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Clinical and Experimental Immunology logoLink to Clinical and Experimental Immunology
. 1984 Jun;56(3):559–566.

Human neutrophils require activation by mononuclear leucocyte conditioned medium to kill the pathogenic free-living amoeba, Naegleria fowleri.

A Ferrante, T J Mocatta
PMCID: PMC1535980  PMID: 6378454

Abstract

Naegleria fowleri is a free-living amoeba which causes a fulminant and rapidly fatal meningoencephalitis in man. Human neutrophils fail to kill the amoeba in vitro, but can do so if they are exposed to conditioned medium (CM) from PHA stimulated mononuclear leucocytes (MNLs). Specific antibody or complement was required to effect amoeba killing by CM modified neutrophils. Only short time exposure of the leucocytes to CM was required to endow them with amoebicidal properties. The CM was also shown to contain neutrophil migration inhibition activity and an activity(ies) which induced a respiratory burst in neutrophils. The results highlight the importance of MNL products other than specific antibody in neutrophil anti-microbial activity.

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Selected References

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  1. Badenoch-Jones P. Lymphokine-induced neutrophil aggregation. Immunology. 1982 Sep;47(1):169–174. [PMC free article] [PubMed] [Google Scholar]
  2. Chess L., Rocklin R. E., MacDermott R. P., David J. R., Schlossman S. F. Leukocyte inhibitory factor (LIF): production by purified human T and B lymphocytes. J Immunol. 1975 Jul;115(1):315–317. [PubMed] [Google Scholar]
  3. Clark R. A., Klebanoff S. J. Neutrophil-mediated tumor cell cytotoxicity: role of the peroxidase system. J Exp Med. 1975 Jun 1;141(6):1442–1447. doi: 10.1084/jem.141.6.1442. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Densen P., Mandell G. L. Phagocyte strategy vs. microbial tactics. Rev Infect Dis. 1980 Sep-Oct;2(5):817–838. doi: 10.1093/clinids/2.5.817. [DOI] [PubMed] [Google Scholar]
  5. Diamantstein T., Klos M., Gold D., Hahn H. Interaction between Entamoeba histolytica and the immune system. I. Mitogenicity of Entamoeba histolytica extracts for human peripheral T lymphocytes. J Immunol. 1981 Jun;126(6):2084–2086. [PubMed] [Google Scholar]
  6. Ehlenberger A. G., Nussenzweig V. The role of membrane receptors for C3b and C3d in phagocytosis. J Exp Med. 1977 Feb 1;145(2):357–371. doi: 10.1084/jem.145.2.357. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Ferrante A., Beard L. J., Thong Y. H. Early decay of human neutrophil chemotactic responsiveness following isolation from peripheral blood. Clin Exp Immunol. 1980 Feb;39(2):532–537. [PMC free article] [PubMed] [Google Scholar]
  8. Ferrante A. Comparative sensitivity of Naegleria fowleri to amphotericin B and amphotericin B methyl ester. Trans R Soc Trop Med Hyg. 1982;76(4):476–478. doi: 10.1016/0035-9203(82)90141-9. [DOI] [PubMed] [Google Scholar]
  9. Ferrante A., Thong Y. H. Antibody induced capping and endocytosis of surface antigens in Naegleria fowleri. Int J Parasitol. 1979 Dec;9(6):599–601. doi: 10.1016/0020-7519(79)90018-3. [DOI] [PubMed] [Google Scholar]
  10. Ferrante A., Thong Y. H. Optimal conditions for simultaneous purification of mononuclear and polymorphonuclear leucocytes from human blood by the Hypaque-Ficoll method. J Immunol Methods. 1980;36(2):109–117. doi: 10.1016/0022-1759(80)90036-8. [DOI] [PubMed] [Google Scholar]
  11. Ferrante A., Thong Y. H. Separation of mononuclear and polymorphonuclear leucocytes from human blood by the one-step Hypaque-Ficoll method is dependent on blood column height. J Immunol Methods. 1982;48(1):81–85. doi: 10.1016/0022-1759(82)90212-5. [DOI] [PubMed] [Google Scholar]
  12. Grewal A. S., Rouse B. T., Babiuk L. A. Mechanisms of recovery from viral infections: destruction of infected cells by neutrophils and complement. J Immunol. 1980 Jan;124(1):312–319. [PubMed] [Google Scholar]
  13. Guerrant R. L., Brush J., Ravdin J. I., Sullivan J. A., Mandell G. L. Interaction between Entamoeba histolytica and human polymorphonuclear neutrophils. J Infect Dis. 1981 Jan;143(1):83–93. doi: 10.1093/infdis/143.1.83. [DOI] [PubMed] [Google Scholar]
  14. Hofstaetter T., Brammsen H. A microassay for nitroblue tetrazolium reduction by human neutrophils. Immunobiology. 1981;159(3):283–292. doi: 10.1016/S0171-2985(81)80086-1. [DOI] [PubMed] [Google Scholar]
  15. Hokland P., Berg K. Interferon enhances the antibody-dependent cellular cytotoxicity (ADCC) of human polymorphonuclear leukocytes. J Immunol. 1981 Oct;127(4):1585–1588. [PubMed] [Google Scholar]
  16. Holbrook T. W., Boackle R. J., Parker B. W., Vesely J. Activation of the alternative complement pathway by Naegleria fowleri. Infect Immun. 1980 Oct;30(1):58–61. doi: 10.1128/iai.30.1.58-61.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Klempner M. S., Rocklin R. E. Specific binding of leukocyte inhibitory factor to neutrophil plasma membranes. J Immunol. 1982 May;128(5):2040–2043. [PubMed] [Google Scholar]
  18. Lomnitzer R., Glover A., Rabson A. R. The effect of PHA-activated MN-cell supernatants on polymorphonuclear leucocyte function. Clin Exp Immunol. 1977 Sep;29(3):501–508. [PMC free article] [PubMed] [Google Scholar]
  19. Nelson R. D., Quie P. G., Simmons R. L. Chemotaxis under agarose: a new and simple method for measuring chemotaxis and spontaneous migration of human polymorphonuclear leukocytes and monocytes. J Immunol. 1975 Dec;115(6):1650–1656. [PubMed] [Google Scholar]
  20. Paton J. C., Ferrante A. Inhibition of human polymorphonuclear leukocyte respiratory burst, bactericidal activity, and migration by pneumolysin. Infect Immun. 1983 Sep;41(3):1212–1216. doi: 10.1128/iai.41.3.1212-1216.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Russell A. S., Miller C. A possible role for polymorphonuclear leucocytes in the defence against recrudescent herpes simplex virus infection in man. Immunology. 1978 Mar;34(3):371–378. [PMC free article] [PubMed] [Google Scholar]
  22. Thong Y. H., Carter R. F., Ferrante A., Rowan-Kelly B. Site of expression of immunity to Naegleria fowleri in immunized mice. Parasite Immunol. 1983 Jan;5(1):67–76. doi: 10.1111/j.1365-3024.1983.tb00724.x. [DOI] [PubMed] [Google Scholar]
  23. Thong Y. H., Ferrante A., Rowan-Kelly B., O'Keefe D. E. Immunization with culture supernatant in experimental amoebic meningoencephalitis. Trans R Soc Trop Med Hyg. 1979;73(6):684–685. doi: 10.1016/0035-9203(79)90021-x. [DOI] [PubMed] [Google Scholar]
  24. Thong Y. H., Ferrante A., Rowan-Kelly B., O'Keefe D. Immunization with live amoebae, amoebic lysate and culture supernatant in experimental Naegleria meningoencephalitis. Trans R Soc Trop Med Hyg. 1980;74(5):570–576. doi: 10.1016/0035-9203(80)90141-8. [DOI] [PubMed] [Google Scholar]
  25. Thong Y. H., Shepherd C., Ferrante A., Rowan-Kelly B. Protective immunity to Naegleria fowleri in experimental amebic meningoencephalitis. Am J Trop Med Hyg. 1978 Mar;27(2 Pt 1):238–240. doi: 10.4269/ajtmh.1978.27.238. [DOI] [PubMed] [Google Scholar]
  26. Vadas M. A., Nicola N. A., Metcalf D. Activation of antibody-dependent cell-mediated cytotoxicity of human neutrophils and eosinophils by separate colony-stimulating factors. J Immunol. 1983 Feb;130(2):795–799. [PubMed] [Google Scholar]
  27. Weisbart R. H., Billing R. Requirement for B-lymphocyte alloantigen in the production of neutrophil migration inhibition factor from T lymphocytes (NIF-T). Immunology. 1980 Apr;39(4):577–582. [PMC free article] [PubMed] [Google Scholar]

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