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a) cg = allograft glomerulopathy, b) ci = interstitial fibrosis, c) ct = tubular atrophy, d) cv = vascular fibrous intimal thickening. There were no significant differences between groups according to Likelihood Ratio Chi- Quadrat test.

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Membagikan "a) cg = allograft glomerulopathy, b) ci = interstitial fibrosis, c) ct = tubular atrophy, d) cv = vascular fibrous intimal thickening. There were no significant differences between groups according to Likelihood Ratio Chi- Quadrat test."

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(1)

Figure S1:

Banff components of chronic lesions in the last biopsy before rituximab in the R and NR cohorts:

a) cg = allograft glomerulopathy, b) ci = interstitial fibrosis, c) ct = tubular atrophy, d) cv = vascular fibrous intimal thickening. There were no significant differences between groups according to Likelihood Ratio Chi- Quadrat test.

a + b

c + d

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Table S1: Individual clinical charts of all patients included in the study;

Abbreviations: autosomal dominant polycystic kidney disease (ADPKD), diabetic nephropathy (diabetic NP), focal and segmental glomerulosclerosis (FSGS), glomerulonephritis (GN), membranoproliferative glomerulonephritis (MPGN), calcineurin inhibitor toxicity (CNI-Tox), reflux nephropathy (Reflux-NP), rapidly progressive glomerulonephritis (RPGN), B=basiliximab, T=tacrolimus, M=mycophenolate mofetil, St=steroids; PS=plasmapheresis (3-4 per patient).

Patient Sex (m) (f)

Age (yr)

Tx Age (months) / Living (l) / Deceased (d) donor / regraft (r)

Renal disease

eGFR / diuresis at

rituximab (ml/min / ml)

Concomitant Findings in the

index biopsy

Maximal proteinuria

(mg/24 h)

Initial immuno- suppression

(IS) at tx

Non responders

1 f 49 4.3 / d Reflux-

nephropathia 28 / 2500 Borderline 380 B, T, M, St, PS

2 f 31 0.3 / d / r Pyelonephritis 13 / 1000 1040 B, T, M, St

3 m 34 6.1 / d Nephro-

nophthisis 12 / 3500 380 B, C, M, St

4 m 29 8.1/ d Chronic GN 28 / 2000 Membranous GN 4.400 B, C, M, St

5 m 18 47.4 / l Unknown 22 / 2000 2310 B, C, M, St

6 f 36 38.2 / d

Mesangio- proliferative GN

17 / 1450 4600 B, T, M, St

7 m 38 5.7/ d

MPGN, CNI- toxicity after heart

transplantation

26 / 1040 Borderline 100 B, T, M, St

8 f 31 187.9 / d RPGN 14 / 1500 9000 B, T, St

9 m 35 1.4/ d / r Pyelonephritis 24 / 600 TCMR 2a 1300 B, T, M, St

10 m 42 28.5 / l Diabetic NP 19 / 2500 4100 B, T, M, St

Responders

11 f 22 57.8 / l Reflux-

nephropathia 27 / 2000 790 B, C, M, St

12 f 48 52.3 / d ADPKD 41 / 2500 180 B, C, M, St

13 m 39 7.1 / d Diabetic NP 39 / 2400 TCMR 2 a 100 B, T, M, St

14 f 41 63.0 / d FSGS 17 / 1810 TCMR 1a 150 B, C, St

15 m 32 62.0 / d Unknown 43 / 3500 1230 B, C, M, St

16 f 48 5.2/ d Chronic GN 27 / 2500

Thrombotic microangiopathy, borderline

1400 B, T, M, St

17 f 40 2.2/ d / r Nephro-

nophthisis 32 / 2300 210 B, T, M, St;

ATG and IVIG

18 m 26 74.8 / l / r IgA-GN 33 / 2100 borderline 1800 T, M, St

19 m 53 144.8 / l / r Chronic GN 62 / 3100 190 B, C, M, St

20 m 45 243.3 / d Diabetic NP 25 / 3100 760 B, C, M, St

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Table S2: Detailed features of AMR in biopsies of patients receiving treatment and HLA DSAs with antigen specificities

Abbreviations: I = indication, R = routine, neg = negative, pos = positive; n. a. = not applicable.

Patient I or R biopsy

g score

Ptc score

C4d PTC score

De novo DSA

Cg score

Antigen- specificity of

DSA

DSA detectable in follow-up Non responders

1 I 1 2 1 neg 0

2 I 1 1 0 pos 0 A31, DQ3 Yes

3 R 2 1 0 neg 0

4 I 3 3 0 pos 0 A24 Yes

5 R 1 1 1 n. a. 1 n. a.

6 R 3 2 1 n. a. 3 n. a.

7 I 1 0 1 neg 1

8 R 0 0 2 pos 2 A24, DQ5 Yes

9 I 0 1 1 neg 0

10 I 2 1 0 n. a. 2 n. a.

Responders

11 I 0 2 3 neg 0

12 I 2 0 0 pos 1 DQ2 No

13 R 1 2 0 neg 0

14 I 0 2 3 n. a. 0 n. a.

15 I 0 1 0 pos 3 DQ7 No

16 R 0 2 0 pos 0 DR4 No

17 I 0 1 3 neg 0

18 I 0 2 3 pos 3 A2 Yes

19 I 2 0 1 pos 1 DQ7 Yes

20 I 3 0 0 pos 3 DQ5, DQ6 Yes

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