Schistosomiasis is a waterborne disease whose life cycle involves freshwater sources conducive for the survival and reproduction of aquatic snails that form a connective link between man and water in the life cycle and transmission of schistosomiasis. The African region has network of rivers with freshwater suggesting the presence of schistosomiasis and difficulty to control. Some communities, due to socioeconomic challenges, have inadequate sanitation and water supply; use of bush toilets for excretion is commonly practiced. These conditions in Africa also promote transmission of soil-transmitted helminthiasis. The World Health Organization (WHO), in response to the public health and socioeconomic impact of neglected tropical diseases, is coordinating strategies for the control and elimination of the diseases including schistosomiasis and soil-transmitted helminthiasis. As one of the milestones, mapping of neglected tropical diseases in the African region has been prioritized for the implementation of control strategies. In countries where mapping has been completed, WHO and its partners are supplying medicines required for annual mass treatment for preventive chemotherapy and encourage countries to take ownership in implementing complementary strategies for morbidity control, elimination and eradication of country-specific neglected tropical diseases. The mainstay of helminthiasis control is preventive chemotherapy, targeting school age children to prevent morbidity and development of pathological manifestations, including urogenital schistosomiasis that is understood to contribute to HIV transmission. Vaccines are still to be discovered and designed, with many possible antigen candidates, but however the immune responses are still to be fully understood. There is need to understand the subtle link between each component of the immune responses and the host immunogenetics impacting on the translated immunological response of cytokines that are delicately controlled for cellular immunity and antibody production. Currently, preventive chemotherapy treatment is the only control method in concert with health education in an attempt to cut the helminthiasis life cycle.
- soil-transmitted helminthiasis
- mass drug administration
Parasitic worms (helminths) are responsible for chronic infections of over two billion people worldwide and impose a huge public health burden. The hallmark of helminth infection is immune modulation of the host's immune response, which both limits immunopathology in the host while allowing the worms to evade host immune attack. The immune modulation of host responses during helminth infection has attracted much interest in terms to understand the generation of protective immunity. Unfortunately, the immune modulation occurring during helminth infection also interferes with the expression of naturally acquired protective immunity against the parasites, resulting in an accumulation of parasites in the host. Experimental Studies suggest manipulating host regulatory responses can enhance helminths vaccine efficacy. In human schistosomiasis, the health impact is not confined to immunopathology but extends to physical damage resulting from the presence of the parasites and the passage of parasite eggs as they are excreted from the host via urine or stool. In the case of urogenital schistosomiasis, infection interferes with child development and health, diminishes female reproductive health and increases susceptibility to sexually transmitted diseases including HIV and can lead to bladder cancer.
Currently available control method is treatment of infected people with the antihelminthic drug praziquantel. Field studies have already demonstrated that praziquantel treatment can induce protective immunity in chronically infected children, while treatment if conducted earlier in life would mean children benefit from the effects of praziquantel earlier, thus avoiding the health costs associated with chronic infections. Praziquantel treatment imparts on molecular and immune responses, mediating resistance in individuals previously with chronic schistosome who became resistant against reinfection by the parasites. This concept of infection-treatment as immunization is used in some veterinary diseases. There is need to investigate the transcriptional and post-translational characteristics underlying resistance to schistosome. Subsequently, regular childhood treatment may induce protective immune responses, that is, treatment of primary infections before it becomes chronic, induces regulatory responses that may reduce the efficacy of the effector responses. More studies are required to understand the activation of regulatory, pro- and anti-inflammatory responses in individuals who remain susceptible to re-infection and the mechanisms by which these regulatory responses modulate effector functions. Such knowledge is important to improving current and future helminth interventions as well as the development of novel therapeutics against immune-mediated pathology arising from parasitic infection or immune dysfunction.
An important constraint for helminths vaccine development is the paucity of information on the induction of appropriate effector pathways mediating protective immunity over the regulatory responses, which modulate them, as well as on mechanisms by which vaccine efficacy and longevity can be enhanced. Experimental studies of other helminths suggest that vaccine efficacy can be improved beyond the typical low protection level by neutralizing immunomodulatory processes. There is missing evidence to identify the key immunomodulators and their functional mechanisms, which can be manipulated to improve the efficacy of helminths vaccines and pathways that can be manipulated to enhance the longevity of vaccine-induced resistance. In addition, there is currently lack of consensus on markers of vaccine-induced protection. However, in the meantime, preventive chemotherapy is the only alternative in concert with health education.
1.1. Human helminthiasis as neglected tropical diseases
Human helminthiasis are part of the neglected tropical diseases (NTDs), which are a diverse group of parasitic, viral and bacterial diseases with distinct characteristics, that thrive mainly among the poorest populations, hinder socioeconomic development and cause substantial illness for more than one billion people globally . Seventeen NTDs (Figure 1) have been specified by the World Health Organization (WHO) and these include dengue, buruli ulcer, cutaneous leishmaniasis, taeniasis/cysticercosis and echinococcosis/hydatidosis, foodborne trematode infections, soil-transmitted helminthiasis (STH), intestinal worms, rabies, blinding trachoma, endemic treponematoses (yaws), leprosy, Chagas disease, Human African trypanosomiasis, visceral leishmaniasis, dracunculiasis, lymphatic filariasis, onchocerciasis and schistosomiasis . These NTDs impair physical and intellectual capacities of the affected persons, thereby perpetuating the cycle of poverty . Forty-seven countries in the African region are endemic to at least one NTD and 37 of them (79%) are coendemic for at least five of these diseases .
Five of the 17 NTDs [lymphatic filariasis, onchocerciasis, schistosomiasis, soil-transmitted helminthiasis (STH) and trachoma] are amenable to preventive chemotherapy. Thus, targeting such disease for control and elimination using available safe medicines and supported by complementary interventions could provide a noticeable quick win on NTD for the African region and in particular for the endemic countries. STHs have been specified as endemic in many countries even though the data collection methods used could be at variance from those recommended by WHO . Countries in the African region through their Ministries of Health have not only endorsed the adoption of the resolutions on NTD by the World Health Assembly (WHA) in 2013, but they also expressed their commitment to scaling up interventions against the major NTDs . With such an increased momentum to eliminate NTDs, it is critical that WHO member states implement NTD strategies demonstrating their commitments.
2. Disease transmission
Schistosomiasis transmission begins most often when people come into contact with bodies of freshwater in which infected people have urinated or defecated and there is a stage of the life cycle in intermediate snail host . Transmission is linked to the life cycle of the schistosome (e.g., egg, miracidium larval form, sporocyst, cercaria, schistosomule, adult schistosome), when an egg comes in contact with freshwater, where it hatches and releases a miracidium. The miracidium swims by ciliary movement toward the snail intermediate host and penetrates its soft tissue. The
2.1. Global public health significance of schistosomiasis
Schistosomiasis remains one of the most prevalent parasitic diseases in the world, found endemic in 76 countries and is a public health concern in the developing world . Schistosomiasis is a chronic disease, poorly recognized at early stages and if untreated the disease debilitates men and women during their most reproductive years. The disease is typically common in areas of the economically disadvantaged people living in areas that have no access to proper sanitation and good water supply systems. The high-risk groups for schistosomiasis are school age children, adolescents, reproductive women and also those whose occupations involve contact with water, for example fishermen, farmers, irrigation workers and women in their domestic tasks . It is estimated that about 652 million people are at risk of infection from the five human schistosome species (
The number of individuals with hydronephrosis due to
Genital schistosomiasis is also common in both males and females in endemic areas. Female genital schistosomiasis (FGS) described as the presence of schistosome eggs on the upper or lower part of the reproductive tract has been demonstrated in up to 75% of females living in schistosomiasis endemic communities (Figure 4A and B) in Africa [10–12]. Reproductive complications due to FGS include low birthweight, abortions, ectopic pregnancies, primary and secondary infertility [13–16]. In African cultures, infertility in married couples is often blamed on women. This leads to rejection by husbands, family and kinship group. The society may not accept women who do not get pregnant . It is also hypothesized that FGS facilitates transmission of HIV [12, 17]. The far-reaching consequences of schistosomiasis infection also include reduced national economic growth and persistent poverty. However, treatment using a single dose is now available, effective and safe to be taken by uninfected children or pregnant mothers and, can easily be incorporated into regular field activities . Any initiative to control schistosomiasis will not only contribute towards morbidity reduction but also to the control of HIV transmission, improvement of school health and performance of children, national economic growth and poverty alleviation.
2.2. Soil-transmitted helminthiasis
Soil-transmitted helminthiases are nematodes transmitted from the soil to humans. These include hookworms (
The conditions that support transmission of STH are similar to those favoring transmission of schistosomiasis (poor sanitation, contamination of the environment with human excreta, poverty leading to lack of protective clothing and safe water supply). These conditions could create an overlap of epidemiological distribution of schistosomiasis and STHs in some regions. There is a high risk of morbidity exacerbation due to mixed infection from schistosomes and STHs. At least 50% of severely ill people due to worm infestation are school age children [19, 24], and infection from STHs and schistosomiasis represent more than 40% of the disease burden due to all tropical diseases, excluding malaria . But these diseases are treatable. The public health significance of schistosomiasis and STH has triggered response from WHO, which in the 54.19th WHA 2001, demanded that all member state endemic to these NTDs should provide regular mass treatment to primary school children at risk of morbidity due to schistosomiasis and STH, with praziquantel and albendazole. There is a major shift in the policy for the control of Preventative Chemotherapeutic Treatment of NTDs to that of control/elimination .
The standard diagnosis for schistosomiasis is detection of viable eggs in urine (
2.4. Global control of helminthiasis
2.4.1. Vector control
The three major species of schistosomes that infect humans,
Indigenous plant extracts are an attractive alternative to chemicals for killing snails. These have low costs due to local availability and the extracts are less toxic to other forms of aquatic life . The plant
2.4.2. Health education
Health education is an important component of effective schistosomiasis prevention and control. Developing health education programs requires that the design, administration and outcomes be adapted to different socioeconomic and cultural settings . Several studies have shown that the individual's behavioral changes facilitating disease prevention and control. Behavior cannot be changed simply with the acquisition of knowledge that can be obtained from health education . Health education programs end up not successful when the socioeconomic and cultural context of communities is not considered. Individuals and communities have to be considered in full their environment and education when developing programs for the control of diseases in an area. The success of programs in reducing high-risk behavior and promoting health-enhancing behavior depends to a considerable degree on whether the life cycle and other biomedical concepts and information are presented in an appropriate, emotional, social, economic and cultural context of target populations. Consideration should be taken when people do not have the means for changing their behavior, for example, inadequate health services, no access to proper sanitation and clean water supply, unavailability of antihelminthic medications and unaffordability of modern treatment.
Observations were made in a longitudinal study conducted in Zimbabwe over 33 months in which parasitology follow-up examination and treatment was done every 6 months for the first year, then a break for almost 24 months. The reinfection was observed to take place in such an endemic setting rising to almost half the levels before treatment (Figures 5A–D). However, after a long break of 24 months, the prevalence was seen to rise to almost pretreatment levels, even though infection intensity was drastically reduced.
Despite several years of mass antiparasitic drug therapy programs and other control measures, helminthiasis still continues to exist. The discovery of a vaccine still remains a pipe dream for the control of human helminthiasis. A vaccine would contribute to the reduction of schistosomiasis morbidity through immune modulation leading to a decrease in parasite load and reduced egg production. A lot of research has been done with a view of controlling and preventing schistosomiasis. Researchers have focused on vaccines, host genetic predisposition, coinfections, autoimmunity and improved diagnostics for surveillance.
Several candidate human schistosomiasis vaccines are in different stages of preclinical and clinical development. The most eligible candidates are egg antigens and the schistosomula tegument membrane antigens (Sm 23, SmTSP-2 and Sm29)  of
The vaccine development strategies are bedeviled with many biological bottlenecks such as the lack of reliable surrogates of protection in humans; immune interactions in coinfections with other diseases in endemic areas; the potential risk of IgE responses to antigens in endemic populations; and paucity of appropriate vaccine efficacy studies in nonhuman primate models. Research is also needed on the role of modern adjuvants targeting specific parts of the innate immune system to tailor a potent and protective immune response for lead schistosome vaccine candidates with the long-term aim to achieve curative worm reduction .
Immune responses during schistosomiasis can be considered in terms of three broad aspects of immunopathogenesis, resistance to reinfection and immunodiagnostics. The development and establishment of chronic infection is impacted by the presence of chronic antigenic exposure as illustrated in Figure 2 and summarized in Figure 3. The immunological regulation associated with the morbidity of schistosomiasis has been studied without completely understanding the impact [45, 46] of the immunological components involved that contribute to failure to design successful vaccines. However, the immune mechanisms related to resistance to reinfection and in response to candidate parasite antigens are not well defined. Adult worms are known to be refractory to immune attack; while immature and developing worms, skin-stage and lung-stage schistosomulae are the probable targets of protective immunity [46, 47] that are safe from drug effects. Whether a protective resistance to reinfection exists is still not well characterized and understood [47, 48], but evidence suggests that such resistance may develop rather slowly [46, 47]. The induction of protective immunity has been shown through immunization of various experimental hosts with irradiated cercariae to work for a short period of time. Data from endemic populations suggest that age-associated decreases in infection result from the development of antiparasite immunity, rather than reduced contact with water . Although the responsible antigens and host immune responses are not fully defined, resistance to reinfection is believed to be associated with IgE antibodies against worm antigens, with low concentrations of IgG4 antibodies to worm antigens and high blood eosinophilia. Resistance to reinfection is partial, which means that protective sterile immunity either does not develop or is rare. Treatment of schistosomiasis increases common correlates of resistance: eosinophilia, parasite-specific IgE and interleukin 5 production in response to worm antigens, while repeated treatment to prevent reinfections can lead to longer intervals before reinfection, even accounting for similar exposure patterns in highly exposed participants .
Neglected tropical diseases are found in areas that have conducive environmental conditions. Schistosomiasis and soil-transmitted helminthiasis often occur alongside each other and with other tropical infectious diseases and with a wide range of coinfecting organisms. In addition to the direct morbidities, schistosomiasis can affect immunological and physiological responses of the host and the coinfecting pathogens. Thus, better control of schistosomiasis could provide adjunctive benefits towards other coinfecting organisms in such areas. The most studied and compelling example is the effect of schistosomiasis on susceptibility to HIV infection. Among women with female genital schistosomiasis, the inflammation of the genital epithelial tissue can lead to a compromised physical barrier to exposure to HIV through sexual activity. In population-based studies, female genital schistosomiasis has been associated with a three to four times increased risk of HIV infection [10–12, 16, 17, 49].
Schistosomiasis alters immune responses directed towards coinfecting pathogens, allergens or vaccines. The immunoregulatory responses during schistosome infection could downregulate T-helper type-1 immune response associated with the control of viral or protozoan infections or interfere with immunization generally made available to children living in affected tropical areas. In one of many studies of schistosomiasis and malaria coinfections it seems to indicate that schistosomiasis modulates malaria; however, studies have yielded conflicting results [50–54]. In some cases, malaria prevalence, anemia and pathological effects are higher in children with schistosomiasis than in children without schistosomiasis, whereas antimalarial immune responses are diminished . However, other studies report no protective effect of schistosome infection on malaria that can be accompanied by increased immune responses [53, 54]. Schistosome and malaria-related antigens can cross react to some extent, further complicating the situation. However, within the host there is need for a delicate but subtle interplay between pro- and anti-inflammatory cytokines that play a major controlling effector role on the antibody production and the cell-mediated antibody dependent cytotoxicity (Figure 6A and B).
3.2. Host immunogenetics
The development of genetic epidemiology methods using recent human genetic mapping information has led to major advances in the identification of host genes in human schistosomiasis and other infections . Determining the role of host genetics in schistosomiasis is complicated by the numerous parasite and environmental factors involved in transmission. Two immunological and pathological phenotypes have been studied so far as schistosomiasis infection levels on the host-parasite as consequences measured by the fecal egg counts and the severe hepatic fibrosis assessed by ultrasound examination. The first study was performed on Brazilian pedigrees and provided strong evidence for a major gene controlling infection levels by
4. Mass drug administration (MDA)
Mass drug administrations (MDA) in affected populations or communities form the basis of current schistosomiasis and soil-transmitted helminthiasis (STH) control and/or management. The MDAs can follow one or more of the following approaches; house-to-house administrations (i.e., mobile teams), booth distribution (i.e., fixed teams), administering drugs in special population groups (e.g., school age children, etc.) and/or areas of community gatherings (e.g., marketplaces, stations, etc.) . Such chemotherapeutic prevention and management strategies of infectious diseases in endemic areas have some significant shortcomings, chief among them being re-infections [59, 60], due to untreated human and animal reservoirs. Prophylactic measures in these areas are difficult as that would mean people will have to take the medicines frequently for life, thus exposing them to potential life-threatening adverse drug events and development of drug resistance. In endemic areas during a five-year round of annual mass treatment of school going age children, before and post-treatment checks revealed that re-infection always takes place (Figure 5). Reinfections were most common in cases where MDA was not accompanied with adequate environmental and health promotion/education interventions. Successful MDA in endemic areas has to be conducted in all age groups. For better coverage, the World Health Organization recommends the utilization of all available medicine distribution channels especially in countries with high levels of infections [60–64].
Repeated MDAs have helped some countries to significantly reduce the disease burden. An example is the 84% reduction of baseline levels of schistosomiasis in a moderately highly endemic region of the northeast of Sierra Leone, with MDA interventions repeated yearly over three years . Communities in Zanzibar, Tanzania also recorded significant reductions in infections levels of soil-transmitted helminthiasis (90–98%) and scabies (68–98%) as additional benefits associated with the annual mass drug administration of ivermectin and albendazole for lymphatic filariasis. Modeling done by Anderson
Despite significant contributions, great optimism and positive outlook; MDA may not lead to total elimination on its own . There is a great need for critical assessments of all MDAs for more positive effects to be realized. Significant community effectiveness of MDA programs stand challenged by issues around; very low coverage (<75%) as about a third of those that really require treatment and/or chemoprophylaxis are receiving it [64, 65]; the utilization of volunteers and/or underpaid workers to distribute or administer medicines; overly relying on fragile healthcare systems in marginalized communities or countries; lack of health and/or pharmacoeconomic evaluations; sustainability questions associated with all chemo-prophylaxis interventions; belief systems, socioeconomic status and general community acceptance; lack of evidence of wider safety and effectiveness of medicines involved in different communities and fears of exerting unnecessary selection pressure, thus promoting drug resistance [63–65]. Despite the noted negative concerns, MDA remain popular in the prevention and/or management of schistosomiasis and soil transmitted helminthiasis. As highlighted above WHO suggests ways by which wider coverage can be attained like utilization of all available medicine distribution channels. Also because in almost all affected and/or poor countries developmental partners and international pharmaceutical companies finance the MDAs, as such the programs remain cost-effective at least from a governmental perspective of pharmacoeconomic evaluations. Issues to do with community acceptance may be addressed by adequate promotional and/or educational programs to clearly explain the aims and objectives of each MDA intervention. Critical evaluation of each MDA intervention on issues to do with safety, drug effectiveness, cost-effectiveness/benefit, sustainability and political will positively feed into the subsequent interventions.
4.1. Helminthiasis management
For schistosomiasis, WHO recommends praziquantel with doses of 40–60 mg/kg body weight in one and/or 2–3 divided dose(s). Praziquantel is effective against all five important species of schistosomes, that is,
The mechanism of action of praziquantel is thought to involve the increased permeability to Ca2+ ions leading to uncontrollable contractions, paralysis and death of the worm. It is also suggested that it leads to vacuolation and blebbing of worm tegumental and subtegumental structures in adults but not juveniles worms [67, 68]. This leads to the exposure of surface antigens to host immune system thus Facilitating immune recognition and clearance of the worm . The drug effect may be explained due to relative differences in sensitivities observed in some settings between adult and juvenile worms . Praziquantel is well absorbed orally (80%), is subjected to first pass effect, metabolized by the liver and excreted via the kidneys . Microsomal enzymes inducers like rifampicin interfere negatively with praziquantel efficacy as they lead to lower than minimum effective concentration of praziquantel in the blood. On the other hand, CYP450 inhibitors like cimetidine, ketoconazole, grape juice, etc. may lead to higher than normal blood levels. It is contraindicated in patients with history of epilepsy and those hypersensitive to it. Operation of machinery or driving by individual after intake is not recommended. There is no evidence linking praziquantel to mutagenesis or harmful effects to fetuses. But as a general rule drugs are best avoided in the first trimester and used during the rest of pregnancy when benefits outweighs risks . The usual mild side effects of praziquantel which generally do not require treatment are malaise, headache, dizziness, abdominal discomfort with or without nausea and/or vomiting, fever and urticarial. Some of these side effects may be altogether the effects of schistosomiasis. These and other side effects may be worse in patients with high worm burden. Resistance to praziquantel by schistosomes has not been reported as yet, as there are no substantiated clinical findings. Reports of resistance are usually misrepresentations of issues like noncompliance or very transient biological phenomena or effects [67, 68].
4.1.1. Management of soil-transmitted helminthiasis
In the management of STH, the WHO recommends any of the following drugs: albendazole (dose of 400 mg); mebendazole (dose of 500 mg); levamisole (dose of 2.5 mgkg−1) and pyrantel (dose of 10 mgkg−1). These drugs are effective against many helminthic infections, for example ascariasis, hookworms, lymphatic filariasis, trichuriasis, strongyloidiasis, zoonotic ancylostomiasis, enterobiasis, among others. Benzimidazoles (i.e., albendazole and mebendazole) are the mostly commonly used [58, 65] in the management of STHs owing to their efficacy, wider spectrum, safety and availability. Benzimidazoles are thought work through inhibiting tubulin polymerisation. Absorption of albendazole is usually very low and the absorbed is subjected to significant first pass effect by the liver. Mebendazole is absorbed almost fourfold better than albendazole, but the rest are similar. May cause bone marrow suppression if taken for a considerable long period as in hydatid disease management were the patient takes three 28 day cycles with 14 day breaks of albendazole. Benzimidazoles are best avoided in pregnancy especially during the first trimester unless good clinical advice benefits outweigh risks . Without having the pharmacokinetic properties changed, praziquantel increases plasma concentration and area under the curve of albendazole sulfoxide (the most active metabolite) by about 50% in healthy subjects. This might be beneficial in coadministration as in MDAs, but also may lead to more side/adverse effects. Side/adverse effects of albendazole depending on the duration of therapy may include, abdominal pain, nausea and vomiting, fever, elevated hepatic enzymes, dizziness, headache, meningeal signs, raised intracranial pressure and vertigo hypersensitivity
Benzimidazoles are active against
4.1.2. Safety of combining praziquantel and benzimidazoles
High safety profile has been observed, in a safety study of praziquantel – albendazole combined treatment of hydatidosis, which require a way more prolonged duration than schistosomiasis and/or STHs . The mild side effects noted were not so different from when monotherapies were used and were transient, disappearing when treatment was withdrawn . There may be need for more evaluations of the severity of side and/or adverse-effects versus worm burden, when worms are localized in the central nervous system and/or in eyes.
4.2. New chemotherapeutic avenues
Mathematical models suggest significant drug resistance by the helminths to current therapies in the new future , the need for new, safer and more effective drugs is apparent. It has been demonstrated that the use of praziquantel and other drugs may enhance the antischistosomal activity. An example of such drugs is lovastatin  (a hypolipidemic agent). Benzodiazepines such as clonazepam are known to have the ability to paralyze adult schistosomes (both males and females) and interfere with egg release . Other promising molecules with antischistosomal activities are the artemisinins and related 1,2,4-trioxolanes . Praziquantel and artemisinin derivatives combined offers better protection  and/or cure rates. Though not 100% effective, MDAs based on WHO guidelines are very important in the fight against many parasitic neglected tropical diseases like schistosomiasis and soil transmitted helminthiasis. MDAs has actually more benefits due to the wider spectrum of both praziquantel and albendazole/mebendazole, as the administration will cover other parasitic infections within targeted communities. Effectiveness is significantly improved if chemoprophylaxis is done together with education and promotion of hygiene and the use of safe water. While praziquantel and albendazole/mebendazole are very effective there is still need to develop new better pharmaceuticals and pursue other avenues like vaccines.
4.3. Schistosomiasis control and elimination: research priorities and capacity building needs
The WHO/TDR Special Program for Research and Training in Tropical Diseases convened diseases reference groups to examine and set research priorities for the neglected tropical diseases. The following research priorities were made: (i) to optimize existing intervention tools so as to maximize impact and sustainability, (ii) to develop novel control tools that will improve impact and sustainability, (iii) to improve diagnostic tests with good sensitivity, specificity, multiplex capacity, and ability to measure infection intensity, and detect drug resistance; especially useful at the current preventive treatment control initiative in which reinfection would be very low. There is also need (iv) to standardize and validate methodologies and cost effective protocols for diagnosis in monitoring and evaluation settings, (v) to develop delivery strategies of multiple interventions to maximize sustainability of control program and integrated neglected tropical diseases control. Recommendation also included the need to develop strategies to increase awareness of ill-health processes, community participation, ownership and empowerment, as well as equity in access to preventive chemotherapeutic control interventions. The application of epidemiological models is required to help monitoring of intervention efficacy including drug resistance tracing. Further to develop new tools for parasite functional genomics in key species, this is believed to assist in vaccine development. A comprehensive research agenda need to be developed from basic sciences to emphasize implementation research and to ensure that control program could be implemented and evaluated based on rigorous scientific evidence. New tools, policies and strategies would lead to strengthened control programs that aim at disease elimination or eradication, where feasible.
4.4. Progress of schistosomiasis preventive chemotherapy in the African region: challenges and research needs
The African region has the highest burden of schistosomiasis, with 4 intermediate host species, endemic in 43 countries. According to WHO statistics at least 220 million people may have schistosomiasis infections. Ten sub-Saharan countries account for more than 70% of the global number of people requiring preventive chemotherapy for schistosomiasis. Prevalence of infection and morbidity are high in school-age children, but high prevalence has also been documented in children less than 5 years of age [71, 72]. The African region has adopted and recommends a comprehensive control strategy for schistosomiasis that includes preventive chemotherapy, health education, access clean water, sanitation and environmental control. These strategies, if implemented vigorously, would lead to the reduction of morbidity and possibly interruption of transmission. However treatment coverage is low in the region and many countries are not yet mapped. Scaling up to reach at least 75% of children is still a challenge because of access to praziquantel. Treatment of pre-school children is also limited by the lack of a pediatric formulation .
Research priorities for schistosomiasis control and elimination in endemic region include, better understanding of the epidemiology and surveillance of infections, implementation research, environmental and social ecology, better use of data and modeling and the basic biology of transmission and snail dynamics . These priorities can only be met through widespread capacity strengthening and collaborative partnerships, transparent interactions between researchers and disease control program managers, learning from areas that have successfully controlled and have experience in research and control of schistosomiasis, for example, China, including intersectorial collaboration and technology transfer and political commitment and funding for disease control and research in each affected country. Conduct of the required research should also be done so as to increase capacity for advanced research as well as to improve disease control. Capacity strengthening should provide personnel able to address gaps from the laboratory to the field, and with skills to properly evaluate interventions, model likely progression and scenarios and quantify impacts of the control program. For schistosomiasis control and elimination, it will be important to rebuild capacity for malacology, which was not stressed when preventive chemotherapy was the main operational component. Other aspects to be strengthened are drug efficacy monitoring, and pharmacovigilance.
4.5. Monitoring and evaluation towards the elimination of schistosomiasis
Monitoring and evaluation (M&E) is a process that helps to improve performance and achieve planned targets. The goal should be to improve current and future management of outputs, outcomes and impact. The results of M&E should help control programs, governments and development partners assess the performance and progress towards schistosomiasis control and elimination. These processes should also document past and current interventions, as well as for planning future activities. Monitoring should be incorporated and implemented from the planning stage of a program as a periodic and recurring task. Documenting results, processes and experiences should steer decision-making and learning processes. Monitoring checks progress against plans. The data acquired through monitoring is used for evaluation.
Evaluations should help to draw conclusions about efficiency, effectiveness, impact, relevance and sustainability of the interventions. The process consolidates information and allows program managers to learn from each other’s experiences, building on expertise and knowledge; generates reports that contribute to transparency and accountability of donated resources. Evaluation may reveal errors and offers alternative ways for improvements. Evaluation documentation provides means by which agencies consolidate and learn from their experiences making policy to guide control and monitoring activities. Evaluations also provide ways to assess the success of the program and the relationship between implementers, decision makers and beneficiaries. Evaluation results provide evidence for raising funds, influencing policy and tracking the success of the program. The assessments of activities depend to a large extent on the manner in which monitoring and evaluation is recommended. Assessment of performance is necessary to select indicators that permit rating of the targeted outputs and outcomes before the implementation of the project.
There should be indicators for other interventions such as health education, water supply and sanitation. Evaluation should inform whether planned tasks are completed or on-going. Quality control and effectiveness of all interventions should be assured.
5. Concluding remarks: mass drug administration for the control of helminthiasis
Tropical and subtropical areas have conducive environment for the flourishing of helminthiasis; these include appropriate temperature, wet and humid soils, abundant fresh flowing river waters and the human factor that continuously contaminates their environment and maintains the life cycle of the parasites. Vaccines are still a long way to be developed since we lack complete understanding of the host-parasite relationship. Host-parasite effects have been observed those leading into severe pathology, in some instances, during the parasite colonization. The effects of helminthiasis are so diverse affecting the health of the host resulting in poor cognitive in school children, affecting reproductive health in childbearing age and reduced work output in economically engaged workforce. The current control strategy is by removing the infection using preventive chemotherapy, ultimately anticipating cutting the life cycle of helminthiasis after several rounds of treatment using mass drug administration. While controlling the life cycle by treatment, much effort should be invested in health education to reduce contamination of the environment. The overall control strategies required should include health education, water and sanitation development, selective chemotherapy, snail control and passive treatment of cases. The options for consideration of water and sanitation development remain a major challenge since this is grossly neglected in most developing areas that are resource limited. While additional environmental and engineering measures for irrigation schemes particularly the small scale irrigation currently being developed require incorporation of the helminthiasis control strategy right from the onset of program development. Use of indigenous and locally available resources in vector control should be included in health education and basic health delivery services (e.g., plant molluscicide —
Finally, recommendations are made for comprehensive, integrated and through multi-disciplinary intervention strategies that include preventive chemotherapy, environmental management, water conservancy, water supply and sanitation development in affected areas and snail control using locally available resources. Such strategies should be evidence-based from research component incorporated in the control activities and use of the most up to date technologies and tools in control. Collaboration would be a platform for capacity strengthening, technology transfer and expertise for the elimination of schistosomiasis from Africa. Above all there is need to obtain government political will for support and sustainability of the programs.
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