Manipulation of apoptosis in the host-parasite interaction

Trends in Parasitology

Volumn 20, Issue 6, 2004, Pages 280-287

  James, Eric R ^a   Green, Douglas R ^b  

^a MEDICAL UNIVERSITY OF SOUTH CAROLINA   (United States)

^b LA JOLLA INSTITUTE FOR ALLERGY AND IMMUNOLOGY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTEMISIN; CERAMIDE; CHLOROQUINE; MEFLOQUINE;

APOPTOSIS; CHEMOTHERAPY; COMET ASSAY; HELMINTH; HOST PARASITE INTERACTION; HUMAN; IMMUNE RESPONSE; IMMUNOCOMPETENT CELL; IRRADIATION; METAZOON; PARASITE; PROTOZOON; REVIEW; VACCINATION;

ANIMALS; APOPTOSIS; HOST-PARASITE RELATIONS; PROTOZOA; PROTOZOAN INFECTIONS; PROTOZOAN VACCINES; VACCINES, ATTENUATED;

ANIMALIA; METAZOA; PROTOZOA; VERMES;

EID: 2442560408     PISSN: 14714922     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pt.2004.04.004     Document Type: Review

References (70)

1. Debrabant A., et al. Programmed cell death in trypanosomatids and other unicellular organisms. Int. J. Parasitol. 33:2003;257-267
2. Heussler V.T., et al. Inhibition of apoptosis by intracellular protozoan parasites. Int. J. Parasitol. 31:2001;1166-1176
3. Luder C.G., et al. Intracellular protozoan parasites and apoptosis: diverse strategies to modulate parasite-host interactions. Trends Parasitol. 17:2001;480-486
4. DosReis G.A., Barcinski M.A. Apoptosis and parasitism: from the parasite to the host immune response. Adv. Parasitol. 49:2001;133-161
5. Inohara N., Nuñez G. NODs: intracellular proteins involved in inflammation and apoptosis. Nat. Rev. Immunol. 3:2003;371-382
6. Nurnberger T., Brunner F. Innate immunity in plants and animals: emerging parallels between the recognition of general elicitors and pathogen-associated molecular patterns. Curr. Opin. Plant Biol. 5:2002;318-324
7. Aravind L., et al. The domains of death: evolution of the apoptosis machinery. Trends Biochem. Sci. 24:1999;47-53
8. Arnoult D., et al. On the evolution of programmed cell death: apoptosis of the unicellular eukaryote Leishmania major involves cysteine proteinase activation and mitochondrion permeabilization. Cell Death Differ. 9:2002;65-81
9. Lee N., et al. Programmed cell death in the unicellular protozoan parasite Leishmania. Cell Death Differ. 9:2002;53-64
10. Al-Olayan E.M., et al. Apoptosis in the malaria protozoan, Plasmodium berghei: a possible mechanism for limiting intensity of infection in the mosquito. Int. J. Parasitol. 32:2002;1133-1143
11. Uren A.G., et al. Identification of paracaspases and metacaspases: two ancient families of caspase-like proteins, one of which plays a key role in MALT lymphoma. Mol. Cell. 6:2000;961-967
12. Ouaissi A. Apoptosis-like death in trypanosomatids: search for putative pathways and genes involved. Kinetoplastid Biol. Dis. 2:2003;5
13. Miller M.B., Bassler B.L. Quorum sensing in bacteria. Annu. Rev. Microbiol. 55:2001;165-199
14. Donlan R.M. Biofilms: microbial life on surfaces. Emerg. Infect. Dis. 8:2002;881-890
15. Petri W.A. Jr, et al. The bittersweet interface of parasite and host: lectin-carbohydrate interactions during human invasion by the parasite Entamoeba histolytica. Annu. Rev. Microbiol. 56:2002;39-64
16. Debrabant A., Nakhasi H. Programmed cell death in trypanosomatids: is it an altruistic mechanism for survival of the fittest? Kinetoplastid Biol. Dis. 2:2003;7
17. Welburn S.C. Apoptosis in procyclic Trypanosoma brucei rhodesiense in vitro. Cell Death Differ. 3:1996;229-236
18. Ameisen J.C. On the origin, evolution, and nature of programmed cell death: a timeline of four billion years. Cell Death Differ. 9:2002;367-393
19. Tibayrenc M., et al. A clonal theory of parasitic protozoa: the population structures of Entamoeba, Giardia, Leishmania, Naegleria, Plasmodium, Trichomonas, and Trypanosoma and their medical and taxonomical consequences. Proc. Natl. Acad. Sci. U. S. A. 87:1990;2414-2418
20. Lewis K. Programmed death in bacteria. Microbiol. Mol. Biol. Rev. 64:2000;503-514
21. Lam E., et al. Programmed cell death, mitochondria and the plant hypersensitive response. Nature. 411:2001;848-853
22. James E.R., Green D.R. Infection and the origins of apoptosis. Cell Death Differ. 9:2002;355-357
23. Hacker G., Fischer S.F. Bacterial anti-apoptotic activities. FEMS Microbiol. Lett. 211:2002;1-6
24. Benedict C.A., et al. To kill or be killed: viral evasion of apoptosis. Nat. Immunol. 3:2002;1013-1018
25. Chen X.M., et al. Cryptosporidium parvum activates nuclear factor kappaB in biliary epithelia preventing epithelial cell apoptosis. Gastroenterology. 120:2001;1774-1783
26. Moore K.J., Matlashewski G. Intracellular infection by Leishmania donovani inhibits macrophage apoptosis. J. Immunol. 152:1994;2930-2937
27. Nash P.B., et al. Toxoplasma gondii-infected cells are resistant to multiple inducers of apoptosis. J. Immunol. 160:1998;1824-1830
28. Nakajima-Shimada J., et al. Inhibition of Fas-mediated apoptosis by Trypanosoma cruzi infection. Biochim. Biophys. Acta. 1475:2000;175-183
29. Green D.R., Evan G.I. A matter of life and death. Cancer Cell. 1:2002;19-30
30. Dobbelaere D.A.E., Rottenberg S. Theileria-induced leukocyte transformation. Curr. Opin. Microbiol. 6:2003;377-382
31. Heussler V.T., et al. Hijacking of host cell IKK signalosomes by the transforming parasite Theileria. Science. 298:2002;1033-1036
32. Kuenzi P., et al. Theileria parva-transformed T cells show enhanced resistance to Fas/Fas ligand-induced apoptosis. J. Immunol. 171:2003;1224-1231
33. Heussler V.T., et al. The intracellular parasite Theileria parva protects infected T cells from apoptosis. Proc. Natl. Acad. Sci. U. S. A. 96:1999;7312-7317
34. Coffer P. OutFOXing the grim reaper: novel mechanisms regulating longevity by forkhead transcription factors. Sci. STKE. 201:2003;PE39
35. Chuenkova M.V., et al. Trypanosoma cruzi trans-sialidase: a potent and specific survival factor for human Schwann cells by means of phosphatidylinositol 3-kinase/Akt signaling. Proc. Natl. Acad. Sci. U. S. A. 98:2001;9936-9941
36. Baumgartner M., et al. Constitutive exclusion of Csk from Hck-positive membrane microdomains permits Src kinase-dependent proliferation of Theileria-transformed B lymphocytes. Blood. 101:2003;1874-1881
37. Piacenza L., et al. L-arginine-dependent suppression of apoptosis in Trypanosoma cruzi: contribution of the nitric oxide and polyamine pathways. Proc. Natl. Acad. Sci. U. S. A. 98:2001;7301-7306
38. Channon J.Y., et al. Toxoplasma gondii induces granulocyte colony-stimulating factor and granulocyte-macrophage colony-stimulating factor secretion by human fibroblasts: implications for neutrophil apoptosis. Infect. Immun. 70:2002;6048-6057
39. Streilein J.W. Ocular immune privilege: the eye takes a dim but practical view of immunity and inflammation. J. Leukoc. Biol. 74:2003;179-185
40. Ferguson T.A., et al. Apoptosis, tolerance, and regulatory T cells - old wine, new wineskins. Immunol. Rev. 193:2003;111-123
41. Eidsmo L., et al. Alteration of Fas and Fas ligand expression during human visceral leishmaniasis. Clin. Exp. Immunol. 130:2002;307-313
42. Nishikawa Y., et al. Mechanisms of apoptosis in murine fibroblasts by two intracellular protozoan parasites, Toxoplasma gondii and Neospora caninum. Parasite Immunol. 24:2002;347-354
43. + B lymphocytes susceptible to Fas/Fas ligand-mediated fratricide. J. Immunol. 168:2002;3965-3973
44. Luder C.G., et al. Toxoplasma gondii inhibits MHC class II expression in neural antigen-presenting cells by down-regulating the class II transactivator CIITA. J. Neuroimmunol. 134:2003;12-24
45. Wei S., et al. Toxoplasma gondii-infected human myeloid dendritic cells induce T-lymphocyte dysfunction and contact-dependent apoptosis. Infect. Immun. 70:2002;1750-1760
46. Matsumoto J., et al. Malaria infection induces rapid elevation of the soluble Fas ligand level in serum and subsequent T lymphocytopenia: possible factors responsible for the differences in susceptibility of two species of Macaca monkeys to Plasmodium coatneyi infection. Infect. Immun. 68:2000;1183-1188
47. Wipasa J., et al. Apoptotic deletion of Th cells specific for the 19-kDa carboxyl-terminal fragment of merozoite surface protein 1 during malaria infection. J. Immunol. 167:2001;3903-3909
48. Gavrilescu L.C., Denkers E.Y. Interleukin-12 p40- and Fas ligand-dependent apoptotic pathways involving STAT-1 phosphorylation are triggered during infection with a virulent strain of Toxoplasma gondii. Infect. Immun. 71:2003;2577-2583
49. + T cells in malaria infection. J. Exp. Med. 195:2002;881-892
50. Freire-de-Lima C.G., et al. Uptake of apoptotic cells drives the growth of a pathogenic trypanosome in macrophages. Nature. 403:2000;199-203
51. de Freitas Balanco J.M., et al. Apoptotic mimicry by an obligate intracellular parasite downregulates macrophage microbicidal activity. Curr. Biol. 11:2001;1870-1873
52. Huston C.D., et al. Caspase 3-dependent killing of host cells by the parasite Entamoeba histolytica. Cell. Microbiol. 2:2000;617-625
53. Kuroda A., et al. Up-regulation of Fas (CD95) and induction of apoptosis in intestinal epithelial cells by nematode-derived molecules. Infect. Immun. 70:2002;4002-4008
54. +) T lymphocytes: a mechanism of immune unresponsiveness in filariasis. Eur. J. Immunol. 32:2002;858-867
55. Chen L., et al. Skin-stage schistosomula of Schistosoma mansoni produce an apoptosis-inducing factor that can cause apoptosis of T cells. J. Biol. Chem. 277:2002;34329-34335
56. + splenocytes undergo apoptosis during an experimental murine infection with Taenia crassiceps. Parasitol. Res. 90:2003;157-163
57. Rumbley C.A., et al. Elimination of lymphocytes, but not eosinophils, by Fas-mediated apoptosis in murine schistosomiasis. Am. J. Trop. Med. Hyg. 65:2001;442-449
58. Sereno D., et al. Antimonial-mediated DNA fragmentation in Leishmania infantum amastigotes. Antimicrob. Agents Chemother. 45:2001;2064-2069
59. Pankova-Kholmyansky I., et al. Ceramide mediates growth inhibition of the Plasmodium falciparum parasite. Cell. Mol. Life Sci. 60:2003;577-587
60. Picot S., et al. Apoptosis related to chloroquine sensitivity of the human malaria parasite Plasmodium falciparum. Trans. R. Soc. Trop. Med. Hyg. 91:1997;590-591
61. Bratosin D., et al. Programmed cell death in mature erythrocytes: a model for investigating death effector pathways operating in the absence of mitochondria. Cell Death Differ. 8:2001;1143-1156
62. Bergquist R., et al. Blueprint for schistosomiasis vaccine development. Acta Trop. 82:2002;183-192
63. Hoffman S.L., et al. Protection of humans against malaria by immunization with radiation-attenuated Plasmodium falciparum sporozoites. J. Infect. Dis. 185:2002;1155-1164
64. Hiramoto R.M., et al. 200 Gy sterilised Toxoplasma gondii tachyzoites maintain metabolic functions and mammalian cell invasion, eliciting cellular immunity and cytokine response similar to natural infection in mice. Vaccine. 20:2002;2072-2081
65. Schumacher B., et al. The C. elegans homolog of the p53 tumor suppressor is required for DNA damage-induced apoptosis. Curr. Biol. 11:2001;1722-1727
66. Flores-Perez I., et al. Apoptosis induced by gamma irradiation of Taenia solium metacestodes. Parasitol. Res. 90:2003;203-208
67. Scheffer S.R., et al. Apoptotic, but not necrotic, tumor cell vaccines induce a potent immune response in vivo. Int. J. Cancer. 103:2003;205-211
68. Harms-Ringdahl M., et al. Radiation induced apoptosis. Mutat. Res. 366:1996;171-179
69. Bickle Q.D., et al. The effects of gamma-irradiation on migration and survival of Schistosoma mansoni schistosomula in mice. Parasitology. 79:1979;223-230
70. Silvie O., et al. Effects of irradiation on Plasmodium falciparum sporozoite hepatic development: implications for the design of pre-erythrocytic malaria vaccines. Parasite Immunol. 24:2002;221-223