Skip to main content
. 2020 Jul 5;47(4):324–328. doi: 10.1111/iji.12505

Table 1.

HLA frequencies in 80 patients with COVID‐19 previously HLA typed to support transplantation

HLA

Allele

Group

COVID‐19 population

Allele group carriage frequency (%; n = 80)

Control Group A

Allele group carriage frequency (%; n = 10,000)

Control Group A

p

Control Group A

p c

Control Group B

Allele group carriage frequency (%) (n = 308)

Control Group B

p

Control Group B

p c

HLA‐A*02 36.3 50.0 .0179 .0536 46.4
HLA‐A*26 11.3 4.0 .0049 .0198 7.5
HLA‐B*44 17.5 32.0 .0052 .0105 19.8
HLA‐C*05 8.8 21.0 .0054 .0215 15.9
HLA‐C*12 12.5 6.0 .0286 11.7
DRB1*15 40.0 28.0 .0238 25.3 .0121
DRB1*04 22.5 35.0 .0185 33.4
DRB1*11 22.5 13.0 .0185 18.8
DRB1*07 16.3 26.0 .0539 20.8
DRB1*10 6.3 1.0 .0014 .0144 4.5
DQB1*05 35.0 27.0 30.5
DQB1*06 52.5 41.0 .0402 36.0 .0010 .0523

The control frequencies are derived from Group A: (n = 10,000) deceased solid organ donors between November 1994 and December 2009 (https://nhsbtdbe.blob.core.windows.net/umbraco‐assets‐corp/2925/antigen.pdf) and Group B: a local (n = 308) wait‐listed renal patient cohort comprising the active wait list from Leeds (n = 150) and a randomly selected cohort (n = 158) from the Manchester centre. Only associations which demonstrated significance, or approached significance when compared with either control population are listed. Significance (Fisher's exact) is shown before (p) and after (p c) Bonferroni correction. Results which are not significant are represented by (−) in the table.