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Infections with the protozoan parasite Toxoplasma gondii are frequent, but one of its main consequences, ocular toxoplasmosis (OT), remains poorly understood. While its clinical description has recently attracted more attention and publications, the underlying pathophysiological mechanisms are only sparsely elucidated, which is partly due to the inherent difficulties to establish relevant animal models. Furthermore, the particularities of the ocular environment explain why the abundant knowledge on systemic toxoplasmosis cannot be just transferred to the ocular situation. However, studies undertaken in mouse models have revealed a central role of interferon gamma (IFNγ) and, more surprisingly, interleukin 17 (IL17), in ocular pathology and parasite control. These studies also show the importance of the genetic background of the infective Toxoplasma strain. Indeed, infections due to exotic strains show a completely different pathophysiology, which translates in a different clinical outcome. These elements should lead to more individualized therapy. Furthermore, the recent advance in understanding the immune response during OT paved the way to new research leads, involving immune pathways poorly studied in this particular setting, such as type I and type III interferons. In any case, deeper knowledge of the mechanisms of this pathology is needed to establish new, more targeted treatment schemes.
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http://dx.doi.org/10.1371/journal.pntd.0008905 | DOI Listing |
Euro Surveill
August 2025
Centre for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.
BACKGROUND is a zoonotic protozoan capable of infecting warm-blooded animal species and humans. Although toxoplasmosis presents mostly as mild or asymptomatic infection in immunocompetent individuals, in unborn children and people with weakened immune systems, the disease can be severe with ocular, neurological or multi-systemic manifestations and even death.AIMWe aimed to collate and analyse data on seroprevalence in humans to model and compare age-dependent prevalence in geographic regions in Europe.
View Article and Find Full Text PDFVet Sci
August 2025
College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China.
is responsible for the disease toxoplasmosis and has the broadest host range among apicomplexan parasites, as it infects virtually all warm-blooded vertebrates. Toxoplasmosis is a zoonotic and emerging public health concern with considerable morbidity and mortality, especially in the developing world, affecting approximately one-third of the world's human population. Clinical presentation varies among species, and the infection establishes lifelong chronicity in hosts.
View Article and Find Full Text PDFJ Pediatric Infect Dis Soc
August 2025
Department of Biological Sciences, Dietrich School of Arts and Sciences, University of Pittsburgh, 4249 Fifth Avenue, Pittsburgh PA 15260, United States.
Toxoplasma gondii is an apicomplexan parasite with an enormous global reach, infecting over a billion people worldwide. An opportunist in humans, T. gondii causes severe disease only in a select few scenarios but is otherwise relatively benign.
View Article and Find Full Text PDFMicrobiol Spectr
August 2025
Laboratório de Biologia Estrutural, Instituto Oswaldo Cruz, Fiocruz, Rio de Janeiro, Brazil.
Unlabelled: Toxoplasmosis is caused by infection with and is one of the most prevalent food-borne parasitic disease worldwide. disseminates through the host organism and forms a latency-specific structure called bradyzoite cysts, found primarily in muscle and neuronal cells. In mice, Toxoplasma leads to sustained brain microvascular abnormalities, including capillary rarefaction, microglial activation, and blood-brain barrier (BBB) breakdown, resulting in synaptic and neuronal loss, behavioral and cognitive damages.
View Article and Find Full Text PDFAnn Med Surg (Lond)
August 2025
Department of Pediatrics and Adolescents Medicine, B.P. Koirala Institute of Health Sciences, Dharan, Sunsari, Nepal.
Introduction And Importance: Dandy-Walker syndrome (DWS) is a rare congenital posterior fossa malformation, affecting 1 in 25 000-30 000 live births. Prenatal diagnosis is possible via ultrasound and MRI. This case highlights a rare Dandy-Walker variant with bilateral optic atrophy and status epilepticus, emphasizing the need for awareness of progressive neurological and visual impairment in Dandy-Walker spectrum disorders.
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