–330. [PubMed] [Google Scholar]
  24. Tosato G., Pike S. E., Blaese R. M. Reversal of infectious mononucleosis-associated suppressor T cell activity by D-mannose. J Exp Med. 1983 Oct 1;158(4):1048–1060. doi: 10.1084/jem.158.4.1048. [DOI] [PMC free article] [PubMed] [Google Scholar]

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