# Case Report: Long-Term Follow-Up of Visceral Leishmaniasis and HIV Coinfected Patients Without Relapse: Lymphoproliferative Response After Stimulation with Soluble Leishmania Antigen

**Authors:** Begoña Monge-Maillo, Daniel Roger-Zapata, Fernando Dronda, Eugenia Carrillo, Javier Moreno, María Dolores Corbacho-Loarte, Diego Gayoso Cantero, Oihane Martín, Sandra Chamorro-Tojeiro, Jose A. Perez-Molina, Francesca Norman, Marta González-Sanz, Rogelio López-Vélez

PMC · DOI: 10.3390/microorganisms13030686 · 2025-03-19

## TL;DR

This case report examines long-term outcomes of three patients coinfected with visceral leishmaniasis and HIV, finding no relapses and varied immune responses.

## Contribution

The study provides long-term follow-up data on VL/HIV coinfected patients and evaluates lymphoproliferative responses as potential markers for relapse risk.

## Key findings

- No relapses were observed in three patients followed for 8 to 19 years.
- Only one patient showed specific cellular immunity against Leishmania.
- Immune response markers showed significant heterogeneity among the cases.

## Abstract

Highly active antiretroviral therapy (HAART) has reduced the incidence of VL/HIV dramatically. However, HAART only partially prevents relapses, with one-year relapse rates ranging from 30 to 60%. Consequently, secondary prophylaxis is recommended for patients with <200 CD4+ cells/μL. In clinical practice, characterizing cellular immune response could help estimate the risk of relapse in VL/HIV coinfected patients. In this study, the lymphoproliferative response after stimulation with soluble Leishmania antigen was assessed in 2022 and 2023 in three cases of VL/HIV coinfection with long-term follow-up (17, 8 and 19 years). PCR and rK-39 results for Leishmania, HIV viral load, CD4 cell count, proliferation index, IFN-γ, IL-2, IP-10, IL-10 and TNF-α were determined. Heterogeneous results were obtained, with only one patient having developed specific cellular immunity against Leishmania. No cases of relapse were observed. The heterogeneity of lymphoproliferative test results in the three cases described highlights the need to identify surrogate markers of cure to guide maintenance or withdrawal of prophylaxis.

## Linked entities

- **Proteins:** IFNG (interferon gamma), IL2 (interleukin 2), CXCL10 (C-X-C motif chemokine ligand 10), IL10 (interleukin 10), TNF (tumor necrosis factor)
- **Diseases:** visceral leishmaniasis (MONDO:0005445)

## Full-text entities

- **Genes:** IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, CXCL10 (C-X-C motif chemokine ligand 10) [NCBI Gene 3627] {aka C7, IFI10, INP10, IP-10, SCYB10, crg-2}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** HIV (MESH:D015658), Visceral Leishmaniasis (MESH:D007898), VL (MESH:C536141)
- **Species:** Leishmania (subgenus) [taxon 38568], Human immunodeficiency virus 1 (no rank) [taxon 11676], Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC11944632/full.md

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Source: https://tomesphere.com/paper/PMC11944632