Acquisition of naturally occurring antibody responses to recombinant protein domains of Plasmodium falciparum erythrocyte membrane protein 1

被引:22
|
作者
Mackintosh, Claire L. [1 ,2 ,3 ]
Christodoulou, Zoe [2 ]
Mwangi, Tabitha W. [1 ]
Kortok, Moses [1 ]
Pinches, Robert [2 ]
Williams, Thomas N. [1 ,3 ,4 ]
Marsh, Kevin [1 ,2 ,3 ]
Newbold, Christopher I. [2 ,3 ]
机构
[1] Kilifi Dist Hosp, Ctr Geog Med Res Coast, Kenya Med Res Inst, Kilifi, Kenya
[2] John Radcliffe Hosp, Weatherall Inst Mol Med, Mol Parasitol Grp, Oxford OX3 9DU, England
[3] John Radcliffe Hosp, Nuffield Dept Med, Oxford OX3 9DU, England
[4] John Radcliffe Hosp, Dept Paediat, Oxford OX3 9DU, England
基金
英国惠康基金;
关键词
D O I
10.1186/1475-2875-7-155
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Antibodies targeting variant antigens expressed on the surface of Plasmodium falciparum infected erythrocytes have been associated with protection from clinical malaria. The precise target for these antibodies is unknown. The best characterized and most likely target is the erythrocyte surface-expressed variant protein family Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1). Methods: Using recombinant proteins corresponding to five domains of the expressed A4 var gene, A4 PfEMP1, the naturally occurring antibody response was assessed, by ELISA, to each domain in serum samples obtained from individuals resident in two communities of differing malaria transmission intensity on the Kenyan coast. Using flow cytometry, the correlation in individual responses to each domain with responses to intact A4-infected erythrocytes expressing A4 PfEMP1 on their surface as well as responses to two alternative parasite clones and one clinical isolate was assessed. Results: Marked variability in the prevalence of responses between each domain and between each transmission area was observed, as wasa strong correlation between age and reactivity with some but not all domains. Individual responses to each domain varied strikingly, with some individuals showing reactivity to all domains and others with no reactivity to any, this was apparent at all age groups. Evidence for possible cross-reactivity in responses to the domain DBL4. was found. Conclusion: Individuals acquire antibodies to surface expressed domains of a highly variant protein. The finding of potential cross-reactivity in responses to one of these domains is an important initial finding in the consideration of potential vaccine targets.
引用
收藏
页数:10
相关论文
共 50 条
  • [41] Antibody Levels to Plasmodium falciparum Erythrocyte Membrane Protein 1-DBLγ11 and DBLδ-1 Predict Reduction in Parasite Density
    Araj, Brittany N.
    Swihart, Bruce
    Morrison, Robert
    Hurtado, Patricia Gonzales
    Teo, Andrew
    Mahamar, Almahamoudou
    Attaher, Oumar
    Diarra, Bacary S.
    Gaoussou, Santara
    Issiaka, Djibrilla
    Dicko, Alassane
    Duffy, Patrick E.
    Fried, Michal
    MSYSTEMS, 2021, 6 (03)
  • [42] Modulation of malaria virulence by determinants of Plasmodium falciparum erythrocyte membrane protein-1 display
    Fairhurst, Rick M.
    Wellems, Thomas E.
    CURRENT OPINION IN HEMATOLOGY, 2006, 13 (03) : 124 - 130
  • [43] An immunoinformatics approach to promiscuous peptide design for the Plasmodium falciparum erythrocyte membrane protein-1
    Khan, Nazam
    Kumar, Rajender
    Chauhan, Shakti
    Farooq, Umar
    MOLECULAR BIOSYSTEMS, 2017, 13 (10) : 2160 - 2167
  • [44] PLASMODIUM FALCIPARUM ERYTHROCYTE MEMBRANE PROTEIN 1 EXPRESSION IN ISOLATES FROM CHILDREN WITH SEVERE MALARIA
    Magistrado, Pamela A.
    Jensen, Anja T.
    Turner, Louise
    Lavstsen, Thomas
    Joergensen, Louise
    John, Davis
    Lusingu, John P.
    Lemnge, Martha
    Olomi, Raimos
    Theander, Thor G.
    AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2010, 83 (05): : 165 - 165
  • [45] EXPRESSION OF PLASMODIUM FALCIPARUM ERYTHROCYTE MEMBRANE PROTEIN 1 (PFEMP1) IS IRON-DEPENDENT
    Ho, May
    Beaudry, Steven D.
    White, Aaron
    Lee, Kristine
    Arie, Takayuki
    Deitsch, Kirk
    Fairhurst, Rick M.
    AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2009, 81 (05): : 95 - 95
  • [46] Erythrocyte protein 4.1 and Plasmodium falciparum phosphoprotein MESA: Membrane-bound transport of parasite protein to the erythrocyte skeleton
    Magowan, C
    Coppel, R
    Mohandas, N
    BLOOD, 1995, 86 (10) : 1865 - 1865
  • [47] Optimized expression of Plasmodium falciparum erythrocyte membrane protein I domains in Escherichia coli -: art. no. 50
    Flick, K
    Ahuja, S
    Chene, A
    Bejarano, MT
    Chen, QJ
    MALARIA JOURNAL, 2004, 3 (1)
  • [48] Mapping the domains of the cytoadherence ligand Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) that bind to the knob-associated histidine-rich protein (KAHRP)
    Waller, KL
    Nunomura, W
    Cooke, BM
    Mohandas, N
    Coppel, RL
    MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2002, 119 (01) : 125 - 129
  • [49] Interaction of Plasmodium falciparum erythrocyte membrane protein 3 with the red blood cell membrane skeleton
    Waller, Karena
    Stubberfield, Lisa
    Nunomura, Wataru
    Mohandas, Narla
    Cooke, Brian
    Coppel, Ross
    AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2006, 75 (05): : 246 - 246
  • [50] B-Cell Responses to Pregnancy-Restricted and-Unrestricted Plasmodium falciparum Erythrocyte Membrane Protein 1 Antigens in Ghanaian Women Naturally Exposed to Malaria Parasites
    Ampomah, Paulina
    Stevenson, Liz
    Ofori, Michael F.
    Barfod, Lea
    Hviid, Lars
    INFECTION AND IMMUNITY, 2014, 82 (05) : 1860 - 1871