Artículo

Purinergic signaling modulates CD4+ T cells with cytotoxic potential during Trypanosoma cruzi infection

Bergero, Gastón Icon; Mazzocco Mariotta, Yanina Luciana Icon; del Rosso, Sebastián Icon; Liu, Ruining ; Cejas Gallardo, Zoé Magalí Icon; Robson, Simon C. ; Rottenberg, Martin ; Aoki, Maria del Pilar Icon

Otros responsables

Fecha

07/2025

Editorial

American Society for Clinical Investigation

Revista

Journal of Clinical Investigation

Título del libro

Nombre del evento

Fecha del evento

Institución organizadora

ISSN

1558-8238

eISSN

ISBN

Idioma

Inglés

Tipo del evento

Clasificación temática

Resumen

Chagas disease, caused by Trypanosoma cruzi, is endemic to Latin America and is characterized by chronic inflammation ofcardiac tissues due to parasite persistence. Hypoxia within infected tissues may trigger the stabilization of HIF-1 and be linkedto ATP release. Extracellular ATP exhibits microbicidal effects but is scavenged by CD39 and CD73 ectonucleotidases, whichultimately generate adenosine (ADO), a potent immunosuppressor. Here, we comprehensively study the importance of HIF-1stabilization and the CD39/CD73/ADO axis, on CD4+ T cells with the cytotoxic phenotype, in facilitating the persistence ofT. cruzi. Myocardial infection induces prominent areas of hypoxia, which is concomitant with HIF-1α stabilization in T cells andlinked to early expansion of CD39+CD73+CD4+ T cell infiltrating population. Functional assays further demonstrate that HIF-1stabilization and CD73 activity are associated with impaired CD4+ T cell cytotoxic potential. RNA-Seq analysis reveals thatHIF-1 and purinergic signaling pathways are overrepresented in cardiac tissues of patients with end-stage Chagas disease. Thefindings highlight a major effect of purinergic signaling on CD4+ T cells with potential cytotoxic capacity in the setting ofT. cruzi infection and have translational implications for therapy.

Aprobación

Revisión

Complementado por

Referenciado por

Licencia Creative Commons

Excepto donde se indique lo contrario, la licencia de este ítem se describe como by-nc-sa