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April 13, 2026Cell Biochemistry and Function0 citationsOpen Access

Brain Involvement in Leishmaniasis

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CFCamila S FreitasECEduardo A. F. CoelhoMCMyron Christodoulides

Key Points

  • This review aims to investigate the neurological aspects of leishmaniasis, particularly brain involvement.
  • Review of clinical descriptions related to brain involvement in leishmaniasis.
  • Analysis of evidence from animal models, particularly canine leishmaniasis.
  • Examination of studies on the blood-brain barrier disruption and inflammatory response in affected hosts.
  • Clinical evidence indicates brain involvement in both human and canine leishmaniasis.
  • Significant findings include the disruption of the blood-brain barrier in infected hosts.
  • The inflammatory response related to cerebral Leishmania infection is explored extensively.

Abstract

ABSTRACT Leishmaniasis is a neglected tropical disease caused by infection with the protozoan parasite Leishmania and it is a significant global health problem. The disease has a wide clinical spectrum, from tegumentary leishmaniasis (TL) that encompasses cutaneous (CL), mucosal (ML) and cutaneous‐diffuse (CDL) forms, to the potentially fatal systemic visceral leishmaniasis (VL). Neurological manifestations are not generally considered as classical clinical signs or symptoms of leishmaniasis, but in this review, we present evidence that this is a false assumption. We examine brain involvement in human and canine leishmaniasis and the contribution of animal models for studying cerebral Leishmania infection. Clinical descriptions of brain involvement are presented, and evidence of Leishmania invasion of the central nervous system. Notably, evidence for brain involvement comes from considerable studies in the dog and covers aspects of disruption of the blood‐brain and blood‐cerebrospinal fluid barriers and the nature of the inflammatory response.

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Cite This Study

Freitas et al. (2026) studied this question.

synapsesocial.com/papers/69dc88583afacbeac03ea328https://doi.org/10.1002/cbf.70209
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