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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.
48 respectively, and 7 eyes developed allograft rejection (0.7%).
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
51 7 [21.9%], P = .007) and biopsy-proven acute rejections (15 [23.4%] vs 31 [48.4%], P = .002).
52  to evaluate the effector mechanisms driving rejection; (2) potential assays to assess the presence o
53                   The incidence of allograft rejection (28% vs 25%; difference, 3% [95% CI, -9% to 15
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) (
58                   Although antibody-mediated rejection (ABMR) has been long recognized as a leading c
59 onfirmed cases of clinical antibody-mediated rejection (ABMR) were present in the population, and str
60 on (TCMR), borderline, and antibody-mediated rejection (ABMR).
61 f between immunological tolerance and embryo rejection accompanied the evolution of unique male pregn
62                    Rationale: Acute cellular rejection (ACR) is common during the initial 3 months af
63 n intestinal transplantation, acute cellular rejection (ACR) remains a significant challenge to achie
64 psy specimens with early AMR, acute cellular rejection (ACR), or acute tubular necrosis (ATN).
65 ular epithelial cells by acute cell-mediated rejection (ACR.
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
70 and lymphatic neovessels and rapid allograft rejection after corneal penetrating keratoplasty.
71 se corticosteroids effectively combats acute rejection after kidney transplantation, but at the cost
72 rgans with lower potential for immunological rejection after transplantation in humans.
73                                              Rejections after conversion were mostly cell-mediated.
74 immunosuppression, balancing risks for graft rejection against risks for infection.
75        Tacrolimus (Tac) is an effective anti-rejection agent in kidney transplantation, but its off-t
76 08-2.62]; P = 0.022) and biopsy-proven acute rejection (aHR, 1.71 [1.13-2.60]; P = 0.012).
77 ft biopsies from 51 ITx patients with severe rejection, alongside 37 stable controls, were analyzed u
78                                              Rejection also occurred if CXCR4 was deleted from donor
79 plicated in the process of chronic allograft rejection, also known as transplant vasculopathy.
80          R2(TCMR) correlated with histologic rejection although with many discrepancies, and R4(late)
81 iated rejection (9.2%) and antibody-mediated rejection (AMR) (13.8%).
82                            Antibody-mediated rejection (AMR) accounts for >50% of kidney allograft lo
83 ti-HLA antibodies (DSA) on antibody-mediated rejection (AMR) and kidney allograft failure is well est
84                            Antibody-mediated rejection (AMR) driven by the development of donor-speci
85                     Active antibody-mediated rejection (AMR) is a potentially devastating complicatio
86 ed for desensitization and antibody-mediated rejection (AMR) treatment by targeting CD20 found on B-l
87 ciation with occurrence of antibody-mediated rejection (AMR) using a recently developed method.
88 l allograft survival after antibody-mediated rejection (AMR).
89 ell-established feature of antibody-mediated rejection (AMR).
90 mmation leading to chronic antibody-mediated rejection (AMR).
91 nt pathway responsible for antibody-mediated rejection (AMR).
92             We used 12% subclinical cellular rejection and 3% subclinical antibody-mediated rejection
93  (AT1R) antibodies have been associated with rejection and allograft loss in solid organ transplantat
94 e allograft dysfunction were associated with rejection and allograft loss.
95            Ablation of LAL suppresses immune rejection and allows growth of human lung cancer cells i
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
99 g IL-6/IL-6R to ameliorate chronic allograft rejection and coronary allograft vasculopathy.
100 del of T-cell-mediated human islet allograft rejection and developed a therapeutic regimen of low-dos
101                                              Rejection and diagnosis of congenital glaucoma were risk
102 ell-mediated rejection and antibody-mediated rejection and discuss the additive value of molecular pr
103 lial cells to eliminate risks of endothelial rejection and failure.
104 isk factor for accelerated cardiac allograft rejection and graft dysfunction .
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
107 antibodies, a factor contributing to chronic rejection and late allograft loss.
108 Additional studies investigating the risk of rejection and long-term graft function are needed before
109 in transplantation by accelerating allograft rejection and preventing tolerance induction.
110 t B cell depletion effectively prevents late rejection and promotes permanent acceptance of islet all
111                                        Graft rejection and rebubbling rates were similar in DMEK-only
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
114 dition to T cells, B cells can mediate graft rejection and transplantation tolerance.
115  shed light on the dynamics of ITx allograft rejection and treatment resistance, peripheral blood sam
116                                          All rejections and clinical borderline rejections in protoco
117                     There were no hyperacute rejections and very infrequent acute rejection in the fi
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
120 -year survival, cardiac or hepatic allograft rejection, and infection.
121 raft and patient survival, episodes of acute rejection, and its response to treatment.
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
125  with cell-mediated and/or antibody-mediated rejection, and portend an adverse outcome.
126  opportunistic viral infections and of graft rejection, and should facilitate point-of-care post-tran
127                       He experienced 6 acute rejections, and none were resistant to steroids.
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
130  compare the risk of CMV infection and acute rejection (AR) among KT recipients by ATG dose.
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
133      In organ transplantation, infection and rejection are major causes of graft loss.
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;
139                         Thereby the risk for rejection because of unnecessary reduction of immunosupp
140 und to be a low-yield screening modality for rejection beyond 6 months post-HT.
141                          Biopsy-proven acute rejection (BPAR) rates and types were compared between i
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
144                  The third was attributed to rejection, but improved after discontinuing the checkpoi
145       ADR-expressing T cells resist cellular rejection by targeting alloreactive lymphocytes in vitro
146 the donor template in yeast, limiting strand rejection by the Sgs1 and Mph1 helicases.
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
151 , not rejection activity, presumably because rejection confers risk via injury.
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
155                                           If rejection criteria were met, a committee mock-refused PC
156                                          PCR rejection criteria, based on white blood cell (WBC) and
157                We hypothesized that clinical rejection defined by concurrent new-onset heart failure
158 ore strongly associated with future CAV than rejection diagnosed on protocol biopsy.
159 ubjects, 106 remained rejection-free, 77 had rejection diagnosed only on protocol biopsy (>=2R cellul
160                                Subjects with rejection diagnosed only on protocol biopsy were not at
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
168                              T cell-mediated rejection episodes tended to be relatively mild-50% (5 e
169 onor-specific human leukocyte antigen Abs or rejection episodes were noted, even though the patients
170                                  Despite the rejection episodes, the vast majority of recipients had
171 of rapamycin immunosuppression, and an acute rejection event were independent risk factors for EW gai
172 entify articles that provide data on mucosal rejection following fVCA.
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
176                   Cox-regression analysis of rejection-free survival revealed better results for mTOR
177          Of 228 study subjects, 106 remained rejection-free, 77 had rejection diagnosed only on proto
178                                      Mucosal rejection frequently occurs; however, the added value of
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
181 fic antibodies (P=0.004), and acute cellular rejection &gt;=2R (P=0.028).
182 re early rejections (<1 y) or any late acute rejection (&gt;1 y) have been associated with coronary arte
183 ansplant cohort (n = 21 no rejection; n = 42 rejection, &gt;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
186 1-1.18), and a higher risk for treated acute rejection (hazard ratio, 1.63; 95% CI, 1.43-1.86).
187 ter surgery with minimal risk of immunologic rejection, herpetic recurrence and graft failure.
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
193 several medications used to prevent or treat rejection in orthotopic heart transplantation.
194       We further demonstrate that late graft rejection in recipients treated with this regimen is ass
195 opic immune mechanisms that facilitate tumor rejection in several tumor models.
196 eracute rejections and very infrequent acute rejection in the first year suggesting no evidence for i
197                        There was no clinical rejection in the first year; subclinical rejection was d
198     Histologic criteria for diagnosing acute rejection in vascularized composite tissue allograft (VC
199       All rejections and clinical borderline rejections in protocol biopsies were treated.
200  melanoma cells is inhibited, up to complete rejection, in Siah2(-/-) mice.
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
203                                 Induction of rejection is a rare event.
204 of immunomonitoring, we found that while ITx rejection is associated with proinflammatory and activat
205                              Renal allograft rejection is more frequent under belatacept-based, compa
206               As a result, antibody-mediated rejection is now widely recognized as the main cause of
207                        The increased bias to rejection is partially explained by changes in synaptic
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.
212                            Two or more early rejections (&lt;1 y) or any late acute rejection (>1 y) hav
213 inflammatory events including acute cellular rejection, lymphocytic bronchiolitis, and Pseudomonas is
214                             Rationale: Acute rejection, manifesting as lymphocytic inflammation in a
215 o ischemia-reperfusion injury (IRI) or graft rejection may be silenced to improve organ quality after
216  transplantation regarding antibody-mediated rejection may not systematically apply to VCA.
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
225                                    The metal rejection obtained was greater than 99%.
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
228                              The majority of rejections occurred within 3 months following HT.
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).
233 (GzmB) expression and the ability to promote rejection of established tumors.
234 fts were rejected at the same time points as rejection of fully allogeneic grafts.
235 E (HLA-E), inhibits antibody-mediated immune rejection of heart allografts.
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
238 e increased by 100% without compromising the rejection of Na(2)SO(4).
239                                  Testing and rejection of noncognate TCs on a sub-ms timescale is ess
240 mmune hemolytic anemia and antibody-mediated rejection of organ transplants.
241 al partners) is strongly associated with the rejection of sacrifices for the greater good (especially
242 arental investment among vertebrates, is the rejection of the nonself-embryo.
243 irst reported small molecule able to prevent rejection of transplanted bone marrow stem cells in vivo
244 itors are immunosuppressants used to prevent rejection of transplanted organs and tissues.
245 he need to develop a model that predicts the rejection of various organics.
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.
248 le control patients were not associated with rejection or allograft loss.
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
251 = 2.67; 95% CI = 1.12-6.32), and acute graft rejection (OR = 3.01; 95% CI = 1.78-5.09).
252 not associated with de novo DSA development, rejection, or allograft loss.
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
255 odies and significantly increase the odds of rejection (P < .1).
256 P=0.04) and mortality (P=0.003), but not for rejection (P=0.6).
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
259                                     Clinical rejection poses a far greater risk for future CAV than r
260 ibe the immunosuppressive regimens and graft rejection rates in living-related HLA-identical (LR HLAi
261                                              Rejection rates in the study and control groups were 19.
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
265 odies and, on prolonged treatment, modulated rejection-related gene-expression patterns.
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
269                          As expected, tumour rejection required cDC1 and CD8(+) T cell priming requir
270 tumor response and T cell-mediated allograft rejection requiring reinitiation of hemodialysis.
271          This approach enables generation of rejection-resistant, 'off-the-shelf', allogeneic T-cell
272 othesized to be secondary to either a tissue rejection response to the haploidentical fetus or from a
273 major issue for MC codes based on acceptance-rejection sampling.
274 jection and 3% subclinical antibody-mediated rejection (SC-ABMR) for the base-case cohort.
275                                  Subclinical rejection (SCR) screening in kidney transplantation (KT)
276                              T cell-mediated rejection seems to form a continuum of alloimmune activa
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
281 ides capable of mediating T cell-based tumor rejection still face important challenges.
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
285 ients suffered an episode of T-cell-mediated rejection (TCMR).
286  kidney BKVN (n = 5) vs pure T cell-mediated rejection (TCMR; n = 10).
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
291  the role of early vascular lesions in graft rejection warrants additional analysis.
292                                              Rejection was associated with proliferation of recipient
293 cal rejection in the first year; subclinical rejection was detected by protocol biopsy in 4 patients.
294                                     Although rejection was not uniform in the belatacept maintenance
295                      Factors associated with rejection were age of recipient (OR, 0.91 [0.84-0.96]; P
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
299                 Two were biopsy-proven acute rejections with subsequent graft failures.
300 mpared to IL2RA, may lower the risk of acute rejection without increasing hepatic complications in HC

 
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