We searched PubMed and Scopus for articles published from 1960 to May, 2012. Studies were identified using search terms “malaria” and “Wuchereria” or “Brugia”. References from the retrieved articles were used to identify other relevant publications that were not identified from the database searches. Each article written in English was assessed for its methodological quality and the relevance of its results.
Personal ViewMalaria and lymphatic filariasis: the case for integrated vector management
Introduction
Several groups have advocated combining control efforts for malaria with those for neglected tropical diseases, lymphatic filariasis in particular.1, 2, 3, 4, 5 Malaria, caused by protozoa of the genus Plasmodium, and lymphatic filariasis, caused by the nematodes Wuchereria bancrofti, Brugia malayi, and Brugia timori, overlap in their distribution in most of Africa, south and southeast Asia, and some parts of Latin America.6, 7 Similarities exist between malaria and lymphatic filariasis in relation to their transmission: both diseases may be transmitted by the same or related vector species, both are potentially controlled by the same vector-control interventions, both have no or almost no hosts other than human beings, and both prevail under conditions of poverty and poor environmental sanitation.
Malaria and lymphatic filariasis cause the highest global burdens of all vector-borne diseases, particularly in Africa and southeast Asia (table 1).7, 8, 9, 10, 11 Malaria is transmitted by Anopheles species in all regions, whereas regional differences exist in the mosquito genera that transmit filarial parasites. In much of Africa and parts of the western Pacific (eg, Papua New Guinea), the anopheline vectors of malaria are also the principal vectors of lymphatic filariasis.12 Culex quinquefasciatus is an important vector in urban areas of east Africa, but in west Africa this species is considered refractory to infection with W bancrofti.13 Elsewhere, members of the Culex pipiens complex (predominantly C quinquefasciatus) and Aedes species are the principal vectors of lymphatic filariasis.7, 11
Integrated vector management is promoted by WHO as the best approach to improve the efficacy, cost-effectiveness, ecological soundness, and sustainability of vector control.14 To achieve integration, vector control should be based on local evidence, adopt a multidisease approach, and combine interventions wherever appropriate and feasible. In its implementation, integrated vector management depends on collaboration between health-sector programmes, other sectors, and communities.15, 16 Here we aim to substantiate a recent statement by WHO on integrated vector management to control malaria and lymphatic filariasis17 by summarising available evidence and suggesting the way forward.
Section snippets
Two global programmes and their challenges
The history of global programmes for the control of malaria and filariasis shows that the emphasis on vector control or drugs changes over time. Vector control, primarily through indoor residual spraying with DDT (dichlorodiphenyltrichloroethane) and dieldrin, was central in the first malaria eradication campaign (1955–69), but lost its significance as financial and technical constraints put eradication out of reach; eradication of malaria was never attempted in sub-Saharan Africa.18, 19, 20
Programme interactions
Vector control to prevent transmission of malaria parasites and mass drug administration to prevent transmission of microfilariae are two strategies that can affect several diseases. Vector control can reduce vector–human contact for more than one disease, particularly where malaria and lymphatic filariasis have the same principal vectors. Mass drug administration campaigns can facilitate the improvement of vector control if linked with the distribution of LLINs.1 In central Nigeria, this
Evidence of combined effects
Several studies have documented the outcome of integrated control of malaria and lymphatic filariasis (table 2).45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55 In some studies, the integration was deliberate; in others, vector control interventions intended for malaria control inadvertently affected lymphatic filariasis. In most reported instances, both diseases had the same anopheline vectors.
In the Solomon Islands, where both diseases had anopheline vectors, indoor residual spraying with DDT
Towards integration
Malaria and lymphatic filariasis have much in common in terms of their geographical distribution, transmission biology, and mutual interactions. Moreover, the global programmes to contain them have matching goals, strategies, and challenges.8, 25 Integration would be required at the level of communities, districts, ministries, and donors.16 The prospects for integration are contingent on the local context of disease epidemiology, vector ecology, and a country's operational capacity. Therefore,
Search strategy and selection criteria
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Cited by (56)
Morbidity hotspot surveillance: A novel approach to detect lymphatic filariasis transmission in non-endemic areas of the Tillabéry region of Niger
2023, Parasite Epidemiology and ControlGenome editing as control tool for filarial infections
2021, Biomedicine and PharmacotherapyCitation Excerpt :The strategies for mitigating vector transmissions include but not limited to indoor spraying with dichlorodiphenyltrichloroethane (DDT), use of long-lasting insecticide-treated nets, applying polystyrene beads to enclosed breeding sites of vectors and improving house designs (improved roofing, and trapdoors with screens). The success stories of effective eradication through the combination of chemotherapy with vector control programs have been extensively discussed elsewhere [36–38]. Despite the success, major vector control strategies are challenged with widespread insecticide resistance, the multiplicity of vector species, changes in vector behaviour, and high cost [39].
Towards global control of parasitic diseases in the Covid-19 era: One Health and the future of multisectoral global health governance
2021, Advances in ParasitologyCitation Excerpt :In other contexts, One Health considerations might lead to the implementation of programme synergies, for instance, within communities where polyparasitism is common, and where interventions could feasibly overlap. Prime examples would include the integration of malaria and lymphatic filariasis vector control initiatives (Kelly-Hope et al., 2013; van den Berg et al., 2013), and concurrent MDA and source control measures for onchocerciasis, soil-transmitted helminthiases and schistosomiasis (Mwinzi et al., 2012; Ndyomugyenyi and Kabatereine, 2003). Perhaps most importantly, the holistic outlook of a One Health approach to parasitic and neglected disease control has the potential to address development objectives beyond control or elimination of disease in humans, including food security (Wielinga and Schlundt, 2014), wildlife conservation (Lu et al., 2017), and tourism (Kasozi et al., 2021).
Clinical, serological and DNA testing in Bengo Province, Angola further reveals low filarial endemicity and opportunities for disease elimination
2020, Parasite Epidemiology and ControlCitation Excerpt :This will save time and resources and consider more appropriate surveillance strategies for low prevalence areas (Riches et al., 2020; Kelly-Hope et al., 2017b), especially in loiasis co-endemic areas where there is increasing evidence of low LF prevalence (Wanji et al., 2019; Kelly-Hope et al., 2018b). Engagement with the national malaria control programme to help increase the bed net coverage in the area will be critical as this can reduce W. bancrofti transmission (Rebollo et al., 2015; Berg et al., 2012; Bockarie et al., 2009), and is a WHO recommended alternative strategy in loiasis co-endemic areas (World Health Organization, 2011; World Health Organization, 2012b). Overall, the number of patients was low and health workers need to be trained to provide care to patients, including home-based self-care for lymphoedema, with subsequent referral if needed for surgical management of hydrocele, as it can improve patient economic and quality of life outcomes (World Health Organization, 2013; World Health Organization, 2019; Betts et al., 2020).
Integrated risk mapping and landscape characterisation of lymphatic filariasis and loiasis in South West Nigeria
2018, Parasite Epidemiology and ControlCitation Excerpt :It may also help to determine if xenomonitoring has a role in delineating risk and endgame surveillance in GPELF (Pedersen et al., 2009). Bed net ownership and usage were associated with lower LF prevalence, suggesting they are an effective vector control tool, as shown in other studies (Nsakashalo-Senkwe et al., 2017; Rebollo et al., 2015; van den Berg et al., 2013; Richards et al., 2013). However, the LF programme could optimise this impact further by increasing coverage among the male population, as they had a higher prevalence and were less likely than their female counterparts to own a bed net.
Excreta flow mapping along the sanitation service chain, a case of Kombolcha town, Ethiopia
2024, Scientific Reports