The Dynamics of Naturally Acquired Immune Responses to Plasmodium falciparum Sexual Stage Antigens Pfs230 & Pfs48/45 in a Low Endemic Area in Tanzania

被引:72
作者
Bousema, Teun [1 ,2 ]
Roeffen, Will [3 ]
Meijerink, Hinta [3 ]
Mwerinde, Harry [4 ]
Mwakalinga, Steve [2 ,5 ]
van Gemert, Geert-Jan [3 ]
van de Vegte-Bolmer, Marga [3 ]
Mosha, Frank [2 ,6 ]
Targett, Geoffrey [1 ]
Riley, Eleanor M. [1 ]
Sauerwein, Robert [3 ]
Drakeley, Chris [1 ,2 ]
机构
[1] Univ London London Sch Hyg & Trop Med, Fac Infect & Trop Dis, Dept Immunol & Infect, London WC1E 7HT, England
[2] Joint Malaria Programme, Moshi, Tanzania
[3] Radboud Univ Nijmegen, Med Ctr, Dept Med Microbiol, NL-6525 ED Nijmegen, Netherlands
[4] Tanzania Plantat Co, TPC Dist Designated Hosp, Lower Moshi, Tanzania
[5] Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, Copenhagen, Denmark
[6] Kilimanjaro Clin Res Inst, Moshi, Tanzania
基金
英国惠康基金;
关键词
TRANSMISSION-BLOCKING IMMUNITY; HUMAN-ANTIBODY RESPONSES; MALARIA TRANSMISSION; SURFACE-ANTIGEN; GAMETOCYTES; AGE; REACTIVITY; REDUCTION; PAPUA; SERA;
D O I
10.1371/journal.pone.0014114
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Naturally acquired immune responses against sexual stages of P. falciparum can reduce the transmission of malaria from humans to mosquitoes. These antigens are candidate transmission-blocking vaccines but little is known about the acquisition of sexual stage immunity after exposure to gametocytes, or their longevity and functionality. We conducted a longitudinal study on functional sexual stage immune responses. Methodology/Principal Findings: Parasitaemic individuals (n = 116) were recruited at a health centre in Lower Moshi, Tanzania. Patients presented with gametocytes (n = 16), developed circulating gametocytes by day 7 (n = 69) or between day 7 and 14 (n = 10) after treatment or did not develop gametocytes (n = 21). Serum samples were collected on the first day of gametocytaemia and 28 and 84 days post-enrolment (or d7, 28, 84 after enrolment from gametocyte-negative individuals). Antibody responses to sexual stage antigens Pfs230 and Pfs48/45 were detected in 20.7% (72/348) and 15.2% (53/348) of the samples, respectively, and were less prevalent than antibodies against asexual stage antigens MSP-1(19) (48.1%; 137/285) and AMA-1 (52.4%; 129/246)(p<0.001). The prevalence of anti-Pfs230 (p = 0.026) and anti-Pfs48/45 antibodies (p = 0.017) increased with longer duration of gametocyte exposure and had an estimated half-life of approximately 3 months. Membrane feeding experiments demonstrated a strong association between the prevalence and concentration of Pfs230 and Pfs48/45 antibodies and transmission reducing activity (TRA, p<0.01). Conclusions/Significance: In a longitudinal study, anti-Pfs230 and Pf48/45 antibodies developed rapidly after exposure to gametocytes and were strongly associated with transmission-reducing activity. Our data indicate that the extent of antigen exposure is important in eliciting functional transmission-reducing immune responses.
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