Background
Currently malaria rapid diagnostic tests (RDTs) detect Plasmodium antigens in blood by antibody-antigen interactions on a nitrocellulose test strip. The targeted antigens include those specific to Plasmodium falciparum (histidine-rich protein-2 (HRP-2) and P. falciparum-specific parasite lactate dehydrogenase (Pf-pLDH)) and antigens common to P. falciparum, Plasmodium vivax, Plasmodium ovale and Plasmodium malariae (pan-species pLDH and aldolase). RDTs combine a control line with one, two or three antigen-detecting test lines, and are referred to as two-, three- and four-band RDTs respectively.
RDTs are being rolled out as an alternative to microscopic diagnosis in malaria endemic settings [
1] and have demonstrated sensitivities close to 100% for the detection of
P. falciparum at densities above 100 asexual parasites/μl or > 0.002% of parasitized red blood cells (RBC). Most false-negative results occur at lower parasite densities. However, false-negative results have been reported also at high parasite densities. Part of those may be ascribed to genetic variations of the HRP-2 [
2‐
6], but the prozone phenomenon may also be involved. Prozone is defined as false-negative or false-low results in antigen-antibody immunological reactions, due to an excess of either antigens or antibodies [
7,
8]. In RDTs, the prozone has been observed in samples with high
P. falciparum parasite densities and dilution of the sample can trace and correct the effect [
9]. In a recent laboratory evaluation, RDT brands were challenged to a panel of clinical samples with
P. falciparum. Prozone was observed among 16 out of 17 HRP-2 RDTs but not among five Pf-pLDH RDTs [
9]. However, as this was a retrospective laboratory study in a reference setting, the frequency and impact of the prozone effect on the diagnosis of malaria in the daily practice of endemic settings remains to be determined.
The main aim of the present study was to assess the frequency of the prozone effect in a malaria endemic field setting. A subsidiary aim was the confirmation of the previous observation that HRP-2 RDTs, but not Pf-pLDH tests, are affected by prozone [
9].
Methods
Study site, study period and patients included
The study was conducted in the emergency ward of the Provincial Hospital of Tete (PHT), located in Central Mozambique. In this area, malaria is predominantly caused by
P. falciparum. Transmission is perennial with peaks during and at the end of the rainy season (February - April)[
10,
11].
The PHT serves as a reference hospital for Tete Province (1,700,000 inhabitants). According to hospital statistics, yearly approximately 50.000 patients present themselves with clinical suspicion of malaria. Diagnosis is confirmed in about 20% of them (either by RDT or microscopy). For this study, all patients suspected of malaria and presenting at the emergency ward of the PHT were prospectively included on a 24 hours/7 days basis from January till April 2010.
Patients, samples and diagnostic work-up
Routine procedures for malaria diagnosis (following national guidelines) at PHT are as follows: EDTA-anticoagulated blood is sampled and a full blood count is performed by an automated haematology analyzer (KX-21N, Sysmex, Kobe, Japan). For children ≤ 5 years, malaria diagnosis is made on a thick blood film (TBF). For patients above five years of age, an RDT is performed and in case of a positive result a TBF is made for confirmation and determination of parasite density. TBFs are stained for 20 minutes at pH 7.2 using Giemsa 3.5% (Merck, KGmA, Darmstadt, Germany). According to the national malaria clinical guidelines, parasite density is scored on a semi-quantitative scale from 1+ (1-9 asexual parasites/100 high power microscopic fields) to 5+ (> 100 asexual parasites/1 high power microscopic field) [
12]. During the study period, three RDT brands (
ICT Malaria, Paracheck-Pf and SD Malaria Antigen Pf FK50) were routinely used (provided by the national malaria programme or a partner NGO).
For the purpose of the study, demographic data, presenting symptoms and clinical signs of severe malaria [
13] were recorded for all patients with clinical suspicion of malaria attending the PHT. In addition, TBFs were performed for all suspected patients, irrespective of their age. For TBFs positive for
P. falciparum and scored as 4+ or 5+, parasite densities were quantitatively assessed: the number of asexual parasites was counted against 200 white blood cells (WBC) and converted to parasites/μl using the WBC count/μl. Hereafter, values were converted to % of parasitized RBC using the RBC count/μl. WBC and RBC counts were those provided by the haematology analyzer.
Samples with a high parasitaemia, defined as ≥ 4% of parasitized RBC [
14,
15], were challenged against a panel of RDTs consisting of four HRP-2 RDTs and two Pf-pLDH RDTs (see below and Table
1). Determination of parasite density and testing of RDTs were done at the latest 48 hours after sampling and samples were stored at 4°C pending RDT testing. Analyses were performed by the regular laboratory staff as well as the authors PG, AS, JS and HC. Left-overs of the EDTA blood samples were stored at -20°C till the end of the study for further analyses.
Table 1
Panel of RDT brands used in the study
ICT Malaria ICT Diagnostics, Cape Town, South Africa Lot n°: 32784 | Two-band: HRP-2 | yes | yes |
Paracheck-Pf Orchid Biomedical Systems, Goa, India Lot n°: A31003, 31672, 32972, 31797 | Two-band: HRP-2 | yes | yes |
SD Malaria Antigen Pf FK50 Standard Diagnostics, Hagal-Dong, Korea Lot n°: 082011, 082012, 080216 | Two-band: HRP-2 | yes | yes |
SD Malaria Ag Pf/Pan FK60 Standard Diagnostics, Hagal-Dong, Korea Lot n°: 090008, 090010, 090026 | Three-band: HRP-2, pan-pLDH | yes | yes |
Hexagon Malaria Combi ‡ Human Wiesbaden, Germany Lot n°: 80930 | Three-band: HRP-2, aldolase | no | yes |
Malaria Pan/Pv/Pf Rapid Device‡ Biotec laboratories Ltd., Ipswitch, UK Lot n°: 91081, 91100 | Four-band: HRP-2, Pan-pLDH, Pv-pLDH | no | no |
CareStart Malaria pLDH Acces Bio, New Jersey, USA Lot n°: B191L, A101L | Three-band: Pf-pLDH, pan-pLDH | no | yes |
SD Malaria pLDH FK40 Standard Diagnostics, Hagal-Dong, Korea Lot n°: 081006 | Three-band: Pf-pLDH, pan-pLDH | no | yes |
First Response Malaria Ag Combo
$
Premier Medical Coorporation Ltd., Daman, India Lot n°: 6900309 | Three-band: HRP-2, Pan-pLDH | yes | yes |
Hexagon Malaria
$
Human, Wiesbaden, Germany Lot n°: 0001 | Two-band:: HRP-2 | no | yes |
ICT Malaria Combo
$
ICT Diagnostics, Cape Town, South Africa Lot n°: 32250 | Three-band: HRP-2, Aldolase | no | yes |
Malaria Total Quick
$
Cypress Diagnostics, Leuven, Belgium Lot n°: 090002 | Three-band:HRP-2, Pan-PLDH | no | no |
Malaria rapid diagnostic tests used and test procedures
Malaria RDTs in cassette format were selected based on demonstrated diagnostic accuracy [
16‐
18], use by national malaria control programmes and non-governmental organizations (NGOs) and availability in Mozambique.
For each sample with high parasitaemia, a 10-fold dilution was made in saline. Both undiluted and diluted sample were assessed with each RDT brand and tests were run in duplicate and read by two observers. The second observer was blinded to the first observer's readings. Tests were performed according to the instructions of the manufacturer, except for the use of an automatic pipette (Finnpipette, Helsinki, Finland) instead of the RDT kits' transfer device. Test line intensities were scored into five categories: none (no line visible), faint (barely visible), weak (paler than the control line), medium (equal to the control line) and strong (stronger than the control line) [
19]. When a control line did not appear, the test was interpreted as invalid and the sample was retested. To assure timely readings, tests were performed in time-controlled batches. Readings were carried out at daylight, within the prescribed reading delay.
Additional analyses
Two additional HRP-2 RDT brands (Hexagon Malaria Combi and Malaria Pan/Pv/Pf Rapid device), not delivered in time for the prospective analysis, were assessed at the end of the study period with samples that had been stored at -20°C (maximum storage duration: 121 days).
In order to investigate the prozone occurrence at parasite densities below 4%, all RDT brands were also assessed with a subset of 45 samples scored as 4+ or 5+ but with parasite densities below 4%.
To confirm the prozone susceptibility of HRP-2 RDTs, an additional panel of four HRP-2 based RDTs was assessed with a subset of stored samples that had demonstrated prozone for at least one of the prospectively assessed HRP-2 RDTs (Table
1). Among the evaluated RDTs, there was also an additional lot number of
Malaria Pan/Pv/Pf Rapid Device. The results of these latter panels were not included for calculation of the frequency of prozone.
Test outcomes and definitions
Samples with high parasitaemia were defined as samples with parasite densities ≥ 4%. Prozone was defined if a sample showed no visible test line or a faint or weak test line when tested undiluted, and a visible test line of higher intensity when tested 10-fold diluted, as observed by two blinded observers and upon duplicate testing [
9].
The frequency of prozone was extrapolated against the total number of samples with high parasitaemia, the total number of P. falciparum positive samples and the total number of patients suspected of malaria.
Quality control
At the start of the study, the laboratory staff received a refresher course on malaria microscopy and RDTs. The study team was trained on study procedures and flow during a pilot phase.
All RDTs were purchased in Belgium and shipped to Tete, except for SD malaria Antigen Pf FK 50 and the lot A31003 of the Paracheck-Pf which were provided locally. During shipment and storage, temperature and humidity were monitored using loggers (Ebro Electronic GmBH, Ingolstadt, Germany). On a daily basis, 10% of TBFs were randomly elected and reread by a member of the study team who was blinded to the original result. All discordances were resolved by a third reader's reading. A photograph was taken from all RDT tests performed and the TBFs were stored for quality control.
Data management and statistical analysis
According to the initial sample size calculation, a total of 5,700 patients suspected of malaria were required for reliable estimation of the frequency of prozone. This was based on the following assumptions and information from hospital statistics: malaria-attributable fraction during the wet season of 30%, prevalence of hyperparasitaemia of 10%, prozone frequency among hyperparasitaemia samples of 30% with 95% confidence intervals (CI) between 20% and 40%.
Data were recorded in registers and on individual case report forms. Data were entered in Microsoft Access (Microsoft Corporation, Redmond, Washington USA) and analyzed in Stata 11.1 (StataCorp LP, College Station, USA). Differences between proportions were tested for significance using the Pearson's Chi-square test or, in case of small sample sizes, a two-tailed Fisher's exact test. Reproducibility and inter-observer reliability for line intensity readings were assessed using the kappa statistic for paired observers and percentage agreements. Differences between medians were tested using the Wilcoxon test. Lot variations for matched pairs of samples were assessed using the McNemar's test. The relation between line intensities of prozone samples across the parasite densities was assessed using the Cuzick's test for trend. A p-value < 0.05 was considered as significant.
Ethical review
The study was approved by the Institutional Review Board of ITM, by the ethical committee of Antwerp University, Belgium and by the Comité Nacional de Bioética para a Saude (MoH), Mozambique. Patients, children's parents or guardians were informed in Portuguese or in the local language (Nhungue) and their written consent was required prior to enrolment.
Discussion
In 2009, an estimated 225 million cases of malaria occurred with 781.000 deaths, mostly due to
P. falciparum in children in Africa [
1]. WHO recommends parasitological diagnostic testing before treatment. When microscopy is not available, RDTs are the alternative. RDTs have been demonstrated to perform equally well or even better than microscopy in field settings [
20‐
23] and are currently deployed at all levels of health facilities [
1].
Some limitations are however to be mentioned. The wet season of 2009-2010 in Mozambique was characterized by irregular rainfall and long dry spells. Due to this low rainfall (30% below expected value in November 2009 up to 60% in March 2010 [
24]) and the impact of local control measures in the months preceding the study, there was less malaria than expected and the originally planned 5% parasite density threshold (defined by WHO as hyperparasitaemia [
13]) was replaced by 4%, also used in other studies [
14,
15]. Although samples below this 4% threshold were included, prozone was not assessed below this threshold, precluding systematic study of possible clinical or laboratory predictors of prozone. Further, due to non-availability of trained staff around the clock, it was not always possible to record all clinical data and to work-up all samples in the laboratory. Likewise, for logistic reasons, two RDTs were assessed with blood samples stored at -20°C and not on fresh samples. However, it should be noted that the HRP-2 antigen is very stable and resistant to harsh conditions [
25]. For three RDTs, storage temperatures slightly exceeded those recommended by the manufacturers. Finally only a minority of undiluted prozone positive samples showed no visible test line, whereas the remaining samples showed faint or weak test lines. However, disregarding faint or even weak test lines as negative is a common error among end-users in field settings [
26‐
28].
There are only few original studies reporting on prozone in malaria RDTs [
9,
29]. Prozone may however explain for the rare but consistent reports of false negative HRP-2 based RDT results in samples with high parasite density: for instance, in a recent study of two RDTs in Sierra Leone, two false-negative samples were observed with the HRP-2 RDT but not with the Pf-pLDH RDT. The parasite densities of both samples were 288,000/μl and 580.000/μl, corresponding to 5.7% and 11.6% parasite density respectively [
30]. Interestingly, the HRP-2 test used in this study was
Paracheck-Pf and the two samples accounted for 1.1% of all malaria positive samples which is in line with the present findings. Similar observations affecting
Paracheck-Pf or other HRP-2 RDT brands have been reported from endemic as well as non-endemic settings [
31‐
33].
In line with previous findings, the present study demonstrated prozone in HRP-2 but not in Pf-pLDH based RDTs frequently used in field settings [
9]. Compared to HRP-2 based RDTs, pLDH based RDTs are ascribed lower sensitivity and lower heat-stability [
23,
34,
35], but according to a recent field study and the second WHO/FIND RDT evaluation round, Pf-pLDH RDTs may perform equally well as HRP-2 RDTs [
17,
36]. The observation of lot-to-lot variations in one HRP-2 RDT brand illustrates that small differences in composition may influence the vulnerability to prozone. In that way, it should be noted that the present data only reflect those of the examined lot numbers and may therefore not be extrapolated to all RDT brands. Although not assessed in the present study, several factors in the design of the individual RDT brands may explain for their different vulnerabilities to the prozone effect. As antigen-antibody interactions are time-related, factors influencing the speed of migration may be involved, such as the pore size of the nitrocellulose membrane and the viscosity and volume of the buffer. In addition, the structure of the antibodies, the affinity and the avidity of the antigen-antibody binding may be of influence. With regard to end-user practice, application of a high blood volume may increase the risk of prozone, as demonstrated previously [
9].
From the present results, it is clear that prozone occurred dispersedly among samples with high parasitaemia. Prozone with non-visible test lines occurred exclusively in samples with parasite densities above 8% and the frequency and intensity of prozone decreased below the 4% threshold. However, the association parasite density - presence of prozone among samples with parasite densities ≥ 4% was not straightforward. This may be ascribed to factors such as capillary sequestration of the parasites, variations in the antigen production during the cycle and strain differences [
4,
37]. Prozone remains a rare phenomenon and although the present study was not designed to trace risk factors of prozone, this study suggests that, apart from hemoglobin level, there are no clear indicators for prozone. This relation can be explained by the high concentration of HRP-2 related to the duration of the disease and/or to the number of malaria crises in the past few weeks.
For the two most affected RDT brand (
Paracheck-Pf and ICT Malaria), prozone with negative or faint HRP-2 test lines (the most dangerous situation) occurred in at least 1.2% of malaria-positive samples and 10.9% of samples with high parasitaemia. At such frequencies, the diagnostic accuracy may be affected and the impact on predictive values will depend on the malaria-attributable fraction of fevers and the proportion of high parasite densities: both factors are related to transmission intensity and pre-existing immunity of the affected population [
38]. For Africa, the
P. falciparum prevalence rate in children aged two to ten years is actually estimated at 17% [
39]. For the distribution of parasite densities, published data are scarce. Two recent studies conducted in children in areas of perennial transmission in Gabon and Sierra Leone reported median parasite densities of 13,860/μl (1,400 - 71,452) and 264,000/μl (1 - 2,136,000) [
22,
30]. When extrapolating for Mozambique, based on the 4,310,086 suspected malaria cases reported in 2009 [
1], a 17% malaria attributable fraction [
39] and a 10% proportion of high parasitaemia, the annual numbers of negative or faint test lines were calculated as 7,694 (CI: 3,883-13,922) and 9,643 (CI: 4,543-15,387) with
Paracheck-Pf and
ICT Malaria (tested with the presently evaluated lots) respectively.
The risk related to false-negative RDT results due to low parasite densities is mitigated by diagnostic algorithms recommending to repeat testing after an unexpected negative RDT result [
40‐
42]. However, such policy will not timely correct for false-negative results due to the prozone, as hyperparasitaemia represents a life-threatening situation. In addition, there is a tendency to roll out RDTs to poorly resourced peripheral health care facilities where there are no further laboratory facilities to perform sample dilution or microscopy in order to correct for prozone [
1,
20]. Possible other measures to address prozone are training of the end-user to understand the problem and to assure interpretation of faint test lines as positive test results. Concerning RDT quality control at the level of national reference laboratories and the FIND/WHO lot testing programme, samples with hyperparasitaemia could be included but in view of the low prozone frequency and its scattered distribution among samples with hyperparasitaemia, it is difficult to assess prozone on a pre-release basis. Post-marketing follow-up including incident reporting could provide further clues. Finally, depending on the distribution of parasite densities in a given population, susceptibility to prozone should be added as a major argument in the strategic choice between Pf-pLDH and HRP-2 RDTs.
In conclusion, prozone is a rare event but it occurs among widely used HRP-2 RDTs at frequencies that may diminish diagnostic accuracy of the affected RDTs.
Authors' contributions
PG, ADW, SM, EB and JJ designed the study; PG, AS, JS, ADW and EB organized laboratory and clinical supervision in Tete; PG, AS, JS, HC and OJV actively participated in the laboratory work in Maputo and Antwerp; PG, AS, ADW, EB and JJ assessed and interpreted the results. All authors contributed to the discussion of the results and the redaction of the manuscript, they all approved the final manuscript.