Assessing the Response of Human NK Cell Subsets to Infection by Clinically Isolated Virus Strains
- PMID: 35344177
- DOI: 10.1007/978-1-0716-2160-8_15
Assessing the Response of Human NK Cell Subsets to Infection by Clinically Isolated Virus Strains
Abstract
Natural killer (NK) cells play a critical role in defending against virus infections.Investigating human NK cell antiviral functions is of prime importance; however, there are challenges such as the human-specific nature of many viruses and differences in NK cell surface markers between humans and rodents. Research on the antivirus response of human NK cells must therefore be carefully planned around species tropism of the viruses of interest and the specific biological questions to be answered. The initial site of many virus infections is a mucosal/epithelial surface. In this context, a clinical virus infection at the ocular surface enables direct analyses on the mechanisms and consequences of infection and immune reactions in situ over the course of disease. For example, the site of infection of a clinical infection in the conjunctiva and cornea can be directly observed in real-time, utilizing split-lamp microscopy, and specimens are readily accessed with minimally invasive techniques.In this chapter, we describe protocols for investigating NK cell responses using clinically isolated viruses in co-culture assays. We also describe procedures for ex vivo analysis of conjunctiva-derived NK cells in adenovirus infection.
Keywords: Antivirus NK cell response; Clinical virus isolates; Human adenovirus infection; Killer cell immunoglobulin-like receptors; Mucosal NK cells; Mucosal immunity in situ; NK cell subsets; Ocular surface.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.
References
-
- Hammer Q, Ruckert T, Romagnani C (2018) Natural killer cell specificity for viral infections. Nat Immunol 19:800–808. https://doi.org/10.1038/s41590-018-0163-6 - DOI - PubMed
-
- Rothenburg S, Brennan G (2020) Species-specific host-virus interactions: implications for viral host range and virulence. Trends Microbiol 28:46–56. https://doi.org/10.1016/j.tim.2019.08.007 - DOI - PubMed
-
- Karre K, Ljunggren HG, Piontek G, Kiessling R (1986) Selective rejection of H-2-deficient lymphoma variants suggests alternative immune defence strategy. Nature 319:675–678. https://doi.org/10.1038/319675a0 - DOI - PubMed
-
- Anfossi N, Andre P, Guia S, Falk CS, Roetynck S, Stewart CA, Breso V, Frassati C, Reviron D, Middleton D, Romagne F, Ugolini S, Vivier E (2006) Human NK cell education by inhibitory receptors for MHC class I. Immunity 25:331–342 - DOI
-
- Kim S, Poursine-Laurent J, Truscott SM, Lybarger L, Song YJ, Yang L, French AR, Sunwoo JB, Lemieux S, Hansen TH, Yokoyama WM (2005) Licensing of natural killer cells by host major histocompatibility complex class I molecules. Nature 436:709–713. https://doi.org/10.1038/nature03847 . [pii] nature03847 - DOI - PubMed
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