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. 2022 Apr 29;13:895209. doi: 10.3389/fimmu.2022.895209

Table 1.

Main baseline demographic, clinical and laboratory data of the patients included in the study.

Variable CVID phenotype (n = 28) BCD (n = 24) Control (n = 14) p-value
Demographics
 Age, yr; median (IQR) 50 (41−68.5) 51 (46−56) 50.5 (30−65) 0.701
 Sex (Male); n (%) 14 (50.0) 11 (45.8) 8 (57.1) 0.800
Biochemical determinations
 Albumin, g/L; median (IQR) 45.3 (42.5−47.5) 46.9 (44.0−47.6) 46.0 (46.0−48.0) 0.279
 Creatinine, μmol/L; median (IQR) 71 (58−82.5) 58.5 (52−71.5) 70.5 (64−85) 0.094
 C-reactive protein, mg/L; median (IQR) 2.43 (1.12−3.93) 1.31 (0.80−2.77) 0.71 (0.60−4.00) 0.075
Haematological determinations
 Leucocytes, x109 cells/L; median (IQR) 6.09 (4.34−8.24) 6.56 (5.64−8.04) 6.60 (5.92−8.10) 0.733
 Neutrophils, x109 cells/L; median (IQR) 3.65 (2.79−5.07) 4.37 (3.48−5.23) 3.83 (3.08−5.38) 0.498
 Lymphocytes, x109 cells/L; median (IQR) 1.43 (1.03−2.39) 1.46 (1.11−1.78) 1.85 (1.64−2.12) 0.055
Immunological determinations
 Immunoglobulin G, mg/L; median (IQR) 8116 (6548−10146) 7836 (6759−9019) 11545 (10300−12315) <0.001
 Immunoglobulin M, mg/L; median (IQR) 207 (52.5−436) 609 (291−781) 921 (554−1383) <0.001
 Immunoglobulin A, mg/L; median (IQR) 50 (50−725) 1639 (1432−2503) 2204 (1882−2634) <0.001
 CD3+, x106/L; median (IQR) 1063 (837−1837) 1208 (940−1474) 1413 (1184−1648) 0.273
 CD3+, %; median (IQR) 81.0 (76.5−86.0) 87.5 (77.5−91.0) 81.0 (76.5−86.0) 0.012
 CD3+CD4+, x106/L; median (IQR) 602 (408−971) 778 (672−1133) 942 (785−1102) 0.012
 CD3+CD4+, %; median (IQR) 42.0 (32.5−48.0) 58.5 (49.5−65.0) 51.0 (47.0−54.0) <0.001
 CD3+CD4+, < 200x106/L; n (%) 1 (3.6) 0 (0.0) 0 (0.0) 0.507
 CD3+CD4+CD45RA, < 10%; n (%) 14 (50.0) 2 (7.1) 3 (21.4) 0.004
 CD3+CD8+; x106/L, median (IQR) 411 (267−782) 281 (202−537) 436 (354−479) 0.266
 CD3+CD8+; %, median (IQR) 31.0 (19.5−48.0) 23.0 (14.0−31.5) 21.5 (17.0−26.0) 0.034
 (CD3+CD4+)/(CD3+CD8+) 1; median (IQR) 1.41 (0.73−2.46) 2.83 (1.49−4.11) 2.33 (1.94−2.79) 0.007
 NK (CD3-CD16+CD56+), x106/L; median (IQR) 118 (68.5−184) 217 (102−295) 203 (171−251) 0.017
 NK (CD3-CD16+CD56+), %; median (IQR) 6.0 (4.0−14.0) 10.5 (7.0−22.0) 10.5 (8.0−13.0) 0.027
 CD19+, x106/L; median (IQR) 123 (40.5−215) 0 (0−0) 237 (195−262) <0.001
 CD19+, ≤ 1%; n (%) 5 (17.9) 24 (100.0) 0 (0.0) <0.001
 Switched memory B cells (CD19+CD27+IgD-IgM-), ≤ 2%; n (%) 15 (53.6) 24 (100.0) 0 (0.0) <0.001
 Transitional B cells (CD19+CD24hiCD27-CD38hi), < 9%; n (%) 25 (89.3) 24 (100.0) 0 (0.0) 0.272
 Activated B cells (CD19+CD21loCD38lo), > 10%; n (%) 1 (3.6) 0 (0.0) 1 (7.1) 0.458
 Absent haemagglutinins; n (%) 8 (29.6) 5 (21.7) 0 (0.0) 0.097
 Salmonella Typhi M vaccine, deficient response; n (%) 25 (89.3) 18 (94.7) 0 (0.0) <0.001
 Complement C3, mg/L; median (IQR) 1225 (1070−1335) 1210 (1020−1415) 1165 (1090−1320) 0.963
 Complement C4, mg/L; median (IQR) 257 (213−352) 260 (223−286) 230 (164−260) 0.152
 Complement B, mg/L; median (IQR) 365 (316−424) 331 (300−423) 347 (274−377) 0.531
SARS-CoV-2 tests
 IgG anti-S, BAU/mL; median (IQR) 0.0 (0.0−1.40) 0.0 (0.0−0.0) 0.0 (0.0−0.0) 0.025
 (IgG+IgA+IgM) anti-N, BAU/mL; median (IQR) 0.079 (0.071−1.22) 0.073 (0.069−0.075) 0.081 (0.074−0.088) 0.871
 IGRA, U/mL; median (IQR) 5.45 (0.00−13.5) 0.53 (0.00−12.1) 2.00 (0.00−41.1) 0.893
Treatments
 Immunoglobulin Replacement Therapy, yes; n (%) 23 (82.1) n.a. n.a. n.a.
 Rituximab, yes; n (%) n.a. 7 (29.2) n.a. n.a.
 Ocrelizumab, yes; n (%) n.a. 17 (70.8) n.a. n.a.
Vaccines
 BNT162b2; n (%) 3 (10.7) 0 (0) 1 (7.1) 0.192
 mRNA-1273; n (%) 24 (85.7) 23 (95.8) 13 (92.9) 0.725
 ChAdOx1 nCoV-19; n (%) 1 (3.6) 1 (4.2) 0 (0) 0.325
 Ad26.COV2.S; n (%) 0 (0) 0 (0) 0 (0) n.a.
Others
 Number of days between the antiCD20 therapy and the first vaccine administration; median (IQR) n.a. 118 (96−139) n.a. n.a.
 Number of days between the vaccine second dose and blood extraction for analysis; median (IQR) 28 (28−34) 29 (28−34) 33 (30−40) 0.235

IQR, interquartile range; n.a, not applicable; BCD, B-cell depleted; CVID, common variable immunodeficiency.

Significant p-values are in bold.