| Literature DB >> 35544009 |
Magali M Moretto1, Imtiaz A Khan2.
Abstract
Microsporidia are a group of pathogens, which can pose severe risks to the immunocompromised population, such as HIV-infected individuals or organ transplant recipients. Adaptive immunity has been reported to be critical for protection, and mice depleted of T cells are unable to control these infections. In a mouse model of infection, CD8 T cells have been found to be the primary effector cells and are responsible for protecting the infected host. Also, as infection is acquired via a peroral route, CD8 T cells in the gut compartment act as a first line of defense against these pathogens. Thus, generation of a robust CD8 T-cell response exhibiting polyfunctional ability is critical for host survival. In this chapter, we describe the effector CD8 T cells generated during microsporidia infection and the factors that may be essential for generating protective immunity against these understudied but significant pathogens. Overall, this chapter will highlight the necessity for a better understanding of the development of CD8 T-cell responses in gut-associated lymphoid tissue (GALT) and provide some insights into therapies that may be used to restore defective CD8 T-cell functionality in an immunocompromised situation.Entities:
Keywords: CD4 T cells; CD8 T cells; Cell-mediated immunity; IFNγ; IL12; IL21; Innate immunity; Microsporidia; γδ T cells
Mesh:
Year: 2022 PMID: 35544009 DOI: 10.1007/978-3-030-93306-7_13
Source DB: PubMed Journal: Exp Suppl ISSN: 1664-431X