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Recurrent visceral leishmaniasis relapses in HIV co-infected patients are characterized by less efficient immune responses and higher parasite load

Visceral leishmaniasis (VL) and HIV co-infection (VL/HIV) has emerged as a significant public health problem in Ethiopia, with up to 30% of patients with VL co-infected with HIV. These patients suffer from recurrent VL relapses and increased mortality. Those with a previous history of VL relapses (r...

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Detalles Bibliográficos
Autores principales: Takele, Yegnasew, Mulaw, Tadele, Adem, Emebet, Womersley, Rebecca, Kaforou, Myrsini, Franssen, Susanne Ursula, Levin, Michael, Taylor, Graham Philip, Müller, Ingrid, Cotton, James Anthony, Kropf, Pascale
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845767/
https://www.ncbi.nlm.nih.gov/pubmed/36685039
http://dx.doi.org/10.1016/j.isci.2022.105867
Descripción
Sumario:Visceral leishmaniasis (VL) and HIV co-infection (VL/HIV) has emerged as a significant public health problem in Ethiopia, with up to 30% of patients with VL co-infected with HIV. These patients suffer from recurrent VL relapses and increased mortality. Those with a previous history of VL relapses (recurrent VL/HIV) experience increased VL relapses as compared to patients with HIV presenting with their first episode of VL (primary VL/HIV). Our aim was to identify drivers that account for the higher rate of VL relapses in patients with recurrent VL/HIV (n = 28) as compared to primary VL/HIV (n = 21). Our results show that the relapse-free survival in patients with recurrent VL/HIV was shorter, that they had higher parasite load, lower weight gain, and lower recovery of all blood cell lineages. Their poorer prognosis was characterized by lower production of IFN-gamma, lower CD4(+) T cell counts, and higher expression of programmed cell death protein 1 (PD1) on T cells.