Visceral Leishmaniasis (VL) is an important protozoan opportunistic disease in HIV patients in endemic areas. East Africa is second to the Indian subcontinent in the global VL caseload and first in VL-HIV coinfection rate. Because of the alteration in the disease course, the diagnostic challenges, and the poor treatment responses, VL with HIV coinfection has become a very serious challenge in East Africa today. Field experience with the use of liposomal amphotericin B in combination with miltefosine, followed by secondary prophylaxis and antiretroviral drugs, looks promising. However, this needs to be confirmed through clinical trials. Better diagnostic and follow-up methods for relapse and prediction of relapse should also be looked for. Basic research to understand the immunological interaction of the two infections may ultimately help to improve the management of the coinfection.
Citation: Diro E, Lynen L, Ritmeijer K, Boelaert M, Hailu A, van Griensven J (2014) Visceral Leishmaniasis and HIV Coinfection in East Africa. PLoS Negl Trop Dis 8(6): e2869. doi:10.1371/journal.pntd.0002869
Editor: Jesus G. Valenzuela, National Institute of Allergy and Infectious Diseases, United States of America
Published: June 26, 2014
Copyright: © 2014 Diro et al. 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.
Funding: ED has received individual PhD scholarship from Belgian development cooperation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Visceral leishmaniasis (VL) is a vector-borne protozoan infection targeting the reticuloendothelial system . Its occurrence is widespread, being prevalent in approximately 70 countries worldwide. East Africa is one of the most affected regions, second only to the Indian subcontinent, with an estimated annual incidence rate of 29,400 to 56,700 cases . The countries most affected in this region are Sudan, South Sudan, and then Ethiopia. Although with much lower VL burden, endemic foci of the disease are also found in Eritrea, Somalia, Kenya, and Uganda . Figure 1 shows the VL-endemic regions in East Africa. The disease typically affects poor communities residing in remote places with poorly functioning health-care systems.
Map taken from “Malaria Consortium; Leishmaniasis control in eastern Africa: Past and present efforts and future needs. Situation and gap analysis, November 2010” .
Historically, East African VL has claimed the lives of many people, with the most infamous epidemic reported from South Sudan by Seaman et al. . Between 1984 and 1994, a devastating epidemic in the western Upper Nile region in South Sudan claimed the lives of an estimated 100,000 people . To date, treatment and care for VL in these resource-poor countries is mainly provided or supported by international organizations such as Médecins Sans Frontières (MSF), Drugs for Neglected Diseases initiative (DNDi), and the World Health Organization (WHO).
The simultaneous infection of humans by HIV and Leishmania almost always leads to a “deadly gridlock,” as they both have the same deleterious effect on the immune response . The majority of VL-HIV coinfections were previously reported from the Mediterranean countries during the pandemic years of HIV/AIDS in the 1990s, with the prevalence of HIV among VL patients reaching up to 60% in intravenous drug users in Spain , . As a consequence of HIV coinfection, atypical presentations of VL, a high rate of treatment failure, and frequent relapses were reported. Only after the introduction of antiretroviral therapy (ART) was a decline in incidence of VL-HIV coinfection observed . With the spread of HIV to other VL-endemic regions of the world, the coinfection is now reported from 35 countries , . Because of the alteration of the disease course, the diagnostic challenges, and the poor treatment response, VL with HIV coinfection has become a very serious challenge in East Africa today.
HIV Epidemiology in East Africa
The prevalence of HIV increased alarmingly from the mid-1980s to the 1990s in most African countries. Since 2000, however, a decline has been seen in the number of new HIV infections, which can be explained by a variety of factors, most notably preventive measures and access to ART , . In Ethiopia, HIV prevalence has declined from 5.6% in 2005 to 2.6% in 2011 (antenatal care sentinel surveillance ), and the estimated prevalence among the adult population is 1.5% (Demographic and Health Survey [DHS] 2011) . However, despite the decreasing prevalence of HIV in the general population, the prevalence of HIV among VL patients has remained proportionally very high. The northwest districts of Ethiopia along the Sudanese border report the highest burden of HIV and VL coinfection rates, with HIV prevalence rates of 20%–40% among VL patients , , . The 2012 annual report from the Leishmaniasis Research and Treatment Centre of the University of Gondar showed that 81/332 (24.4%) of all admitted VL cases were HIV coinfected (unpublished data). The rates of coinfection from different studies in Ethiopia are summarized in Table 1.
The particularly high HIV coinfection rate in northwest Ethiopia could be due to the massive population movement in the region . In this area of cash-crop farming, there is a high labour demand, and 300,000 to 500,000 highlanders from urban and semiurban areas seasonally move in and out of the region. When these Leishmania-nonimmune highlanders go to the VL-endemic regions, they become exposed and infected. Internal migration is also a risk factor for HIV, and those infected with HIV will develop overt disease (VL) more rapidly than those who are not infected . The HIV prevalence rate among migrant workers at the MSF Holland voluntary counselling and testing services at Humera and Abdurafi was 8%–12% during 2008 and 2012 (MSF, unpublished data). Over the period from 2009 to 2012, MSF treated 1,255 primary VL cases, out of which 235 (18.7%) were HIV positive. The HIV prevalence among primary VL cases in the other MSF treatment areas in the same period were as follows: South Sudan 61/2,426 (2.5%); Sudan 19/1,455 (1.3%); and Kenya 22/1,595 (1.4%).
In Sudan, a hospital-based study in Khartoum reported a coinfection rate of 9.4% in 2002. Reports from southeast Sudan (Gedarif state), a region characterised by population movements, found HIV coinfection in 3.6% of VL cases in 2003 . Systematic testing of VL patients for HIV in MSF programs in Sudan and South Sudan between 2009 and 2012 showed an HIV coinfection rate of 2%–2.5% (MSF, unpublished data). In the other neighbouring countries and endemic regions, mainly children are affected, and the HIV coinfection rate is very low . MSF experience in Kacheliba in Western Pokot, Kenya, showed 1.4% HIV coinfection rate between 2006 and 2012. However, only 1,595 of the total 3,007 primary VL cases during the period were tested for HIV (MSF, unpublished data).
VL in East Africa is caused by Leishmania donovani and is transmitted by a sand fly of the species Phlebotomus orientalis or P. martini in a predominantly anthroponotic cycle (i.e., from man to man without animal reservoir) , . Although less virulent parasites (nonhuman pathogenic trypanosomatids and etiologic agents of the cutaneous form of the disease) were isolated from VL cases in some HIV-coinfected cases in zoonotic transmission regions , there are no reports of such cases from this region to date.
VL Clinical Manifestations
Patients with VL typically present with prolonged fever, weight loss, prostration, splenomegaly, and pancytopenia . While these manifestations are common for both non-HIV and HIV coinfected patients, patients can present with atypical clinical symptoms in cases of severe immunosuppression. Leishmania parasites, which are normally concentrated in the reticuloendothelial organs, are often disseminated, and high parasite loads can be found in peripheral locations such as the skin, gut, lungs, peripheral blood, peritoneal fluid, and other organs and glands. Most of these atypical manifestations have been described in Europe with L. infantum as the etiologic agent –. Although in Ethiopia coinfected patients generally present with the classical signs and symptoms , atypical manifestations have also been reported , . Gastrointestinal tract and skin involvement was frequently described.
Atypical presentations of VL can easily be confused with several other opportunistic conditions that occur in HIV patients and therefore cause a diagnostic challenge. Oral and skin lesions might be misdiagnosed as Kaposi sarcoma or skin tumours. Patients with disseminated disease often have a very weak immune response and may die even before the diagnosis is established. In resource-poor settings where case detection and management according to the existing guidelines are based on clinical case definitions and a syndromic approach , these atypical VL presentations in HIV patients might be missed and underreported.
In L. donovani-transmission regions, a number of patients develop a maculopapular or nodular skin rash following successful treatment for VL. This syndrome, called post-kala-azar dermal leishmaniasis (PKDL), starts around the paranasal and perioral areas and spreads to the rest of the body. PKDL is reported in up to 50% of VL-treated patients in Sudan . While most PKDL case reports from Sudan were in HIV-negative patients, a study in Ethiopia indicated that PKDL was more frequent among HIV patients, with an incidence of moderate–severe PKDL of 27.3% in HIV patients and 13.3% among non-HIV patients by the sixth month after VL treatment . It presents as a different clinical presentation, showing nodular lesions that contain an abundance of parasites. In contrast to the immune-competent host where PKDL develops after treatment, in HIV patients it may occur during VL (para-kala-azar dermal leishmanias [para-KDL]). However, skin lesions concomitant with visceral disease have been reported among HIV patients with the same parasite strain isolated both from the skin and the spleen . As a consequence of severe immunosuppression, distinguishing para-KDL from VL with dissemination to the skin is complicated during this kind of presentation. The possible visceralization of dermatotropic species prevalent in the region (L. major, L. tropica, and L. aethiopica) requires confirmation by molecular tests.
Main diagnostic methods used for VL in East Africa.
The commonly available serological tests in the region, the rK39 rapid diagnostic test (RDT) and the direct agglutination test (DAT), showed inconsistent and generally lower performance in comparison to the Indian subcontinent in immunocompetent VL. A meta-analysis examining the diagnostic performance of the rK39 RDT reported an average sensitivity of 79% and specificity of 85% . The rK39 test's accuracy also depends on the format of the test used. The DiaMed-ITLEISH (Bio-Rad Laboratories) showed satisfactory sensitivity (85%–90%) and specificity (90%–99%) in immunocompetent patients in East Africa and performs significantly better than the Kalazar Detect (Inbios International) , . The few studies available suggest DAT performance to be slightly better than the rK39 RDT , . However, DAT is often not available in the public health sector in this region. MSF currently uses an algorithm with serial serological testing (rK39 followed by DAT if rK39 is negative) conducted at the first stage and invasive procedures restricted to those who remain with diagnostic uncertainty .
Studies on other serological tests (indirect fluorescent antibody test [IFAT], enzyme-linked immunosorbent assay [ELISA], western blotting), on urine antigen, and on molecular diagnosis are hardly available .
Diagnosis of VL in HIV-coinfected individuals.
Few studies have assessed the performance of the main serological tests in HIV-positive patients in East Africa. Compared to HIV-negative individuals, sensitivity of the rK39 RDT (DiaMed-IT LEISH) was lower (77% versus 87%) among parasitologically confirmed cases in a study in Ethiopia. The sensitivity of DAT was generally higher but still lower among HIV-coinfected patients (89% versus 95%). Of interest, rK39 and DAT combined in a serial algorithm yielded a sensitivity of 98%, probably due to partly nonoverlapping sensitivity of both tests . A high positive predictive value of DAT (93.8%) was found in another study, but sensitivity and specificity were not reported . Other studies have also demonstrated that DAT titers in HIV-positive and HIV-negative individuals are comparable , , . Overall, the performance of serological tests in HIV-coinfected individuals in East Africa is still better than what has been reported in European studies , . While the lower sensitivities of rK39 and DAT may be due to the impact of HIV on antibody production, it has been proposed that the performance of serological tests in HIV-coinfected individuals may also depend on which infection was acquired first .
The suboptimal sensitivity of the commonly available serological test (rK39 RDT) explains the continued reliance on parasitological tests that can only be provided in a limited number of hospitals in the endemic areas. Some studies suggest that higher tissue parasite densities occur in HIV-coinfected patients , , . Parasite detection is also often the only way to diagnose atypically localized manifestations of VL  and allows for further study on the strain type. Given the overall poor and unpredictable treatment response, parasitological diagnosis is also necessary to assess treatment response and to decide on the need of treatment extension or change of drugs. The standard means of parasitological diagnosis in VL entails microscopy and/or culture from spleen, bone marrow, or lymph nodes. While highly accurate, the procedure is invasive, painful, and carries the risk of potentially fatal bleeding. Due to high treatment failure and the relapsing nature of the disease, VL-HIV patients will be repeatedly exposed to these tests. Other parasite detection methods not yet thoroughly explored rely on the microscopic detection of parasites in the peripheral blood. Such methodology could help avoid invasive procedures and could be easily applied in basic laboratory settings. Studies conducted in European HIV-positive individuals infected with L. infantum have shown promising results when using concentrated blood (sensitivity 78% and specificity 100%) , . A diagnostic study in which different peripheral blood concentration and visualization techniques are being evaluated is currently ongoing in Ethiopia. Preliminary data suggested high specificity but low sensitivity (close to 40%) . Finally, the performance of a commercially available kala-azar latex agglutination urine antigen test (KAtex) to monitor treatment response (as test of cure) is being evaluated in Ethiopian HIV-infected patients (http://clinicaltrials.gov/show/NCT01360762).
Molecular testing (polymerase chain reaction [PCR] on peripheral blood and/or on bone marrow aspirate) has been used in first-line diagnosis for VL in HIV-coinfected individuals in European countries and Brazil and merits further exploration in East Africa . Ongoing or planned diagnostic studies focusing on HIV-coinfected individuals in East Africa are summarized in Box 1.
Box 1. VL Diagnosis and Treatment in HIV-Coinfected Individuals in East Africa: Current Knowledge and Practice and Ongoing or Planned Initiatives
Diagnosis: Current knowledge and practice
- Lower accuracy of rK39 RDT and DAT in East Africa in the general VL patient population compared to other L. donovani-endemic regions (Indian subcontinent)
- The limited data on HIV-coinfected individuals suggest somewhat lower accuracy of serological tests
- Sequential diagnostic algorithms combining serological (rK39 followed by DAT) and parasitological testing achieve high accuracy with less need for invasive procedures
- Diagnosis in HIV-coinfected patients still often relies on invasive procedures for parasitological diagnosis and for monitoring of treatment response
Diagnosis: Ongoing or planned VL diagnostic studies in HIV-coinfected individuals (Ethiopia)
- Noninvasive parasitological diagnosis using peripheral blood microscopy
- Microculture inoculation of peripheral blood mononuclear cells
- Urine antigen tests: Evaluation of KAtex for diagnosis and treatment response, test of cure (TOC)
- Molecular methods: reverse transcription loop mediated isothermal amplification (RT-LAMP) assay to be evaluated in 2013 (Foundation for Innovative New Diagnostics [FIND])
VL treatment in HIV coinfection in East Africa.
Striking differences exist in VL treatment response in the general VL patient population across and within regions –. Higher doses of paromomycin and liposomal amphotericin B appear necessary for treatment of L. donovani in East Africa than in the Indian subcontinent. Of interest, within East Africa, clear differences in efficacy were seen with these drugs in between and within different countries, with the lowest cure rates noted in northern Ethiopia and Sudan. Possibly, these observations could extend to VL-HIV coinfection as well.
For decades, antimonials have been the cornerstone of VL treatment in Africa. Although these drugs still maintain good efficacy in East Africa, their use is associated with unacceptably high and potentially fatal toxicity in VL-HIV coinfection . Reported death rates during antimonial treatment typically have been 4- to 10-fold higher compared to HIV-negative individuals , ,  and have varied between 6.5% and 24.5% in a more recent study . In a recent Ethiopian study, high parasitologically confirmed treatment-failure rates (30%) were observed in HIV-infected patients treated with antimonials . Table 2 summarizes the studies showing the treatment outcomes of VL and VL-HIV for different antileishmanial drugs from 1998 on.
In the search for a safer alternative, liposomal amphotericin B has increasingly been explored in East Africa. While studies have consistently reported an excellent tolerability, cure rates in HIV-infected individuals have been rather disappointing in this continent. At a total dose of 30 mg/kg, around 16% of primary VL and 56% of VL relapse cases demonstrate parasitological failure in northern Ethiopia . This is in clear contrast with a report from India in which high (100%) cure rates were achieved at a total dose of 20 mg/kg . Current WHO guidelines recommend a cumulative dose of 40 mg/kg, with 8 to 10 doses of 3–5 mg/kg taken daily or intermittently, for VL-HIV coinfection in East Africa , although this has not yet been evaluated in the region.
Miltefosine has been evaluated in only one clinical trial in Ethiopia . In comparison with antimonials, it was found safer but less effective, with 17.5% parasitological treatment failure. Interestingly, a compassionate use of miltefosine in combination with liposomal amphotericin B (at 30 mg/kg total dose) in 111 HIV-coinfected VL patients seems to suggest substantially higher cure rates and lower failure rates both in primary VL and VL relapse . Based on this emerging evidence, a clinical trial is planned to start in northwest Ethiopia by the end of 2013, evaluating in parallel two treatment options: (1) combination therapy: miltefosine (2.5 mg/kg per day) for 28 days combined with liposomal amphotericin B (6 doses of 5 mg/kg; total dose 30 mg/kg) and (2) a high dose of liposomal amphotericin B (8 doses of 5 mg/kg; total dose 40 mg/kg).
Whereas the combination of antimonials and paromomycin (for 17 days) is now recommended by WHO as first-line treatment in immunocompetent individuals in East Africa, experience with it as a first-line treatment for HIV-coinfected individuals is limited . This regimen is now used in some programs for VL-HIV coinfected patients as a second-line treatment (in case of intolerance or failure of liposomal amphotericin B)  or as a first-line treatment if access to and availability of liposomal amphotericin B is limited. Current national and international treatment recommendations for VL-HIV coinfection are summarized in Table 3.
Risk of relapse and secondary prophylaxis in VL-HIV coinfection.
Given the high rates of lost to follow-up in most reported studies (often above 50%) , , , reliable data on the risk of relapse in VL-HIV-coinfected individuals are very scarce. In the most complete study, the reported risk of relapse at six months varied between 25.4% for the miltefosine group and 11.4% for the sodium stibogluconate (SSG) group . Another study estimated a one-year relapse risk of close to 20% for individuals with primary VL and CD4 cell counts of around 200 cells/µL and around 60% for those with multiple previous VL episodes and CD4 cell counts below 100 cells/µL . However, the potential bias caused by the high proportion of patients not receiving ART who were lost to follow-up in this study compromises the generalizability of these estimates. In line with European data, use of ART was associated with an estimated 50% reduced risk of relapse in this study. VL relapse was also associated with persistently low CD4 counts while on ART.
A recent systematic review, mainly containing data on L. infantum in Europe, suggested that secondary prophylaxis could reduce the risk of relapse in VL-HIV coinfection by at least 50% , . Whereas secondary prophylaxis against VL is indeed recommended by WHO for VL-HIV coinfection in areas with zoonotic transmission, this is less clear when transmission is human to human (antroponotic transmission) . In such a situation, use of any of the few available VL treatment drugs for secondary prophylaxis carries the risk of emergence and spread of drug resistance. Pentamidine has been proposed for secondary prophylaxis in such a situation, since it exerts antileishmanial effect, is currently not used for VL treatment, and has been found to be relatively safe in a prophylactic dose –. An open-label multicentre clinical trial recruiting HIV coinfected adults at high risk of VL relapse is currently ongoing in Ethiopia to evaluate the feasibility, safety, and effectiveness of monthly intravenous administration of pentamidine (4 mg/kg) for a period of 12 to 18 months. Main outcome data are expected before the end of 2014 (http://clinicaltrials.gov, NCT01360762).
Antiretroviral treatment in VL-HIV coinfection.
Within Europe, the widespread use of ART in VL-endemic areas has had a major epidemiological effect on VL-HIV coinfection, with a pronounced reduction of new cases and prolonged disease-free survival for established VL-HIV coinfection. The effect on relapse has been more modest, with an estimated 50% reduction. Although ART has now been scaled up in most African countries, access to ART in the generally remote and underresourced VL-endemic areas remains challenging. Only in Ethiopia do all (major) VL treatment sites provide ART. Usually, ART is initiated as soon as the patient is clinically stable, typically during the second week after initiation of VL treatment.
There is only one retrospective study on the effect of ART on survival in VL-HIV coinfection in East Africa, which did not demonstrate an effect . However, this might be due to the high proportion of lost to follow-up patients who were interrupting their ART. It was also not assessed whether HIV viral suppression was achieved .
Overall and in clear contrast with TB-HIV, the immune reconstitution inflammatory syndrome (IRIS) appears to be an exception in VL-HIV coinfection. Only a handful of clear-cut case reports of (ART-associated) VL-IRIS have been reported at the global level –. Whether the overall dampening effect of the Leishmania parasite on the immune system could relate to this requires further study. The lack of a clear case definition of IRIS in VL-HIV could further add to this lack of reporting. In East Africa, a few cases of VL have been reported after ART initiation (including seroconversion), but it is not clear to what extent these are true “unmasking” IRIS cases . While PKDL is assumed to be an immune-mediated condition , in HIV patients on ART, it may indicate IRIS , . Two cases were reported from Ethiopia with exacerbation of skin lesions after ART initiation, described as PKDL or PKDL-like lesions . Detailed prospective studies are required to characterize IRIS in VL-HIV coinfection, with a special focus on skin manifestations.
With the global scaling-up of ART, HIV-1 protease inhibitors (PIs) are increasingly available in VL-HIV-endemic regions, including regions in Africa. Several lines of evidence suggest that HIV-1 protease inhibitors might directly exert antiparasitic effects, including effects against Leishmania. One potential approach could consist of using PI-based ART instead of non-nucleoside reverse transcription inhibitor (NNRTI)-based ART in VL-HIV-endemic regions. However, with detailed animal or clinical studies lacking, additional research is required before HIV-1 PIs should be taken forward towards this goal .
The Role of VL-HIV Coinfections as Reservoirs for Transmission of L. donovani
The infectiousness of HIV-coinfected patients to sand flies in endemic areas of anthroponotic foci has not been studied. However, coinfected patients were found to have higher tissue parasite loads and higher rates of PKDL ,  potentially acting as reservoirs. Given the high rate of treatment failure and risk of relapse ,  and the associated repeated and prolonged exposure to antileishmanial drugs, HIV-coinfected individuals are also at increased risk of developing drug resistance and could possibly serve as a source of resistant parasites. Ideally, xenodiagnosis studies should be conducted in East Africa as well in order to better define the epidemiological impact of HIV coinfection in this region.
Discussion and Conclusions
As a neglected disease, the significance of Leishmania infection in HIV patients was recognized late. The poorest segments of the population, such as migrant daily laborers, are affected. Thus, the diagnostic and treatment challenges of VL-HIV coinfection have continued to date, especially in East Africa , .
The control of VL requires a combined effort at vector control, improved living standards and case detection, and early treatment . The feasibility of transmission prevention methods like impregnated bed nets, blankets, and protective clothing should be evaluated. In the case of VL-HIV, targeting the most at-risk population groups (e.g., the migrant population) and improving their awareness through health education and counseling for both diseases should be pursued. Health professions should also be regularly updated about VL.
Case detection and management is especially challenging for HIV-infected persons. To have a larger impact on VL-HIV coinfection, a comprehensive and multipronged approach will be required. Better diagnostic and curative options would help to improve case detection and patient management. As with other HIV-associated coinfections (for instance, tuberculosis and cryptococcal meningitis), preventive strategies should be explored. As the experience in Europe testifies, the preventive effect of large-scale introduction of ART merits exploration. Although the current WHO guidelines now recommend early ART initiation , the most challenging part will be early HIV diagnosis and retention in care in a typically highly mobile and difficult to reach population.
Diagnosing VL in HIV patients relies mainly on parasite detection from tissue aspiration. This is due to the insufficiently sensitive serological tests that also do not help to diagnose relapsed cases, which are very common in HIV patients. However, tissue aspiration is associated with potential risk of fatal bleeding that requires experience and health facilities equipped to handle this potential complication. Thus, a simple-to-use but reliable antigen-detection diagnostic procedure or tool that can be applicable for treatment monitoring and diagnosing relapses is urgently required.
For VL-HIV case management, field experience favors the use of the following combination treatment: liposomal amphotericin B and miltefosine  followed by secondary prophylaxis , ,  and ART. However, studies are urgently needed to strengthen the evidence for this treatment and improve its outcome in patients in field conditions in East Africa. To date, there is no clear evidence regarding the interaction of ARV drugs and antileishmanial medications. Basic research to understand the immunological interaction of the two infections, as well as the immune modulatory effects of drugs, may ultimately help to improve the management of the coinfection.
Tackling VL-HIV coinfection in the long run, along with combating VL in general, will strongly depend on the strength and commitment of the national programs. However, to date, the national programs still rely on substantial external support in most East African countries. Moreover, a strong link with the national HIV program will be needed for efficient and integrated program management. Though the HIV prevalence is declining in Ethiopia, the unstable socioeconomic and political situations in South Sudan and the high population migrations in the region warrant continuous effort for the control of both diseases.
Box 2. Key Learning Points
- Northwest Ethiopia has the highest known burden of VL-HIV coinfection rates in the world.
- VL-HIV coinfection is associated with diagnostic and treatment challenges that still need additional research.
- Atypical clinical presentations and poor performance of rapid serological tests among the HIV co-infected VL patients poses a diagnostic challenge.
- There is a high rate of treatment failure and relapse of VL among HIV-coinfected patients.
- Combination treatment with liposomal amphotericin B and miltefosine followed by secondary prophylaxis and ART seems to be a promising standard of care that needs clinical trials.
Box 3. Five Key Papers in the Field
- Hurissa Z, Gebre-Silassie S, Hailu W, Tefera T, Lalloo DG, et al. (2010) Clinical characteristics and treatment outcome of patients with visceral leishmaniasis and HIV co-infection in northwest Ethiopia. Trop Med Int Health 15: 848–855. doi: 10.1111/j.1365-3156.2010.02550.x
- ter Horst R, Tefera T, Assefa G, Ebrahim AZ, Davidson RN, et al. (2009) Field evaluation of rK39 test and direct agglutination test for diagnosis of visceral leishmaniasis in a population with high prevalence of human immunodeficiency virus in Ethiopia. Am J Trop Med Hyg 80: 929–934.
- ter Horst R, Collin SM, Ritmeijer K, Bogale A, Davidson RN (2008) Concordant HIV infection and visceral leishmaniasis in Ethiopia: the influence of antiretroviral treatment and other factors on outcome. Clin Infect Dis 46: 1702–1709. doi: 10.1086/587899
- Ritmeijer K, ter Horst R, Chane S, Aderie EM, Piening T, et al. (2011) Limited effectiveness of high-dose liposomal amphotericin B (AmBisome) for treatment of visceral leishmaniasis in an Ethiopian population with high HIV prevalence. Clin Infect Dis 53: e152–e158. doi: 10.1093/cid/cir674
- Ritmeijer K, Dejenie A, Assefa Y, Hundie TB, Mesure J, et al. (2006) A comparison of miltefosine and sodium stibogluconate for treatment of visceral leishmaniasis in an Ethiopian population with high prevalence of HIV infection. Clin Infect Dis 43: 357–364. doi: 10.1086/505217
- 1. van Griensven J, Diro E (2012) Visceral leishmaniasis. Infect Dis Clin North Am 26: 309–322 doi:10.1016/j.idc.2012.03.005.
- 2. Alvar J, Velez ID, Bern C, Herrero M, Desjeux P, et al. (2012) Leishmaniasis worldwide and global estimates of its incidence. PLoS One 7: e35671 doi: 10.1371/journal.pone.0035671.
- 3. Seaman J, Mercer AJ, Sondorp E (1996) The epidemic of visceral leishmaniasis in western upper Nile, Southern Sudan: Course and impact from 1984 to 1994. Int J Epidemiol 25: 862–871.
- 4. Olivier M, Badaro R, Medrano FJ, Moreno J (2003) The pathogenesis of Leishmania/HIV co-infection: cellular and immunological mechanisms. Ann Trop Med Parasitol 97 Suppl 1: 79–98 doi: 10.1179/000349803225002561.
- 5. Alvar J, Aparicio P, Aseffa A, den Boer M, Canavate C, et al. (2008) The relationship between leishmaniasis and AIDS: the second 10 years. Clin Microbiol Rev 21: 334–359 table. doi:10.1128/CMR.00061-07.
- 6. Jarvis JN, Lockwood DN (2013) Clinical aspects of visceral leishmaniasis in HIV infection. Curr Opin Infect Dis 26: 1–9 doi: 10.1097/QCO.0b013e32835c2198.
- 7. World Health Organization (2010 March 22) Control of the Leishmaniases. In: WHO Technical Report Series 949: Report of a meeting of the WHO Expert Committee on the Control of Leishmaniases, Geneva, 22–26 March 2010. Geneva, Swetzerland: World Health Organization.
- 8. Joint United Nations Programme on HIV/AIDS [UNAIDS] (2013) Global Report: UNAIDS report on the global AIDS epidemic. Available: http://www.unaids.org/en/media/unaids/contentassets/documents/epidemiology/2013/gr2013/UNAIDS_Global_Report_2013_en.pdf. Accessed 22 May 2014.
- 9. Merson MH, O'Malley J, Serwadda D, Apisuk C (2008) The history and challenge of HIV prevention. Lancet 372: 475–488 doi: 10.1016/S0140-6736(08)60884-3.
- 10. Ethiopian Health and Nutrition Research Institute (EHNRI) (2011) Report on the 2009 Round Antenatal Care Sentinel HIV Surveillance in Ethiopia. Available: http://www.ehnri.gov.et/newsletter/ANC%202009_Final_Report.pdf. Accessed 22 May 2014.
- 11. Federal Democratic Republic of Ethiopia (2012) Country progress report on HIV/AIDS response. Available: http://www.unaids.org/en/dataanalysis/knowyourresponse/countryprogressreports/2012countries/GAP%20Report%202012.pdf. Accessed 22 May 2014.
- 12. Mengistu G, Ayele B (2007) Visceral leishmaniasis and HIV co-infection in patients admitted to Gondar University Hopsital, North West Ethiopia. Ethiop J Health Dev 21: 53–60.
- 13. Argaw D, Mulugeta A, Herrero M, Nombela N, Teklu T, et al. (2013) Risk factors for visceral Leishmaniasis among residents and migrants in Kafta-Humera, Ethiopia. PLoS Negl Trop Dis 7: e2543 doi: 10.1371/journal.pntd.0002543.
- 14. Gelanew T, Kuhls K, Hurissa Z, Weldegebreal T, Hailu W, et al. (2010) Inference of population structure of Leishmania donovani strains isolated from different Ethiopian visceral leishmaniasis endemic areas. PLoS Negl Trop Dis 4: e889 doi: 10.1371/journal.pntd.0000889.
- 15. Malaria Consortium (2010) Leishmaniasis control in eastern Africa: Past and present efforts and future needs. Situation and gap analysis. Available: http://www.malariaconsortium.org/userfiles/file/NTD%20Resources/VL%20EA%20Situation%20Analysis%20Fina_Janl.pdf. Accessed 22 May 2014.
- 16. Catorce G (2010) Leishmania infantum/HIV co-infection: cuteneous lesions following treatment of visceral leishmaniasis. Ann Dermatol Venereol 133: 39–42.
- 17. Fenske S, Stellbrink HJ, Albrecht H, Greten H (1991) Visceral leishmaniasis in an HIV-infected patient: clinical features and response to treatment. Klin Wochenschr 69: 793–796.
- 18. Garcia-Samaniego J, Laguna F (1997) [Intestinal leishmaniasis in AIDS patients]. Rev Esp Enferm Dig 89: 145.
- 19. Hurissa Z, Gebre-Silassie S, Hailu W, Tefera T, Lalloo DG, et al. (2010) Clinical characteristics and treatment outcome of patients with visceral leishmaniasis and HIV co-infection in northwest Ethiopia. Trop Med Int Health 15: 848–855 doi: 10.1111/j.1365-3156.2010.02550.x.
- 20. Gelanew T, Hurissa Z, Diro E, Kassahun A, Kuhls K, et al. (2011) Disseminated cutaneous leishmaniasis resembling post-kala-azar dermal leishmaniasis caused by Leishmania donovani in three patients co-infected with visceral leishmaniasis and human immunodeficiency virus/acquired immunodeficiency syndrome in Ethiopia. Am J Trop Med Hyg 84: 906–912 doi:10.4269/ajtmh.2011.11-0055.
- 21. Diro E, Hurissa Z, van Griensven J, Hailu A (2011) Unusual presentations of visceral leishmania in the era of HIV. In: Proceedings of the 16th International Conference on AIDS and STIs in Africa (ICASA); 4–8 December 2011; Addis Ababa, Ethiopia.
- 22. Zijlstra EE, Musa AM, Khalil EA, el-Hassan IM, el-Hassan AM (2003) Post-kala-azar dermal leishmaniasis. Lancet Infect Dis 3: 87–98.
- 23. Ritmeijer K, Veeken H, Melaku Y, Leal G, Amsalu R, et al. (2001) Ethiopian visceral leishmaniasis: generic and proprietary sodium stibogluconate are equivalent; HIV co-infected patients have a poor outcome. Trans R Soc Trop Med Hyg 95: 668–672.
- 24. Chappuis F, Rijal S, Soto A, Menten J, Boelaert M (2006) A meta-analysis of the diagnostic performance of the direct agglutination test and rK39 dipstick for visceral leishmaniasis. BMJ 333: 723 doi: 10.1136/bmj.38917.503056.7C.
- 25. Chappuis F, Mueller Y, Nguimfack A, Rwakimari JB, Couffignal S, et al. (2005) Diagnostic accuracy of two rK39 antigen-based dipsticks and the formol gel test for rapid diagnosis of visceral leishmaniasis in northeastern Uganda. J Clin Microbiol 43: 5973–5977 doi: 10.1128/JCM.43.12.5973-5977.2005 [doi].
- 26. Cunningham J, Hasker E, Das P, El SS, Goto H, et al. (2012) A global comparative evaluation of commercial immunochromatographic rapid diagnostic tests for visceral leishmaniasis. Clin Infect Dis 55: 1312–1319 doi:10.1093/cid/cis716.
- 27. Diro E, Techane Y, Tefera T, Assefa Y, Kebede T, et al. (2007) Field evaluation of FD-DAT, rK39 dipstick and KATEX (urine latex agglutination) for diagnosis of visceral leishmaniasis in northwest Ethiopia. Trans R Soc Trop Med Hyg 908–914 doi: 10.1016/j.trstmh.2007.05.002.
- 28. ter Horst R, Tefera T, Assefa G, Ebrahim AZ, Davidson RN, et al. (2009) Field evaluation of rK39 test and direct agglutination test for diagnosis of visceral leishmaniasis in a population with high prevalence of human immunodeficiency virus in Ethiopia. Am J Trop Med Hyg 80: 929–934.
- 29. Adams ER, Schoone GJ, Ageed AF, Safi SE, Schallig HD (2010) Development of a reverse transcriptase loop-mediated isothermal amplification (LAMP) assay for the sensitive detection of Leishmania parasites in clinical samples. Am J Trop Med Hyg 82: 591–596 doi: 10.4269/ajtmh.2010.09-0369.
- 30. Hailu A, Berhe N (2002) The performance of direct agglutination tests (DAT) in the diagnosis of visceral leishmaniasis among Ethiopian patients with HIV co-infection. Ann Trop Med Parasitol 96: 25–30.
- 31. Ritmeijer K, Dejenie A, Assefa Y, Hundie TB, Mesure J, et al. (2006) A comparison of miltefosine and sodium stibogluconate for treatment of visceral leishmaniasis in an Ethiopian population with high prevalence of HIV infection. Clin Infect Dis 43: 357–364 doi: 10.1086/505217.
- 32. Deniau M, Canavate C, Faraut-Gambarelli F, Marty P (2003) The biological diagnosis of leishmaniasis in HIV-infected patients. Ann Trop Med Parasitol 97 Suppl 1: 115–133 doi: 10.1179/000349803225002598.
- 33. Izri MA, Deniau M, Briere C, Rivollet D, Petithory JC, et al. (1996) Leishmaniasis in AIDS patients: results of leukocytoconcentration, a fast biological method of diagnosis. Bull World Health Organ 74: 91–93.
- 34. Yansouni CP, Diro E, Lynen L, van Griensven J, Takele Y, et al.. (2012) Diagnosis of visceral leishmaniasis using peripheral blood microscopy in Ethiopia: a phase-III diagnostic study evaluating 3 parasite concentration techniques compared to tissue aspiration. In: Proceedings of the 61st Annual Meeting of the American Society of Tropical Medicine and Hygiene, 11–15 November 2012; Atlanta, Georgia, United States.
- 35. Cota GF, de Sousa MR, Demarqui FN, Rabello A (2012) The diagnostic accuracy of serologic and molecular methods for detecting visceral leishmaniasis in HIV infected patients: meta-analysis. PLoS Negl Trop Dis 6: e1665 doi: 10.1371/journal.pntd.0001665.
- 36. Hailu A, Musa A, Wasunna M, Balasegaram M, Yifru S, et al. (2010) Geographical variation in the response of visceral leishmaniasis to paromomycin in East Africa: a multicentre, open-label, randomized trial. PLoS Negl Trop Dis 4: e709 doi: 10.1371/journal.pntd.0000709.
- 37. Musa AM, Younis B, Fadlalla A, Royce C, Balasegaram M, et al. (2010) Paromomycin for the treatment of visceral leishmaniasis in Sudan: a randomized, open-label, dose-finding study. PLoS Negl Trop Dis 4: e855 doi: 10.1371/journal.pntd.0000855.
- 38. Ritmeijer K, ter Horst R, Chane S, Aderie EM, Piening T, et al. (2011) Limited effectiveness of high-dose liposomal amphotericin B (AmBisome) for treatment of visceral leishmaniasis in an Ethiopian population with high HIV prevalence. Clin Infect Dis 53: e152–e158 doi: 10.1093/cid/cir674.
- 39. Diro E, Lynen L, Mohammed R, Boelaert M, Hailu A, et al.. (2013) Increasing parasitological failure rate of visceral leishmaniasis to sodium stibogluconate among HIV co-infected patients in East Africa. In: Proceedings of the Fifth World Leishmaniasis Congress; 13–17 May 2013; Porto de Galhinas, Brazil.
- 40. Sinha PK, van Griensven J, Pandey K, Kumar N, Verma N, et al. (2011) Liposomal amphotericin B for visceral leishmaniasis in human immunodeficiency virus-coinfected patients: 2-year treatment outcomes in Bihar, India. Clin Infect Dis 53: e91–e98 doi: 10.1093/cid/cir521.
- 41. Ritmeijer K (2013) Old and new treatments for HIV/VL co-infection. In: Proceedings of the Fifth World Leishmaniasis Congress, 13–17 May 2013; Porto de Galhinas, Brazil.
- 42. Musa A, Khalil E, Hailu A, Olobo J, Balasegaram M, et al. (2012) Sodium stibogluconate (SSG) & paromomycin combination compared to SSG for visceral leishmaniasis in East Africa: a randomised controlled trial. PLoS Negl Trop Dis 6: e1674 doi: 10.1371/journal.pntd.0001674.
- 43. Federal Ministry of Health, Ethiopia (2013) Guidelines for diagnosis, treatment and prevention of leishmaniasis in Ethiopia, 2nd edition. Addis Adaba, Ethiopia: Federal Ministry of Health, Ethiopia.
- 44. Hailu W, Weldegebreal T, Hurissa Z, Tafes H, Omollo R, et al. (2010) Safety and effectiveness of meglumine antimoniate in the treatment of Ethiopian visceral leishmaniasis patients with and without HIV co-infection. Trans R Soc Trop Med Hyg 104: 706–712 doi: 10.1016/j.trstmh.2010.07.007.
- 45. ter HR, Collin SM, Ritmeijer K, Bogale A, Davidson RN (2008) Concordant HIV infection and visceral leishmaniasis in Ethiopia: the influence of antiretroviral treatment and other factors on outcome. Clin Infect Dis 46: 1702–1709 doi: 10.1086/587899.
- 46. Cota GF, de Sousa MR, Rabello A (2011) Predictors of visceral leishmaniasis relapse in HIV-infected patients: a systematic review. PLoS Negl Trop Dis 5: e1153 doi: 10.1371/journal.pntd.0001153.
- 47. Lopez-Velez R, Videla S, Marquez M, Boix V, Jimenez-Mejias ME, et al. (2004) Amphotericin B lipid complex versus no treatment in the secondary prophylaxis of visceral leishmaniasis in HIV-infected patients. J Antimicrob Chemother 53: 540–543 doi: 10.1093/jac/dkh084.
- 48. Calza L, Marinacci G, Manfredi R, Colangeli V, Fortunato L, et al. (2001) Pentamidine isethionate as treatment and secondary prophylaxis for disseminated cutaneous leishmaniasis during HIV infection: case report. J Chemother 13: 653–657.
- 49. Ena J, Amador C, Pasquau F, Carbonell C, Benito C, et al. (1994) Once-a-month administration of intravenous pentamidine to patients infected with human immunodeficiency virus as prophylaxis for Pneumocystis carinii pneumonia. Clin Infect Dis 18: 901–904.
- 50. Yeung KT, Chan M, Chan CK (1996) The safety of i.v. pentamidine administered in an ambulatory setting. Chest 110: 136–140.
- 51. ter Horst R, Collin SM, Ritmeijer K, Bogale A, Davidson RN (2008) Concordant HIV infection and visceral leishmaniasis in Ethiopia: the influence of antiretroviral treatment and other factors on outcome. Clin Infect Dis 46: 1702–1709 doi: 10.1086/587899.
- 52. Petter A, Shetty-Lee A, Kofler G, Huemer HP, Larcher C (2001) Visceral leishmaniasis in an AIDS patient on successful antiretroviral therapy: failure of parasite eradication despite increase in CD4+ T-cell count but low CD8+ T-cell count. Scand J Infect Dis 33: 236–238.
- 53. Ramos A, Cruz I, Munez E, Salas C, Fernandez A, et al. (2008) Post-kala-azar dermal Leishmaniasis and uveitis in an HIV-positive patient. Infection 36: 184–186 doi: 10.1007/s15010-007-6279-5.
- 54. Antinori S, Longhi E, Bestetti G, Piolini R, Acquaviva V, et al. (2007) Post-kala-azar dermal leishmaniasis as an immune reconstitution inflammatory syndrome in a patient with acquired immune deficiency syndrome. Br J Dermatol 157: 1032–1036 doi: 10.1111/j.1365-2133.2007.08157.x.
- 55. Bittencourt A, Silva N, Straatmann A, Nunes VL, Follador I, et al. (2003) Post-kala-azar dermal leishmaniasis associated with AIDS. Braz J Infect Dis 7: 229–233.
- 56. Stark D, Pett S, Marriott D, Harkness J (2006) Post-kala-azar dermal leishmaniasis due to Leishmania infantum in a human immunodeficiency virus type 1-infected patient. J Clin Microbiol 44: 1178–1180 doi: 10.1128/JCM.44.3.1178-1180.2006.
- 57. Ridolfo AL, Gervasoni C, Antinori S, Pizzuto M, Santambrogio S, et al. (2000) Post-kala-azar dermal leishmaniasis during highly active antiretroviral therapy in an AIDS patient infected with Leishmania infantum. J Infect 40: 199–202.
- 58. Gilad J, Borer A, Hallel-Halevy D, Riesenberg K, Alkan M, et al. (2001) Post-kala-azar dermal leishmaniasis manifesting after initiation of highly active anti-retroviral therapy in a patient with human immunodeficiency virus infection. Isr Med Assoc J 3: 451–452.
- 59. Khalil EA, Khidir SA, Musa AM, Musa BY, Elfaki ME, et al. (2013) Post-Kala-Azar Dermal Leishmaniasis: A Paradigm of Paradoxical Immune Reconstitution Syndrome in Non-HIV/AIDS Patients. J Trop Med 2013: 275253 doi: 10.1155/2013/275253.
- 60. Tadesse A, Hurissa Z (2009) Leishmaniasis (PKDL) as a case of immune reconstitution inflammatory syndrome (IRIS) in HIV-positive patient after initiation of anti-retroviral therapy (ART). Ethiop Med J 47: 77–79.
- 61. van GJ, Diro E, Lopez-Velez R, Boelaert M, Lynen L, et al. (2013) HIV-1 protease inhibitors for treatment of visceral leishmaniasis in HIV-co-infected individuals. Lancet Infect Dis 13: 251–259 doi: 10.1016/S1473-3099(12)70348-1.
- 62. Word Health Organization (2013) Consolidated Guidelines on Use of Antiretroviral Drugs for Treating and Preventing HIV Infection Recommendations for a Public Health Approach. Geneva, Switzerland: World Health Organization.
- 63. CDC (2009) Guidelines for Prevention and Treatment of Opportunistic Infections in HIV-Infected Adults and Adolescents. MMWR Morb Mortal Wkly Rep 58: RR–4.
- 64. Hailu A, Gebre-Michael T, Berhe N, Balkew M (2006) Leishmaniasis in Ethiopia. In: The Ecology and Epidemiology of Health and Disease in Ethiopia. Addis Ababa, Ethiopia: Shama Books. pp. 615–634.
- 65. Lyons S, Veeken H, Long J (2003) Visceral leishmaniasis and HIV in Tigray, Ethiopia. Trop Med Int Health 8: 733–739.