Abstract
Sera (BCG-lipopolysaccharide [LPS] serum) were obtained from mice infected with Mycobacterium bovis BCG 2 h after intravenous administration of bacterial endotoxin (LPS). Varying concentrations of sera were added to cultures of Plasmodium falciparum-infected human erythrocytes; parasite viability was assessed by hypoxanthine incorporation after 4 days in culture. At concentrations of 1 to 3%, cultures treated with BCG-LPS serum showed a two- to threefold increase in hypoxanthine incorporation; at higher concentrations (4 to 8%), hypoxanthine incorporation fell to 2 to 5% of that in control cultures. Concurrent assays with control sera (from untreated mice or mice treated with BCG or LPS alone) caused some stimulation but no inhibition at up to 8% concentration. Examination of cultures treated with BCG-LPS serum showed morphological, deterioration of parasites within erythrocytes. The presence of tumor necrosis factor in the BCG-LPS serum was confirmed by using a standard L-cell cytotoxicity assay. In addition, rabbit antiserum against partially purified tumor necrosis factor protected intraerythrocytic forms of P. falciparum from the toxic effects of BCG-LPS serum. These data suggest that the factor in BCG-LPS serum that is toxic to P. falciparum in human erythrocytes is antigenically similar or identical to tumor necrosis factor. This nonantibody mediator of killing may play a role in human malaria.
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- Baldwin R. W., Pimm M. V. BCG in tumor immunotherapy. Adv Cancer Res. 1978;28:91–147. doi: 10.1016/s0065-230x(08)60647-8. [DOI] [PubMed] [Google Scholar]
- Berry L. J. Bacterial toxins. CRC Crit Rev Toxicol. 1977 Nov;5(3):239–318. doi: 10.3109/10408447709082601. [DOI] [PubMed] [Google Scholar]
- Carswell E. A., Old L. J., Kassel R. L., Green S., Fiore N., Williamson B. An endotoxin-induced serum factor that causes necrosis of tumors. Proc Natl Acad Sci U S A. 1975 Sep;72(9):3666–3670. doi: 10.1073/pnas.72.9.3666. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chulay J. D., Haynes J. D., Diggs C. L. Inhibition of in vitro growth of Plasmodium falciparum by immune serum from monkeys. J Infect Dis. 1981 Sep;144(3):270–278. doi: 10.1093/infdis/144.3.270. [DOI] [PubMed] [Google Scholar]
- Chulay J. D., Haynes J. D., Diggs C. L. Plasmodium falciparum: assessment of in vitro growth by [3H]hypoxanthine incorporation. Exp Parasitol. 1983 Feb;55(1):138–146. doi: 10.1016/0014-4894(83)90007-3. [DOI] [PubMed] [Google Scholar]
- Clark I. A. Does endotoxin cause both the disease and parasite death in acute malaria and babesiosis? Lancet. 1978 Jul 8;2(8080):75–77. doi: 10.1016/s0140-6736(78)91386-7. [DOI] [PubMed] [Google Scholar]
- Clark I. A., Virelizier J. L., Carswell E. A., Wood P. R. Possible importance of macrophage-derived mediators in acute malaria. Infect Immun. 1981 Jun;32(3):1058–1066. doi: 10.1128/iai.32.3.1058-1066.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gentry M. K., Dalrymple J. M. Quantitative microtiter cytotoxicity assay for Shigella toxin. J Clin Microbiol. 1980 Sep;12(3):361–366. doi: 10.1128/jcm.12.3.361-366.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hammerstrøm J. Human adherent mononuclear blood cells: cytolytic and cytostatic activity and characterization of effector cells during in vitro culture. Acta Pathol Microbiol Scand C. 1981 Apr;89(2):115–122. doi: 10.1111/j.1699-0463.1981.tb02674.x. [DOI] [PubMed] [Google Scholar]
- Hammerstrøm J. Human monocyte-mediated cytotoxicity to K-562 cells: activation by lymphokines. Scand J Immunol. 1979;10(6):575–584. doi: 10.1111/j.1365-3083.1979.tb01392.x. [DOI] [PubMed] [Google Scholar]
- Hoffmann M. K., Oettgen H. F., Old L. J., Mittler R. S., Hammerling U. Induction and immunological properties of tumor necrosis factor. J Reticuloendothel Soc. 1978 Apr;23(4):307–319. [PubMed] [Google Scholar]
- Jensen J. B., Boland M. T., Akood M. Induction of crisis forms in cultured Plasmodium falciparum with human immune serum from Sudan. Science. 1982 Jun 11;216(4551):1230–1233. doi: 10.1126/science.7043736. [DOI] [PubMed] [Google Scholar]
- Jensen J. B., Boland M. T., Hayes M., Akood M. A. Plasmodium falciparum: rapid assay for in vitro inhibition due to human serum from residents of malarious areas. Exp Parasitol. 1982 Dec;54(3):416–424. doi: 10.1016/0014-4894(82)90051-0. [DOI] [PubMed] [Google Scholar]
- Jensen J. B., Trager W. Plasmodium falciparum in culture: establishment of additional strains. Am J Trop Med Hyg. 1978 Jul;27(4):743–746. doi: 10.4269/ajtmh.1978.27.743. [DOI] [PubMed] [Google Scholar]
- Kutner S., Baruch D., Ginsburg H., Cabantchik Z. I. Alterations in membrane permeability of malaria-infected human erythrocytes are related to the growth stage of the parasite. Biochim Biophys Acta. 1982 Apr 23;687(1):113–117. doi: 10.1016/0005-2736(82)90178-x. [DOI] [PubMed] [Google Scholar]
- Lambros C., Vanderberg J. P. Synchronization of Plasmodium falciparum erythrocytic stages in culture. J Parasitol. 1979 Jun;65(3):418–420. [PubMed] [Google Scholar]
- Loose L. D., Trejo R., Di Luzio N. R. Impaired endotoxin detoxification as a factor in enhanced endotoxin sensitivity of malaria infected mice. Proc Soc Exp Biol Med. 1971 Jul;137(3):794–797. doi: 10.3181/00379727-137-35669. [DOI] [PubMed] [Google Scholar]
- Matthews N., Watkins J. F. Tumour-necrosis factor from the rabbit. I. Mode of action, specificity and physicochemical properties. Br J Cancer. 1978 Aug;38(2):302–309. doi: 10.1038/bjc.1978.202. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Milas L., Scott M. T. Antitumor activity of Corynebacterium parvum. Adv Cancer Res. 1978;26:257–306. doi: 10.1016/s0065-230x(08)60090-1. [DOI] [PubMed] [Google Scholar]
- Moore R. N., Goodrum K. J., Berry L. J. Mediation of an endotoxic effect by macrophages. J Reticuloendothel Soc. 1976 Mar;19(3):187–197. [PubMed] [Google Scholar]
- Männel D. N., Falk W., Meltzer M. S. Inhibition of nonspecific tumoricidal activity by activated macrophages with antiserum against a soluble cytotoxic factor. Infect Immun. 1981 Jul;33(1):156–164. doi: 10.1128/iai.33.1.156-164.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Männel D. N., Meltzer M. S., Mergenhagen S. E. Generation and characterization of a lipopolysaccharide-induced and serum-derived cytotoxic factor for tumor cells. Infect Immun. 1980 Apr;28(1):204–211. doi: 10.1128/iai.28.1.204-211.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ojo-Amaize E. A., Salimonu L. S., Williams A. I., Akinwolere O. A., Shabo R., Alm G. V., Wigzell H. Positive correlation between degree of parasitemia, interferon titers, and natural killer cell activity in Plasmodium falciparum-infected children. J Immunol. 1981 Dec;127(6):2296–2300. [PubMed] [Google Scholar]
- Pasvol G., Wilson R. J. The interaction of malaria parasites with red blood cells. Br Med Bull. 1982 May;38(2):133–140. doi: 10.1093/oxfordjournals.bmb.a071749. [DOI] [PubMed] [Google Scholar]
- Ruddle N. H., Waksman B. H. Cytotoxicity mediated by soluble antigen and lymphocytes in delayed hypersensitivity. 3. Analysis of mechanism. J Exp Med. 1968 Dec 1;128(6):1267–1279. doi: 10.1084/jem.128.6.1267. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SUTER E., ULLMAN G. E., HOFFMAN R. G. Sensitivity of mice to endotoxin after vaccination with BCG (Bacillus Calmette-Guérin). Proc Soc Exp Biol Med. 1958 Oct;99(1):167–169. doi: 10.3181/00379727-99-24282. [DOI] [PubMed] [Google Scholar]
- Taverne J., Dockrell H. M., Playfair J. H. Endotoxin-induced serum factor kills malarial parasites in vitro. Infect Immun. 1981 Jul;33(1):83–89. doi: 10.1128/iai.33.1.83-89.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wright S. C., Bonavida B. Selective lysis of NK-sensitive target cells by a soluble mediator released from murine spleen cells and human peripheral blood lymphocytes. J Immunol. 1981 Apr;126(4):1516–1521. [PubMed] [Google Scholar]

