Skip to main content
. 2023 Jan 12;23(3):423–428. doi: 10.1016/j.ajt.2022.11.002

Table.

Clinical, transplant, and vaccination characteristics of solid organ transplant recipients who received tixagevimab and cilgavimab.

N 36
T+C dose, n (%)
 2 150 + 150 doses 13 (36%)
 1 300 + 300 dose 23 (64%)
Age (y), median (IQR) 60.7 (58.1, 66.1)
Transplanted organ(s), n (%)
 Kidney 20 (56%)
 Liver 3 (8%)
 Lung 5 (14%)
 Heart 4 (11%)
 Multiplea 4 (11%)
Sex, n (%)
 Male 16 (44%)
 Female 20 (56%)
Race, n (%)
 White 33 (92%)
 Other 3 (8%)
Years since transplant, median (IQR) 4.1 (1.7, 9.2)
Maintenance immunosuppression, n (%)
 Triple immunosuppressionb 19 (53%)
 Mycophenolate 30 (83%)
 Corticosteroids 23 (64%)
 Calcineurin inhibitor 30 (83%)
 mTOR inhibitors 6 (17%)
 Belatacept 1 (3%)
Number of vaccine doses prior to T+C, n (%)
 3 8 (22%)
 4 27 (75%)
 5 1 (3%)
Days from last vaccination to T+C, median (IQR) 38.5 (26, 114.5)
History of prior COVID-19c, n (%) 2 (6%)

Abbreviations: COVID-19, coronavirus disease 2019; IQR, interquartile range; mTOR, mammalian target of rapamycin inhibitor; T+C, tixagevimab and cilgavimab.

a

Includes heart-kidney (1), liver-kidney (1), and kidney-pancreas (2).

b

Defined as corticosteroids plus calcineurin or mTOR inhibitor plus antimetabolite.

c

Defined as self-reported prior to a positive COVID-19 test or baseline (pre-T+C)-positive antinucleocapsid antibody.