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1 n increased incidence of biopsy-proven acute rejection.
2 o or in the setting of help-dependent tumour rejection.
3 contain host endothelium, a source of immune rejection.
4 ) lymph nodes and improves human cancer cell rejection.
5 n and restricted T cell activation and graft rejection.
6 ells with donor leukocytes in the absence of rejection.
7 jection does not occur in absence of mucosal rejection.
8 be explained by the signaling value of this rejection.
9 els of inflammatory arthritis and lung-graft rejection.
10 r evidence that PCs were affected throughout rejection.
11 an transplantation and preventing hyperacute rejection.
12 RNase alone could be insufficient for pollen rejection.
13 executes a key role in the evolution towards rejection.
14 antation remains profoundly limited by graft rejection.
15 2 months postweaning or at concern for acute rejection.
16 n early allograft dysfunction and consequent rejection.
17 cular for the diagnosis of antibody-mediated rejection.
18 e allogeneic response and control transplant rejection.
19 localized skin inflammation consistent with rejection.
20 rammed cell death-1 (PD-1)-related allograft rejection.
21 ients at both elevated and standard risk for rejection.
22 atients experiencing acute kidney transplant rejection.
23 ears, deciphering pathophysiology of cardiac rejection.
24 ized CD8(+) T cell response to bolster tumor rejection.
25 raft infection and the possible induction of rejection.
26 Two patients presented concomitantly CDI and rejection.
27 outcome in KTRs independent of graft loss or rejection.
28 ide effects in patients with renal allograft rejection.
29 is not sufficient for either type of pollen rejection.
30 ence of clinical or histological evidence of rejection.
31 ry and attenuates kidney and heart allograft rejection.
32 tion of corticosteroid boluses used in acute rejection.
33 ctivation had limited effects on controlling rejection.
34 DNA mutations in cancer cells lead to tumor rejection.
35 isolation and transplantation, and allograft rejection.
36 ith an antioxidant may delay immune-mediated rejection.
37 alues >=2.5 are predictive of late allograft rejection.
38 e, despite their higher rates of early acute rejection.
39 tibody responses and accelerated heart graft rejection.
40 dentify antibodies associated with allograft rejection.
41 or antibody-mediated), and 45 had a clinical rejection.
42 loss, but this was in the context of a mixed rejection.
43 raft recipients at the time of biopsy-proven rejection.
44 ipients due to a perceived increased risk of rejection.
45 ith regards to possible social acceptance or rejection.
46 ies cardiac transplant recipients at risk of rejection.
47 < 0.01), with an excess of antibody-mediated rejections.
49 of DGF (29.3% versus 29.2%, P = 0.9), acute rejection (11.2% versus 11.7%, P = 0.8), and median LOS
50 was associated with a similar rate of acute rejection (13% vs 9%, P = 0.08) but increased rate of ea
52 to evaluate the effector mechanisms driving rejection; (2) potential assays to assess the presence o
54 gnificantly increased in patients with acute rejection: 3.89 (1.36) versus 2.32 (1.82), P = 0.021.
55 dnDSAs had a higher rate of organ allograft rejection (45.4% vs 13.8%, P = .03) compared to those wi
56 18.2% prevalence) from acute and subclinical rejection (67.4%); interstitial fibrosis and tubular atr
57 relatively low incidence of T cell-mediated rejection (9.2%) and antibody-mediated rejection (AMR) (
59 onfirmed cases of clinical antibody-mediated rejection (ABMR) were present in the population, and str
61 f between immunological tolerance and embryo rejection accompanied the evolution of unique male pregn
63 n intestinal transplantation, acute cellular rejection (ACR) remains a significant challenge to achie
66 9 patients diagnosed with TCMR 1A/borderline rejection across 11 US centers with a simultaneous measu
67 ed to molecular AKI and CKD and to eGFR, not rejection activity, presumably because rejection confers
68 95% confidence interval 0.62-1.58) or acute rejection (adjusted odds ratio 0.89, 95% confidence inte
69 experienced more early rejection, more acute rejection after 90 days, and a clinically significant de
71 se corticosteroids effectively combats acute rejection after kidney transplantation, but at the cost
77 ft biopsies from 51 ITx patients with severe rejection, alongside 37 stable controls, were analyzed u
83 ti-HLA antibodies (DSA) on antibody-mediated rejection (AMR) and kidney allograft failure is well est
86 ed for desensitization and antibody-mediated rejection (AMR) treatment by targeting CD20 found on B-l
93 (AT1R) antibodies have been associated with rejection and allograft loss in solid organ transplantat
96 pe of both acute and chronic T cell-mediated rejection and antibody-mediated rejection and discuss th
97 Neutralizing Tnfa should help in avoiding rejection and associated tissue injury in the allograft
98 i-INT was predicted by prior T-cell-mediated rejection and BKVAN, human leukocyte antigen mismatch, c
100 del of T-cell-mediated human islet allograft rejection and developed a therapeutic regimen of low-dos
102 ell-mediated rejection and antibody-mediated rejection and discuss the additive value of molecular pr
105 Tacrolimus (Tac) is widely used to prevent rejection and graft loss in solid organ transplantation.
106 in the setting of diagnosing renal allograft rejection and how this will improve transplant patient c
108 Additional studies investigating the risk of rejection and long-term graft function are needed before
110 t B cell depletion effectively prevents late rejection and promotes permanent acceptance of islet all
112 atients need to be aware of the high risk of rejection and the poor remission rate with the use of ch
113 le in developing the concepts of immunologic rejection and tolerance, which led to him receiving the
115 shed light on the dynamics of ITx allograft rejection and treatment resistance, peripheral blood sam
118 d graft survival using Cox regression, acute rejection, and delayed graft function (DGF) using logist
119 ing social conflict, isolation, devaluation, rejection, and exclusion historically increased risk for
122 s from respiratory specimens, acute cellular rejection, and lymphocytic bronchiolitis are associated
123 lyses, Pseudomonas isolation, acute cellular rejection, and lymphocytic bronchiolitis remained indepe
124 se score >=40, postoperative hospital stays, rejection, and nonanastomotic biliary strictures were hi
126 opportunistic viral infections and of graft rejection, and should facilitate point-of-care post-tran
128 uired for prior authorizations, the frequent rejections, and the perception of being excluded from th
129 ESW was associated with increased acute rejection (aOR=(1.09)1.16(1.23)), slightly increased gra
131 cted (HIV+) persons are excellent, yet acute rejection (AR) is common and optimal immunosuppressive r
132 mation in a perivascular (acute perivascular rejection [AR]) or peribronchiolar (lymphocytic bronchio
134 y allografts undergoing acute and/or chronic rejection are typically T cells and monocyte/macrophages
135 occurs; however, the added value of mucosal rejection assessment for patient management is unknown.
136 Peli1 ablation profoundly promotes tumor rejection, associated with increased tumor-infiltrating
137 ll as CXCL9 messenger RNA (a marker of graft rejection) at elevated levels in urine samples from pati
138 primary endpoint was biopsy-confirmed acute rejection (BCAR) within 60 weeks after transplantation;
142 low-up, the incidence of biopsy-proven acute rejection (BPAR) was 77% (37/48) and 66% (31/47) (P = 0.
143 genes related to inflammation and allograft rejection but downregulation of oxidative phosphorylatio
147 be compromised by chronic antibody-mediated rejection (CAMR), leading to irreversible necrosis of th
148 to prevent errors and could be replaced by a rejection comment specifying clinical situations that mi
149 who received ATG were at lower risk of acute rejection compared to those who received IL2RA (1-y crud
150 therapy was associated with fewer deaths and rejections, compared with standard immunosuppression tri
152 ity class II or CD40 in cDC1 impaired tumour rejection, consistent with a role for cognate CD4(+) T c
153 cimens showed grade 2A acute T cell-mediated rejection, cortical infarction, or acute tubular injury.
154 raphy in a memory paradigm assessing correct rejection (CR) of lures, item recognition (IR) and assoc
159 ubjects, 106 remained rejection-free, 77 had rejection diagnosed only on protocol biopsy (>=2R cellul
161 but it is unknown whether the type of acute rejection differs between these patient groups or whethe
162 The data indicates that higher-grade skin rejection does not occur in absence of mucosal rejection
163 factors associated with biopsy-proven acute rejection during the first post-transplant year in a pre
164 asive biomarkers to identify the presence of rejection, endoscopy and biopsy remain the gold standard
165 tive probabilities of infection, first acute rejection episode, malignancy, de novo donor specific an
166 Of the 196, 37 (18.9%) had a previous acute rejection episode; 96 (49%) had concurrent i score = 0.
167 ndependent predictors of CAV were: number of rejection episodes (cause-specific hazard ratio [95% con
169 onor-specific human leukocyte antigen Abs or rejection episodes were noted, even though the patients
171 of rapamycin immunosuppression, and an acute rejection event were independent risk factors for EW gai
173 of FcgammaRIIB correlated with freedom from rejection following withdrawal from immunosuppression in
174 mbranes; however, challenges such as low ion rejection for high salinity water, low water flux, and l
175 Secondary endpoints included death-censored rejection-free survival and the frequency of extracorpor
179 quantified the association of ESW with acute rejection, graft failure, and mortality using multivaria
180 were treatment failure (biopsy-proven acute rejection, graft loss, or death), delayed graft function
182 re early rejections (<1 y) or any late acute rejection (>1 y) have been associated with coronary arte
183 ansplant cohort (n = 21 no rejection; n = 42 rejection, >1R) with an area under the curve of 0.87 (P
184 nalysis of liver transplant biopsies detects rejection, has the potential to resolve ambiguities, and
185 i versus MPA in terms of biopsy-proven acute rejection (hazard ratio [confidence interval], 0.32 [0.1
188 (RA), endothelial cell density, immunologic rejection, herpetic recurrence, and graft failure rates.
189 ificant volumetric changes during ion uptake/rejection, i.e., during doping/de-doping and charging/di
190 eer influence and hypersensitivity to social rejection in adolescence increase the likelihood of both
191 G12C inhibitor AMG 510 can potentiate immune rejection in combination with immune checkpoint blockade
192 ein S-RNase contributes to S-specific pollen rejection in conspecific crosses, as well as to rejectin
196 eracute rejections and very infrequent acute rejection in the first year suggesting no evidence for i
198 Histologic criteria for diagnosing acute rejection in vascularized composite tissue allograft (VC
201 in 188 of 1763 (10.7%) blood samples and any rejection (including borderline changes) in 614 of 1763
202 pulations in ischemia-reperfusion injury and rejection, including their interaction with allograft-in
204 of immunomonitoring, we found that while ITx rejection is associated with proinflammatory and activat
208 ithin kidney transplants or play any role in rejection is unknown, however, in part because of limite
209 maintenance therapy groups, the frequency of rejection limits the practical implementation of this st
210 face of the cornea, there was an endothelial rejection line (Khodadoust line) with keratic precipitat
211 othelial graft rejection with an endothelial rejection line occurring 1 year after the procedure.
213 inflammatory events including acute cellular rejection, lymphocytic bronchiolitis, and Pseudomonas is
215 o ischemia-reperfusion injury (IRI) or graft rejection may be silenced to improve organ quality after
217 fers between these patient groups or whether rejection mediates the effect between ethnicity, death-c
218 other VCA patients, vascular injury in mild rejection might warrant a different clinical approach.
219 hereas DC-GF patients experienced more early rejection, more acute rejection after 90 days, and a cli
220 5), persistent infection (n = 14) or de novo rejection (n = 11) 6 months following a standardized red
221 ry allograft vasculopathy (n=86, 70%), prior rejection (n=76, 62%), presence of donor-specific antibo
222 t adult cardiac transplant cohort (n = 21 no rejection; n = 42 rejection, >1R) with an area under the
223 hin 10 years, 4% of eyes developed allograft rejection, no primary graft failures occurred, and 6% of
224 of endoscopic evaluation, episodes of acute rejection, nutritional therapy, and renal function betwe
226 similar in DMEK-only and triple-DMEK groups: rejection occured in 8.8% and 8.75% of cases respectivel
227 s 2.7% (P < .0001), and future or persistent rejection occurred in 9 of 42 patients (21.4%) vs 0% (P
229 aching 234.9 +/- 8.1 kg m(-2) h(-1) and salt rejection of 99.7 +/- 0.2 %, outperforming existing memb
230 constant expression of CD28 accelerated the rejection of allogeneic skin grafts in young RAG2(-/-) r
231 ed from mutations, and leads to an effective rejection of both virus-injected and distant tumors.
232 defense of cultural worldviews, and violent rejection of democratic principles and the rule of law).
236 marrow stem cell transplantation where early rejection of immunologically mismatched grafts is driven
237 t chemical contaminants and the insufficient rejection of low-molecular-weight neutral organics by RO
241 al partners) is strongly associated with the rejection of sacrifices for the greater good (especially
243 irst reported small molecule able to prevent rejection of transplanted bone marrow stem cells in vivo
246 icular, we show that acceptance (compared to rejection) of curiosity-driven or incentive-driven gambl
247 poses a far greater risk for future CAV than rejection on protocol biopsy in pediatric HT recipients.
249 rs resulted in CD8 and PD-L1-dependent tumor rejection or growth inhibition and a reduction in myeloi
250 ACR compared to acute tubular injury without rejection or pretransplant "normal kidney" biopsy sample
253 ransition from low rejection to near-perfect rejection over a solute size range smaller than half Ang
254 prior allograft failure as a result of acute rejection (P < .001) or disease recurrence (P = .003), b
257 to proteasome inhibitor-based therapy for 4 rejection phenotypes and to determine factors that predi
258 highest mortality and post-mortem inspection rejections, poorest walking ability, most hock burn and
260 ibe the immunosuppressive regimens and graft rejection rates in living-related HLA-identical (LR HLAi
262 (93.8% vs 80.9% HLA non-ID LDKTx, p<0.001), rejection rates were lower (after 1 year 9.6% vs 27.1%;
263 Primary outcomes included graft survival and rejection rates, and secondary outcomes included rates o
264 drate antigens (Ags) are critical drivers of rejection reactions to ABO-incompatible allogeneic graft
266 based on expression of previously annotated rejection-related transcripts identified 4 groups: norma
267 ul strategies to induce suppression of graft rejection relies on inhibition of T-cell activation.
268 Endothelial failure and immunological graft rejection remain long-term complications leading to late
272 othesized to be secondary to either a tissue rejection response to the haploidentical fetus or from a
277 l En/DMT correlated significantly with graft rejection severity (r = 0.972, r = 0.729, and r = 0.823,
278 lets maintained euglycemia and delayed graft rejection significantly longer than those receiving none
279 leukocyte donor/recipient ratio varied with rejection status for macrophages and with time post-tran
280 ation of recipient leukocytes, regardless of rejection status, and in tolerant mixed hematopoietic ch
282 ood histocompatibility with no immunological rejection, support vascularized tissue ingrowth, and pro
283 mal "R1(normal) " (N = 129), T cell-mediated rejection (TCMR) "R2(TCMR) " (N = 37), early injury "R3(
284 eria for chronic active (CA) T cell-mediated rejection (TCMR), borderline, and antibody-mediated reje
287 ially overlooked in favor of T cell-mediated rejection, the importance of the humoral alloimmune resp
288 nock-ins enables the visualization of tissue rejection through individual target cell-killing events
289 es, yielding a step-wise transition from low rejection to near-perfect rejection over a solute size r
290 t of whether the fine balance between immune rejection versus tolerance is achieved with various appl
293 cal rejection in the first year; subclinical rejection was detected by protocol biopsy in 4 patients.
296 Here, we present a case of endothelial graft rejection with an endothelial rejection line occurring 1
297 tcomes were excellent; a trend toward higher rejection with D+ raises concerns that merit further inv
298 n/DMT maps can diagnose active corneal graft rejection with excellent accuracy, sensitivity, and spec
300 mpared to IL2RA, may lower the risk of acute rejection without increasing hepatic complications in HC