Clonally diverse CD38+ HLA-DR+ CD8+ T cells persist during fatal H7N9 disease

Nature Communications
Zhongfang WangKatherine Kedzierska

Abstract

Severe influenza A virus (IAV) infection is associated with immune dysfunction. Here, we show circulating CD8+ T-cell profiles from patients hospitalized with avian H7N9, seasonal IAV, and influenza vaccinees. Patient survival reflects an early, transient prevalence of highly activated CD38+HLA-DR+PD-1+ CD8+ T cells, whereas the prolonged persistence of this set is found in ultimately fatal cases. Single-cell T cell receptor (TCR)-αβ analyses of activated CD38+HLA-DR+CD8+ T cells show similar TCRαβ diversity but differential clonal expansion kinetics in surviving and fatal H7N9 patients. Delayed clonal expansion associated with an early dichotomy at a transcriptome level (as detected by single-cell RNAseq) is found in CD38+HLA-DR+CD8+ T cells from patients who succumbed to the disease, suggesting a divergent differentiation pathway of CD38+HLA-DR+CD8+ T cells from the outset during fatal disease. Our study proposes that effective expansion of cross-reactive influenza-specific TCRαβ clonotypes with appropriate transcriptome signatures is needed for early protection against severe influenza disease.

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Datasets Mentioned

BETA
E-MTAB-6379

Methods Mentioned

BETA
dissection
dissections
RNAseq
scRNAseq
reverse transcription PCR
PCR
Genotyping
scRNA-seq

Software Mentioned

CuffQuant
TCRdist
FastQC
Ensembl
TopHat2
pheatmap
FACS Diva
DAVID
SC3
R

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