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. 2022 Jun 7;76(3):e299–e307. doi: 10.1093/cid/ciac458

Table 1.

Characteristics of Study Participants at Baseline

Characteristic Participants Tested Using ELISA and sVNT Random Subset of 20 Participants Tested Using ELISA, sVNT, and PRNT
(N = 312) (N = 20)
n (%) n (%)
Female 120 (38) 9 (45)
Age (median, IQR), years 54 (47–62) 55 (47–64)
Ethnicity
ȃChinese 306 (98) 20 (100)
Obesity (for Asian populations), body mass index
ȃUnderweight (<18.5) 6 (2) 0 (0)
ȃNormal (18.5–22.9) 114 (37) 5 (25)
ȃOverweight (23.0–24.9) 84 (27) 7 (35)
ȃObese (≥25.0) 108 (35) 8 (40)
Chronic medical conditions
ȃAny 98 (32) 6 (30)
ȃLung disease, including chronic obstructive pulmonary disease and asthma 1 (0) 0 (0)
ȃHeart disease 7 (2) 0 (0)
ȃHypertension 57 (18) 5 (25)
ȃDiabetes 22 (7) 1 (5)
ȃHypercholesterolemia 42 (13) 3 (15)
ȃKidney disease 4 (1) 0 (0)
ȃLiver disease 4 (1) 1 (5)
ȃCancer 5 (2) 1 (5)
Prior COVID-19 vaccination
ȃ2-dose CoronaVac (Sinovac) 305 (98) 20 (100)
ȃ2-dose BIBP (Sinopharm) 7 (2) 0 (0)
Days between first and second dose of COVID-19 vaccination, median (IQR) 28 (28–29) 28 (28–29)
Days between second and third (study) dose of COVID-19 vaccination, median (IQR) 206 (192–217) 197 (172–208)
Smoking
ȃEver 33 (11) 5 (25)
ȃCurrent 22 (7) 3 (15)

We enrolled 315 adults who previously received 2 doses of inactivated COVID-19 vaccine and administered the BNT162b2 vaccine as a third vaccine dose. Among them, ELISA and sVNT against ancestral severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus were performed in paired day 0 and day 28 sera available from 312 vaccinated participants, and we randomly selected 20 participants and also performed PRNT against the ancestral SARS-CoV-2 virus and the Omicron variant.

Abbreviations: COVID-19, coronavirus disease 2019; ELISA, enzyme-linked immunosorbent assay; IQR, interquartile range; PRNT, plaque reduction neutralization test; sVNT, surrogate virus neutralization test.