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      Ten failings in global neglected tropical diseases control

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      PLoS Neglected Tropical Diseases
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          Abstract

          Over the course of the last decade, the global community has made tremendous progress towards neglected tropical disease (NTD) control or even elimination, especially for some of the 20 conditions now recognized by the World Health Organization (WHO) [1]. However, there remain important and substantive gaps in our achievements. Some of these gaps are glaring and obvious, and the fact that they continue to be ignored by global leaders and policymakers approaches a moral failing or outrage. Listed here are 10 of what I consider to be our greatest missed opportunities, including some that I previously highlighted as priorities for the new WHO Director-General, Dr. Tedros [2]. The first group of failings is linked to the geopolitics of the NTDs and is listed below. 1 NTDs of regional importance. There are several NTDs that have enormous regional importance in the areas where they occur. But because these diseases are not widely or globally distributed, they do not rise to the top in terms of disease burden estimates and are largely ignored by the global community. Examples include Buruli ulcer in West Africa, loiasis in Central Africa, and podoconiosis (nonfilarial elephantiasis) in East Africa. New World regional diseases include paracoccidioidomycosis, mucocutaneous leishmaniasis, and Oroya fever (Carrion’s disease). However, the example of dracunculiasis and efforts towards its eradication show that these diseases do not necessarily have to be ignored. 2 Political destabilization in the “Old World”: Leishmaniasis and cholera arising from the killing fields. Next to poverty, conflict may be the biggest social determinant of NTDs. Both cutaneous and visceral leishmaniasis outbreaks are now arising from horrific battles and collapsed health system infrastructures in Syria, Iraq, Afghanistan, Sudan, and South Sudan [2–4], while cholera is causing a dramatic and lethal epidemic in Yemen. Cutaneous leishmaniasis has now reached hyperendemic proportions in current and former ISIS occupation zones, and through forced human emigrations, this NTD may spill over into Lebanon, Turkey, Jordan, and elsewhere [3]. Visceral leishmaniasis is killing an unknown number of people in war-torn Sudan and South Sudan [4]. During the 1980s and 1990s, visceral leishmaniasis killed tens of thousands of people from the conflicts happening in some of the same locations in East Africa. It’s happening again. 3 Political destabilization in the “New World”: Venezuela. As Venezuela’s health system slowly collapses, we have seen the resurgence or reemergence of malaria and NTDs such as dengue and other arthropod-borne virus (arbovirus) infections, Chagas disease, and schistosomiasis, just to name a few [5]. Even though Venezuela’s reemerging NTDs now threaten to spread to neighboring Latin American countries or even reverse global goals in the region, the leaders of the Organization of American States (OAS) have so far not seriously worked to tackle this emerging health crisis. 4 Climate change and its impact on vector-borne and zoonotic NTDs. We’ve seen the rapid introduction or reemergence and then spread of dengue, chikungunya, yellow fever, and Zika virus infection in the Western Hemisphere—together with the appearance of mosquito-transmitted and snail-borne diseases in parts of Europe, including arbovirus infections and schistosomiasis—and also an uptick of diseases in Central Asia and the Middle East [2, 6]. Former Vice President Al Gore and others have pointed out that climate change can work in concert with poverty, war, and population movements to produce its detrimental effects, and in this case, the combination appears to promote the increase and spread of NTDs [2, 6]. There is a lot of global interest in climate change, but we could do more to redirect some of this energy towards interventions in the areas of greatest vulnerability. 5 Blue marble health: NTDs in “wealthy” nations. “Blue marble health” refers to new and somewhat paradoxical findings that the poor living in wealthy group of 20 (G20) nations—and also Nigeria (richer than the bottom three or four G20 nations)—account for a majority of the world’s disease burden for the poverty-related neglected diseases and NTDs [2, 7, 8]. These numbers include millions of Americans living in the United States with an NTD and a significant but mostly hidden level of poverty and disease in Europe and Australia [7, 8]. Thus far, it’s not been possible to get this concept on the agendas of G20 summits. But we urgently need a commitment from the G20 leaders to provide treatments for their own vulnerable populations and to commit to research and development (R&D) investments [9]. The bottom line is that the G20 leaders are missing a chance to simultaneously eliminate disease and improve their own economies. The second group is more linked to closing coverage gaps and providing universal access and is listed below. 6 Female genital schistosomiasis. By now almost everyone connected to global health NTDs should know that female genital schistosomiasis (FGS) is one of the most common gynecologic conditions of women who live in poverty in Africa [10]. They should know that FGS has emerged as one of Africa’s most important cofactors in its AIDS epidemic. However, the leaders of the global HIV/AIDS communities continue to ignore these findings and act as if they simply want this problem to go away and not trouble them any further. 7 Patient access to Chagas disease essential medicines. Chagas disease affects millions of impoverished people in the Americas. Today, most of the cases of Chagas disease occur in Latin America’s three large economies—Argentina, Brazil, and Mexico—and yet more than 90 percent of people with Trypanosoma cruzi infection do not have access to treatment [2, 11]. They include tens of thousands of T. cruzi–infected pregnant women that may pass their infection vertically to their unborn fetus. Chagas disease ranks among the most glaring health disparities in the Americas. The disease is also globalizing to Southern Europe and elsewhere. So far, well-intentioned efforts to raise the awareness of this disease have made little impact [12]. When it comes to Chagas disease, the OAS and the Inter-American Development Bank are both conspicuous by their absence. 8 Closing the gap on mass drug administration (preventive chemotherapy)—And then there’s yaws and scabies. We’re making good but not great progress on providing NTD essential medicines used for mass treatment of the three soil-transmitted helminth infections, lymphatic filariasis, and onchocerciasis. WHO now finds that we’re covering less than two-thirds of the global population requiring treatment for these diseases, but we may not be doing as well for trachoma and schistosomiasis [2, 13]. Also, the major mass drug administration and preventive chemotherapy partners and donors are still mostly silent about extending these programs to also eliminate yaws (azithromycin) and scabies (ivermectin) [2, 14]. These two cutaneous neglected diseases are not exactly “low-hanging fruit,” but we can certainly accelerate progress towards their elimination. 9 R&D “one shot on goal.” I’m not quite sure how this happened. For diseases such as HIV/AIDS, tuberculosis (TB), and malaria, it’s understood that we will need multiple new approaches to control and eliminate these diseases. It’s also accepted that for AIDS, TB, and malaria, we will need to pursue (and fund) several avenues of R&D simultaneously, including new drugs, diagnostics, vaccines, and—for malaria—vector control approaches [15]. But for the NTDs, it seems we only get one shot on goal. If a mass drug administration approach is being funded, we can’t fund a vaccine, or vice versa [15]. There is a terrible and unacceptable double standard for our diseases. History teaches us that we will not eliminate an NTD through only one-dimensional strategies. 10 Leprosy elimination. The community of leprosy scientists and public health experts has incredible passion and commitment. The good news is that in 2016 WHO launched a new leprosy strategy, which hopefully will redouble global efforts for control and elimination. Certainly, these 10 items are not the only NTD challenges for our global leaders and political institutions. At PLOS Neglected Tropical Diseases, we look forward to hearing from you regarding things I might have missed or ignored.

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          Chagas Disease: “The New HIV/AIDS of the Americas”

          Endemic Chagas disease has emerged as an important health disparity in the Americas. As a result, we face a situation in both Latin America and the US that bears a resemblance to the early years of the HIV/AIDS pandemic. Neglected tropical diseases (NTDs) are among the most common conditions afflicting the estimated 99 million people who live on less than US$2 per day in the Latin American and Caribbean (LAC) region [1]. Almost all of the “bottom 100 million” living in the Americas suffer from at least one NTD [1], and according to some estimates, the NTDs cause a burden of disease in the LAC region that closely approximates or even exceeds that resulting from HIV/AIDS [2]. Chagas disease (American trypanosomiasis) is a vector-borne disease and a leading cause of the deaths and disability-adjusted life years (DALYs) lost that result from NTDs in the LAC region [2]. With approximately 10 million people living with Chagas disease, this condition is one of the most common NTDs affecting the bottom 100 million in the region, a prevalence exceeded only by hookworm and other soil-transmitted helminth infections [1], [2]. Moreover, among the NTDs in the Americas, Chagas disease ranks near the top in terms of annual deaths and DALYs lost [1], [2]. While most of the world's cases of Chagas disease occur in the LAC region, there is increasing recognition that many people with Trypanosoma cruzi infection also live in the US and Europe [3]. In practical terms, the “globalization” of Chagas translates to up to 1 million cases in the US alone, with an especially high burden of disease in Texas and along the Gulf coast [4], [5], although other estimates suggest that there are approximately 300,000 cases in the US [6], in addition to thousands of cases documented in Canada, Europe, Australia, and Japan [3]. Among those living with Chagas disease around the world today, 20%–30% (roughly 2–3 million people) are either currently suffering from Chagasic cardiomyopathy or will develop this clinical sequela [7]. Chagasic cardiomyopathy is a highly debilitating condition characterized by cardiac arrhythmias, heart failure, and risk of sudden death from ventricular fibrillation or tachycardia or thromboembolic events [7]. Another estimate suggests that up to 5.4 million people living today will develop Chagasic cardiomyopathy [8], [9]. Damage to the gastrointestinal tract can also produce debilitating megaesophagus and megacolon [7]. There are a number of striking similarities between people living with Chagas disease and people living with HIV/AIDS, particularly for those with HIV/AIDS who contracted the disease in the first two decades of the HIV/AIDS epidemic. Both diseases are health disparities, disproportionately affecting people living in poverty [1], [2]. Both are chronic conditions requiring prolonged treatment courses: a lifetime of antiretroviral therapy for HIV/AIDS patients, and one to three months of therapy for those with Chagas disease [7]. Treatment for HIV/AIDS is lifesaving, although it seldom if ever results in cure, while for Chagas disease, the treatment has proven efficacy only for the acute stages of the infection or in children up to 12 years of age during the early chronic phase of the infection [10]. For both diseases the treatment is expensive—in the case of Chagas disease, the expected cost of treatment per patient year is $1,028, with lifetime costs averaging $11,619 per patient [11]. Exacerbating costs, Chagas disease itself is a serious opportunistic infection of people living with HIV/AIDS, and is associated with meningoencephalitis, cerebral lesions, and high mortality [7]. As with patients in the first two decades of the HIV/AIDS epidemic, most patients with Chagas disease do not have access to health care facilities. A recent analysis indicates that many patients do not have access to the essential medicines for Chagas disease, in particular, the first line of therapy, the drug benznidazole [12]. According to Médecins Sans Frontières (MSF, Doctors Without Borders), many highly endemic countries, including Paraguay and Bolivia, face acute shortages of benznidazole, forcing thousands of newly diagnosed patients to postpone treatment [12]. Both diseases are also highly stigmatizing, a feature that for Chagas disease further complicates access to benznidazole and other essential medicines, as well as access to serodiagnosis and medical counseling. For some individuals with T. cruzi living in the US, immigration status presents an additional challenge to seeking care and prevention services. Just as stigma due to sexual orientation has been a barrier to HIV care and prevention, especially in the beginning of the epidemic, immigration status may function as a deterrent to Chagas disease care and prevention. Based on the assertions outlined above—the chronic morbidities and high mortalities, the prolonged and expensive treatment courses, the lack of therapeutic options, and barriers to access to essential medicines—a patient living with Chagas disease faces formidable challenges that resemble those faced by someone living with HIV/AIDS, especially the challenges that occurred in the early years of the HIV/AIDS epidemic. Shown in Table 1 is a quantitative comparison between people living with Chagas disease [2], [4], [6], [13], [14] and those living with HIV/AIDS in the LAC region and the Americas [13]–[17]. Briefly, the roughly 10 million people living with Chagas disease (including 2–5 million individuals with Chagasic cardiomyopathy) is comparable in number to the 1.6 million people living with HIV/AIDS in the LAC region and the 1–2 million living with HIV/AIDS in North America (including Mexico). However, based on current estimates, both the number of annual DALYs lost and the attributed deaths are about five times higher for HIV/AIDS. The morbidity and mortality estimates for both Chagas disease and HIV/AIDS are undergoing revision by the University of Washington Institute of Health Metrics and Evaluation. 10.1371/journal.pntd.0001498.t001 Table 1 Comparison of Chagas disease versus HIV/AIDS. Disease Estimated Number of Cases in LAC [Reference] Estimated Number of Cases in North America [Reference] Estimated DALYs in the Americas [Reference] Estimated Annual Deaths in the Americas [Reference] Countries Most Affected [Reference] Chagas disease 8–9 million (2–5 million cases of Chagasic cardiomyopathy) [2] 0.3–1.0 million in the US [4], [6] 0.7 million [13] 14,000 [14] Bolivia, Mexico, Colombia, Central America [2] HIV/AIDS 1.6 million [15], [16] 2.3 milliona [17] 3.2 million [13] 105,000a [15]–[17] Brazil, Mexico, Colombia, United States [15]–[17] a The UNAIDS data for North America also includes Western and Central Europe. According to the US Centers for Disease Control and Prevention, at the end of 2008 an estimated 1.2 million people were living with HIV in the US [40]. There are additional parallels. Chagas disease has emerged as an important blood transfusion–related risk throughout the Americas just as HIV/AIDS did in the early 1980s, prior to the implementation of widespread blood screening and testing [18]–[20]. Moreover, mother-to-child transmission leading to congenital Chagas disease and other adverse neonatal outcomes is increasingly recognized [21]–[24] (Table 2). Both congenital Chagas disease and HIV/AIDS have a recognized clinical syndrome [21], [25], with adverse birth outcomes as well as deleterious maternal effects in pregnancy [22], [23], [26]. During pregnancy, the rate of vertical transmission of T. cruzi infection is approximately 5% (although some investigators believe the rate could be as high as 10%), whereas it is 15%–40% for untreated HIV/AIDS [27] and 1%–2% for mothers who receive antiretroviral therapy [28]. The Pan American Health Organization estimates that there are over 14,000 cases of congenital Chagas disease in Latin America [29], with 2,000 newborns infected annually in North America alone [24], compared to 36,000 pediatric HIV/AIDS cases in Latin America [15]. 10.1371/journal.pntd.0001498.t002 Table 2 Comparison of congenital Chagas disease and HIV/AIDS. Category Congenital Chagas Disease [Reference] Congenital HIV/AIDS [Reference] Major clinical features Hepatosplenomegaly, hydrops, neonatal death [21]. Failure to thrive, opportunistic infections, lymphocytic interstitial pneumonitis, developmental delays [25]. Effects in pregnancy Pregnancy enhances parasitemia [22]. Increased risk of miscarriage, preterm birth, neonatal infection [23]. Increased spontaneous abortion, chorioamnionitis, low birth weight, prematurity [26]. Vertical transmission Vertical transmission of 5% from seropositive mothers [23], although some investigators believe the transmission rate may be higher. Vertical transmission of 15%–40% without maternal treatment [27]. Vertical transmission of 1%–2% on antiretroviral treatment [28]. Number of cases 14,000 cases in Latin America [29]. 40,000 pregnant women in North America, 2,000 newborns are infected annually [24]. 36,000 pediatric HIV/AIDS cases in Central and South America [15]. It is only appropriate to point out that there are important differences between Chagas disease and HIV/AIDS. Whereas HIV/AIDS is almost always a fatal condition in the absence of antiviral therapy, up to 70%–80% of people with Chagas disease do not progress to cardiomyopathy. Moreover, Chagas disease is a true NTD and there is a paucity of anti-protozoan drugs available for this condition, whereas HIV/AIDS can no longer be considered neglected in this sense as there is an armamentarium of antiretroviral drugs currently available (although for both conditions, patients in developing countries suffer from lack of access to essential medicines). As another contrast between the two diseases, there is also evidence for oral transmission of Chagas through food contamination in the Amazon basin [30]. Over the last three decades of the global HIV/AIDS pandemic, an aggressive and committed activist community has achieved success in promoting widespread access to antiretroviral drugs in developed and developing countries. As a result, at present millions of people living with HIV/AIDS receive antiretroviral therapy, and pediatric HIV/AIDS has been nearly eliminated as a public health problem in the US [31]. Patient advocacy and global efforts to promote access to benznidazole and other therapies for Chagas disease, on the other hand, are at a much earlier stage. In the last decade, MSF has launched efforts to screen more than 80,000 people in Bolivia, Colombia, Guatemala, Honduras, Nicaragua, and Paraguay, having diagnosed and treated more than 6,000 and 4,000 individuals, respectively [12]. Other non-governmental organizations have also been engaged in Chagas disease treatments. Of great concern is a looming shortage of benznidazole, as well as the over-reliance on a single drug manufacturer, and inadequate international efforts to organize global production and distribution of the drug in Latin America [12]. Nifurtimox, another drug commonly used in the treatment of Chagas disease, should also be made available for the LAC region. In parallel with global advocacy efforts, expansion of operational research activities is crucial to optimize the efficacy of existing control and elimination efforts, including the testing of more field-adapted tools [12]. There are also requirements to expand vector control activities and health education in the communities affected by Chagas disease, in addition to providing training for local health care providers in endemic areas [12]. The importance of a research and development agenda to develop new and improved Chagas disease drugs cannot be overlooked. As noted above, both antitrypanosomal drugs used for the treatment of Chagas disease, benznidazole and nifurtimox, require prolonged and expensive treatment courses; moreover, the efficacy of either drug for the treatment of late chronic infection and Chagasic cardiomyopathy still remains uncertain and unproven [32], [33]. Toxicities and the frequency of side effects of both medicines frequently require patients to interrupt or halt treatments, and both drugs are contraindicated in pregnancy [34]–[36]. In response to this crisis, the product development partnership (PDP) Drugs for Neglected Diseases initiative (DNDi) is accelerating the development of new Chagas disease drugs in the non-profit sector, in parallel with a small group of academic laboratories that are pursuing several drug targets [37], [38]. Finally, just as the International AIDS Vaccine Initiative (IAVI) PDP is developing several experimental HIV/AIDS vaccines, the Sabin Vaccine Institute PDP is accelerating the development of a new therapeutic Chagas disease vaccine in collaboration with several key universities and public sector biotechnology and manufacturing institutions in Mexico [1]. In further support of this research, a recent analysis by Lee and his colleagues confirms the potential cost effectiveness of Chagas disease vaccines [39]. Stark similarities exist between today's global Chagas disease epidemic and the first two decades of the HIV/AIDS epidemic. This translates into a humanitarian catastrophe for the poorest people in the Americas and elsewhere. This perceptible health disparity demands urgent attention by global health policy makers to prioritize Chagas disease and develop a comprehensive strategy for control and elimination efforts, blood screening and point-of-care testing, maternal and child interventions, health education, and parallel research and development. Successfully addressing the vast burden of Chagas disease will require overcoming the current lack of available drugs, together with expanding vector control strategies and developing new and innovative control tools. To this end, eliminating Chagas disease will require a commitment from international health agencies, governments of the disease-endemic countries, PDPs, and patient advocacy groups.
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            Old World Cutaneous Leishmaniasis and Refugee Crises in the Middle East and North Africa

            The Syrian refugee crisis has precipitated a catastrophic outbreak of Old World cutaneous leishmaniasis now affecting hundreds of thousands of people living in refugee camps or trapped in conflict zones. A similar situation may also be unfolding in eastern Libya and Yemen. Leishmaniasis has been endemic in Syria for over two centuries, with the first case ever reported being as early as 1745, when it was known as the “Aleppo boil” [1,2]. Old World cutaneous leishmaniasis (CL) is characterized most notably by disfiguring skin lesions, nodules, or papules, and in the Middle East and North Africa (MENA) region it is primarily caused either by Leishmania tropica (anthroponotic) or L. major (zoonotic), with some sporadic cases also caused by L. infantum (Box 1) [3–5]. In North Africa, a chronic form of CL also can be caused by L. killicki [6–7]. Box 1. Old World Cutaneous Leishmaniasis (CL) in the MENA Region Anthroponotic CL Major etiologic agent: Leishmania tropica [4,5,7] Major vector: Phlebotomus sergenti [4,5] Zoonotic CL Major etiologic agent: L. major [4,5,7] Minor etiologic agent: L. infantum [4,5] Vectors: Ph. papatasi for L. major; Ph. perfiliewi, Ph. perniciosus, Ph. longicuspis, and Ph. ariasi for L. infantum [5] Major animal reservoirs: Rodents (L. major) and dogs (L. infantum) [4,7] Although Old World CL is generally not fatal, clinical symptoms can lead to disfiguring scars that result in social stigmatization and psychological consequences. The World Health Organization (WHO) has estimated that around 2.4 million disability-adjusted life years (DALYs) are lost due to CL and visceral leishmaniasis (VL) globally [8]; however, the number of DALYs attributed to CL is still under evaluation. The 2013 Global Burden of Disease Study determined that CL causes only 41,700 DALYs [9], while other studies have found that these figures may represent profound underestimates [10,11]. Studies observing the impact of marring CL facial scars have found that the social stigmatization involved leads to anxiety, depression, and decreased quality of life for patients [12]. The scars can lead to a changed perception of self and can limit individuals’ abilities to participate in society, further decreasing their social, psychological, and economic well-being, as employment opportunities become scarce. Women, adolescents, and children are particularly susceptible to the social stigmatization of disfiguring scars [13]. The hardships caused by CL extend beyond physical symptoms and manifest most prominently in patients’ social, psychological, and economic well-being. Like many neglected tropical diseases (NTDs), CL not only occurs in settings of poverty but the disease also has the ability to perpetuate and reinforce poverty, catalyzing a positive feedback loop between disease and poverty [14]. For many of these reasons, the WHO classifies leishmaniasis as one of 17 NTDs [15], although the cutaneous form is often not prioritized in major global health initiatives, unlike the NTDs now targeted by integrated preventive chemotherapy [11]. Pre-Conflict Old World CL in Syria Even before the current crisis, the Syrian government has struggled to contain endemic CL. After a 30-year hiatus during which CL was mostly restricted to Aleppo and Damascus [16], CL re-emerged in northwestern Syria in 1988 [1,17]. In 1991, the incidence of CL dropped temporarily due to insecticide spraying, but it began to rapidly rise again even as insecticide spraying continued [18]. The increased number of cases may have been accounted for in part by increased awareness and reporting of the disease; however, the most likely explanation for the dramatic increase and distribution of CL starting in the early 1990s stems from socioeconomic and environmental factors [1]. During this time, Syria experienced rapid and decentralized urbanization as city suburbs expanded and the population density increased [19]. People began to migrate from rural to urban areas, and municipal departments, overwhelmed by these changes, were no longer able to provide adequate hygiene and sanitation services such as trash collection and disposal, as well as insecticide spraying [1,19]. As populations migrated, individuals with no immunity became exposed to CL and the disease spread [1]. Such factors may account for a steep rise in the apparent number of CL cases in Syria beginning in 2008 as reported previously by Salam et al. in PLOS Neglected Tropical Diseases (Fig 1) [20]. 10.1371/journal.pntd.0004545.g001 Fig 1 Year-wise trend of CL cases reported in Middle East (from Salam et al 2014, PLOS Neglected Tropical Diseases) [20]. The numbers of CL cases in Syria began to increase even further following the onset of the Syrian Civil War in March, 2011, with new cases appearing in regions previously thought to be non-endemic. War, Refugees, and the Emergence of Catastrophic NTDs While CL is by no means new to Syria [7], the war in Syria has greatly increased the risk for CL and reports have indicated sharp increases in the number of CL cases in Syria and in surrounding areas of the Middle East [2]. Armed conflict enables outbreaks of serious NTDs [4,14,21,22] due to a combination of factors—most notably, collapsed health care infrastructures and population displacement. As populations migrate to endemic and non-endemic regions, they are exposed to infections for the first time or introduce diseases into new areas, respectively [4,20,23]. Additionally, the chaos and instability often lends to poor living conditions, which further exacerbate the risk for rapid transmission of infectious diseases [4,14]. In recent years, such factors were notable for producing catastrophic NTD outbreaks of cholera in the Democratic Republic of Congo and kala-azar in Sudan [24,25]. Additionally, human migration can be accompanied by deforestation or tumultuous urbanization, which often exacerbate disease outbreaks [26]. In West Africa, all of these factors combined to create a “perfect storm” for the 2014–2015 Ebola virus infection epidemic [27]. The ongoing Syrian conflict has escalated similar factors of instability and chaos that have been shown by past events, such as the Ebola epidemic in West Africa, to facilitate infectious disease outbreaks. As the conflict in Syria approaches its fifth year, over 50% of the public hospitals in Syria have been destroyed and the health care infrastructure is bordering on nonexistent [28]. Thus far, an estimated 6.5 million Syrians have been internally displaced [29,30] and an additional 4.4 million Syrians have been externally displaced [31]. Due to the violence, Syrians have been forced to flee from their homes and seek refuge across the Middle East, North Africa, and, more recently, Europe [31]; currently, 95% of the over 4 million refugees who have fled Syria reside in Turkey, Jordan, Lebanon, Iraq, and Egypt (Fig 2) [31]. The mass migration of people within Syria and the MENA region has put a strain on resources. Internally displaced individuals have reported that they are in need of non-food items (including personal hygiene products), health care services, food, shelter, water, and education [32]. Similarly, externally displaced individuals are often living in overcrowded and unhygienic spaces, commonly without access to many necessary resources, including basic sanitation and waste disposal services, food, electricity, as well as health care [33–36]; in Lebanon, refugee camps consist mostly of makeshift houses built out of scrap and rubble or tents [33]. Syria is now the leading producer of refugees in the world and has contributed significantly to what is considered to be the largest global refugee crisis since World War II [37,38]. 10.1371/journal.pntd.0004545.g002 Fig 2 The displacement of Syrian refugees (data from UNHCR, Syria Regional Refugee Response: Inter-agency Information Sharing Portal) [31]. Both inside and outside of Syria, conditions of poverty and malnutrition are prevalent and living situations are grim as adequate municipal services and necessary resources remain scarce [33]. The socioeconomic and environmental circumstances created by the conflict in Syria facilitate risk factors for the continued transmission of CL, and they not only potentiate increased incidence of CL but also exacerbate the morbidity and mortality of CL after transmission [14,33]. Ongoing violence in Syria has corresponded with infrastructural instability and chaotic population migration. It has created a setting in which we have seen the re-emergence of polio and measles, as well as tuberculosis, hepatitis A, and other infections in Syria and among displaced Syrian refugees [30,39]. However, the pathognomonic and obvious clinical features of Old World CL caused by both L. tropica and L. major possibly make it the most visible sign of disease emerging under the current circumstances. Old World CL and the Current Syrian Crisis With settings enabling transmission of Old World CL as a backdrop, the number of new cases has continued to rise. Within Syria, a 2013 study published by the Ministry of Health reported an incidence rate more than twice as high as the incidence rate reported in Syria between 2004 and 2008 by the WHO. The annual incidence of CL in Syria between 2004 and 2008 was estimated to be 23,000 cases per year [40]. In 2012, 53,000 cases were reported, and in the first half of 2013 alone, 41,000 cases were reported [41]. Additionally, the number of cases of CL has most likely been severely underreported [42]; the WHO estimated that the actual incidence of CL in Syria between 2004 and 2008 was three to five times higher than the reported incidence [40]. The true number of annual incident and prevalent cases in Syria may therefore exceed 100,000. Along its border with Syria, Turkey—which has taken more Syrian refugees than any country thus far [31]—has shown indications of increased prevalence of CL among already endemic existing populations in correlation with the influx of refugees from Syria [23]. Old World CL has emerged in Lebanon as well, although the outbreak to date has been largely contained to refugee populations [33,43,44]. A new report indicates that among the cases of CL observed in refugee communities in Lebanon, 85% of the cases are caused by L. tropica, with the remainder caused by L. major [33]. This may complicate treatment in the long term as L. tropica patients tend to be more refractory to the main CL drug, sodium stibogluconate (SSG) [45–47]. In the countries that have observed new cases of CL, younger age groups, due to their lack of previous exposure to the disease, have been the most affected [23,33]. Non-immune existing individuals also are at great risk of contracting CL as their immune systems are not equipped to fend off the parasite. Few countries have mandated reporting of CL [33], and the resultant weak reporting system promotes a lack of disease awareness and public policies for treatment and prevention. Compounding this problem is the absence of rapid diagnostics and the requirement to have highly skilled dermatologists and pathologists establish a diagnosis on the basis of clinical presentation and confirmatory microscopy, respectively. Even then, the sensitivity of microscopy is not particularly high (68% for L. major and 45% for L. tropica) [48]. The CL clinical presentation is also often accompanied by a wide spectrum of clinical manifestations that can mimic other inflammatory and neoplastic diseases, further complicating the diagnosis and reporting of CL [49,50]. If Old World CL is not addressed promptly, experience warns of a likely outbreak that may have unanticipated consequences if allowed to erupt. In the early 2000s, an outbreak of CL was observed after the Iraq War that spread beyond endemic populations and included foreign troops in the area [43,51]. The 1990s Afghani civil war experience also was notable for its outbreak of CL [52]. The war is estimated to have caused hundreds of thousands of CL cases in Afghanistan and among refugee populations in Pakistan [52,53]. Old World CL and Other Conflict Zones in MENA Knowledge of Old World CL in Syria and among its refugees is limited; however, we know even less about the situation in areas of Libya now controlled by the self-proclaimed Islamic State, or Daesh, and its allied extremist groups [54]. Both zoonotic and anthroponotic disease cycles have been identified in Libya; however, most of the published literature on CL in Libya focuses on the zoonotic form, which is caused by L. major. This form is responsible for the majority of CL cases in Libya, with Ph. papatasi as the main vector, and Psymommys obesus (fat sand rat) and Meriones libycus (Libyan jird) reported as disease reservoirs [55]. However, L. tropica anthroponotic CL has also been identified in Nalut and Bani Walid. Interestingly, both L. infantum and L. donovani have been identified in Nalut as causative for CL [55,56]. Outdoor activities like farming and construction work are highly correlated with disease emergence as a result of increasing exposure to sandfly bites [57,58]. Recently, the United Nations High Commissioner for Refugees (UNHCR) reported that 363,067 individuals have been displaced in Libya due to the ongoing unrest [59]. Re-emergence of CL from mass displacement could occur in areas that have had experience with CL, including Siret, Nalut, Garyan, Bani Walid, Kikla, and Ghudamis. Furthermore, about one million Libyan refugees have been displaced to Tunisia. Anecdotal reports from Tunisia, where refugee camps have been established [60], indicate that cases of leishmaniasis are on the rise, but there is minimal, if any, documentation. Leishmaniasis is a hidden NTD in Yemen as well. Approximately 10,000 new cases are reported annually [61]. These cases are caused by both L. tropica and L. infantum in high altitude regions, including Sa’da, Amr’an, Al Bayda, Ibb, Al Dhale’a, Dhamar, and Sana’a [62,63]. Furthermore, L. donovani, L. tropica, and L. infantum cause CL in regions that belong to the Tihama Coastal Plain, such as Al Hudaydah, Hajjah, and Ta’izz [62]. The Regional Leishmaniasis Control Centre (RLCC) reports that half of the clinically resembling CL cases are mucocutaneous leishmaniasis and that Yemeni CL patients suffer from both shortage of CL treatment and inadequate response to treatment [64]. Moreover, the access to health care has been reduced significantly due to conflict in Yemen and absence of aid. As CL in Yemen is thought to be caused exclusively by an anthroponotic cycle, the disease prevalence will likely increase as the rubbish accumulation and lack of sewage system foster the perfect breeding sites for Ph. sergenti vector. Although no refugee camps have been deployed as a result of the current Yemeni conflict, many people are migrating to neighboring countries such as Saudi Arabia, which may lead to the spreading of anthroponotic CL in the southern Saudi regions. The situations in Libya and Yemen will need further monitoring. Discussion and Preliminary Recommendations Areas of conflict provide for complex circumstances that make accurate data collection and humanitarian aid inaccessible and impractical. Additionally, there is ongoing dialogue about the efficacy of humanitarian aid in areas of conflict [65]. Especially with the loss of governmental control in many areas of Syria, Iraq, and parts of Libya to Daesh, policy recommendations are nearly impossible to implement in many regions of MENA [2]. Despite the difficulties of navigating current geopolitical circumstances in MENA, more can be done to address the CL situation in this region. Interventions to prevent and control the spread of CL must be multilateral in dimension and specific to local circumstances [66]. The following list of preliminary recommendations to prevent and control CL outbreaks highlights general policies that have already been proposed by organizations such as the WHO and the Centers for Disease Control [66–68], and emphasizes refugee camps and communities of displaced individuals living in regions of stability in MENA. The utmost priority of all interventions is to do no harm. Continued improvement of living conditions and hygiene infrastructure for refugees. Clean water, food, and sanitation services aid basic survival while also aiding the prevention and control of CL among endemic refugee populations. Implementation of mobile teams in refugee camps consisting of medical professionals experienced in diagnosing and treating CL. Responsibilities for mobile teams would include disease (and vector) detection, active surveillance, and providing health care treatment for patients with CL. Treatment includes sodium stibogluconate (Pentostam) and meglumine antimoniate (Glucantime), as well as alternatives therapies, such as cryotherapy, if there is a treatment shortage. Collection of health impact assessments prior to the establishment of refugee camps in neighboring areas of conflict zones. For example, the extermination of animal reservoirs before settling displaced individuals can help avoid emerging outbreaks among refugee communities [7]. Implementation of services to address psychological and economic impacts of CL. The most devastating consequences of contracting CL are often socioeconomic and psychological. Initiatives addressing community stigma surrounding skin lesions and papules associated with CL. Additional educational programs in refugee communities to raise awareness of CL also may be beneficial in preventing outbreaks. Distribution of insecticide treatment, particularly in areas known to be endemic with anthroponotic cycle, to help prevent contagion. A recent Cochrane analysis has concluded that insecticides may be effective at reducing the incidence of CL; however, whether insecticides are best applied through indoor spraying, treatment of clothing and bed sheets, or use of nets remains undetermined [69]. Research and development to improve diagnosis, treatment, and prevention methods, as well as ongoing operational research, monitoring, and evaluation to confirm the effectiveness of existing approaches. All research and development initiatives should give due considerations to ethical issues of working with refugee populations. The full extent of the Old World CL epidemic in Syria and in bordering countries, as well as in Libya and Yemen, remains mostly unknown. An adequate disease burden analysis depends on programs of active surveillance and disease detection, but these are few and far between due to the violence and instability. We may be witnessing an epidemic of historic and unprecedented proportions, but it has largely been hidden due to lack of specific information. The biggest limitation of this paper is the inability to access data due to the difficulties of gathering accurate and current information from regions of instability. Surveillance is even more challenging in the current refugee crises due to the unprecedented magnitude of population migration. The most effective policies in addressing the potentially devastating CL situation that is emerging from some conflict zones in MENA are initiatives that will promote disease control while simultaneously promoting the survival of refugees. Provisions of clean water, food, hygiene services, and adequate shelter will improve the living conditions of refugees while simultaneously addressing many of the socioeconomic and environmental risk factors that make refugees highly susceptible to infectious diseases. For example, makeshift houses allow sandflies to come in close proximity to human beings and the lack of municipal services creates conditions that facilitate poor health outcomes. Recommendations for research include the development of improved rapid diagnosis tests, possibly similar to the point-of-care diagnostic tests under development for VL [70]. Currently, diagnoses are performed by specialized dermatologists and can only be confirmed by a stained smear or culture from a skin lesion, which require laboratory settings. The lack of a rapid diagnosis test slows the process of diagnosis and leads to delayed treatment and greater risk for misdiagnosis of CL. Development of a commercially available vaccine for Old World CL should also be made a priority, as one does not currently exist even though it would enhance efficacy of disease and vector control programs [71,72]. A recent analysis confirms the cost-effectiveness for a vaccine that targets either New World CL [72] or Old World VL [73]. Additionally, research assessing how best to address the socioeconomic and psychological impacts of CL on patients as well as the cultural stigma of papules left by CL would facilitate a more well-rounded approach to confronting the consequences of CL outbreaks. These research projects should be specific to the dynamics of local communities and cultures. Micro-financing programs may alleviate some of the economic hardships often associated with CL; however, the feasibility of micro-financing programs in conflict-affected communities is still being debated [74]. A multifaceted, collaborative approach must be taken to control the incidence of CL [7,75], with priority given to initiatives that will not only aid in the prevention and control of CL but also improve the living conditions and survival of refugee populations. The World Health Assembly already adopted a resolution in 2007 to address the global burden of leishmaniasis [67], but immediate action must be taken to address the spreading burden of CL in the Middle East. By no fault of their own, refugees and displaced individuals are often fleeing from one unimaginable circumstance of horror and violence to another of poverty and disease. International communities have a responsibility to pay greater attention to this pressing issue, and it is imperative that proactive measures are taken to establish efficient and sustainable initiatives aimed at diagnosing, treating, and preventing CL as the conflicts in Syria, Iraq, Libya, and Yemen continue.
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              A review of visceral leishmaniasis during the conflict in South Sudan and the consequences for East African countries

              Background Visceral leishmaniasis (VL), caused predominantly by Leishmania donovani and transmitted by both Phlebotomus orientalis and Phlebotomus martini, is highly endemic in East Africa where approximately 30 thousands VL cases are reported annually. The largest numbers of cases are found in Sudan - where Phlebotomus orientalis proliferate in Acacia forests especially on Sudan’s eastern border with Ethiopia, followed by South Sudan, Ethiopia, Somalia, Kenya and Uganda. Long-standing civil war and unrest is a dominant determinant of VL in East African countries. Here we attempt to identify the correlation between VL epidemics and civil unrest. Objective and methodology In this review, literature published between 1955 and 2016 have been gathered from MSF, UNICEF, OCHA, UNHCR, PubMed and Google Scholar to analyse the correlation between conflict and human suffering from VL, which is especially apparent in South Sudan. Findings Waves of forced migration as a consequence of civil wars between 1983 and 2005 have resulted in massive and lethal epidemics in southern Sudan. Following a comprehensive peace agreement, but especially with increased allocation of resources for disease treatment and prevention in 2011, cases of VL declined reaching the lowest levels after South Sudan declared independence. However, in the latest epidemic that began in 2014 after the onset of a civil war in South Sudan, more than 1.5 million displaced refugees have migrated internally to states highly endemic for VL, while 800,000 have fled to neighboring countries. Conclusion We find a strong relationship between civil unrest and VL epidemics which tend to occur among immunologically naïve migrants entering VL-endemic areas and when Leishmania-infected individuals migrate to new areas and establish additional foci of disease. Further complicating factors in East Africa’s VL epidemics include severe lack of access to diagnosis and treatment, HIV/AIDS co-infection, food insecurity and malnutrition. Moreover, cases of post-kala-azar dermal leishmaniasis (PKDL) can serve as important reservoirs of anthroponotic Leishmania parasites.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Negl Trop Dis
                PLoS Negl Trop Dis
                plos
                plosntds
                PLoS Neglected Tropical Diseases
                Public Library of Science (San Francisco, CA USA )
                1935-2727
                1935-2735
                21 December 2017
                December 2017
                : 11
                : 12
                : e0005896
                Affiliations
                [1 ] Texas Children’s Center for Vaccine Development, National School of Tropical Medicine, Baylor College of Medicine, Houston, Texas, United States of America
                [2 ] James A Baker III Institute for Public Policy, Rice University, Houston, Texas, United States of America
                [3 ] Scowcroft Institute for International Affairs, The Bush School of Government and Public Service, College Station, Texas, United States of America
                New York Blood Center, UNITED STATES
                Author notes

                The author is principal investigator on several vaccines against neglected tropical diseases that are in development or in clinical trials.

                Author information
                http://orcid.org/0000-0001-8770-1042
                Article
                PNTD-D-17-01105
                10.1371/journal.pntd.0005896
                5739381
                29267282
                4de1115b-d7be-4959-8155-82be21a67ec2
                © 2017 Peter J. Hotez

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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                Funding
                The author received no specific funding for this work.
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