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. 2023 Mar 27;7(14):3403–3415. doi: 10.1182/bloodadvances.2022009054

Table 4.

Demographic, clinical, and vaccination response data for participants grouped based on the vaccination scheme

Variable Vector based, n = 28 Only 1, n = 25 2× mRNA-based, n = 168 P value
Age (y) 53 (45; 60) 55 (48; 61) 60 (47; 69) .05
Sex .2
 Female 13 (46%) 8 (32%) 87 (52%)
 Male 15 (54%) 17 (68%) 81 (48%)
WBC 5.5 (4.5; 6.1) 5.7 (4.7; 7.1) 6.3 (4.8; 8.2) .1
Study cohort .07
 Healthy control 13 (46%) 16 (64%) 62 (37%)
 Lymphoid neoplasms 4 (14%) 1 (4%) 37 (22%)
 Myeloid neoplasms 11 (39%) 8 (32%) 69 (41%)
Prior SARS-CoV-2 infection < .001
 Yes 0 (0%) 7 (28%) 2 (1.2%)
 No 28 (100%) 18 (72%) 166 (98.8%)
Current cancer treatment .4
 Yes 11 (39%) 6 (24%) 64 (38%)
 No 17 (61%) 19 (76%) 104 (62%)
Spike-specific IgG detectable (n [%] of participants) 26 (93%) 23 (96%) 159 (95%) .9
Spike-specific CD4+ T cells detectable (n [%] of participants) 27 (96%) 15 (60%) 102 (61%) .001
Spike-specific CD8+ T cells detectable (n (%) of participants) 20 (71%) 8 (32%) 48 (29%) < .001

Vaccination success is expressed as percentage of study participants with detectable spike-specific IgG, CD4+, and CD8+ responses, respectively. WBC, white blood cell count.

Significant (<0.05) P values are highlighted in bold.

Median (Q1 and Q3); n (%).

Summarizes in-label Ad26.COV2.S (Janssen) and off-label single-shot immunization using either mRNA vaccine.

Kruskal-Wallis rank sum test; Fisher exact test.