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. 2021 Oct 6;210(5-6):291–304. doi: 10.1007/s00430-021-00722-5

Table 3.

Comparison of clinical and virological parameters between recipients infected with single or multiple HCMV strains

Recipients with single-strain infection (n = 9) Recipients with multiple-strain infection (n = 7) p value
Sex male, n (%) 5 (56) 4 (57) 1
Mean age (range), years 51 (24–63) 51 (19–62) 0.633
Donor/recipient HCMV serostatus, n (%) 0.358
 D + R +  4 (44) 5 (71)
 D − R +  5 (56) 2 (29)
In vivo T cell depletion, n (%) 7 (78) 6 (85) 1
aGvHD, n (%) 5 (56) 3 (42) 1
Median time to onset of aGvHD (range), days after HSCT 35 (10–66) 36 (28–47) 0.786
Fatal outcome, n (%) 3 (33) 2 (29) 1
Median time to fatal outcome (range), days after HSCT 254 (211–1445) 423 (134–711) 0.8
More than one reactivation episode, n (%) 4 (44) 1 (14) 0.308
DNAaemia detected at day 80, n (%) 5 (56) 0 (0) 0.034
Median HCMV load (range), IU/ml plasmaa 1680 (303–5790) 2010 (348–398,000) 0.374
Median viral load peak value (range), IU/ml 2550 (463–5790) 1630 (692–398,000) 0.918
Median duration of individual antigenaemia episodes (range), days after HSCT 15 (0–38) 11 (7–19) 0.202
Median duration of overall HCMV-antigenaemia (range), days 25 (0–49) 14 (9–22) 0.142
Median antigenaemia peak value (range), pp65 positive cells/400 000 leukocytes 33 (0–400) 88 (13–303) 0.837

Bold value indicates statistically significant p values of < 0.05

D donor, aGvHD acute graft-versus-host disease, HSCT haematopoietic stem cell transplantationm, R recipient

aFor all plasma samples with sequence data of the respective group