2004, Número 1
<< Anterior Siguiente >>
salud publica mex 2004; 46 (1)
Gametocitos de Plasmodium vivax y Plasmodium falciparum: etapas relegadas en el desarrollo de vacunas
Contreras-Ochoa C, Ramsey JM
Idioma: Español
Referencias bibliográficas: 61
Paginas: 64-70
Archivo PDF: 115.43 Kb.
RESUMEN
Los gametocitos de
Plasmodium son los responsables de la transmisión del huésped vertebrado al mosquito vector. Sufren un proceso de desarrollo complejo a partir de parásitos asexuales, que no está completamente entendido, expresando proteínas y moléculas de adhesión especificas. Son capaces de inducir una respuesta inmune humoral específica con anticuerpos IgG, y celular específica, con producción de TNFα, IFNγ y proliferación de linfocitos γδ
+, aun cuando existen respuestas inducidas en contra de las etapas previas del parásito (esporozoito, exo-eritrocítica y eritrocítica). Las vacunas destinadas a bloquear la transmisión del parásito no contemplan a los gametocitos circulantes en el huésped como blancos de acción, sino que van enfocadas contra antígenos expresados en los gametos y en las etapas posfertilización. El estudio de los mecanismos que regulan la producción de gametocitos y de la respuesta inmune contra éstos, ofrece una oportunidad para el desarrollo de estrategias adicionales para el control de la transmisión.
REFERENCIAS (EN ESTE ARTÍCULO)
Lobo CA, Kumar N. Sexual differentiation and development in the malaria parasite. Parasitol Today 1998;14(4):146-150.
Dier M, Day KR. Commitment to gametocytogenesis in Plasmodium falciparum. ParasitoToday 2000;16(3):102-107.
Paul R, Brey P, Robert V. Plasmodium sex determination and transmission to mosquitoes.Trends Parasitol 2002;18(1):32-38.
Day K, Hayward R, Smith D, Culvenor J. CD-36 dependent adhesion and knob expression of the transmission stages of Plasmodium falciparum is stage specific. Mol Biochem Parasitol 1998;93(2):166-177.
Sinden RE. Sexual development of malarial parasites.Adv Parasitol 1983;22:153-216.
Rogers N, Daramola O,Targett G, Hall B. CD36 and intercellular adhesion molecule mediate adhesion of developing Plasmodium falciparum gametocytes. Infect Immun 1996;64(4):1480-1483.
Smalley ME,Abdalla S, Brown J.The distribution of Plasmodium falciparum in the peripheral blood and bone marrow of Gambian children.Trans R Sot Trop Med Hyg 1981;75(1):103-105.
Rogers N, Hall B, Obiero J,Targett G, Sutherland C.A model for sequestration of the trasmission stages of Plasmodium falciparum: Adhesion of gametocyte-infected erythrocytes to human bone marrow cells. Infect Immun 2000;68(6):3455-3462.
Sinden RE, Butcher GA, Billker O, Fleck SL. Regulation of infectivity of Plasmodium to the mosquito vector.Adv Parasitol 1996;38:53-117.
Mendis KN, David PH, Carter R. Human immune responses against sexual stages of malaria parasites: Considerations for malaria vaccines. Int J Parasitol 1990;20(4):497-502.
Carter R.Transmission blocking malaria vaccines. Vaccine 2001;19(17-19):2309-2314.
12.Miller LH, Hoffman SL. Research toward vaccines against malaria. Nat Med 1998;4(5 Suppl):520-524.
Healer JD, McGuinness P, Hoperoft S, Haley R, Carter C, Riley E. Complement-mediated lysis of Plasmodium falciparum gametes by malaria-immune human sera is associated with antibodies to the gamete surface antigen Pfs230. Infect Immun 1997;65(8):3017-3023.
Kwiatkowski D, Marsh K. Development of a malaria vaccine. Lancet 1997;350(9092): 1696-1701.
ScherfA, Carter R, Petersen C,Alano P, Nelson R,Aikawa M et al. Gene activation of Pfl I-I of Plasmodium falciparum by chromosome breakage and healing: Identification of gametocyte-specific protein with a potential role in gametogenesis. EMBO J 1992;11(6):2293-2301.
Mendis K, Munesinnghe Y, de Silva Y, Keragalla I, Carter R. Malaria transmission-blocking immunity induced by natural infections of Plasmodium vivax in humans. Infect Immun I 987;55(2):369-372.
Gamage-Mendis AC, Rajakaruna, Carter R, Mendis KN.Transmission blocking immunity to human Plasmodium vivax malaria in an endemic population in Kataragama, Sri Lanka. Parasite Immunol 1992;14(4):385-396.
Ramsey J, Salinas E, Rodríguez MH.Acquired transmission-blocking immunity to Plasmodium vivax in a human population of Southern coastal Mexico.Am J Trop Med Hyg 1996;54(5):458-563.
19.Naonatune T, Karunaweera ND, Del Giudice G, Kularatne MU, Grau GE, Carter R et al. Cytokines kill malaria parasites during infection crisis: Extracellular complementary factors are essential.) Exp Med 1991;173(3):523-529.
Karunaweera N, Carter R, Grau G, Kniatkowski D, Del Guidice G, Mendis K. Tumour necrosis factor-dependent parasite-killing effects during paroxysm in non-immmune Plasmodium vivax malarial patients. Clin Exp Immunol I 992;88(3):499-505.
Good MF, Quakyi A, Berzofsky R, Carter R, Miller L. Human cell clones reactive to the sexual stages of Plasmodium falciparum malaria:High frequency of gamete-reactiveT cells in peripheral blood from nonexposed donors.) Immunol 1987;138(1):306-31 I.
Goodier M,Targett G. Polyclonal T-cell responses to Plasmodium falciparum gametocytes in malaria nonexposed donors. Parasite Immunol 1997;19(9):419-425.
Riley E, Ong C, Olerup O, Eida S, Allen S, Bennett S et al. Cellular and humoral immune responses to Plasmodium falciparum gametocyte in malaria-immune individuals.) Immunol 1990;144(12):4810-4816.
Riley EM, Allen SJ,Wheeler J, Blackman M, Bennett S,Takacs B et al. Naturally acquired cellular and humoral responses to the major merozoite surface antigen (PfMSPI) of Plasmodium falciparum are associated with reduced malaria morbidity. Parasite Immunol 1992;14(3):321-337.
Baird JK,JonesTR, Danudirgo EW,Annis BA, Bangs MJ, Basri H et al. Age-dependent acquired protection against Plasmodium falciparum in people having two years exposure to hyperendemic malaria.Am J Trop Med Hyg 1991;45(1):65-76.
Jakobsen PH. Plasmodium falciparum malaria parasite exoantigens: Their role in disease and in immunity. Dan Med Bull 1995;42(1):22-39.
Luty A), Mayombo J, Lekoulou F, Mshana R. Immunologic responses to soluble exoantigens of Plasmodium falciparum in Gabonese children exposed to continuous intense infection.Am J Trop Med Hyg 1994;51(6):720-729.
Kristensen G, Jakobsen PH. Plasmodium falciparum: Characterization of toxin-associated proteins and identification of a hemoglobin containing parasite cytokine stimulator. Exp Parasitol 1996;82(2):147-1
Ramsey JM,Tello A, Contreras CO, Ordóñez R, Chirino N, Rojo J et al. Plasmodium falciparum and P. vivax gametocyte-specific exoantigens stimulate proliferation ofTCR gd+ lymphocytes.) Parasitol 2002:88(I ):59-68.
30.Behr C, Poupot R, Peyrat MA, PoquetY, Constant 9 Dubois P et al. Plasmodium falciparum stimuli for human gamma deltaT cells are related to phosphorylated antigens of mycobacteria. Infect Immun 1996;64(8):2892-2896.
Pichyangkul S, Saengkrai P,Yongvanitchit K, Stewart A, Heppner DG. Activation of gamma deltaT cells in malaria: Interaction of cytokines and a schizont-associated Plasmodium falciparum antigen. Infect Dis 1997;176(1):233-241.
Waterfall M, Black A, Riley E. Gamma delta+T cells preferentially respond to live rather than killed malaria parasites. Infect Immun I 998;66(5):2393-2398.
Hensmann M, Kwiatkowski D. Cellular basis of early cytokine response to Plasmodium falciparum. Infect Immun 2001;69(4):2364-2371.
Worku S, Bjorkman A,Troye-Blomberg M,Jemaneh L, FarnertA, Christensson B. Lymphocyte activation and subset redistribution in the peripheral blood in acute malaria illness: Distinct gamma delta+ T cell patterns in Plasmodium falciparum and P. vivax infections. Clin Exp Immunol 1997;108(1):34-41.
Hviid L, Kurtzhals JA,Adabayeri V, Loizon S, Kemp K, Goka BQ et al. Perturbation and proinflammatory type activation of V delta I (+) gamma delta T cells in African children with Plasmodium falciparum malaria. Infect Immun 2001;69(5):3190-3196.
Rzepczyk CM,Anderson K, Stamatiou S,Townsend E,Allworth A, McCormack J et al. Gamma deltaT cells:Their immunobiology and role in malaria infections. Inc j Parasitol 1997;27(2):191-200.
Troye-Blomberg M,Worku S,Tangteerawatana 9 Jamshaid R, Soderstrom K, Elghazali G et al. Human gamma deltaT cells that inhibit the in vitro growth of the asexual blood stages of the Plasmodium falciparum parasite express cytolytic and proinflammatory molecules. Scand J Immunol I999;50(6):642-650.
Carding SR, Egan PJ. Gamma deltaT cells: Functional plasticity and heterogeneity. Nature Rev Immunol 2002;2(5):336-345.
Chien YH, Jores R, Crowley MP. Recognition by gamma/deltaT cells. Annu Rev Immunol 1996;14:511-532.
Chen ZW. Comparative biology of gamma delta T cells. Sci Prog 2002;85(Pt4):347-358.
Dieli F,Troye-Blomberg M, Ivanyi J, Fournie JJ, Bonneville M, Peyrat MA et al. Vgamma9/Vdelta2 T lymphocytes reduce the viability of intracellular Mycobacterium tuberculosis. Eur J Immunol 2000;30(5):1512-1519.
Ferrero E, Biswas P,Vettoretto K, Ferrarini M, Uguccioni M, Piali L et al. Macrophages exposed to Mycobacterium tuberculosis release chemokines able to recruit selected leucocyte subpopulations: Focus on gamma delta cells. Immunology 2003;108(3):365-374.
Nakano Y, Hisaeda H, Sakai T, Ishikawa H, Zhang M, MaekawaY et al. Roles of NKT cells in resistance against infection with Toxoplasma gondii and in expression of heat shock protein 65 in the host macrophages. Microbes Infect 2002;4(1): I - I I .
Lagler H,Willheim M,Traunmuller F,Wah1 K,Winkler H, Ramharter M et al. Cellular profile of cytokine production in a patient with visceral leishmaniasis: Gamma delta+ T cells express both type 1 cytokines and interleukin-10. Stand J Immunol 2003;57(3):291-295.
Cardona AE, González PA,Teale JM. CC chemokines mediate leukocyte trafficking into the central nervous system during murine neurocysticercosis: Role of gamma delta T cells in amplification of the host immune response. Infect Immun 2003;71(5):2634-2642.
Poccia F, Gougeon ML,Agrati C, Montesano C, Martini F, Pauza CD et al. Innate T-cell immunity in HIV infection:The role of Vgamma9Vdelta2 T lymphocytes. Curr Mol Med 2002;2(8):769-78 I.
Sciammas R, Bluestone JA.TCR gamma delta cells and viruses. Microbes Infect 1999; I (3):203-212.
López RD. Human gamma delta-T cells in adoptive immunotherapy of malignant and infectious diseases. Immunol Res 2002;26(1-3):207-221
Playfair jH,Taverne J, Bate CA. Don't kill the parasite: Control the disease. Acta Leiden 1991;60(1):157-165.
50.Ambroise-Thomas P.Vaccination against malaria. Disappointments and hopes. Bull Acad Natl Med 1997;181(8):1637-1650.
Taylor-Robinson A.Vaccination against malaria:Targets, strategies and potentiation of immunity to blood stage parasites. Front Biosci 2000;5:16-29.
Scherf A, Behr C, Sarthou JL, Pla M, Rogier C,Trape JF et al. Immune response in mouse and malaria-exposed humans to peptides derived from Pf1I-I, a highly repetitive megadalton protein of Plasmodium falciparum. Eur J Immunol 1993;23:1574-1581.
Baker DA,Thompson J, Daramola O, Carlton JM,Targett G. Sexual stage specific RNA expresssion of a new Plasmodium falciparum gene detected by in situ hybridization. Mol Biochem Parasitol 1995;72:193-201.
54.Premawansa S, Gamage-Mendis A, Perera L, Begarnie S, Mendis K, Carter R. Plasmodium falciparum malaria transmission-blocking immunity under conditions of low endemicity as in Sri Lanka. Parasite Immunol 1994;16:35-42.
Duffy PE, Kaslow DC.A novel malaria protein, Pfs28 and Pfs25 are genetically linked and synergistic as falciparum malaria transmission-blocking vaccines. Infect Immun 1997;65:1109-1113.
Hisaeda H, Stowers A,Tsuboi T, Collins W, Sattabongkot J, Suwanabun N et al. Antibodies to malaria vaccine candidates Pvs25 and Pvs28 completely block the ability of Plasmodium vivax to infect mosquitoes. Infect Immun 2000;68:6618-6623.
Silvestrini F,Alano P,Williams J. Commitment to the production of male and female gametocytes in the human malaria parasite Plasmodium falciparum. Parasitology 2000; 121(Pt 5):465-471.
Eksi S,Williamson KC. Male-specific expression of the paralog of malaria transmissionblocking target antigen Pfs230, PfB0400w. Mol Biochem Parasitol 2002;122(2):127-30.
Piper K, Hayward R, Cox M, Day K. Malaria transmission and naturally acquired immunity to PfEMP-I. Infect Immun 1999;67:6369-6374. 60. Abdel-WahabA,Abdel-Muhsin AM, Ali E, Suleiman S, Ahmed S, Walliker D et al. Dynamics of gametocytes among Plasmodium falciparum clones in natural infections in an area of highly seasonal transmission.) Infect Dis 2002;185(12):1838-1842.
Delrieu l,Waller CC, Mota MM, Grainger M, Langhorne J, Holder AA. PSLAP, a protein with multiple adhesive motifs, is expressed in Plasmodium falciparum gametocytes. Mol Biochem Parasito I 2002;121(1):11-20.
Healer J, Graszynski A, Riley EM. Phagocytosis does not play a mayor role naturally acquired transmission-blocking immunity to Plasmodium falciparum malaria. Infect Immun I 999;67(5):2334-2339.