Expression of Plasmodium falciparum 3D7 STEVOR proteins for evaluation of antibody responses following malaria infections in naive infants

被引:19
作者
Schreiber, N. [2 ]
Khattab, A. [1 ]
Petter, M. [1 ]
Marks, F. [2 ,3 ]
Adjei, S. [4 ]
Kobbe, R. [2 ]
May, J. [2 ]
Klinkert, M. -Q. [1 ]
机构
[1] Bernhard Nocht Inst Trop Med, Dept Mol Med, D-20359 Hamburg, Germany
[2] Bernhard Nocht Inst Trop Med, Infect Dis Epidemiol Grp, D-20359 Hamburg, Germany
[3] Int Vaccine Inst, Seoul 151600, South Korea
[4] KNUST Univ PO, Kumasi Ctr Collaborat Res Trop Med, Kumasi, Ghana
关键词
recombinant STEVOR; Plasmodium falciparum; immune responses; infants;
D O I
10.1017/S0031182007003794
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Clinical immunity to Plasmodium falciparum malaria develops after repeated exposure to the parasite. At least 2 P. falciparum variant antigens encoded by multicopy gene families (var and rif) are targets of this adaptive antibody - mediated immunity. A third multigene family of variant antigens comprises the stevor genes. Here, 4 different stevor sequences were selected for cloning and expression in Escherichia coli and His(6)-tagged fusion proteins were used for assessing the development of immunity. In a cross-sectional analysis of clinically immune adults living in a malaria endemic area in Ghana, high levels of anti-STEVOR IgG antibody titres were determined in ELISA. A cross-sectional study of 90 nine-month-old Ghanaian infants using I recombinant STEVOR showed that the antibody responses correlated positively with the number of parasitaemia episodes. In a longitudinal investigation of 17 immunologically naive 9-month-old infants, 3 different patterns of anti-STEVOR antibody responses could be distinguished (high, transient and low). Children with high anti-STEVOR-antibody levels exhibited an elevated risk for developing parasitaemia episodes. Overall, a protective effect could not be attributed to antibodies against the STEVOR proteins chosen for the study presented here.
引用
收藏
页码:155 / 167
页数:13
相关论文
共 39 条
[1]   Antibodies to Plasmodium falciparum rifin proteins are associated with rapid parasite clearance and asymptomatic infections [J].
Abdel-Latif, MS ;
Dietz, K ;
Issifou, S ;
Kremsner, PG ;
Klinkert, MQ .
INFECTION AND IMMUNITY, 2003, 71 (11) :6229-6233
[2]   Recognition of variant rifin antigens by human antibodies induced during natural Plasmodium falciparum infections [J].
Abdel-Latif, MS ;
Khattab, A ;
Lindenthal, C ;
Kremsner, PG ;
Klinkert, MQ .
INFECTION AND IMMUNITY, 2002, 70 (12) :7013-7021
[3]   Induction of cross-reactive immune responses to NTS-DBL-1α/x of PfEMP1 and in vivo protection on challenge with Plasmodium falciparum [J].
Ahuja, Sanjay ;
Pettersson, Fredrik ;
Moll, Kirsten ;
Jonsson, Cathrine ;
Wahlgren, Mats ;
Chen, Qijun .
VACCINE, 2006, 24 (35-36) :6140-6154
[4]   Analysis of multiple Plasmodium falciparum infections in Tanzanian children during the phase III trial of the malaria vaccine SPf66 [J].
Beck, HP ;
Felger, I ;
Huber, W ;
Steiger, S ;
Smith, T ;
Weiss, N ;
Alonso, P ;
Tanner, M .
JOURNAL OF INFECTIOUS DISEASES, 1997, 175 (04) :921-926
[5]   Field epidemiological studies on malaria in a low endemic area in the Philippines [J].
Belizario, VY ;
Saul, A ;
Bustos, MDG ;
Lansang, MA ;
Pasay, CJ ;
Gatton, M ;
Salazar, NP .
ACTA TROPICA, 1997, 63 (04) :241-256
[6]   STEVOR - a multifunctional protein? [J].
Blythe, JE ;
Surentheran, T ;
Preiser, PR .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2004, 134 (01) :11-15
[7]   Expression profiling of the schizont and trophozoite stages of Plasmodium falciparum with a long-oligonucleotide microarray -: art. no. R9 [J].
Bozdech, Z ;
Zhu, JC ;
Joachimiak, MP ;
Cohen, FE ;
Pulliam, B ;
DeRisi, JL .
GENOME BIOLOGY, 2003, 4 (02)
[8]   Plasmodium falciparum antigenic variation:: Relationships between in vivo selection, acquired antibody response, and disease severity [J].
Bull, PC ;
Pain, A ;
Ndungu, FM ;
Kinyanjui, SM ;
Roberts, DJ ;
Newbold, CI ;
Marsh, K .
JOURNAL OF INFECTIOUS DISEASES, 2005, 192 (06) :1119-1126
[9]   Parasite antigens on the infected red cell surface are targets for naturally acquired immunity to malaria [J].
Bull, PC ;
Lowe, BS ;
Kortok, M ;
Molyneux, CS ;
Newbold, CI ;
Marsh, K .
NATURE MEDICINE, 1998, 4 (03) :358-360
[10]   The sickle cell trait is associated with enhanced immunoglobulin G antibody responses to Plasmodium falciparum variant surface antigens [J].
Cabrera, G ;
Cot, M ;
Migot-Nabias, F ;
Kremsner, PG ;
Deloron, P ;
Luty, AJF .
JOURNAL OF INFECTIOUS DISEASES, 2005, 191 (10) :1631-1638