High dimensional analysis defines multicytokine T‐cell subsets and supports a role for IL‐21 in atopic dermatitis
2021
BACKGROUND Flow cytometry is a well-accepted approach for immune profiling, however its value is restricted by the limited number of markers that can be analyzed simultaneously. Mass cytometry/CyTOFoffers broad-scale immune characterization integrating large number of parameters. While partial blood phenotyping was reported in atopic dermatitis (AD), patients' comprehensive profiling, critical for leveraging new targeted treatments, is not available. IL-21 may be involved in inflammatory skin diseases but its role in AD is not well established. METHODS We studied T-cell polarization in the blood of 20 moderate-to-severe AD and 15 controls. Using CyTOF and an unsupervised analysis we measured the frequencies and mean metal intensities of activated polar CD4+ /CD8+ T-cell subsets. Immunohistochemistry, immunofluorescence and qRT-PCR were used to analyze skin samples. RESULTS Examining24 surface, intracellular markers and transcription factors, we identified six CD4+ and five CD8+ T-cell metaclusters. A CD4+ skin homing IL-13+ monocytokineand a novel IL-13+ IL-21+ multicytokinemetaclusterswere increased in AD vs. controls (P<0.01). While IL-13 signature characterized both clusters, levels were significantly higher in the IL-21+ group. Both clusters correlated with AD severity (r=0.49, P=0.029). Manual gating corroborated these results and identified additional multicytokinesubsets in AD. Immunohistochemistry and immunofluorescence, validated by mRNA expression,displayed significantly increasedIL-21 counts and colocalization with IL-13/IL-4R in AD skin. CONCLUSION Amulticytokine signature characterizesmoderate-to-severe AD, possibly explaining partial therapeutic responses to one cytokine targeting, particularly in severe patients. Prominent IL-21 signature in blood and skinhints for a potential pathogenic role of IL-21 in AD.
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