Skip to main content
. Author manuscript; available in PMC: 2022 Sep 1.
Published in final edited form as: J Invest Dermatol. 2021 Mar 23;141(9):2208–2218.e14. doi: 10.1016/j.jid.2021.02.749

Figure 2. Vδ2+γδ T and iNKT-cells are enriched in PN patients.

Figure 2.

PBMCs from PN (n=4) and healthy subjects (n=5) (67% African American) were stimulated with PMA and Ionomycin in combination with protein transport inhibitor for 4hrs. The differentiation of T-cell subtypes was assessed by flow cytometry. a, Representative flow cytometry plots for γδ T-cells (CD3+CD4 CD8γδTCR+ cells). b, Percentage of CD3+ γδ T-cells (median ± ICR). c, Representative flow cytometry plots for Vδ1+ and Vδ2+ subsets of γδ – T cells. d, Percentage of sub-population of γδ-T cells (CD3+γδ-TCR+Vδ1+ or Vδ2+) (median ± ICR). e, Representative flow cytometry plots for iNKT-cells (CD3+CD4CD8CD56+). f, Percentage of CD3+ iNKT – cells (median ± ICR). g, Heat map representing geometric mean expression of T-cell populations from healthy and PN subjects as represented by CD4+ T helper (CD3+CD4+CD8) cells, CD8+ T cytotoxic cells (CD3+CD8+ CD4), γδ T-cells (CD3+CD4CD8 TCR+ cells), iNKT-cells (CD3+CD4CD8 CD56+). h, Representative flow cytometry plots for CD8 Naïve (CD3+CD8+CD45RA+) cells and CD8 Memory (CD3+CD8+CD45RO+) cells. i, Percentage of CD8 Naïve and CD8 Memory cells (median ± ICR). *P<0.05, healthy controls versus PN subjects, as calculated by a non-parametric Mann Whitney U-test. ns = non-significant.