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. 2022 Mar 25;9:826537. doi: 10.3389/fmed.2022.826537

Table 1.

Patient characteristics.

MPN-Ruxo MPN-no Ruxo p HCs
(n = 20) (n = 54) (n = 81)
Age, median (range) 71.5 (41–85) 73 (44–92) 0.669 74 (55–92)
Sex, n, male (%) 14 (70.0) 25 (46.2) 0.06 34 (42.0)
Diagnosis, n (%)
ET 3 (15.0) 29 (53.7) NA
PV 3 (15.0) 17 (31.5) NA
MF 13 (65.0) 6 (11.1) <0.001
Primary MF/secondary MF 6 (30.0)/7 (35.0) 4 (7.4)/2 (3.7)
MPN-U 1 (5.0) 2 (3.7) NA
Time from diagnosis, years, 6.7 (4.1–11.6) 5.8 (2.8–9.4) 0.642
median (IQR)
Driver mutation, n (%)
JAK2 11 (55.0) 36 (66.7) 0.41
CALR 3 (15.0) 8 (14.8) NA
MPL 2 (10.0) 0 (0) NA
Triple-negative 3 (15.0) 10 (18.5)
NA 1 (5.0)
WBC (×103/μL), median (IQR) 6.6 (3.6–9.7) 6.3 (3.8–8.6) 0.039 NA
Lymphocyte (×103/μL), median (IQR) 1.1 (0.9–1.6) 1.4 (1.1–1.9) 0.039 NA
Treatment, n (%) NA
Ruxolitinib 20 (100)
Cytoreductive therapy 34 (63.0)
No treatment 20 (37.0)
Time of exposition to NA
ruxolitinib, n (%)
<1 year 11 (55.0)
≥1 year 9 (45.0)
Dose of ruxolitinib, n (%) NA
≤20 mg 13 (65.0)
>20 mg 7 (35.0)
Interval from 2nd vaccine to 42.5 (22.5–74.5) 41.5 (27–64.75) 0.642 41 (29–55)
Ab analysis, median (IQR)
Anti-S Ab level, median (IQR) 11.35 319.5 <0.001 677
(2.06–68.17) (170.25–689.0) (362–1,191)
Seroconversion, n (%) 16 (80.0) 52 (96.3) 0.036 81 (100)
Achieving protective value, n (%) 2 (10.0) 31 (57.4) <0.001 71 (87.6)
Anti-N antibody positivity, n (%) 0 (0) 0 (0) 1 0 (0)

MPN-Ruxo, myeloproliferative neoplasms with ruxolitinib; MPN-no Ruxo, myeloproliferative neoplasms without ruxolitinib; HCs, healthy controls; ET, essential thrombocythaemia; PV, polycythaemia vera; MF, myelofibrosis; MPN-U, myeloproliferative neoplasms, unclassifiable; JAK2, Janus kinase 2; CALR, calreticulin; MPL, thrombopoietin receptor; WBC, white blood cells; IQR, interquartile range; Anti-S Ab, anti-spike-receptor binding domain antibody; Anti-N IgG, anti-nucleocapsid protein IgG, NA: not assessed.