VSTM1-v2 does not drive human Th17 cell differentiation: A replication study

Publication date

2023-04

Authors

von Richthofen, Helen J
Hafkamp, Florianne M.J.
van Haperen, Anouk
de Jong, Esther C.
Meyaard, L.ORCID 0000-0003-0707-4793ISNI 000000039582950X

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Abstract

Signal inhibitory receptor on leukocytes-1 (SIRL-1) is an immune inhibitory receptor expressed on human myeloid cells. We previously showed that dendritic cell (DC)-driven Th17 cell differentiation of human naive CD4+ T cells requires presence of neutrophils, which is inhibited by SIRL-1 ligation. VSTM1-v2 is a soluble isoform of SIRL-1, which was previously proposed to function as a Th17 polarizing cytokine. Here, we investigated the effect of VSTM1-v2 on DC-driven Th17 cell development. Neutrophils induced DC-driven Th17 cell differentiation, which was not enhanced by VSTM1-v2. Similarly, we found no effect of VSTM1-v2 on cytokine-driven Th17 cell development. Thus, our results do not support a role for VSTM1-v2 in Th17 cell differentiation.

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Citation

von Richthofen, H J, Hafkamp, F M J, van Haperen, A, de Jong, E C & Meyaard, L 2023, 'VSTM1-v2 does not drive human Th17 cell differentiation : A replication study', PLoS ONE, vol. 18, no. 4, e0284404. https://doi.org/10.1371/journal.pone.0284404