Figure 1.
Inhibition of aPL prothrombotic and proinflammatory response by NAPc2. (A) Thrombus formation in mice treated with immunoglobulin (10 μg) fractions either alone or together with NAPc2; platelets are shown in red, and leukocytes are shown in green. Quantification of thrombus size in the vena cava inferior 3 hours after injection of immunoglobulin isolated from healthy controls (n = 4) or patients with COVID-19 (n = 6) and flow restriction. Mean ± standard deviation (SD), ∗∗∗∗P < .0001, t test following Shapiro-Wilk test for normal distribution. (B) MM1 cells were cultured in human serum or plasma and then stimulated for 1 hour with HL5B or HL7G (400 ng/mL each), rJGG9 or IgG (1 μg/mL each), LPS (10 ng/mL) or IgG from patients with COVID-19 (10 μg/mL). (C) Suppression of TF, TNF, GBP6 and IRF8 mRNA induction by NAPc2 (200 nM) and NAP5 (200 nM) after 1 hour of stimulation with immunoglobulin (10 μg/mL) isolated from patients with COVID-19 (n = 10), ∗P < .0001; 1-way analysis of variance (ANOVA).

Inhibition of aPL prothrombotic and proinflammatory response by NAPc2. (A) Thrombus formation in mice treated with immunoglobulin (10 μg) fractions either alone or together with NAPc2; platelets are shown in red, and leukocytes are shown in green. Quantification of thrombus size in the vena cava inferior 3 hours after injection of immunoglobulin isolated from healthy controls (n = 4) or patients with COVID-19 (n = 6) and flow restriction. Mean ± standard deviation (SD), ∗∗∗∗P < .0001, t test following Shapiro-Wilk test for normal distribution. (B) MM1 cells were cultured in human serum or plasma and then stimulated for 1 hour with HL5B or HL7G (400 ng/mL each), rJGG9 or IgG (1 μg/mL each), LPS (10 ng/mL) or IgG from patients with COVID-19 (10 μg/mL). (C) Suppression of TF, TNF, GBP6 and IRF8 mRNA induction by NAPc2 (200 nM) and NAP5 (200 nM) after 1 hour of stimulation with immunoglobulin (10 μg/mL) isolated from patients with COVID-19 (n = 10), ∗P < .0001; 1-way analysis of variance (ANOVA).

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