Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1995 Nov;63(11):4290–4294. doi: 10.1128/iai.63.11.4290-4294.1995

Survival of immunoglobulin G-opsonized Toxoplasma gondii in nonadherent human monocytes.

C E Fadul 1, J Y Channon 1, L H Kasper 1
PMCID: PMC173609  PMID: 7591060

Abstract

Toxoplasma gondii is a protozoan parasite that is able to penetrate human monocytes by either passive uptake during phagocytosis or active penetration. It is expected that immunoglobulin G (IgG) opsonization will target the parasite to macrophage Fc gamma receptors for phagocytic processing and subsequent degradation. Antibody-opsonized T. gondii tachyzoites were used to infect nonadherent and adherent human monocytes obtained from the peripheral blood of seronegative individuals. The infected monocytes were evaluated for the presence of intracellular parasites and the degree of parasiticidal activity. A marked difference in both the numbers of infected macrophages and numbers of parasites per 100 macrophages was observed in the nonadherent cells when compared with those of the adherent cell population. When macrophage Fc gamma receptors were down-modulated, opsonized tachyzoites retained their ability to penetrate the host cell at a rate similar to that observed for unopsonized parasites. These results suggest that antibody opsonization of T. gondii does not prevent active penetration of human monocytes by the parasite and, furthermore, has little effect on intracellular replication of the parasite.

Full Text

The Full Text of this article is available as a PDF (238.6 KB).

Selected References

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

  1. Anderson S. E., Jr, Bautista S. C., Remington J. S. Specific antibody-dependent killing of Toxoplasma gondii by normal macrophages. Clin Exp Immunol. 1976 Dec;26(3):375–380. [PMC free article] [PubMed] [Google Scholar]
  2. Anderson S. E., Jr, Remington J. S. Effect of normal and activated human macrophages on Toxoplasma gondii. J Exp Med. 1974 May 1;139(5):1154–1174. doi: 10.1084/jem.139.5.1154. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Beaman M. H., Subauste C. S., Wong S. Y., Remington J. S. Toxoplasma-macrophage interactions. Immunol Ser. 1994;60:475–493. [PubMed] [Google Scholar]
  4. Berón W., Alvarez-Dominguez C., Mayorga L., Stahl P. D. Membrane trafficking along the phagocytic pathway. Trends Cell Biol. 1995 Mar;5(3):100–104. doi: 10.1016/s0962-8924(00)88958-8. [DOI] [PubMed] [Google Scholar]
  5. Brown D. L., Phillips D. R., Damsky C. H., Charo I. F. Synthesis and expression of the fibroblast fibronectin receptor in human monocytes. J Clin Invest. 1989 Jul;84(1):366–370. doi: 10.1172/JCI114166. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Dubremetz J. F., Rodriguez C., Ferreira E. Toxoplasma gondii: redistribution of monoclonal antibodies on tachyzoites during host cell invasion. Exp Parasitol. 1985 Feb;59(1):24–32. doi: 10.1016/0014-4894(85)90053-0. [DOI] [PubMed] [Google Scholar]
  7. Graziano R. F., Fanger M. W. Human monocyte-mediated cytotoxicity: the use of Ig-bearing hybridomas as target cells to detect trigger molecules on the monocyte cell surface. J Immunol. 1987 Feb 1;138(3):945–950. [PubMed] [Google Scholar]
  8. Grimwood J., Smith J. E. Kinetics of the growth and variation in infectivity of Toxoplasma gondii in mice. Ann Trop Med Parasitol. 1991 Dec;85(6):659–661. doi: 10.1080/00034983.1991.11812622. [DOI] [PubMed] [Google Scholar]
  9. Hauser W. E., Jr, Remington J. S. Effect of monoclonal antibodies on phagocytosis and killing of Toxoplasma gondii by normal macrophages. Infect Immun. 1981 May;32(2):637–640. doi: 10.1128/iai.32.2.637-640.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Joiner K. A., Fuhrman S. A., Miettinen H. M., Kasper L. H., Mellman I. Toxoplasma gondii: fusion competence of parasitophorous vacuoles in Fc receptor-transfected fibroblasts. Science. 1990 Aug 10;249(4969):641–646. doi: 10.1126/science.2200126. [DOI] [PubMed] [Google Scholar]
  11. Kasper L. H., Crabb J. H., Pfefferkorn E. R. Isolation and characterization of a monoclonal antibody-resistant antigenic mutant of Toxoplasma gondii. J Immunol. 1982 Oct;129(4):1694–1699. [PubMed] [Google Scholar]
  12. Kasper L. H., Mineo J. R. Attachment and invasion of host cells by Toxoplasma gondii. Parasitol Today. 1994 May;10(5):184–188. doi: 10.1016/0169-4758(94)90026-4. [DOI] [PubMed] [Google Scholar]
  13. Lee M. T., Kaushansky K., Ralph P., Ladner M. B. Differential expression of M-CSF, G-CSF, and GM-CSF by human monocytes. J Leukoc Biol. 1990 Mar;47(3):275–282. doi: 10.1002/jlb.47.3.275. [DOI] [PubMed] [Google Scholar]
  14. McCabe R. E., Catterall J. R., Remington J. S. Unique differences in infectivity and seroreactivity of Toxoplasma harvested from mice infected for different lengths of time. J Parasitol. 1987 Dec;73(6):1152–1157. [PubMed] [Google Scholar]
  15. McLeod R., Estes R., Mack D. G., McLeod E. G. Effects of human alveolar macrophages and peripheral blood monocytes on Toxoplasma gondii. J Infect Dis. 1983 May;147(5):957–957. doi: 10.1093/infdis/147.5.957. [DOI] [PubMed] [Google Scholar]
  16. Michl J., Pieczonka M. M., Unkeless J. C., Silverstein S. C. Effects of immobilized immune complexes on Fc- and complement-receptor function in resident and thioglycollate-elicited mouse peritoneal macrophages. J Exp Med. 1979 Sep 19;150(3):607–621. doi: 10.1084/jem.150.3.607. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Mineo J. R., McLeod R., Mack D., Smith J., Khan I. A., Ely K. H., Kasper L. H. Antibodies to Toxoplasma gondii major surface protein (SAG-1, P30) inhibit infection of host cells and are produced in murine intestine after peroral infection. J Immunol. 1993 May 1;150(9):3951–3964. [PubMed] [Google Scholar]
  18. Owen C. A., Campbell E. J., Stockley R. A. Monocyte adherence to fibronectin: role of CD11/CD18 integrins and relationship to other monocyte functions. J Leukoc Biol. 1992 Apr;51(4):400–408. doi: 10.1002/jlb.51.4.400. [DOI] [PubMed] [Google Scholar]
  19. Pelloux H., Chumpitazi B. F., Santoro F., Polack B., Vuillez J. P., Ambroise-Thomas P. Sera of patients with high titers of immunoglobulin G against Toxoplasma gondii induce secretion of tumor necrosis factor alpha by human monocytes. Infect Immun. 1992 Jul;60(7):2672–2676. doi: 10.1128/iai.60.7.2672-2676.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Remington J. S., Krahenbuhl J. L., Mendenhall J. W. A role for activated macrophages in resistance to infection with Toxoplasma. Infect Immun. 1972 Nov;6(5):829–834. doi: 10.1128/iai.6.5.829-834.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Sharma S. D., Catterall J. R., Remington J. S. Parasiticidal activity of macrophages against Toxoplasma. Methods Enzymol. 1986;132:626–637. doi: 10.1016/s0076-6879(86)32046-9. [DOI] [PubMed] [Google Scholar]
  22. Sibley L. D., Weidner E., Krahenbuhl J. L. Phagosome acidification blocked by intracellular Toxoplasma gondii. 1985 May 30-Jun 5Nature. 315(6018):416–419. doi: 10.1038/315416a0. [DOI] [PubMed] [Google Scholar]
  23. Sporn S. A., Eierman D. F., Johnson C. E., Morris J., Martin G., Ladner M., Haskill S. Monocyte adherence results in selective induction of novel genes sharing homology with mediators of inflammation and tissue repair. J Immunol. 1990 Jun 1;144(11):4434–4441. [PubMed] [Google Scholar]
  24. Wilson C. B., Remington J. S. Activity of human blood leukocytes against Toxoplasma gondii. J Infect Dis. 1979 Dec;140(6):890–895. doi: 10.1093/infdis/140.6.890. [DOI] [PubMed] [Google Scholar]
  25. Wilson C. B., Tsai V., Remington J. S. Failure to trigger the oxidative metabolic burst by normal macrophages: possible mechanism for survival of intracellular pathogens. J Exp Med. 1980 Feb 1;151(2):328–346. doi: 10.1084/jem.151.2.328. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Woof J. M., Partridge L. J., Jefferis R., Burton D. R. Localisation of the monocyte-binding region on human immunoglobulin G. Mol Immunol. 1986 Mar;23(3):319–330. doi: 10.1016/0161-5890(86)90059-3. [DOI] [PubMed] [Google Scholar]
  27. Wright S. D. Methods for the study of receptor-mediated phagocytosis. Methods Enzymol. 1986;132:204–221. doi: 10.1016/s0076-6879(86)32009-3. [DOI] [PubMed] [Google Scholar]
  28. Zhou P., Thomassen M. J., Pettay J., Deodhar S. D., Barna B. P. Human monocytes produce monocyte chemoattractant protein 1 (MCP-1) in response to a synthetic peptide derived from C-reactive protein. Clin Immunol Immunopathol. 1995 Jan;74(1):84–88. doi: 10.1006/clin.1995.1012. [DOI] [PubMed] [Google Scholar]

Articles from Infection and Immunity are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES