Abstract

CD8 T cell memory offers critical antiviral protection, even in the absence of neutralizing antibodies. The paradigm is that CD8 T cell memory within the lung tissue consists of a mix of circulating TEM cells and non-circulating TRM cells. However, based on our analysis, the heterogeneity within the tissue is much higher, identifying TCM, TEM, TRM, and a multitude of populations which do not perfectly fit these classifications. Further interrogation of the populations shows that TRM cells that express CD49a, both with and without CD103, have increased and diverse effector potential compared with CD49a negative populations. These populations function as a one-man band, displaying antiviral activity, chemokine production, release of GM-CSF, and the ability to kill specific targets in vitro with delayed kinetics compared with effector CD8 T cells. Together, this study establishes that CD49a defines multiple polyfunctional CD8 memory subsets after clearance of influenza infection, which act to eliminate virus in the absence of direct killing, recruit and mature innate immune cells, and destroy infected cells if the virus persists.

Highlights

  • CD8 T cell memory is critical for host protection from previously encountered and related pathogens [1, 2]

  • The cells were stained for classical effector and memory surface markers, allowing for the discrimination of TEFF (CD44posCD62LnegKLRG1pos), TCM (CD44posCD62Lpos), TEM (CD44posCD62LnegKLRG1negCCR7negCX3CR1pos/neg), and TRM (CD44posCD69posCD49aposCD103pos) [2, 5, 8, 32, 33]

  • Since CD69 did not appear to be the defining feature of lung TRM, we focused on further subsetting the memory CD8 T cells based on CD49a and CD103 expression

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Summary

Introduction

CD8 T cell memory is critical for host protection from previously encountered and related pathogens [1, 2]. TRM are heralded for their ability to rapidly respond upon instances of reinfection, limiting disease severity and improving survival [2, 6,7,8] They are predominantly observed at epithelial barrier surfaces of non-lymphoid tissues, maintained in close proximity to the cells often targeted by viruses [2, 8]. This memory population has been described in many organs including, but not limited to skin, intestines, lung, female reproductive tract, salivary glands, and tonsils [9,10,11,12,13,14].

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