Plasmodium falciparum malaria parasite var gene expression is modified by host antibodies: longitudinal evidence from controlled infections of Kenyan adults with varying natural exposure

被引:22
作者
Abdi, Abdirahman I. [1 ,2 ]
Hodgson, Susanne H. [3 ]
Muthui, Michelle K. [1 ]
Kivisi, Cheryl A. [1 ,2 ]
Kamuyu, Gathoni [1 ]
Kimani, Domtila [1 ]
Hoffman, Stephen L. [6 ]
Juma, Elizabeth [4 ,5 ]
Ogutu, Bernhards [4 ,5 ]
Draper, Simon J. [3 ]
Osier, Faith [1 ]
Bejon, Philip [1 ]
Marsh, Kevin [1 ]
Bull, Peter C. [7 ]
机构
[1] CGMRC, KEMRI Wellcome Trust Res Programme, POB 230-80108, Kilifi, Kilifi County, Kenya
[2] Pwani Univ, POB 195-80108, Kilifi, Kenya
[3] Univ Oxford, Jenner Inst, Oxford, England
[4] Kenya Govt Med Res Ctr, Clin Res Ctr, Nairobi, Kenya
[5] Strathmore Univ, Ctr Res Therapeut Sci, Nairobi, Kenya
[6] Sanaria Inc, Rockville, MD USA
[7] Univ Cambridge, Dept Pathol, 17 Tennis Court Rd, Cambridge CB2 1QP, England
基金
英国惠康基金;
关键词
PfEMP1; Antibodies; P; falciparum; Immunity; Controlled human malaria infection (CHMI); Sporozoite; VARIANT SURFACE-ANTIGENS; NATURALLY ACQUIRED-IMMUNITY; SEVERE DISEASE; ERYTHROCYTES; ADHESION; TARGETS; BINDING; CONSERVATION; PROTECTION; SEQUENCE;
D O I
10.1186/s12879-017-2686-0
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: The PfEMP1 family of Plasmodium falciparum antigens play a key role in pathogenesis of severe malaria through their insertion into the surface of parasite infected erythrocytes, and adhesion to host cells. Previous studies have suggested that parasites expressing PfEMP1 subclasses group A and DC8, associated with severe malaria, may have a growth advantage in immunologically naive individuals. However, this idea has not been tested in longitudinal studies. Methods: Here we assessed expression of the var genes encoding PfEMP1, in parasites sampled from volunteers with varying prior exposure to malaria, following experimental infection by sporozoites (PfSPZ). Using qPCR, we tested for associations between the expression of various var subgroups in surviving parasite populations from each volunteer and 1) the levels of participants' antibodies to infected erythrocytes before challenge infection and 2) the apparent in vivo parasite multiplication rate. Results: We show that 1) expression of var genes encoding for group A and DC8-like PfEMP1 were associated with low levels of antibodies to infected erythrocytes (aIE) before challenge, and 2) expression of a DC8-like CIDRa1.1 domain was associated with higher apparent parasite multiplication rate in a manner that was independent of levels of prior antibodies to infected erythrocytes. Conclusions: This study provides insight into the role of antibodies to infected erythrocytes surface antigens in the development of naturally acquired immunity and may help explain why specific PfEMP1 variants may be associated with severe malaria.
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页数:11
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