Frontiers in Cellular and Infection Microbiology · 2022 · 21 citations · 41 references
Life SciencesImmunologyMicrobiologyHost-pathogen InteractionsImmunology Of Infectious DiseasesImmunopathologyCell-mediated ImmunityCellular Immune ResponsesHost-parasite Immune InteractionsParasitic Disease PathogenesisParasitic PathogenesisT-cell Responses To ParasitesCellular Immune Response To ParasitesInfection EstablishmentLocal Immune ResponseParasite Chronic InfectionParasitic Cyst FormationT Cell-mediated Immune ResponseT-cell Immune ResponsesT-cell Mediated Immune Response
The larval stage of the tapeworm Echinococcus granulosus sensu lato ( E. granulosus s.l. ) caused a chronic infection, known as cystic echinococcosis (CE), which is a worldwide public health problem. The human secondary CE is caused by the dissemination of protoscoleces (PSCs) when fertile cysts are accidentally ruptured, followed by development of PSCs into new metacestodes. The local immune mechanisms responsible for the establishment and established phases after infection with E. granulosus s.l . are not clear. Here, we showed that T cells were involved in the formation of the immune environment in the liver in CE patients and Echinococcus granulosus sensu strict ( E. granulosus s.s. ) - infected mice, with CD4 + T cells being the dominant immune cells; this process was closely associated with cyst viability and establishment. Local T2-type responses in the liver were permissive for early infection establishment by E. granulosus s.s. between 4 and 6 weeks in the experimental model. CD4 + T-cell deficiency promoted PSC development into cysts in the liver in E. granulosus s.s. -infected mice. In addition, CD4 + T-cell-mediated cellular immune responses and IL-10-producing CD8 + T cells play a critical role in the establishment phase of secondary E. granulosus s.s. PSC infection. These data contribute to the understanding of local immune responses to CE and the design of new therapies by restoring effective immune responses and blocking evasion mechanisms during the establishment phase of infection.
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CD4+ T cells are required for secondary expansion and memory in CD8+ T lymphocytes
Edith M. Janssen, Edward E. Lemmens, Tom Wolfe et al. · Nature · 2003 · 1.6K citations