# Clinical, Laboratory, and Therapeutic Characteristics of Visceral Leishmaniasis with Emphasis on Immune Status: A Multicentre Cohort Study in Greece

**Authors:** Aristos Aristodimou, Achilleas Gikas, Maria Antoniou, Karolina Akinosoglou, Nikolaos Partalis, Angelos Pefanis, Periklis Panagopoulos, Charalambos Christofidis, Evangelos I. Kritsotakis

PMC · DOI: 10.3390/pathogens15020141 · Pathogens · 2026-01-28

## TL;DR

This study examines the clinical features and treatment outcomes of visceral leishmaniasis in Greece, highlighting differences in immunocompromised patients.

## Contribution

The study provides detailed clinical data on visceral leishmaniasis in Greece, emphasizing immune status as a key factor in treatment outcomes.

## Key findings

- Immunocompromised patients with visceral leishmaniasis had distinct clinical features and higher treatment failure rates.
- Liposomal amphotericin B was the primary treatment, with a 10% treatment failure rate linked to immunosuppression.
- Mortality from visceral leishmaniasis was low, with only one death directly attributed to the disease.

## Abstract

Visceral leishmaniasis (VL) is an endemic zoonotic disease in southern Europe with increasing clinical relevance among immunocompromised populations; however, detailed clinical data remain scarce. This retrospective multicentre cohort study analysed patients with confirmed VL treated at seven hospitals in Greece over a 26-year period. Clinical, treatment, and outcome data were collected with a minimum follow-up of 18 months to assess cure, treatment failure, relapse, and mortality. A total of 144 patients were enrolled (59% male; mean age 41.8 years, range 0.1–84 years), most of whom were Greek nationals (85%) and resided in rural areas (61%). Fever was the primary reason for hospital admission in 95% of patients. At diagnosis, 42 patients (29%) were immunocompromised. These patients were significantly older than immunocompetent individuals and more likely to present with diarrhoea and arthralgia, whereas hepatomegaly was less frequent. Liposomal amphotericin B was administered to 90% of patients. Treatment failure occurred in 14 patients (10%) and was significantly associated with immunosuppression and leukaemia. Relapse within 18 months occurred in 5.5% of patients. Overall mortality was relatively low (7 patients, 5%), with one death directly attributable to VL. This study demonstrates that VL remains endemic in Greece, affects patients across all age groups, and is primarily autochthonous. Immunosuppression is associated with distinct clinical features and poorer treatment outcomes in VL, underscoring the need for heightened clinical vigilance, combined diagnostic approaches, and extended follow-up in vulnerable populations.

## Linked entities

- **Diseases:** Visceral leishmaniasis (MONDO:0005445), leukaemia (MONDO:0004355)

## Full-text entities

- **Diseases:** diarrhoea (MESH:D003967), deterioration of renal function (MESH:D058186), pneumonia (MESH:D011014), pleural effusion (MESH:D010996), leukopenia (MESH:D007970), inherited or acquired immunodeficiency condition (MESH:D000163), hypogammaglobulinemia (MESH:D000361), autoimmune (MESH:D001327), cytomegalovirus (CMV) viraemia (MESH:D003586), febrile (MESH:D000071072), splenomegaly (MESH:D013163), impaired immune status (MESH:D013226), vomiting (MESH:D014839), Fever (MESH:D005334), VL (MESH:D007898), influenza (MESH:D007251), impaired immunity (MESH:D020274), HLH (MESH:D051359), respiratory tract infection (MESH:D012141), bacteraemia (MESH:C531821), injury to (MESH:D014947), Q fever (MESH:D011778), inflammatory (MESH:D007249), Pneumocystis jirovecii pneumonia (MESH:D011020), hepatosplenomegaly (MESH:C535727), weakness (MESH:D018908), pancytopenia (MESH:D010198), Klebsiella pneumoniae meningitis (MESH:D007710), Thoracic Diseases (MESH:D013896), haematological malignancies (MESH:D009369), Leishmania infection (MESH:D007896), Anaemia (MESH:D000743), leukaemia (MESH:D015458), peripheral oedema (MESH:D010523), Polyclonal hypergammaglobulinemia (MESH:D006942), non-Hodgkin lymphoma (MESH:D008228), allergic reactions (MESH:D004342), parasitic disease (MESH:D010272), bacterial infections (MESH:D001424), lymph node enlargement (MESH:D000072717), Mycobacterium avium infection (MESH:D015270), CL (MESH:D016773), HIV infection (MESH:D015658), septic shock (MESH:D012772), Salmonella typhi infection (MESH:D014435), rotavirus infection (MESH:D012400), Haematological abnormalities (MESH:D006402), neutropenia (MESH:D009503), malnutrition (MESH:D044342), impaired cellular immunity (MESH:D007153), death (MESH:D003643), hepatomegaly (MESH:D006529), organomegaly (MESH:D016878), arthralgia (MESH:D018771), urinary tract infection (MESH:D014552), weight loss (MESH:D015431), tropical diseases (MESH:D015493), acute myeloid leukaemia (MESH:D054218), infection (MESH:D007239), chronic kidney failure (MESH:D007676)
- **Chemicals:** L (MESH:D007930), methotrexate (MESH:D008727), azathioprine (MESH:D001379), meglumine antimonate (MESH:D000077485), prednisone (MESH:D011241), L-AMB (MESH:C068538), etoposide (MESH:D005047), AMB (MESH:D000666)
- **Species:** Human immunodeficiency virus 1 (no rank) [taxon 11676], Leishmania infantum (species) [taxon 5671], Klebsiella pneumoniae (species) [taxon 573], Canis lupus familiaris (dog, subspecies) [taxon 9615], Human immunodeficiency virus (species) [taxon 12721], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942823/full.md

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Source: https://tomesphere.com/paper/PMC12942823