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. 2023 Dec 10;11(12):1835. doi: 10.3390/vaccines11121835

Table 3.

Evolution of anti-RBD antibody titers in study participants.

Estimated Anti-RBD Antibody Titers (AU/mL), GMT (95% CI)
Months from 2nd Dose of the BNT162b2 Vaccine a
1.5 3 7 9 13 16 19 26
All participants 5384
(4556–6363)
4432
(3785–5165)
1325 *
(1169–1503)
1305
(1151–1479)
13,966 *
(11,962–16,906)
20,601 *
(18,039–23,528)
20,214
(17,451–23,415)
17,040
(13,938–20,832)
Age
<47 years 5869
(4811–7161)
4764
(3938–5764)
1473 *
(1245–1742)
1223
(1019–1467)
12,581 *
(10,371–15,262)
18,639
(15,457–22,476)
18,997
(15,558–23,195)
17,128
(13,328–22,013)
≥47 years 4931
(4023–6044)
4098
(3375–4975)
1153 *
(973–1367)
857
(717–1026)
15,532 *
(12,703–18,992)
22,812
(18,978–27,420)
21,534
(17,851–25,977)
16,950
(13,275–21,643)
Gender
Male 5659
(4534–7064)
4734
(3817–5873)
1485 *
(1221–1805)
1228
(998–1511)
16,068 *
(12,767–20,223)
26,695
(21,539–33,086)
22,564
(18,183–28,000)
20,656
(15,671–27,229)
Female 5232
(4334–6314)
4250
(3558–5077)
1211 *
(1040–1410)
924
(784–1089)
12,880 *
(10,783–15,385)
17,740
(15,026–20,945)
18,972
(15,865–22,687)
15,249
(12,126–19,177)
Previous SARS-CoV-2 infection b
No 4570
(3828–5455)
3632
(3076–4289)
1076
(937–1236)
853
(734–991)
14,691
(12,411–17,389)
22,600
(19,526–26,158)
22,421
(19,188–26,200)
19,907 **
(16,105–24,608)
Yes 10,658 **
(8010–14,181)
10,028 **
(7587–13,254)
2909 **
(2230–3795)
2210 **
(1664–2933)
11,312
(8382–15,265)
14,009
(10,321–19,014)
13,128
(9447–18,244)
8916
(6205–12,810)
SARS-CoV-2 infections during the study c
No 5562
(4136–7478)
4528
(3362–6100)
1080
(815–1431)
808
(596–1097)
11,851
(8308–16,903)
14,001
(9247–21,199)
10,008
(6750–14,839)
8814
(5370–14,466)
Yes 5354
(4493–6380)
4403
(3737–5188)
1348
(1177–1543)
1068
(922–1237)
14,365
(12,217–16,891)
22,013
(19,539–26,619)
22,806 **
(19,539–26,619)
19,081
(15,445–23,573)

Abbreviations: Anti-RBD: antibodies against the receptor-binding domain of the S1 subunit of the spike protein of SARS-CoV-2; AU/mL: arbitrary units per milliliter; GMT, geometric mean titer; 95% CI: 95% confidence interval. a All participants received two doses of BNT162b2. A booster dose of mRNA-1273 was administered to 248 (93%) study participants immediately after the 9-month time point; the bivalent Omicron-adapted BNT162b2 vaccine was administered to 93 (35%) study participants between the 19-month and the 26-month time points. b Fifty (17%) participants had documented SARS-CoV-2 infections either before the first dose of BNT162b2 (n = 37) or prior to the 1.5-month time point (n = 13). c SARS-CoV-2 infections occurring before the first dose of BNT162b2, prior to the 1.5-month time point, or during follow-up; 53 (20%) subjects who were naïve at the 1.5-month time point remained uninfected throughout the entire study. * Significant difference (p < 0.05) compared with the previous time point. ** Significant difference (p < 0.05) among groups at indicated time points.