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. Author manuscript; available in PMC: 2018 Feb 1.
Published in final edited form as: J Allergy Clin Immunol. 2016 Jun 16;139(2):628–633.e10. doi: 10.1016/j.jaci.2016.04.049

Appendix Table 1.

aGVHD in TME(+) patients compared to aGVHD in TME(−) patients, restricted to subsets of (a) all patients, (b) patients with no history of pre-transplant GVHD, (c) patients receiving transplants from maternal donors, (d) patients receiving T cell depleted transplants, (e) patients receiving cytotoxic chemotherapy, (f) patients receiving serotherapy, (g) patients for whom TME was determined by STR method, (h) patients receiving transplants from non-maternal donors.

a
All Patients N (%) TME+
N (%)
TME−
N(%)
RR (95%CI) p
74 35 39
aGVHD I–IV 27 (36.5) 20 (57.1) 7 (17.9) 3.2 (1.5–6.6) 0.0006
aGVHD II–IV 21 (28.4) 15 (42.9) 6 (15.4) 2.8 (1.2–6.4) 0.011
aGVHD III–IV 7 (9.5) 5 (14.3) 2 (5.1) 2.8 (0.58–13) 0.24
cGVHD (N=35, 37)^ 6 (8.1) 4 (11.4) 2 (5.4) 2.1 (0.41–11) 0.42
b
No Pre-Transplant
GVHD
N (%) TME+
N (%)
TME−
N(%)
RR p
66 27 39
aGVHD I–IV 24 (36.4) 16 (59.3) 8 (20.5) 2.9 (1.4–5.8) 0.0018
aGVHD II–IV 19 (28.8) 13 (48.1) 6 (15.4) 3.1 (1.4–7.2) 0.0057
aGVHD III–IV 6 (9.1) 4 (14.8) 2(5.1) 2.9 (0.57–15) 0.22
cGVHD (N=27, 37)^ 5 (7.6) 3 (11.1) 2 (5.4) 2.1 (0.37–11) 0.64
c
Maternal Donors N (%) TME+
N (%)
TME−
N(%)
RR p
44 29 15
aGVHD I–IV 22 (50.0) 19(65.5) 3(20.0) 3.8 (1.2–9.3) 0.0097
aGVHD II–IV 17(38.6) 14(48.3) 3 (20.0) 2.4 (0.82–7.1) 0.10
aGVHD III–IV 5 (11.4) 5 (17.2) 0 (0) 7.0 (0.36–135) 0.15
cGVHD (N=29, 14)^ 4 (9.1) 3 (10.3) 1 (7.1) 1.4 (0.17–13) 0.74
d
TCD N (%) TME+
N (%)
TME−
N(%)
RR p
50 30 20
aGVHD I–IV 25 (50.0) 20 (66.6) 5 (25.0) 2.7 (1.2–5.9) 0.009
aGVHD II–IV 19 (38.0) 15 (50) 4 (20.0) 2.5 (0.97–6.4) 0.04
aGVHD III–IV 6 (12.0) 5 (16.6) 1 (5.0) 3.3 (0.42–28) 0.38
cGVHD (N=30, 18)^ 5 (10.0) 4 (13.3) 1 (5.6) 2.7 (0.32–22) 0.64
e
Cytotoxic Conditioning N (%) TME+
N (%)
TME−
N(%)
RR p
23 7 16
aGVHD I–IV 8 (34.8) 5 (71.4) 3 (18.8) 3.8 (1.2–12) 0.026
aGVHD II–IV 5 (21.7) 3 (42.9) 2 (12.5) 3.4 (0.73–16) 0.14
aGVHD III–IV 2 (8.7) 2 (28.6) 0 (0) NA NA
cGVHD (N=7, 15)^ 2 (9.1) 1 (14.3) 1 (6.7) 2.1 (0.16–30) 1.0
f
Serotherapy
Conditioning
N (%) TME+
N (%)
TME−
N(%)
RR p
31 10 21
aGVHD I–IV 7 (22.6) 3 (30.0) 4 (19.0) 1.6 (0.43–5.7) 0.65
aGVHD II–IV 4 (12.9) 2 (20.0) 2 (9.5) 2.1 (0.34–13) 0.58
aGVHD III–IV 1 (3.2) 1 (10.0) 0 (0) NA 0.32
cGVHD (N=10, 20)^ 3 (9.7) 1 (10.0) 2 (10.5) 1.0 (0.08 – 13) 1.0
g
STR Analysis N (%) TME+
N (%)
TME−
N(%)
RR p
38 19 19
aGVHD I–IV 17 (44.8) 14 (73.7) 3 (15.8) 4.7 (1.6 – 14) 0.0008
aGVHD II–IV 11 (28.9) 9 (47.4) 2 (10.5) 4.5 (1.1–18) 0.03
aGVHD III–IV 5 (13.2) 4 (21.1) 1 (5.3) 4.0 (0.49–33) 0.34
cGVHD (N=19, 17)^ 4 (11.1) 2 (10.5) 2 (11.8) 0.89 (0.14 –
5.7)
1.0
h
Non-Maternal Donors N (%) TME+
N (%)
TME−
N(%)
RR p
30 6 24
aGVHD I–IV 6 (20) 1 (16.7) 5 (20.1) 0.8 (0.11–5.6) 0.82
aGVHD II–IV 4 (13.3) 1 (16.7) 3 (12.5) 1.3 (0.17–10.7) 0.79
aGVHD III–IV 2 (6.7) 0 (0) 2 (8.3) 0.7 (0.04 – 13) 0.82
cGVHD (N=6, 23)^ 2 (6.9) 1 (16.7) 1 (4.3) 4.6 (0.34–62) 0.25
^

cGVHD outcome was restricted to evaluable patients surviving >100 days post-HSCT.