Differential regulation of β-chemokines in children with Plasmodium falciparum malaria

Infection and Immunity

Volumn 73, Issue 7, 2005, Pages 4190-4197

  Ochiel, Daniel O ^a   Awandare, Gordon A ^a   Keller, Christopher C ^a   Hittner, James B ^b   Kremsner, Peter G ^c,d   Weinberg, J Brice ^e   Perkins, Douglas J ^a,f  

^a UNIVERSITY OF PITTSBURGH   (United States)

^b School of Business   (United States)

^c UNIVERSITY OF TÜBINGEN   (Germany)

^d ALBERT SCHWEITZER HOSPITAL   (Gabon)

^e DUKE UNIVERSITY MEDICAL CENTER   (United States)

^f UNIVERSITY OF PITTSBURGH GRADUATE SCHOOL OF PUBLIC HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BETA CHEMOKINE; HEMATIN; HEMOZOIN; MACROPHAGE INFLAMMATORY PROTEIN 1ALPHA; MACROPHAGE INFLAMMATORY PROTEIN 1BETA; MALARIA PIGMENT; PIGMENT; RANTES; UNCLASSIFIED DRUG;

ANEMIA; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; EX VIVO STUDY; GENE EXPRESSION; HOST PATHOGEN INTERACTION; HUMAN; HUMAN CELL; IMMUNE RESPONSE; IN VITRO STUDY; MALARIA; PARASITEMIA; PERIPHERAL BLOOD MONONUCLEAR CELL; PLASMODIUM FALCIPARUM; PRIORITY JOURNAL; PROTEIN DETERMINATION;

CHILD; CHILD, PRESCHOOL; FEMALE; GENE EXPRESSION PROFILING; HEMEPROTEINS; HEMOGLOBINS; HUMANS; MACROPHAGE INFLAMMATORY PROTEIN-1; MALARIA, FALCIPARUM; MALE; RANTES;

EID: 21544468019     PISSN: 00199567     EISSN: None     Source Type: Journal    
DOI: 10.1128/IAI.73.7.4190-4197.2005     Document Type: Article

References (49)

1. Abrams, E. T., H. Brown, S. W. Chensue, G. D. Turner, E. Tadesse, V. M. Lema, M. E. Molyneux, R. Rochford, S. R. Meshnick, and S. J. Rogerson. 2003. Host response to malaria during pregnancy: placental monocyte recruitment is associated with elevated beta chemokine expression. J. Immunol. 170:2759-2764.
2. Bacon, K., M. Baggiolini, H. Broxmeyer, R. Horuk, I. Lindley, A. Mantovani, K. Maysushima, P. Murphy, H. Nomiyama, J. Oppenheim, A. Rot, T. Schall, M. Tsang, R. Thorpe, J. Van Damme, M. Wadhwa, O. Yoshie, A. Zlotnik, and K. Zoon. 2002. Chemokine/chemokine receptor nomenclature. J. Interferon Cytokine Res. 22:1067-1068.
3. Breman, J. G., A. Egan, and G. T. Keusch. 2001. The intolerable burden of malaria: a new look at the numbers. Am. J. Trop. Med. Hyg. 64:iv-vii.
4. Brenier-Pinchart, M. P., H. Pelloux, D. Derouich-Guergour, and P. Ambroise-Thomas. 2001. Chemokines in host-protozoan-parasite interactions. Trends Parasitol. 17:292-296.
5. Broxmeyer, H. E. 2001. Regulation of hematopoiesis by chemokine family members. Int. J. Hematol. 74:9-17.
6. Burgmann, H., U. Hollenstein, C. Wenisch, F. Thalhammer, S. Looareesuwan, and W. Graninger. 1995. Serum concentrations of MIP-1 alpha and interleukin-8 in patients suffering from acute Plasmodium falciparum malaria. Clin. Immunol. Immunopathol. 76:32-36.
7. Cantor, A. B., and S. H. Orkin. 2002. Transcriptional regulation of erythropoiesis: an affair involving multiple partners. Oncogene 21:3368-3376.
8. Chaisavaneeyakorn, S., J. M. Moore, L. Mirel, C. Othoro, J. Otieno, S. C. Chaiyaroj, Y. P. Shi, B. L. Nahlen, A. A. Lal, and V. Udhayakumar. 2003. Levels of macrophage inflammatory protein 1α (MIP-1α) and MIP-1β in intervillous blood plasma samples from women with placental malaria and human immunodeficiency virus infection. Clin. Diagn. Lab. Immunol. 10: 631-636.
9. Chaiyaroj, S. C., A. S. Rutta, K. Muenthaisong, P. Watkins, M. Na Ubol, and S. Looareesuwan. 2004. Reduced levels of transforming growth factor-beta 1, interleukin-12 and increased migration inhibitory factor are associated with severe malaria. Acta Trop. 89:319-327.
10. Chomczynski, P., and N. Sacchi. 1987. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162:156-159.
11. Cook, I. F. 1985. Herpes zoster in children following malaria. J. Trop. Med. Hyg. 88:261-264.
12. Dallalio, G., M. North, S. W. McKenzie, and R. T. Means, Jr. 1999. Cytokine and cytokine receptor concentrations in bone marrow supernatant from patients with HIV: correlation with hematologic parameters. J. Investig. Med. 47:477-483.
13. Dodoo, D., F. M. Omer, J. Todd, B. D. Akanmori, K. A. Koram, and E. M. Riley. 2002. Absolute levels and ratios of proinflammatory and anti-inflammatory cytokine production in vitro predict clinical immunity to Plasmodium falciparum malaria. J. Infect. Dis. 185:971-979.
14. Egan, T. J., W. W. Mavuso, and K. K. Ncokazi. 2001. The mechanism of beta-hematin formation in acetate solution. Parallels between hemozoin formation and biomineralization processes. Biochemistry 40:204-213.
15. Francis, S. E., D. J. Sullivan, Jr., and D. E. Goldberg. 1997. Hemoglobin metabolism in the malaria parasite Plasmodium falciparum. Annu. Rev. Microbiol. 51:97-123.
16. Goldie, P., E. Roth Jr., J. Oppenheim, and J. Vanderberg. 1990. Biochemical characterization of Plasmodium falciparum hemozoin. Am. J. Trop. Med. Hyg. 43:584-596.
17. Graham, G. J., and I. B. Pragnell. 1992. SCI/MIP-1 alpha: a potent stem cell inhibitor with potential roles in development. Dev. Biol. 151:377-381.
18. Graham, G. J., E. G. Wright, R. Hewick, S. D. Wolpe, N. M. Wilkie, D. Donaldson, S. Lorimore, and I. B. Pragnell. 1990. Identification and characterization of an inhibitor of haemopoietic stem cell proliferation. Nature 344:442-444.
19. Hanum, P. S., M. Hayano, and S. Kojima. 2003. Cytokine and chemokine responses in a cerebral malaria-susceptible or -resistant strain of mice to Plasmodium berghei ANKA infection: early chemokine expression in the brain. Int. Immunol. 15:633-640.
20. Jaramillo, M., I. Plante, N. Ouellet, K. Vandal, P. A. Tessier, and M. Olivier. 2004. Hemozoin-inducible proinflammatory events in vivo: potential role in malaria infection. J. Immunol. 172:3101-3110.
21. 2 biosynthesis in Plasmodium falciparum malaria occurs through hemozoin-induced suppression of blood mononuclear cell cyclooxygenase-2 gene expression via an interleukin-10-independent mechanism. Mol. Med. 10:45-54.
22. Keller, C. C., P. G. Kremsner, J. B. Hittner, M. A. Misukonis, J. B. Weinberg, and D. J. Perkins. 2004. Elevated nitric oxide production in children with malarial anemia: hemozoin-induced nitric oxide synthase type 2 transcripts and nitric oxide in blood mononuclear cells. Infect. Immun. 72:4868-4873.
23. Kun, J., R. Schmidt-Ott, L. Lehman, B. Lell, D. Luckner, B. Greve, P. Matousek, and P. Kremsner. 1998. Merozoite surface antigen 1 and 2 genotypes and rosetting of Plasmodium falciparum in severe and mild malaria in Lambaréné, Gabon. Trans. R. Soc. Trop. Med. Hyg. 92:110-114.
24. Lillard, J. W., Jr., U. P. Singh, P. N. Boyaka, S. Singh, D. D. Taub, and J. R. McGhee. 2003. MIP-1 alpha and MIP-1beta differentially mediate mucosal and systemic adaptive immunity. Blood 101:807-814.
25. Lord, B. I., C. M. Heyworth, and L. B. Woolford. 1993. Macrophage inflammatory protein: its characteristics, biological properties and role in the regulation of haemopoiesis. Int. J. Hematol. 57:197-206.
26. Luster, A. D. 2002. The role of chemokines in linking innate and adaptive immunity. Curr. Opin. Immunol. 14:129-135.
27. Luty, A. J. F., D. J. Perkins, B. Lell, R. Schmidt-Ott, L. G. Lehman, D. Luckner, B. Greve, P. Matousek, K. Herbich, D. Schmid, J. B. Weinberg, and P. G. Kremsner. 2000. Low interleukin-12 activity in severe Plasmodium falciparum malaria. Infect. Immun. 68:3909-3915.
28. Mabey, D. C., A. Brown, and B. M. Greenwood. 1987. Plasmodium falciparum malaria and Salmonella infections in Gambian children. J. Infect. Dis. 155: 1319-1321.
29. Machado, F. S., G. A. Martins, J. C. Aliberti, F. L. Mestriner, F. Q. Cunha, and J. S. Silva. 2000. Trypanosoma cruzi-infected cardiomyocytes produce chemokines and cytokines that trigger potent nitric oxide-dependent trypanocidal activity. Circulation 102:3003-3008.
30. Mackay, C. R. 2001. Chemokines: immunology's high impact factors. Nat. Immunol. 2:95-101.
31. Maitland, K., P. Bejon, and C. R. Newton. 2003. Malaria. Curr. Opin. Infect. Dis. 16:389-395.
32. Malaguarnera, L., R. M. Imhesi, S. Pignatelli, J. Simpore, M. Malaguarnera, and S. Musumeci. 2002. Increased levels of interleukin-12 in Plasmodium falciparum malaria: correlation with the severity of disease. Parasite Immunol. 24:387-389.
33. Musumeci, M., L. Malaguarnera, J. Simpore, A. Messina, and S. Musumeci. 2003. Modulation of immune response in Plasmodium falciparum malaria: role of IL-12, IL-18 and TGF-beta. Cytokine 21:172-178.
34. Othoro, C., A. Lal, B. Nahlen, D. Koech, A. Orago, and V. Udhayakumar. 1999. A low interleukin-10 tumor necrosis factor-α ratio is associated with malaria anemia in children residing in a holoendemic region in western Kenya. J. Infect. Dis. 179:279-282.
35. 2 and blood mononuclear cell cyclooxygenase-2 with disease severity in children with Plasmodium falciparum malaria. J. Infect. Dis. 183:113-118.
36. Perkins, D. J., J. B. Weinberg, and P. G. Kremsner. 2000. Reduced interleukin-12 and transforming growth factor-beta1 in severe childhood malaria: relationship of cytokine balance with disease severity. J. Infect. Dis. 182: 988-992.
37. Santiago H. D. C., C. F. Oliveira, L. Santiago, F. O. Ferraz, D. D. G. de Souza, L. A. De-Freitas, L. C. C. Afonso, M. M. Teixeira, R. T. Gazzinelli, and L. Q. Vieira. 2004. Involvement of the chemokine RANTES (CCL5) in resistance to experimental infection with Leishmania major. Infect. Immun. 72:4918-4923.
38. Sarfo, B. Y., S. Singh, J. W. Lillard, A. Quarshie, R. K. Gyasi, H. Armah, A. A. Adjei, P. Jolly, and J. K. Stiles. 2004. The cerebral-malaria- associated expression of RANTES, CCR3 and CCR5 in post-mortem tissue samples. Ann. Trop. Med. Parasitol. 98:297-303.
39. Scott, J. G. 1944. Herpes simplex cornea in malaria. Br. Med. J. 2:212-215.
40. Sherry, B. A., G. Alava, K. J. Tracey, J. Martiney, A. Cerami, and A. F. Slater. 1995. Malaria-specific metabolite hemozoin mediates the release of several potent endogenous pyrogens (TNF, MIP-1 alpha, and MIP-1 beta) in vitro, and altered thermoregulation in vivo. J. Inflamm. 45:85-96.
41. Su, S. B., N. Mukaida, J. B. Wang, Y. Zhang, A. Takami, S. Nakao, and K. Matsushima. 1997. Inhibition of immature erythroid progenitor cell proliferation by macrophage inflammatory protein-1-alpha by interacting mainly with a C-C chemokine receptor, CCR1. Blood 90:605-611.
42. Suguitan, A. L., Jr., R. G. Leke, G. Fouda, A. Zhou, L. Thuita, S. Metenou, J. Fogako, R. Megnekou, and D. W. Taylor. 2003. Changes in the levels of chemokines and cytokines in the placentas of women with Plasmodium falciparum malaria. J. Infect. Dis. 188:1074-1082.
43. Torre, D., F. Speranza, M. Giola, A. Matteelli, R. Tambini, and G. Biondi. 2002. Role of Th1 and Th2 cytokines in immune response to uncomplicated Plasmodium falciparum malaria. Clin. Diagn. Lab. Immunol. 9:348-351.
44. Villalta, F., Y. Zhang, K. E. Bibb, J. C. Kappes, and M. F. Lima. 1998. The cysteine-cysteine family of chemokines RANTES, MIP-1α, and MIP-1β induce trypanocidal activity in human macrophages via nitric oxide. Infect. Immun. 66:4690-4695.
45. Weinberg, J. B., J. J. Muscato, and J. E. Niedel. 1981. Monocyte chemotactic peptide receptor. Functional characteristics and ligand-induced regulation. J. Clin. Investig. 68:621-630.
46. Whittle, H. C., J. Brown, K. Marsh, M. Blackman, O. Jobe, and F. Shenton. 1990. The effects of Plasmodium falciparum malaria on immune control of B lymphocytes in Gambian children. Clin. Exp. Immunol. 80:213-218.
47. Whittle, H. C., J. Brown, K. Marsh, B. M. Greenwood, P. Seidelin, H. Tighe, and L. Wedderburn. 1984. T-cell control of Epstein-Barr virus-infected B cells is lost during P. falciparum malaria. Nature 312:449-450.
48. Winkler, S., M. Willheim, K. Baier, D. Schmid, A. Aichelburg, W. Graninger, and P. G. Kremsner. 1998. Reciprocal regulation of Th1- and Th2-cytokine-producing T cells during clearance of parasitemia in Plasmodium falciparum malaria. Infect. Immun. 66:6040-6044.
49. World Health Organization, Communicable Diseases Cluster. 2000. Severe falciparum malaria. Trans. R. Soc. Trop. Med. Hyg. 94(Suppl. 1):S1-S90.