Microvascular inflammation and endothelial cell activation in kidney antibody mediated rejection
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Transcript of Microvascular inflammation and endothelial cell activation in kidney antibody mediated rejection
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Microvascular inflammation and endothelial cell activation in kidney antibody mediated
rejection
Michael Mengel
Department of Laboratory Medicine and Pathology University of Alberta, Edmonton, Canada
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Three Pathways to Antibody-Mediated Injury
Antibody Alone ComplementMediated
Cell Mediated (FcR)
Farkash and Colvin, Nat Rev Nephrol 8:255, 2012
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Classical complement pathway activation:Antibody + Antigen C1
C4 C4a + C4b
C4d binds covalently to local
siteHelmut Feucht Clin Exp Immunol 86:464, 1991
Mannose binding lectin/MASP1
Role of C4d in antibody-mediated rejection
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Detection of C4d is crucial for diagnosing antibody mediated rejection
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Microcirculation inflammation in AMR
CD3 CD68
HeartKidney
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Phenotype of glomerulits
CD15 – early AMR
CD68 – late AMR
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Diagnosis of AMR
Mengel M et al. Transpl Int. 2012 Jun;25(6):611-22
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Follow up of C4d positive biopsies and the development of TX-Glomerulopathy
• Significant more often associated with Transplant Glomerulopathy (53% vs. 14%)
• Significant more often associated with Transplant Capillaropathy (71% vs. 13%)
• Significantly associated with progression of Transplant Glomerulopathy in follow-up biopsy (82% vs. 27%, median after 23 months)
Regele et al.
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Pathogenesis of Capillaropathy
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Transplant-Capillaropathy
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antibody-mediated injury and microcirculation inflammation
glomerulitis glomerulopathy
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Sequential development of CHR in non-human primates
No CHR Stage I Stage II Stage III Stage IV
Days post-transplant106 182 225 352 371
Smith et al (Boston) AJT 8:1662, 2008
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C4d versus microcirculation inflammation in biopsies prior to AMR treatment (1996-2001)
Verghese et al. Clin. Transplant 2013 in press
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Gaston et al Transplant 90:68,2010
C4d-DSA-
C4d-DSA+
C4d+DSA-
C4d+DSA+
N=173
DeKAF StudyBiopsies for late graft dysfunction
Months post-bx
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unsupervised Principal Component Analysis
Banff lesionsGraft Survival
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Limited specificity of microcirculation inflammation
Fahim et al. Am J Transplant. 2007 Feb;7(2):385-93.
no rejection (n=453)
borderline (n=105)
TCMR (n=76)0
1020304050607080
14.1
45.7
68.4
% c
ases
with
cap
illar
itis
Gibson et al. Am J Transplant. 2008 Apr;8(4):819-25.
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The association of TG (D) (n=44) with antibody (A), PTCBMML (B), and C4d (C).
TG phenotype* A B C D n (%) “ABCD” + + + + 10 (27) “ABD” + + - + 12 (32)
“ACD” + - + + 2 (5)
“AD” + - - + 1 (3)
“BCD” - + + + 1 (3)
“BD” - + - + 9 (24)
“CD” - - + + 1 (3)
“D” - - - + 1 (3)
Sis et al. AJT 2007; 7: 1743-1752
73% of Tg cases show some signs of humoral rejection
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Loupy et al: Subclinical progressive microcirculation injury in presensitized patients, despite C4d negativity
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Potential causes for C4d negativity
C4d+ ABMR
C4d negative ABMR
Complement activationComplement dependent cell injuryEndothelial activationRecruitment and activation of leukocytes
Is C4d deposited in low amounts (Thus not detectable by current methods)Treatment effects?
Do HLA antibodies in a complement-independent way cause EC activation and subsequent inflammation and Fc receptor mediated graft injury?
?
?
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Three Pathways to Antibody-Mediated Injury
Antibody Alone ComplementMediated
Cell Mediated (FcR)
Farkash and Colvin, Nat Rev Nephrol 8:255, 2012
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endothelial genes are increased in AMR
Red arrows indicate genes that are known to be involved in endothelial cell activation
N ABMR TCMRGene Symbol Normalized Signal Normalized Signal Normalized Signal
VWF 1.05 115.36 6.39 738.30 3.39 419.08CAV1 1.17 206.07 5.35 857.90 2.99 494.11RHOJ 0.99 27.60 2.94 85.27 1.65 53.58MCAM 1.12 192.50 2.93 476.93 2.02 326.45CDH5 1.00 75.34 2.58 201.54 1.61 123.20SELE 1.06 23.25 2.23 55.26 1.20 28.66
PALMD 0.93 78.15 2.12 182.35 1.36 122.61PECAM1 0.93 294.26 2.00 638.35 1.60 514.29
KLF4 1.11 236.31 1.52 318.70 1.00 216.59CYYR1 1.04 162.34 1.52 238.68 1.15 182.55CD34 1.05 138.33 1.50 198.87 1.12 148.89TEK 1.04 190.45 1.47 275.89 1.04 198.66
SOX18 1.02 13.48 1.46 19.92 1.08 14.41ZNF521 0.92 37.82 1.38 55.56 0.80 33.75RASIP1 0.98 80.80 1.37 114.53 0.97 80.99HOXD4 1.02 372.75 1.33 495.27 1.02 378.73RAI14 0.95 273.72 1.21 347.63 0.87 256.99
PODXL 1.11 1489.49 1.06 1404.16 0.74 1067.37DLC1 0.95 273.83 0.98 287.39 0.74 221.40FGD5 0.88 212.06 0.97 233.58 0.71 170.90FOXF2 1.02 12.59 0.86 10.61 0.99 12.25EMCN 1.01 700.89 0.85 600.32 0.64 459.15KDR 0.94 307.06 0.77 244.78 0.60 197.55
CETP 1.04 26.61 0.72 18.27 1.06 29.67MAOB 0.97 1450.68 0.69 1031.30 0.52 795.14
Welch t testFDR 0.05
Sis et al. AJT 2009;9:2312-23
Also not in our strictdefinition of ENDAT list, but increased in ABMR:
CDH13Duffy blood groupSOX7THBDMALL
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Endothelial Cell-Associated Transcripts correlate with pathologic
features of AMR (in 173 biopsies)
Endothelial TranscriptsCorrelation coefficient p
C4d deposition .376 p<0.001Peritubular capillaritis .252 0.002
PTCBMML .266 0.004g .248 0.001
i .358 p<0.001t .135 NSv .092 NS
cg .261 0.001mm .173 0.02ci .330 p<0.001ct .286 p<0.001cv .014 NSah -.050 NS
Sis et al. AJT 2009;9:2312-23
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n=81
Inci
denc
e of
tran
spla
nt g
lom
erul
opat
hy (*
%)
No Ab n=30
Ab with no E n=21
Ab with E n=30
C4d+ Transplant GlomerulopathyC4d Negative Transplant Glomerulopathy
0102030405060
no Ab Ab with noENDAT
Ab with ENDAT
6.7%19%
43%
C4d is negative in 60% of chronic active ABMR biopsies
Sis et al. Am J Transplant. 2009 Oct;9(10):2312-23.
No Abn=30
Ab with no En=21
Ab with En=30Tr
ansp
lant
Glo
mer
ulop
athy
scor
e ( c
g, m
ean
+ 95
% C
I)
n=81
p=0.01
p=0.53
Cum
ulat
ive
Surv
ival
No No AbAbAbAb with no Ewith no EAbAb with Ewith E
Post-biopsy time (months)
p=0.001p=0.001
Ab with E
No Ab or Ab with no E
60% C4d negative
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Transcripts selectively associated with DSA:Endothelial and NK cell transcripts
Hidalgo et al. AJT 2010; 10: 1812–1822
NK
endothelial
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CD56 ABMR
CD56 TCMR
CD68 ABMR
CD68 TCMR
CD3 ABMR
CD3 TCMR
0
1
2
3A. B.
C. D.
E.
C4d+ ABMR
C4d- ABMR
TCMR
CD56+ CD68+ CD3+
Mea
n nu
mbe
r of p
ositi
ve c
ells
in
five
per
itubu
lar c
apill
arie
s
p=0.006 p=0.03 p=0.09
CD3CD68CD56
NK cells and macrophages in antibody mediated peritubular capillaritis
Hidalgo et al. AJT 2010; 10: 1812–1822
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Hirohashi and Colvin et al. Am J Transplant. 2012 Feb;12(2):313-21. Akiyoshi and Colvin at al. Human Immunology Volume 73, Issue 12 2012 1226 - 1232
Role of complement and NK cells in antibody mediated rejection
NK cell
stain
AMR AMR + anti NK
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A molecular classifier for diagnosing AMR
Sellares et al. Am J Transplant. 2013 Apr;13(4):971-83.
Classifier score correlates with:• Pathology (ptc, g, cg, I, cv, ah,
ct, ci)• Consensus amongst
pathologists• Presence of DSA• outcome
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Sellares et al. Am J Transplant. 2013 Apr;13(4):971-83.
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Dean et al. Am J Transplant 2012; 12:1551-1563
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Summary
• Donor-specific antibody acting on the allograft is associated with endothelial cell and local complement activation [ in most cases]
• DSA acting on the allograft is associated with microcirculation inflammation as the morphological correlate [notion: the antigen is expressed in the microcirculation]
• DSA acting on the allograft is associated with increased expression of inflammation (T cells, macrophages, g-interferon), endothelial, and NK cell associated transcripts as the molecular correlate
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C4d C4d30 minutes
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Objective
• To review the current knowledge of mechanisms, diagnostics and clinical management of patients with antibody-mediated rejection.
• Since the vast majority of experience in this area has been accumulated in renal transplant patients, this group of patients will be the main focus of the presentation, but relevant lessons applicable to other types of organ transplants will be discussed as well.
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Intragraft gene expression in positive crossmatch kidney allografts
Dean et al. Am J Transplant 2012; 12:1551-1563
Class – Comparisons:
• A and B: no significant differences in gene expression
• C and D: over-expression of inflammatory transcripts (T cells, macrophages, g-interferon) in XM+ biopsies
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Limited specificity of capillaritis
no rejection (n=453) borderline (n=105) TCMR (n=76)0
10
20
30
40
50
60
70
80
14.1
45.7
68.4
% c
ases
with
cap
illar
itis
Gibson et al. Am J Transplant. 2008 Apr;8(4):819-25.
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AMR and vasculopathy