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Clinical and Experimental Immunology logoLink to Clinical and Experimental Immunology
. 1993 Oct;94(1):140–144. doi: 10.1111/j.1365-2249.1993.tb05991.x

Triggering of respiratory burst by phagocytosis in monocytes of patients with systemic lupus erythematosus.

E Gyimesi 1, M Kavai 1, E Kiss 1, I Csipö 1, G Szücs 1, G Szegedi 1
PMCID: PMC1534380  PMID: 8403496

Abstract

The triggering of the respiratory burst by phagocytosis via different receptors in monocytes of patients with systemic lupus erythematosus (SLE) was investigated. The superoxide anion synthesis was assayed by reduction of ferricytochrome C that was inhibited by superoxide dismutase. The mononuclear cell suspensions were triggered by IgG-coated latex, C3 complement fragment-coated and uncoated yeast (Saccharomyces cerevisiae). Superoxide generation induced by phagocytosis via Fc gamma R was decreased in monocytes of patients with SLE. On the other hand, MoAbs against Fc gamma RI, Fc gamma RII and especially CR3 could also induce superoxide anion synthesis. At the same time, superoxide generation induced by anti-CR3 could be inhibited with C3-coated yeast.

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Selected References

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  1. Anderson C. L., Guyre P. M., Whitin J. C., Ryan D. H., Looney R. J., Fanger M. W. Monoclonal antibodies to Fc receptors for IgG on human mononuclear phagocytes. Antibody characterization and induction of superoxide production in a monocyte cell line. J Biol Chem. 1986 Sep 25;261(27):12856–12864. [PubMed] [Google Scholar]
  2. Arthur M. J., Kowalski-Saunders P., Gurney S., Tolcher R., Bull F. G., Wright R. Reduction of ferricytochrome C may underestimate superoxide production by monocytes. J Immunol Methods. 1987 Apr 2;98(1):63–69. doi: 10.1016/0022-1759(87)90436-4. [DOI] [PubMed] [Google Scholar]
  3. Casellas A. M., Prat A., Llera A., Manni J., Boveris A., Sarano J. F. Increased superoxide production by polymorphonuclear leukocytes in systemic lupus erythematosus. Clin Exp Rheumatol. 1991 Sep-Oct;9(5):511–514. [PubMed] [Google Scholar]
  4. Frank M. M., Fries L. F. The role of complement in inflammation and phagocytosis. Immunol Today. 1991 Sep;12(9):322–326. doi: 10.1016/0167-5699(91)90009-I. [DOI] [PubMed] [Google Scholar]
  5. Kimberly R. P., Ahlstrom J. W., Click M. E., Edberg J. C. The glycosyl phosphatidylinositol-linked Fc gamma RIIIPMN mediates transmembrane signaling events distinct from Fc gamma RII. J Exp Med. 1990 Apr 1;171(4):1239–1255. doi: 10.1084/jem.171.4.1239. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Kimberly R. P., Meryhew N. L., Runquist O. A. Mononuclear phagocyte function in SLE. I. Bipartite Fc- and complement-dependent dysfunction. J Immunol. 1986 Jul 1;137(1):91–96. [PubMed] [Google Scholar]
  7. Kávai M., Csipö I., Sonkoly I., Csongor J., Szegedi G. Y. Defective immune complex degradation by monocytes in patients with systemic lupus erythematosus. Scand J Immunol. 1986 Nov;24(5):527–532. doi: 10.1111/j.1365-3083.1986.tb02167.x. [DOI] [PubMed] [Google Scholar]
  8. Kávai M., Gyimesi E., Szücs G., Szegedi G. Binding and endocytosis of erythrocytes sensitized with rabbit IgG via Fc gamma receptors of human monocytes. Immunology. 1991 Dec;74(4):657–660. [PMC free article] [PubMed] [Google Scholar]
  9. Kávai M., Lukács K., Sonkoly I., Jókay I. J., Berndt A., Szegedi G. Loss of monocyte membrane receptors in patients with SLE. Clin Exp Immunol. 1980 Apr;40(1):66–71. [PMC free article] [PubMed] [Google Scholar]
  10. Kávai M., Sándor M., Szegedi G., Gergely J. Ligand-specific cross-inhibition of monocyte phagocytosis. Scand J Immunol. 1988 Oct;28(4):397–402. doi: 10.1111/j.1365-3083.1988.tb01468.x. [DOI] [PubMed] [Google Scholar]
  11. Nakagawara A., Nathan C. F., Cohn Z. A. Hydrogen peroxide metabolism in human monocytes during differentiation in vitro. J Clin Invest. 1981 Nov;68(5):1243–1252. doi: 10.1172/JCI110370. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Nathan C. F., Cohn Z. A. Antitumor effects of hydrogen peroxide in vivo. J Exp Med. 1981 Nov 1;154(5):1539–1553. doi: 10.1084/jem.154.5.1539. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Ross G. D., Medof M. E. Membrane complement receptors specific for bound fragments of C3. Adv Immunol. 1985;37:217–267. doi: 10.1016/s0065-2776(08)60341-7. [DOI] [PubMed] [Google Scholar]
  14. Salmon J. E., Kimberly R. P., Gibofsky A., Fotino M. Defective mononuclear phagocyte function in systemic lupus erythematosus: dissociation of Fc receptor-ligand binding and internalization. J Immunol. 1984 Nov;133(5):2525–2531. [PubMed] [Google Scholar]
  15. Tan E. M., Cohen A. S., Fries J. F., Masi A. T., McShane D. J., Rothfield N. F., Schaller J. G., Talal N., Winchester R. J. The 1982 revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum. 1982 Nov;25(11):1271–1277. doi: 10.1002/art.1780251101. [DOI] [PubMed] [Google Scholar]
  16. Yu C. L., Chang K. L., Chiu C. C., Chiang B. N., Han S. H., Wang S. R. Defective phagocytosis, decreased tumour necrosis factor-alpha production, and lymphocyte hyporesponsiveness predispose patients with systemic lupus erythematosus to infections. Scand J Rheumatol. 1989;18(2):97–105. doi: 10.3109/03009748909099924. [DOI] [PubMed] [Google Scholar]

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