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. 2015 Apr 14;15(8):2170–2179. doi: 10.1111/ajt.13241

Table 3.

TCRβ repertoire diversity and clinical correlation

CD4+ T cells
CD8+ T cells
Donor TCRβ repertoire >Mean <Mean Total p-value χ2-test >Mean <Mean Total p-value χ2-test
Donor type MUD 9 5 14 8 7 15
SIB 5 3 8 0.933 2 5 7 0.277
Donor age <40 5 2 7 5 2 7
>40 8 5 13 0.658 3 10 14 0.035
Patient
Survival Alive 9 7 16 8 9 17
Dead 5 1 6 0.240 2 3 5 0.781
TRM Alive 11 7 18 9 10 19
Dead 3 1 4 0.601 1 2 3 0.650
Relapse No 10 6 16 6 10 16
Yes 4 2 6 0.856 4 2 6 0.221
EBV reactivation No 12 3 15 7 8 15
Yes 2 5 7 0.020 3 4 7 0.867
CMV reactivation No 10 2 12 5 6 11
Yes 4 6 10 0.035 5 6 11 1.000
aGvHD No 4 2 6 2 4 6
Yes 10 6 16 0.856 8 8 16 0.484

Contingency table of donor CD4+ and CD8+ T cell diversity post–G-CSF mobilization in correlation with clinical parameters of the recipients. Groups were divided according to their clonotype numbers above or below the compartment mean (CD4+ mean = 2490 clonotypes; CD8+ mean = 1661 clonotypes). According to this classification, a correlation between lower donor CD4+ TCRβ diversity and virus reactivation (CMV and EBV) was significant. In addition, a significant correlation could be demonstrated between lower CD8+ TCRβ diversity and the age of the donor.

aGvHD, acute graft-versus-host disease; χ2-test, chi-squared test; TRM, transplant-related mortality.