Epidemiology, disease patterns, immunology, diagnosis, treatment and control measures of leishmaniasis are described. Various issues relating to leishmaniasis are highlighted: the relative lack of importance given to this disease compared with other infections, climate change and its possible impact on extension of endemicity of this infection, and new diagnostic tests which are improving diagnosis, especially in resource poor areas. Other important aspects discussed include the potential for newer oral therapy to change the way this disease is managed; Leishmania–HIV coinfection and groups at risk; and development of an effective vaccine.
- IFN, interferon
- PCR, polymerase chain reaction
- PKDL, post-kala azar dermal leishmaniasis
- Th, T helper
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Infectious diseases steal the headlines on a regular basis and are ranked high among other major news items like natural disasters, conflict situations and terrorism. Emerging infectious diseases with wide threatening potential such as severe acute respiratory syndrome and pandemic influenza, are usually the ones which get best coverage and consequently better funding. Diseases with high prevalence such as HIV/AIDS and malaria (table 1) should bring better financial returns from investing research into new treatments and developing vaccinations than similar investment into lower prevalence infections. Leishmaniasis is one such infection which rarely shares this limelight and thus remains largely a neglected disease.1,2
This article is being reprinted as there were a number of errors in the original version. The publisher apologises unreservedly to the authors and readers for any confusion these errors may have caused.
Despite this, several issues regarding leishmaniasis merit discussion: resistance to conventional drug treatment has developed in certain areas of the world, necessitating a change of first-line agents; rapid, less invasive diagnostic procedures have been developed which are most useful in poorly resourced parts of the world; despite advances in the understanding of the immunology of the disease and the unravelling of the Leishmania genome, a vaccine has not yet been developed; and the extent of disease in different individuals stresses the complex immunology of leishmaniasis, brought to the fore more recently with the advent of HIV–Leishmania coinfection, and its difficult eradication in this scenario.
This review is based on information from bibliographic research, Entrez-Pubmed searches on leishmaniasis, review articles and papers in their reference lists, and from the authors’ personal archives.
Leishmaniasis is endemic in more than 60 countries worldwide,1 including Southern Europe, North Africa, the Middle East, Central and South America and the Indian subcontinent. It is not endemic in South East Asia and Australia.4 The burden of disease (90% of cases) is borne by Afghanistan, Pakistan, Syria, Saudi Arabia, Algeria, Iran, Brazil, and Peru in the case of cutaneous leishmaniasis, and by India, Bangladesh, Nepal, Sudan, and Brazil in the case of visceral leishmaniasis.3 Recently the number of reported cases and geographical areas have increased,5 and this has sparked concern regarding the contribution that global warming might have on this observation.6,7
One of the causative organisms of leishmaniasis, Leishmania donovani, was first described in 1903 by Leishman and Donovan almost simultaneously.4Leishmania is a protozoon, able to infect animals, humans and sandflies. There are at least 20 species of Leishmania. Each may cause a disease specific to the species and the host response. Organism prevalence differs by geographical distribution. Thus disease patterns differ by geographical area (table 2).
The reservoirs of the disease are animals like canines and rodents (zoonotic cycle) and, in countries such as Sudan, humans (anthroponotic cycle).10 The sandfly is the vector of the disease and ingests the organism, as an amastigote, into its digestive tract when feeding on an infected animal. The amastigote develops into a promastigote in its digestive tract, and will then be injected into the susceptible host at the next feed. The promastigote then infects macrophages and develops into amastigotes (fig 1).
About 70 different species of sandfly can transmit leishmaniasis.11 The species are mainly Lutzomyia in the Americas and Phlebotomous elsewhere.12 The sandfly characteristically feeds at dusk, and being a weak flier, tends to remain close to its breeding area, not too high from the ground. Different species have different feeding and resting patterns. These different characteristics are important in formulating control strategies (see below).
The incidence and prevalence can be seen in table 1. Infection is more common in men than in women, but this may reflect increased exposure to sandflies. Although disease occurs irrespective of age, children aged 1–4 years are particularly at risk of infection in the Mediterranean regions, and childhood infection may account for more than half of all cases in some of these countries.13 Untreated visceral leishmaniasis carries a mortality of 75–95%, while cutaneous leishmaniasis can disseminate to involve the mucosa, resulting in death from secondary infection.8
Three main types of disease patterns occur: visceral, cutaneous and mucocutaneous leishmaniasis (table 3). The type of disease expressed depends both on the type of Leishmania species and on the zymodeme (electrophoretic isoenzyme pattern) expressed on that species. Thus one zymodeme may cause visceral leishmaniasis while another zymodeme of the same species may cause cutaneous leishmaniasis.14
The incubation period varies from 3 to 8 months15,16 (range 10 days17 to 34 months18). Features include fever, weight loss, hepatosplenomegaly (usually spleen much larger than liver), lymphadenopathy, pancytopenia and hypergammaglobulinaemia.10 Skin pigmentation may be a feature (“kala azar”: black disease). It may be asymptomatic and self-resolving, but usually runs a chronic course and may be fatal without or despite treatment.19 Death usually occurs because of severe secondary bacterial infections in advanced disease.
Some cases of visceral leishmaniasis present atypically and cases have been reported which involve the lungs, pleura, oral mucosa, larynx, oesophagus, stomach, small intestine, skin and bone marrow.12
Box 1: Current issues in Leishmania infection
Leishmania is given less importance than other more prevalent infectious diseases.
Climate change may be responsible for the extension of endemicity of leishmaniasis to previously non-endemic countries.
New diagnostic tests should improve diagnosis, especially in the field in resource-poor areas.
Leishmania may relapse in HIV patients and is difficult to eradicate, if at all in this setting. There have been calls for Leishmania infection to be officially recognised as an AIDS-defining illness.
Anthroponotic transmission may occur in intravenous drug users who share needles.
The Leishmania genome has been unravelled, but an effective vaccine is not yet available.
Variations of visceral leishmaniasis
Post-kala azar dermal leishmaniasis (PKDL) develops after resolution of visceral leishmaniasis. The time interval to development of PKDL is variable. PKDL occurs in a small percentage of patients in Africa and India.12 This is usually due to infection by the L donovani sensu stricto cluster.20 The skin lesions are macular, maculo-papular or nodular, and usually spread from the perioral area to other areas of the body.
This initially starts as a papule at the site of a sandfly bite which then increases in size, crusts (fig 2), and eventually ulcerates. It may take 3–18 months to heal in over 90% of cases.12 The incubation period lasts from 2 weeks to several months and cases up to 3 years have been reported in Old World cutaneous leishmaniasis.17,21 In New World cutaneous leishmaniasis, the incubation period is usually 2–8 weeks.22
Variations of cutaneous leishmaniasis
Leishmaniasis recidivans is characterised by tuberculoid lesions developing around scars of healed cutaneous ulcers, revealing a low parasite count on biopsy. Infections tend to be resistant to treatment.
In diffuse cutaneous leishmaniasis, dissemination of skin lesions rarely occurs over the face, hands and feet, revealing high parasite numbers due to poor cell-mediated immune response. This is more common in the New World Leishmania but also occurs with L aethiopica in East Africa.23
The incubation period is 1–3 months, but mucocutaneous leishmaniasis may occur many years after the initial cutaneous ulcer has healed. Mucosal involvement occurs in South American cases of cutaneous leishmaniasis (espundia) involving the nose, oral cavity and pharynx. This causes difficulty with eating and an increased risk of secondary infection which carries a significant mortality.
The immune response (box 2) to Leishmania infection is cell mediated. The organism lies exclusively intracellularly, mainly inside macrophages as replicating amastigotes. The outcome of infection will depend on whether the host mounts primarily a T-helper (Th)-1 or Th2 response.24 Studies in animals suggest that the same parasite epitope can induce a Th1 response in animals with resolving infection or a Th2 response in others with disease progression.25 Other animal studies have shown that Th1 and natural-killer cells produce interferon γ (IFNγ), which mediates resistance, whilst interleukin (IL)4-producing Th2 cells confer susceptibility to infection.26 Human studies have also shown that IL4, a component of the Th2 response, may also be associated with disease progression.27
Box 2: The immune response
Th1 immune response
T-helper CD4 cells producing IL2, IL3, IFNγ
Will promote immune responses that are primarily cell mediated/inflammatory by activating cytotoxic T cells, natural killer cells and macrophages
In leishmaniasis, associated with disease resolution
Th2 immune response
Th2 cells produce IL4, IL5, IL6, IL10 which favour induction of antibody responses by B cells
In leishmaniasis, associated with disease progression
In the Th1 response, promastigotes attach to reticuloendothelial cells and T helper CD4 cells produce IL2, IL3 and IFNγ which activate macrophages. IL12 and tumour necrosis factor (TNF) are also important in this type of response. The promastigotes are then phagocytosed by the activated macrophages into vacuoles which then fuse with lysosomes.
Host genetics inevitably influence the type of immune response. Studies in mice and humans have shown that genes such as those coding for natural resistance associated macrophage protein 1 (NRAMP1), TNF or the major histocompatibility complex are thought to play a major role in the outcome of infection.28 The parasite itself can affect the macrophage and dendritic cell responses. Specific gene loci such as the A2 gene can code for products which promote L donovani infectivity.11 Thus the interplay between the host-determined delayed-type hypersensitivity, antigen-specific T-cell reactivity, and cytokine secretion, and the type and virulence of the particular infecting Leishmania species determine what type of disease expression develops in the host.
Some cases are believed to harbour Leishmania organisms for indefinite periods before the disease is expressed, suggesting latent infection.29 Parasites have also been detected in lymph nodes after clinical cure.30 This is probably the basis of recrudescence of leishmaniasis which can occur decades after the initial infection, if cell-mediated immunity becomes disturbed. It is thought that “sterile” immunity—that is, complete eradication of the organism, probably rarely develops in visceral infection.
Diagnosis in visceral leishmaniasis is usually based on microscopic detection of amastigotes in smears of tissue aspirates or biopsy samples. Bone marrow aspirates or biopsy are frequently the tissues of choice with sensitivities in the 55–97% range (fig 1). Lymph node aspirate smears (sensitivity 60%) or biopsy, and splenic aspirates (sensitivity >97%)11 may also be taken for diagnosis, though the latter may give rise to life-threatening haemorrhage (table 4).
Sometimes the parasite can be cultured from microscopy negative tissue samples on special media like Novy, McNeal, Nicolle (NNN) medium or inoculated into animals such as hamsters.
Leishmania antibody (direct agglutination test) may be detected with a sensitivity of 72% and a specificity of 94%.10 Some cross-reactions in leprosy, Chagas disease, malaria, and schistosomiasis may occur. In HIV, antibodies to Leishmania may become undetectable.
Immunochromatographic strip testing of blood from a finger prick for leishmanial anti-K39 antibody has been used successfully in field serodiagnosis31 with a sensitivity of 90–100% in symptomatic patients. This test is useful in clinical management in resource-poor areas.1
Leishmania DNA can also be detected in tissue aspirates and peripheral blood by polymerase chain reaction (PCR), with some series giving a sensitivity of 70–93% in peripheral blood.10 High sensitivities down to the level of one parasite have been recorded.32 Newer methods with high sensitivity and specificity include the detection of Leishmania antigen and antibody in the urine.33,34
Diagnosis is usually based on microscopic examination of skin scrapings or biopsy specimens, usually taken from the edge of lesions. This is rapid and low-cost, but has limited sensitivity, especially in chronic lesions.35
Cultures of the lesions, while more sensitive, may become contaminated by bacterial and fungal elements in the biopsy specimen itself. Also, different species have different growth requirements. Leishmania species may be identified using isoenzyme electrophoresis, but this is lengthy and expensive and necessitates cultivation of parasites on a large scale. Monoclonal antibodies can also be used for identification of species in cultured strains, but direct analysis of clinical specimens is better achieved by using PCR, which is rapid, with high specificity and sensitivity. Detection and genetic characterisation of Leishmania can also be accomplished simultaneously.35. One study on American cutaneous leishmaniasis yielded a PCR sensitivity rate of 100%.36
Antibody detection is poorly sensitive due to a lack of significant antibody production in cutaneous leishmaniasis. Moreover, in American cutaneous leishmaniasis there have been reports of cross-reactivity of leishmanial antigens with antibodies induced by other kinetoplastids such as Trypanosoma cruzi.37
Other available means of diagnosing cutaneous leishmaniasis include the Montenegro (leishmanin) skin test which detects specific cutaneous delayed-type hypersensitivity. It involves intradermal injection of Leishmania antigen, for example L Mexicana, and monitoring for a local reaction.38 Limitations of this test include its inability to distinguish between current and past infection, as well as reports of false positivity in other skin infections.39
Recommended treatment regimens are summarised in table 5.
Treatment is largely based on pentavalent antimonials. Increasing resistance to antimonials is a major problem, and this is most evident in North Bihar, India, where the failure rate for this treatment is more than 50%.11,40 Pentavalent antimony (Sb(V)) can take the form of sodium stibogluconate (Sb(V) 100 mg/ml) or meglumine antimonate (Sb(V) 85 mg/ml). These can be given intravenously or intramuscularly with equal efficacy. It is usually administered at a dose of Sb(V) 20 mg/kg for 28 days, depending on the species and the clinical syndrome. A recent randomised trial in US military personnel showed a shorter, 10-day course to be equally effective.41 A maximum dose of 850 mg daily has been recommended42 in order to minimise side effects such as arrhythmias. Some experts, however, feel that this might predispose to resistance, and advocate higher doses. In some resistant cases of both visceral leishmaniasis and cutaneous leishmaniasis, IFN-gamma has been added successfully to Sb(V) to induce remission.43
Amphotericin B is an effective treatment used in Sb(V)-resistant cases. It is toxic and needs to be given for a prolonged period on an inpatient basis. The alternative is to use the liposomal form, which is highly effective and less toxic, although up to now prohibitively expensive. The trend in Southern Europe is shifting towards using liposomal amphotericin B as first-line treatment, even though the response rate is still around 90% for antimonials. However, a recent trend in increasing resistance to pentavalent antimonials in this area has been recorded, possibly attributed to using meglumine antimonate to treat infected dogs.44 The effectiveness of short courses of this liposomal amphotericin B is resulting in improved cost-benefits.40,45 Studies using lower doses of this agent are also showing promise to improve cost-effective treatment in resource poor areas with high antimonial resistance.46
Miltefosine is the first effective orally active drug against leishmaniasis. Studies of treatment with this drug for 3 or 4 weeks have shown a cure rate of 95–100%.47,48 It has also compared very well (cure rate of 94%) with amphotericin B (cure rate 97%) at 6 months’ follow-up. It has the added benefit of a very good safety profile.49 The potential for this drug for treatment of large numbers of patients as outpatients in resource-poor areas is high, though concerns about compliance and eventual resistance have been expressed.11
Other effective drugs have been used in treating leishmaniasis. Pentamidine can be used in treatment-resistant cases of visceral leishmaniasis.50 Its use is limited by its substantial toxicity, necessitating close inpatient monitoring.51 Paromomycin (aminosidine) has been used effectively in resistant cases in North Bihar.52 Pending commercial availability, this treatment should offer cost savings, though issues of potential toxicity such as nephrotoxicity or ototoxicity may need further evaluation.53 Sitamaquine, another oral agent, is currently being evaluated in phase II studies in India.11 This drug has been associated with a 50–67% cure rate.54,55 The imidazole and triazole drugs are not recommended for use in visceral leishmaniasis.
In PKDL, treatment is indicated only for those who have severe and prolonged disease. Pentavalent antimonials (2-month course usually sufficient) and liposomal amphotericin B are both effective.20
In deciding the best mode of treatment of cutaneous leishmaniasis, some facts need to be considered. Old World cutaneous leishmaniasis is not a life threatening disease and >90% of patients heal spontaneously within 3–18 months. The outcome of cutaneous leishmaniasis in the New World depends on the infecting species and may vary from benign to more severe manifestations. It is thus important to try to identify the infecting species, either by knowing the endemic species of the specific geographical area, or by means of diagnostic procedures. This can throw light on the prognosis and management options.
Treatment of cutaneous leishmaniasis will accelerate cure and reduce scarring. This is especially important at cosmetically important sites. Options in the treatment of cutaneous leishmaniasis include local or systemic treatment. Criteria in favour of local treatment56 include: Old World cutaneous leishmaniasis; small, single lesions; lack of risk of development of mucocutaneous leishmaniasis, lack of lymph node metastases; and L mexicana lesions. New World lesions except L mexicana, mucosal or lymph node involvement and lesions refractory to local treatment would be indications for systemic treatment.
Local treatment of cutaneous leishmaniasis
Physical modes of treatment including cryotherapy have been employed with success ranging from 77% to 100% at 4 weeks.57,58 Local infrared heat lamps have also produced good results, although invariably accompanied by skin bulla formation.59
Paromomycin (aminosidine) ointment is produced in two different formulations. When combined with methylbenzethonium chloride, it gives cure rates of 74–85%, which is more effective than when combined with urea.60 However, paromomycin-methylbenzethonium causes more severe local inflammatory reactions than paromomycin-urea.61
Intralesional infiltration of the dermis and base of the lesion with pentavalent antimony may be performed. This is a relatively painful procedure which needs to be performed regularly every 1–2 weeks for about 3–8 times. The cure rate with this procedure is about 75%.11 If this is not effective, systemic therapy should be considered.
Imiquimod, a topical immunomodulator has been successfully used in combination with meglumine antimonate in cases resistant to meglumine alone.62
Systemic treatment of cutaneous leishmaniasis
Systemic treatment with antimonials in general requires a 20-day course. L major, L tropica and L mexicana usually respond to a 10-day course.11 Pentamidine has been used as first line therapy in L guyanensis infection, but studies with L panamensis, L brasiliensis and L mexicana have also given a cure rate of 96%, comparable to 91% with meglumine antimonate.63,64
Of the imidazole/triazole drugs, oral fluconazole and has been found useful in L major infections, with a cure rate of 79%.65 Ketoconazole has been studied in L braziliensis panamensis with efficacy (74%) similar to that of stibogluconate (68%).66
Oral miltefosine has been studied in Colombia and Guatemala, with short-term cure rates of 91% in areas where L (V) panamensis is common. In areas where L (V) braziliensis and L mexicana mexicana are common, the cure rate fell to 53%.67
Liposomal amphotericin B has not been extensively studied in cutaneous leishmaniasis, but isolated reports of its use in resistant cases show its effectiveness.68,69 Similarly, systemic aminosidine has not been commonly used, and a study comparing it to antimonials for L braziliensis cutaneous leishmaniasis was not in favour of its use in this form.70
Allopurinol has shown some enhancing of antimonial activity, but its use alone has not shown any significant benefit.71
Treatment of mucocutaneous leishmaniasis with antimonials is unsatisfactory, especially in severe disease.72 Amphotericin B73 and more recently liposomal amphotericin B have been used in difficult cases with success.74 Steroids may have to be used in cases where respiratory compromise is possible.
There needs to be a high index of suspicion in patients with HIV with the typical presentations of visceral leishmaniasis such as pyrexia, pancytopenia and hepatosplenomegaly. However, splenomegaly may be absent in HIV.75 Uncommon sites of infection, such as the gastrointestinal tract or the upper respiratory tract, are more frequent. Diagnosis is reached as for non-HIV patients except that the Leishmania antibody test (direct agglutination test) is frequently (42.6%) negative.76,77 The highest prevalence of coinfection occurs in southwestern Europe, mostly in Spain.76 The main risk group is intravenous drug users and an anthroponotic cycle has been suggested where Leishmania organisms present in used syringes78 are inoculated intravenously.
The importance of cell-mediated immunity in controlling leishmaniasis in the long term is best illustrated in Leishmania–HIV coinfection. When visceral leishmaniasis occurs in a known HIV-positive patients or when someone with a history of visceral leishmaniasis acquires HIV, there is a high risk that the Leishmania infection will become intractable. Even after appropriate treatment of visceral leishmaniasis, Leishmania–HIV is associated with a high relapse rate of 52% after 1 month to 3 years.76 Visceral leishmaniasis in HIV infection is being proposed for inclusion in the Centers for Disease Control and Prevention CDC clinical category C for the definition of AIDS as an indicator disease.79
Although treatment of coinfection has not been adequately studied, pentavalent antimonials are still used widely. The relapse rate does not appear to be affected by the type of treatment given according to a head-to-head study between meglumine antimonate and amphotericin B.80 Meglumine antimonate and liposomal amphotericin have only been compared in smaller studies; no differences were found.81 One study suggested a role for oral miltefosine when the above treatments have failed in coinfected individuals.82
Secondary prophylaxis prevents relapse and improves survival.79,83 Both pentavalent antimonials administered once every 28 days84 and liposomal amphotericin B every 21 days may be used;83 no differences in efficacy have been found. Secondary prophylaxis should be continued at CD4 counts below 200/μl. It may be safe to stop secondary prophylaxis at CD4 counts above 350/μl and possibly even above 200/μl while on effective antiretroviral treatment.84 Antiretroviral treatment has been effective in decreasing relapses of visceral leishmaniasis.85
Control of leishmaniasis depends on the prevalent local epidemiological characteristics. Thus in areas where sandflies are mostly endophilic (rest mostly indoors after feeding), spraying houses with insecticide is effective in reducing the likelihood of contracting cutaneous leishmaniasis.86,87 Treated and untreated bed nets have been used effectively in environments where sandflies are endophagic (feed mainly indoors).88 In some areas where the disease is transmitted anthroponotically, nets have also been used to prevent transmission from infected patients with cutaneous leishmaniasis. Other control strategies, including insecticide impregnated curtains, and insecticide treatment of dogs and dog collars have been used with good effect.89
In Brazil, dogs are culled if they test positive for Leishmania, but this strategy has not been effective.90 In southwestern Europe, where leishmaniasis is closely linked with intravenous drug abuse and HIV, control of HIV has yielded positive results.91 Needle-exchange interventions should have similar results.
In India, where anthroponotic transmission is important, effective treatment of patients, especially those with PKDL (who may act as long-term reservoirs), has been found to be effective in controlling transmission when combined with vector control.2
There is no effective vaccine for prevention of leishmaniasis. The closest effective alternative to vaccination follows from the traditional “leishmanisation” technique adopted in the Middle East and Eastern Europe. This involved the encouragement of sandfly bites on traditionally unexposed areas of skin, such as the buttocks. The resulting lesion would heal spontaneously, in the process providing immunity against cutaneous leishmaniasis in less acceptable areas, such as the face. Early studies recommended using L tropica inoculations to induce immunity.92 This technique has been further developed in Iran, where scientists have produced standardised and stable L major populations which can produce more consistent and acceptable iatrogenically-induced lesions.89
The safety and efficacy of live-attenuated and killed vaccines has been debated and shifts in favour of development some of these has been recorded in recent years. Killed vaccines were favoured in the 1990s because of safety problems with live-attenuated vaccines; however, recent advances in manipulation of the Leishmania genome may make development of a live attenuated vaccine more feasible.93
Work on recombinant DNA derived antigen vaccines and protein or peptide-based vaccines is a more recent approach, made possible by the Leishmania Genome Project (www.sanger.ac.uk/Projects/L_major/). The realisation that CD8 cells are as important as CD4 cells in inducing resistance94 and maintaining immunity has led to a shift in vaccine research.95 Most vaccine research is targeted against cutaneous leishmaniasis; any effectiveness against visceral leishmaniasis is uncertain. Work on a vaccine against human visceral leishmaniasis has been less successful,96 but should be boosted following success with a cutaneous leishmaniasis vaccine. Work on a canine visceral leishmaniasis vaccine seems to be more advanced.97
Leishmaniasis remains a problematic infection requiring either potentially toxic treatments or less toxic, but expensive drugs. However, the availability of newer oral agents may change the way this disease is managed. Relapse may occur, especially in situations where immunosuppression is present; secondary prophylaxis needs to be given in this setting. The combination of Leishmania, HIV and anthroponotic transmission between injecting drug users heralds a potential for higher incidence rates in endemic countries with severe drug abuse problems. In the absence of an effective vaccine, and with extension of endemicity, possibly due to climate change, these problems may become worse.
MULTIPLE CHOICE QUESTIONS (TRUE/FALSE (T/F); ANSWERS AT END OF REFERENCES)
Leishmania is endemic in Australasia
Leishmania can be transmiited through infected syringes
The epidemiology of Leishmania is tightly knit with the epidemiology of the sandfly
The sandfly usually bites during the day
The number of countries where Leishmania is endemic is set to increase with global warming
2. Visceral leishmaniasis
Is characterised by splenomegaly and pancytopenia
Carries a low mortality if not treated
The organism is characteristically extracellular
Fatalities are usually the result of secondary bacterial infections
Almost always responds to antimony products
An effective vaccine is available
The body’s response to infection is T-cell mediated
The disease manifestation depends on Leishmania species and host response
Immunosuppression predisposes to Leishmania infection
Leishmania organisms can remain dormant for years in the reticulo-endothelial system
Liposomal amphotericin is effective but very expensive
There are no oral medications to effectively treat Leishmania
Oral miltofisine is very effective in the treatment of kala azar
Cutaneous Leishmania can be treated both by physical and pharmacological means
Leishmania in the immunosuppressed usually necessitates secondary prophylaxis
Identification of amastigotes in tissue smears or histology are commonly used methods of diagnosis
Antibody towards K39 antigen is proving useful, especially in field diagnosis of visceral leishmaniasis
Tissue cultures are used routinely
Splenic aspirates are very sensitive and usually safe
Leishmania PCR is useless on blood samples
1. (A) F, (B) T, (C) T, (D) F, (E) T; 2. (A) T, (B) F, (C) F, (D) T, (E) F; 3. (A) F, (B) T, (C) T, (D) T, (E) T; 4. (A) T, (B) F, (C) T, (D) T, (E) T; 5. (A) T, (B) T, (C) F, (D) F, (E) F.
We are grateful to Dr Paul Cuschieri, Consultant Microbiologist St Luke’s Hospital, Malta, for his helpful comments during production of this review.
Competing interests: None.
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