Background
Plasmodium vivax, the most frequent cause of recurring malaria, is widely distributed throughout Latin America, some parts of Africa and Southeast Asian countries [
1‐
3]. An estimated 2.85 billion people worldwide are at risk of vivax malaria and approximately 65% of cases are from Asian and South American regions [
4]. The major features of
P. vivax that distinguish it from other
Plasmodium species are its high transmission potential from early and continuous gametocyte production, its hibernating behaviour in the liver in the form of hypnozoites, its shorter life cycle and its high infectivity in vectors, which are the primary obstacles to controlling this type of malaria [
5]. In this regard, the development of a vaccine to attack vivax malaria is urgently needed to reduce morbidity and mortality related to malaria. However, due to technical limitations such as lack of continuous culture, the development of effective vivax vaccine has been delayed, and the eradication of vivax malaria is still challenging.
Among three types of vaccine candidates-pre-erythrocytic, erythrocytic and transmission blocking-the erythrocytic approach is targeted primarily toward minimizing the morbidity, mortality and parasitaemia levels. Blood stage antigens such as apical membrane protein 1 (AMA-1), merozoite surface protein 1 (MSP-1) and Duffy-binding protein (DBP) are major targets for blood-stage vaccine development because they are responsible for the clinical manifestation and merozoite invasion of red blood cells in humans [
6]. It is possible to acquire immunity against blood stage antigens in natural exposure-derived
P. vivax infections. Similarly, protection against
P. vivax infection could be induced by numerous immunization strategies [
7]. However, the rapid mutation of the blood-stage antigens is the primary challenging problem in its vaccine development. In fact, an effective vaccine must be able to induce both humoral and cellular immune responses without having any genetic restriction while stimulating memory cells. Therefore, the discovery of potential vaccine antigens and a better understanding of the underlying immune mechanisms against parasites in natural infections will guide us to progress further in developing this vaccine.
Recently, a new vaccine candidate has emerged for blood stage vivax malaria infections called
Plasmodium vivax merozoite surface protein 1 paralog (PvMSP1P-19), which is located at the upstream locus of the MSP1 gene. It was identified as a paralog of PvMSP1, and it showed similarities in the size, molecular mass, number and location of cystine residue, whereas it was not expressed as a highly polymorphic protein as was PvMSP1 [
8,
9]. Interestingly, PvMSP1P-19 was found to contain double epidermal growth factor (EGF)-like domains, which assist in merozoite invasions of erythrocytes. As a consequence, the rosette forms of PvMSP1P-19-transfected COS7 cells and human erythrocyte binding observed during in vitro study was stronger than those seen in PvMSP1-infected cells. This result assures us that the function of PvMSP1P-19 is to play a role as a parasite ligand for invasion. Additionally, another advantage of PvMSP1P-19 is that both the N- and C-terminal regions have high potential for inducing host immune responses, and the resulting antibodies inhibit PvMSP1P-19-erythrocyte binding [
10]. Another study also reported that PvMSP1P-19 strongly induces the activation of IFN-γ-producing effector cells following natural
P. vivax exposure, suggesting that it has the potential to activate the recall response of Th1 effector memory cells [
11]. These data all suggested that PvMSP1P-19 is reliable at inducing the inhibitory antibody and at promoting good immunogenicity. However, to be sure that PvMSP1P-19 antigen has the ability as a vaccine candidate, further studies are needed. Hence, in this study, the longevity of a naturally acquired antibody against the PvMSP1P-19 antigen was evaluated because it would be an important factor for determining the qualifications of the vaccine. Another objective of this study is to observe the specific memory B cell (MBC) response to PvMSP1P-19 in
P. vivax-infected patients to acquire a better understanding of the underlying immune mechanisms and to develop an effective malaria vaccine in the future.
Methods
Study area and sample collection
To observe the antigenicity of PvMSP1P-19 antigen during acute and convalescence phase and the maintenance of anti-PvMSP1P-19 responses after recovery from P. vivax infection, both cross-sectional survey and longitudinal cohort study were performed between May 2014–October 2016 in a low-malaria-transmission area, Rap Ro malaria clinic, Chumphon Province, which is located in the southern part of Thailand where both P. vivax and Plasmodium falciparum commonly occur.
The antigenicity of PvMSP1P-19 in induction of antibody response in natural infection at acute malaria infection and after recovery from infection was explored. Ten milliliters of heparinized peripheral blood samples were collected from P. vivax acutely infected patients (n = 40) and from P. vivax subjects who had recovered from the infection at 3 months (n = 27), 9 months (n = 15) and 12 months (n = 14). In addition, the malaria endemic villagers (n = 15) who lived in the same village as acutely infected patients for more than 5 years showed negative parasitaemia in blood smears at the time of collection as well as have no history of malaria infection was recruited in this survey. The ages of subjects ranged from 18 to 63 years old.
The maintenance of anti-PvMSP1P-19 response after recovery from infection was demonstrated from a longitudinal analysis. Among 40 P. vivax infected patients, 16 infected individuals were followed antibody response at acute phase and after they recovered from infection for 3 months. Moreover, five infected individuals were followed anti-PvMSP1P-19 responses after 3, 9 and 12 months recovery from infection. Giemsa staining by thick and thin peripheral blood films was used for diagnosis, and nested PCR was performed to confirm the P. vivax infection. Individual samples were taken for plasma preparation and used for enzyme-linked immunosorbent assays (ELISA) and erythrocyte binding inhibition assays (EBIA).
The presence of memory B cell responses to the PvMSP1P-19 antigen after recovery from P. vivax infection was demonstrated by collecting peripheral blood mononuclear cell (PBMC) samples (n = 11) from individuals during acute phase and after 9 months recovery from infection with P. vivax between June 2016 and March 2017. Blood samples from healthy persons (n = 22) from the Faculty of Medical Technology, Mahidol University who had never been exposed to malaria in their lives were collected as healthy controls for this study. The study was approved by the Committee on Human Rights Related to Human Experimentation, Mahidol University, and the Ministry of Health, Thailand (MUIR 2012/079.2408).
Recombinant PvMSP1P-19 protein expression
The recombinant protein PvMSP1P-19 was expressed and purified as previously described [
10]. Briefly, the gene fragment encoding PvMSP1P-19, which was obtained from the genomic DNA of the
P. vivax SalI strain sequence, was amplified by PCR and cloned into the
XhoI and
NotI sites of the pEU-E01-His-TEV-MCS vector (Cell Free Sciences, Matsuyama, Japan). An ABI PRISM 310 Genetic Analyzer and a BigDye Terminator v1.1 Cycle Sequencing kit (Applied Biosystems, Foster City, CA, USA) were used to confirm the inserted nucleotide sequence. For the in vitro transcription and subsequent translation, highly purified plasmid DNA was prepared by using a Maxi Plus™ Ultrapure plasmid extraction system (Viogene, Taipei, Taiwan) in accordance with the manufacturer’s instructions. For recombinant protein expression, the purified DNA was eluted in 0.1× TE buffer (10 mM Tris–HCl, pH 8.0, 1 mM EDTA) and used in a wheat germ cell-free (WGCF) system (CellFree Sciences) as described previously [
12,
13]. After that, the newly synthesized recombinant PvMSP1P-19-19 protein was purified using a nickel-nitrilotriacetic acid (Ni–NTA) column (Qiagen, Hilden, Germany).
Detection of total IgG responses to PvMSP1P-19
The levels of the antibody response against PvMSP1P-19 in individuals with P. vivax exposure were measured by indirect ELISA. In brief, 5 μg/mL of recombinant PvMSP1P-19 protein was used to coat 96-well ELISA plates overnight at 4 °C. Then, 100 μL of 5% skim milk was added to each well and incubated for 2 h. Next, the plates were washed twice with washing buffer (0.05% Tween-20 in 1× PBS), and 50 μL of 1:200 diluted plasma was added to specific wells of the coated plate and incubated for 1 h. After that, the wells were washed again, followed by the addition of 50 μL of affinity-purified peroxidase-labelled goat anti-human IgG (H+L) antibody, which was diluted 1:1000 with blocking buffer. After 90 min of incubation at room temperature, another washing step was needed. After that, 50 μL of 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) substrate solution was added. The ELISA plates were incubated for 45 min in the dark at room temperature. Finally, the optical density (OD) of each sample well was measured with an ELISA plate reader (SYNERGY™ HTX multi-mode reader, BioTek) at 405 nm (OD405). All the samples were analysed in duplicate and mean values were used in the analyses. The cut-off value was obtained from the mean plus two standard deviations (SDs) of the OD of all of the non-exposed Thai plasma samples. Based on ELISA data, the seropositive samples were classified into the following two groups: high responders (OD ≥ mean + 4SD of non-exposed Thai control plasma; 0.039–0.137) and low responders (OD < mean + 4SD of non-exposed Thai control plasma; 0.022–0.037).
Erythrocyte binding inhibition assay of anti-PvMSP1P-19 antibody
In this study, human embryonic kidney 293 cells carrying the SV40 large T antigen (HEK293-T) were used in an EBIA specific to PvMSP1P-19. The cells were grown in Dulbecco’s modified Eagle medium (DMEM) (Gibco, Invitrogen, Paisley, UK) with 10% fetal bovine serum (FBS) (Gibco) at 37 °C with 5% atmospheric CO2. The cells were passaged when they reached 90–100% confluence. A 2 × 104 concentration of cells was transferred into each well of a 24-well culture plate (Corning Inc., Corning, NY, USA). Next, the cells were transfected with 50 μL of DNA-liposome complex, and 100 ng of diluted plasmid pEGFP-MSP1P was mixed with 2% Lipofectamine®2000 (Invitrogen, Carlsbad, CA, USA) and incubated at 37 °C in a 5% CO2 chamber for 42–44 h. The transfection efficiencies were determined by observing the expression of green fluorescence protein (GFP) under an inverted fluorescence microscopy. The HEK293-T cells with transfection efficiencies of >80% were used for the EBIA.
To test the inhibition of the antibodies, 250 μL of 1:10 diluted plasma was added to transfected HEK293-T cells containing culture plate wells and incubated for 1 h at 37 °C. Then, 50 μL of 10% Duffy-positive human packed red blood cells was added to each well. The plates were incubated for 2 h, followed by the removal of the non-adherent erythrocytes by washing them with washing buffer (1× PBS with Mg2+ and Ca2+). Rosette-forming transfected HEK293-T cells in which adherent erythrocytes covered >50% of the HEK293-T cell surface were quantified under the 20× magnified objective lens of an inverted microscope (Olympus, CKX41, UK) for 30 fields per well. The plasma samples obtained from non-malaria naive individuals were considered negative controls, and mouse monoclonal antibodies against PvMSP1P-19 were used as the positive control. The percent binding-inhibition of each subjects was determined by assessing the number of rosettes in wells of transfected HEK293-T cells in the presence of P. vivax human plasma relative to rosettes in wells of transfected cells in presence of non-exposed Thai control plasma. Individual samples were dispensed into duplicate wells, and the whole experiment was repeated three times.
Preparation of peripheral blood mononuclear cells
To demonstrate the presence of MBCs specific to the PvMSP1P-19 antigen, PBMC samples from individuals who had recovered from P. vivax infection for 9 months (n = 11) were taken for MBC phenotyping and ELISPOT assays. The PBMCs were prepared from heparinized blood, for which the blood was diluted with incomplete RPMI 1640 medium (Gibco, Invitrogen, Paisley, UK) at a 1:1 proportion. To separate the PBMCs, diluted blood was overlaid on Ficoll-Hypaque (Stemcell Technologies, Vancouver, Canada). The overlaid blood sample was centrifuged for 30 min at 2000 rpm and 18 °C. The lymphocytes were harvested and washed twice at 1500 rpm for 10 min at 4 °C, then resuspended in R10 medium (incomplete RPMI media supplement with 10% FBS and 100 units/mL penicillin, with 100 μg/mL streptomycin). Later, the cell counting process and cell viability evaluation were performed by Trypan blue exclusion test.
Phenotyping memory B cells
To phenotype the MBCs, approximately 1 × 106 PBMCs were stained with a panel of fluorochrome-conjugated monoclonal antibodies that consisted of anti-human CD19-FITC (Biolegend®, San Diego, CA, USA), anti-human CD10-PE Cy7 (Biolegend®) and anti-human CD27-PE (Biolegend®) and incubated for 15 min at 4 °C. The cells were washed with 500 μL of FACS buffer at 1500 rpm for 5 min at 4 °C. Then, the cells were resuspended in 250 μL of FACS buffer. Finally, the stained cells were phenotyped by flow cytometry (BD FACSCanto™; Becton–Dickinson, Oxford, UK) and the resulting data were analysed by FlowJo (v. 7.0; Tree Star Inc., San Carlos, CA, USA).
PBMCs from stimulation for the ELISPOT assay
Before the ELISPOT assay was performed, PBMCs were first stimulated with polyclonal activator R848 and recombinant human IL-2 (Mabtech AB, Stockholm University, Sweden). During the cell stimulation process, 1 × 106 cells per mL were seeded into the 24-well culture plate (Corning Inc.). In parallel to the stimulated samples, non-stimulated samples were also employed. All the samples were incubated at 37 °C in a humidified 5% CO2 incubator for 72 h.
ELISPOT assay
MultiScreen Filter PVDF Immobilon plates (Merck Millipore, Darmstadt, Germany) were treated with 35% ethanol for 1 min prior to being washed five times with sterile water. The wells were then coated overnight at 4 °C with 15 µg/mL of monoclonal antibodies of anti-human IgG (clones MT91/145; Mabtech), 10 µg/mL of recombinant PvMSP1P-19 or PvMSP1 antigen, or 5 µg/mL of tetanus toxoid (TT) antigen (Merck Millipore, Darmstadt, Germany) diluted in sterile PBS. The plates were washed with 200 µL of sterile PBS five times and blocked with 200 µL of R10 for at least 30 min at 37 °C in 5% CO2. Both the stimulated and non-stimulated cells were harvested from the culture plates, counted and seeded in duplicate to yield 5 × 104 cells per anti-human IgG-coated well and 1 × 106 cells per specific antigen-coated well. After 24 h of incubation at 37 °C and 5% CO2, the plates were then washed with PBS five times. Then, 1 µg/mL of detection monoclonal antibodies MT78/145 (Mabtech) diluted in PBS-0.5% FBS were added and incubated for 2 h at room temperature. After five washes with PBS, the immobilized IgG was labelled using streptavidin–horseradish peroxidase (HRP)-conjugated polyclonal goat anti-human IgG (Mabtech) diluted to 1:1000 in PBS-0.5% FBS; Mabtech) and incubated for 1 h at room temperature. Following a thorough washing with PBS, tetramethylbenzidine (TMB) substrate (Mabtech) was added. The filtered plates were rinsed with deionized water after distinct spots emerged. Antigen-specific MBCs were expressed as spot-forming cells (SFC) in the wells. The plates were then left to dry and stored to protect them from light until they could be analysed with a Bioreader 5000 Pro-F gamma ELISPOT Reader (BioSys GmbH, Karben, Germany). PBMCs from P. vivax subjects that were cultured without stimulation and then incubated overnight with PvMSP1P-19 antigens were used as negative controls. The positive ELISPOT response was defined when spots were detected in duplicate wells and the total spots in the specific antigen-coated well reached at least twice the number of spots detected in the negative controls.
Statistical analysis
The data were analysed using GraphPad Prism software (Systat Software, San Jose, CA, USA) and Microsoft Excel 2007. The nonparametric Mann–Whitney U test was used to determine the significant difference of the antibody titre level against PvMSP1P-19 antigen in P. vivax malaria-exposed subjects, endemic villagers and healthy controls. An unpaired t-test was used to measure the significant difference between the acute phase and after 3 months recovery from infection groups from same individual. The CD19+ total B cells and MBC frequencies between different time points in the same individual were compared by paired t-test. MBCs specific to PvMSP1P-19 antigens and TT antigens between stimulated PBMCs and the non-stimulated negative control were compared by using a Wilcoxon matched-pairs signed rank test. In all the analyses, P values of less than 0.05 (P < 0.05) were deemed to indicate statistical significance.
Discussion
The aim of the blood stage malaria vaccine is to limit parasite growth during the stage that occurs within red blood cells and to prevent the clinical symptoms and pathology of malaria. However, most of the vaccines that are currently under development are in a pre-clinical study. The high polymorphisms of many leading candidate blood stage antigens are a major challenge for developing an effective vaccine against diverse strain of the parasites [
14,
15]. The PvMSP1 paralog is GPI-anchored protein that is expressed on the merozoite surface, which is involved erythrocyte receptor binding [
8]. In comparison with PvMSPs, it has a limited number of polymorphisms and is highly conserved [
8]. For the ability in immune stimulation, cellular and antibody mediated immune responses against PvMSP1P-19 was developed in
P. vivax-exposed patients [
10,
11]. The antibody from antisera and
P. vivax human plasma strongly blocked the binding to human erythrocytes, indicating PvMSP1P-19 antigen contain epitope recognized by inhibitory antibodies. To consider PvMSP1P-19 as a blood-stage vaccine candidate, better understanding long-lived immune response against this protein could be useful for vivax malaria protection.
In this study, the follow up seroprevalence of anti-PvMSP1P responses demonstrated a high prevalence of antibody responses, approximately 72.5, 70.4 and 67.9% at acute phase, 3 months recovery and 9 months recovery phases, respectively. Furthermore, a longitudinal cohort study of anti-PvMSP1P-19 response in 16 individuals at acutely infected phase and after 3-month recovery from infection showed the stability of antibody titres in the absence of reinfection. Interestingly, some patients maintained their antibody response up to 12-month recovery from infection. These data were in line with other studies which showed the maintenance of antibody response to PfMSP1
19 and PfMSP-1
42 and PvRAMA after recovery from infection in individuals who were living in low-transmission areas [
16‐
19]. However, in endemic areas with high malaria infection rate had an impact on the efficiency of the antibody response development. Anti-PfMSP1 response was not sustained during the long dry season in Sudan following anti-malarial drug treatment and parasite clearance. Here, the data support the persistence of antibody response to malaria antigen after recovery from infection in low-transmission areas.
Antibody to PvMSP1P-19 had inhibitory activity against erythrocyte binding, approximately 75% of high responders and 30.76% of low responders strongly inhibited PvMSP1P-19 binding to erythrocytes. Importantly, the inhibitory activity was maintained after 12 months recovery from infection in some individuals, suggesting
P. vivax patients could produce antibodies against PvMSP1P-19 binding to erythrocytes during acute phase, and they can maintain this antibody after recovering from the infection. With regard to the association between the in vitro inhibition assay of antibodies and the clinical protection in malaria infection, the cohort study had been demonstrated in PvDBP vaccine candidates. The maintenance of naturally acquired inhibitory antibody responses decreased the risk of
P. vivax malaria in rural Amazonians [
20] and conferred protection from blood stage
P. vivax infection [
21]. Here, the functional assay of anti-PvMSP1P-19 inhibitory antibody was well demonstrated, further study is required to demonstrate the association between stability of inhibitory antibody responses and its protection from
P. vivax malaria.
The association between long-lived anti-PvMSP1P-19 responses and the persistence of peripheral CD19
+ B cells after recovery from infection was observed. However, during acute phase, the total CD19
+ B cells were reduced compared to non-malaria naive and during convalescence. This data was consistent with previous findings of
P. falciparum infection study [
22,
23]. The reduction of total CD19
+ B cells could be explained by the temporary reallocation of lymphocytes from the peripheral circulation to the tissues or lymphoid organs following infection [
24], or it might occur through the evasive mechanism of
Plasmodium upon the disruption of B cell lymphopoiesis and the induction of B cell apoptosis as reported in a mouse model [
25,
26]. In addition, the expansion of CD19
+ B cell frequency at 3-month recovery phase may explain the homeostatic regulation of immune system after parasite clearance as there was no significant difference of CD19
+ B cells population between 3-month recovery from infection and malaria naive individuals, and the expansion of CD19
+ B cell was not correlated with antibody levels in this recovery phase.
After recovery from
P. vivax infection, the maintenance of CD10
−CD19
+CD27
+ MBCs was associated with positive PvMSP1P-19-specific MBC responses and circulating antibody titre. However, the positive correlation between peripheral CD10
−CD19
+CD27
+ MBCs and the number of positive spots for PvMSP1P-specific MBC response was not observed. These data suggest that the natural infection could induce PvMSP1P-19-specific MBC development, and those MBCs are able to differentiate among antibody-secreting cells to maintain the long-term antibody responses to this antigens in the absence of reinfection as parasitaemia at 3 and 9 months recovery from infection showed negative by nested PCR. However, the persistence of specific MBCs to the malaria antigens is still unclear. In low-transmission areas, MBCs specific to
P. falciparum MSP-1 antigen and the
P. vivax antigens, AMA1 and MSP1-19 was retained after recovery from infection [
16,
17,
27]. By contrast, some data from high-malaria-transmission regions showed the expansion of
P. falciparum AMA1- and MSP1-specific MBCs in acute infection, and then memory cells were contracted to a point slightly higher than pre-infection levels after 6 months of decreased
P. falciparum exposure [
28]. Here, the persistence of PvMSP1P-19-specific MBC response after recovery from infection supports the hypothesis that MBC responses are more stable in low-malaria-transmission areas. In addition, the positive PvMSP1P-19-specific MBC response but negative for antibody titre in 2 adult children suggests that immunity to PvMSP1P-19 can develop persisting MBC responses in some individuals since the initial infection of malaria.
Authors’ contributions
HMKM, SC and PTS: performed the experiments, analysed the data and wrote the paper. JHH, FM and SKL: expressed the recombinant protein. PC and ETH: conceived and designed the experiments. All the authors read and approved the final manuscript.