Plasmodium falciparum rhoptry protein RSP2 triggers destruction of the erythroid lineage

Blood

Volumn 106, Issue 10, 2005, Pages 3632-3638

  Layez, Corinne ^b   Nogueira, Paulo ^b   Combes, Valery ^b   Costa, Fabio T M ^b   Juhan Vague, Irène ^b   Pereira Da Silva, Luiz H ^b   Gysin, Jürg ^a  

^a AIX MARSEILLE UNIVERSITY   (France)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

MONOCLONAL ANTIBODY; PROTOZOAL PROTEIN; RHOPTRY PROTEIN RING SURFACE PROTEIN 2; UNCLASSIFIED DRUG;

ANEMIA; ARTICLE; BONE MARROW; CELL DESTRUCTION; CELL LINEAGE; COMPLEMENT ACTIVATION; CONTROLLED STUDY; DYSERYTHROPOIESIS; ERYTHROCYTE; ERYTHROID CELL; HOST CELL; HUMAN; HUMAN CELL; IN VITRO STUDY; MALARIA; MALARIA FALCIPARUM; PHAGOCYTOSIS; PLASMODIUM FALCIPARUM; PRIORITY JOURNAL; SERUM; STEM CELL;

EID: 27744463413     PISSN: 00064971     EISSN: 00064971     Source Type: Journal    
DOI: 10.1182/blood-2005-04-1574     Document Type: Article

References (38)

1. Abdalla S, Weatherall DJ, Wickramasinghe SN, Hughes M. The anaemia of P. falciparum malaria. Br J Haematol. 1980;46:171-183.
2. Phillips RE, Pasvol G. Anaemia of Plasmodium falciparum malaria. Baillieres Clin Haematol. 1992;5:315-330.
3. Looareesuwan S, Merry AH, Phillips RE, et al. Reduced erythrocyte survival following clearance of malarial parasitaemia in Thai patients. Br J Haematol. 1987;67:473-478.
4. Dondorp AM, Kager PA, Vreeken J, White NJ. Abnormal blood flow and red blood cell deformability in severe malaria. Parasitol Today. 2000;16:228-232.
5. Dondorp AM, Angus BJ, Chotivanich K, et al. Red blood cell deformability as a predictor of anemia in severe falciparum malaria. Am J Trop Med Hyg. 1999;60:733-737.
6. Douki JB, Sterkers Y, Lepolard C, et al. Adhesion of normal and Plasmodium falciparum ring-infected erythrocytes to endothelial cells and the placenta involves the rhoptry-derived ring surface protein-2. Blood. 2003;101:5025-5032.
7. Saul A. Towards a malaria vaccine: riding the rollercoaster between unrealistic optimism and lethal pessimism. Southeast Asian J Trop Med Public Health. 1992;23:656-671.
8. Trager W, Jensen JB. Human malaria parasites in continuous culture. Science. 1976;193:673-675.
9. Lambros C, Vanderberg JP. Synchronization of Plasmodium falciparum erythrocytic stages in culture. J Parasitol. 1979;65:418-420.
10. Robert C, Pouvelle B, Meyer P, et al. Chondroitin-4-sulphate (proteoglycan), a receptor for Plasmodium falciparum-infected erythrocyte adherence on brain microvascular endothelial cells. Res Immunol. 1995;146:383-393.
11. Pouvelle B, Buffet PA, Lepolard C, Scherf A, Gysin J. Cytoadhesion of Plasmodium falciparum ring-stage-infected erythrocytes. Nat Med. 2000;6:1264-1268.
12. Andrews KT, Pirrit LA, Przyborski JM, et al. Recovery of adhesion to chondroitin-4-sulphate in Plasmodium falciparum varCSA disruption mutants by antigenically similar PfEMP1 variants. Mol Microbiol. 2003;49:655-669.
13. Gysin J, Pouvelle B, Fievet N, Scherf A, Lepolard C. Ex vivo desequestration of Plasmodium falciparum-infected erythrocytes from human placenta by chondroitin sulfate A. Infect Immun. 1999;67:6596-6602.
14. Chen P, Lamont G, Elliott T, et al. Plasmodium falciparum strains from Papua New Guinea: culture characteristics and drug sensitivity. Southeast Asian J Trop Med Public Health. 1980;11:435-440.
15. Baldi DL, Andrews KT, Waller RF, et al. RAP1 controls rhoptry targeting of RAP2 in the malaria parasite Plasmodium falciparum. EMBO J. 2000;19:2435-2443.
16. Oduola AM, Milhous WK, Weatherly NF, Bowdre JH, Desjardins RE. Plasmodium falciparum: induction of resistance to mefloquine in cloned strains by continuous drug exposure in vitro. Exp Parasitol. 1988;67:354-360.
17. Baldi DL, Good R, Duraisingh MT, Crabb BS, Cowman AF. Identification and disruption of the gene encoding the third member of the low-molecular-mass rhoptry complex in Plasmodium falciparum. Infect Immun. 2002;70:5236-5245.
18. Martin P, Papayannopoulou T. HEL cells: a new human erythroleukemia cell line with spontaneous and induced globin expression. Science. 1982;216:1233-1235.
19. Okano H, Okamura J, Yagawa K, Tasaka H, Motomura S. Human erythroid cell lines derived from a patient with acute erythremia. J Cancer Res Clin Oncol. 1981;102:49-55.
20. Groux H, Gysin J. Opsonization as an effector mechanism in human protection against asexual blood stages of Plasmodium falciparum: functional role of IgG subclasses. Res Immunol. 1990;141:529-542.
21. Sabchareon A, Burnouf T, Ouattara D, et al. Parasitologic and clinical human response to immunoglobulin administration in falciparum malaria. Am J Trop Med Hyg. 1991;45:297-308.
22. Gysin J, Moisson P, Pereira da Silva L, Druilhe P. Antibodies from immune African donors with a protective effect in Plasmodium falciparum human infection are also able to control asexual blood forms of the parasite in Saimiri monkeys. Res Immunol. 1996;147:397-401.
23. Letestu R, Valensi F. Bone marrow aspiration for diagnostic purposes [in French]. Ann Biol Clin (Paris). 2003;61:655-665.
24. Holm I, Nato F, Mendis KN, Longacre S. Characterization of C-terminal merozoite surface protein-1 baculovirus recombinant proteins from Plasmodium vivax and Plasmodium cynomolgi as recognized by the natural anti-parasite immune response. Mol Biochem Parasitol. 1997;89:313-319.
25. Friedman MJ, Blankenberg T, Sensabaugh G, Tenforde TS. Recognition and invasion of human erythrocytes by malarial parasites: contribution of sialoglycoproteins to attachment and host specificity. J Cell Biol. 1984;98:1672-1677.
26. Baum J, Ward RH, Conway DJ. Natural selection on the erythrocyte surface. Mol Biol Evol. 2002;19:223-229.
27. Looareesuwan S, Davis TM, Pukrittayakamee S, et al. Erythrocyte survival in severe falciparum malaria. Acta Trop. 1991;48:263-270.
28. Knuttgen HJ. The bone marrow of non-immune Europeans in acute malaria infection: a topical review. Ann Trop Med Parasitol. 1987;81:567-576.
29. Wickramasinghe SN, Abdalla SH. Blood and bone marrow changes in malaria. Baillieres Best Pract Res Clin Haematol. 2000;13:277-299.
30. Facer CA, Brown J. Monocyte erythrophagocytosis in falciparum malaria. Lancet. 1981;1:897-898.
31. Goka BQ, Kwarko H, Kurtzhals JA, et al. Complement binding to erythrocytes is associated with macrophage activation and reduced haemoglobin in Plasmodium falciparum malaria. Trans R Soc Trop Med Hyg. 2001;95:545-549.
32. Waitumbi JN, Opollo MO, Muga RO, Misore AO, Stoute JA. Red cell surface changes and erythrophagocytosis in children with severe Plasmodium falciparum anemia. Blood. 2000;95:1481-1486.
33. Ekvall H. Malaria and anemia. Curr Opin Hematol. 2003;10:108-114.
34. Stowers A, Taylor D, Prescott N, Cheng Q, Cooper J, Saul A. Assessment of the humoral immune response against Plasmodium falciparum rhoptry-associated proteins 1 and 2. Infect Immun. 1997;65:2329-2338.
35. Rogerson SJ, Pollina E, Getachew A, Tadesse E, Lema VM, Molyneux ME. Placental monocyte infiltrates in response to Plasmodium falciparum malaria infection and their association with adverse pregnancy outcomes. Am J Trop Med Hyg. 2003;68:115-119.
36. Omodeo-Sale F, Motti A, Dondorp A, White NJ, Taramelli D. Destabilisation and subsequent lysis of human erythrocytes induced by Plasmodium falciparum haem products. Eur J Haematol. 2005;74:324-332.
37. Weatherall DJ, Abdalla S, Pippard MJ. The anaemia of Plasmodium falciparum malaria. Ciba Found Symp. 1983;94:74-97.
38. Perrin LH, Loche M, Dedet JP, Roussilhon C, Fandeur T. Immunization against Plasmodium falciparum asexual blood stages using soluble antigens. Clin Exp Immunol. 1984;56:67-72.