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. 2022 Mar 24;13:829228. doi: 10.3389/fimmu.2022.829228

Table 4.

Combined analysis of NKG2C (KLRC2) and FcγRIIIA (FCGR3A) genotypes – cohort 1 (BORTEJECT).

Number of risk genotypes
(KLRC2 wt/wt and/or FCGR3A-V/V158 or -V/F158)
Parameters Two risk genotypes One risk genotype No risk genotype P value
n=47 n=31 n=7
DSA characteristics
MFI of the immunodominant DSA, median (IQR) 3,470 (1,753–9,602) 2,239 (1,360–4,837) 1,508 (1,087–1,946) 0.071
Biopsy results a,b
Banff ABMR, n (%) 33 (70) 14 (45) 2 (29) 0.024
g+ptc scorec, median (IQR) 2 (0–4) 0 (0–2) 0 (0–1) 0.006
MMDx results
ABMR archetype, n (%) 27 (60) 13 (43) 1 (14) 0.052
ABMR score c , median (IQR) 0.43 (0.14–0.72) 0.23 (0.08–0.60) 0.11 (0.10–0.22) 0.043
NK cell burden-associated PBT (NKB), median (IQR) 1.01 (0.50–1.35) 0.61 (0.43–1.22) 0.43 (0.32–0.69) 0.074
IFN-γ-associated PBT (GRIT1), median (IQR) 0.79 (0.46–0.98) 0.57 (0.29–0.94) 0.28 (-0.10–0.44) 0.012

ABMR, antibody-mediated rejection; DSA, donor-specific antibody; g, glomerulitis; IQR, interquartile range; MFI, mean fluorescence intensity; PBT, pathogenesis-based transcripts; ptc, peritubular capillaritis.

a

Morphologic lesions were scored according to the Banff 2017 classification of renal pathology.

b Gene expression analysis was performed in 83 of the 86 study patients.

c

For 2 and 4 recipients, biopsy material was not sufficient for ptc, and g scoring, respectively.