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1. |
THE HUMAN BONE MARROW AS AN IMMUNOREGULATORY ORGAN1 |
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Transplantation,
Volume 68,
Issue 8,
1999,
Page 1079-1090
Joshua Miller,
James Mathew,
Rolando Garcia-Morales,
Keith Zucker,
Manuel Carreno,
Yide Jin,
Laphalle Fuller,
George Burke,
Gaetano Ciancio,
Andreas Tzakis,
Camillo Ricordi,
Les Olson,
Anne Rosen,
David Roth,
Violet Esquenazi,
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ISSN:0041-1337
出版商:OVID
年代:1999
数据来源: OVID
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2. |
MAXIMIZING THE BENEFITS OF HLA MATCHING FOR RENAL TRANSPLANTATION: ALLELES, SPECIFICITIES, CREGS, EPITOPES, OR RESIDUES? |
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Transplantation,
Volume 68,
Issue 8,
1999,
Page 1093-1094
Craig Taylor,
Philip Dyer,
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ISSN:0041-1337
出版商:OVID
年代:1999
数据来源: OVID
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3. |
HEPATITIS C LINKS HEPATOLOGISTS, NEPHROLOGISTS AND TRANSPLANT SURGEONS |
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Transplantation,
Volume 68,
Issue 8,
1999,
Page 1094-1095
Orla Crosbie,
Graeme Alexander,
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ISSN:0041-1337
出版商:OVID
年代:1999
数据来源: OVID
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4. |
PERSISTENCE OF DONOR ANTIGEN IS NECESSARY FOR MAINTENANCE OF XENOTOLERANCE-A PARALLEL TO ALLOGENEIC SYSTEMS? |
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Transplantation,
Volume 68,
Issue 8,
1999,
Page 1095-1096
Bruce Rosengard,
Abraham Shaked,
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ISSN:0041-1337
出版商:OVID
年代:1999
数据来源: OVID
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5. |
EVALUATION OF HLA MATCHING FOR CREG ANTIGENS IN EUROPE1 |
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Transplantation,
Volume 68,
Issue 8,
1999,
Page 1097-1099
Thomas Wujciak,
Gerhard Opelz,
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摘要:
Background.In North America, cross-reactive antigen group (CREG) matching was introduced recently for cadaver kidney allocation. This is expected to result in improved graft outcome and an increased number of transplants for patients with rare HLA antigens.Methods.We analyzed the impact of CREG matching using the data of the Collaborative Transplant Study for 59,516 first cadaver transplants performed in Western Europe. The 10 HLA class I CREGs described by Takemoto et al. were used for a comparison with the conventional HLA-A+B mismatching scheme.Results.Transplant outcome depends primarily on the number of HLA-A+B mismatches and not on the CREG match grades. In a retrospective analysis, CREG mismatches correlated with the number of HLA-A+B mismatches. However, in computer simulations, we found that prospective CREG matching is not associated with beneficial HLA-A+B matching.Conclusion.The positive CREG matching effect observed in retrospective analyses is caused by the underlying effects of conventional HLA-A+B matching. CREG-oriented cadaver kidney allocation in Europe would, therefore, be inferior to the current conventional HLA-A+B+DR allocation.
ISSN:0041-1337
出版商:OVID
年代:1999
数据来源: OVID
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6. |
A PHASE I STUDY OF A 4-WEEK COURSE OF SDZ-RAD (RAD) IN QUIESCENT CYCLOSPORINE-PREDNISONE-TREATED RENAL TRANSPLANT RECIPIENTS1,2 |
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Transplantation,
Volume 68,
Issue 8,
1999,
Page 1100-1106
Barry Kahan,
Robert Wong,
Catherine Carter,
Stephen Katz,
Janet Von Fellenberg,
Charles Van Buren,
Silke Appel-Dingemanse,
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摘要:
Background and Methods.This phase I, randomized, blinded, placebo-controlled study assessed the safety profile and pharmacokinetics of a 4-week course of once-daily, sequential ascending doses (0.75, 2.5, or 7.5 mg/day) of SDZ-RAD (RAD) capsules in renal transplant recipients on a stable regimen of cyclosporine (CsA; Neoral®) and prednisone.Results.RAD displayed a similar spectrum of side effects as observed with rapamycin, namely, an increased incidence of infection associated with the augmented immunosuppression and a dose-related occurrence of thrombocytopenia, hypercholesterolemia, and hypertriglyceridemia, particularly at the 7.5-mg dose. The pharmacokinetic parameters of RAD showed dose proportionality, a good correlation between trough and area under the curve (AUC) concentrations, and a moderate accumulation of 2.5-fold. The drug was absorbed within 2 hr and displayed a 16-19-hr half-life, which is shorter than that of rapamycin. RAD reached steady state at 4 days. Preliminary kinetic-dynamic correlations indicate a correlation between thrombocytopenia (but not hyperlipidemia) and AUC, as well as maximum drug concentrations, and weight-adjusted dose. At the end of a 4-week course of simultaneous dosing, there was no evidence of a pharmacokinetic interaction between CsA and RAD.Conclusion.This study suggests that the shorter half-life of RAD compared to rapamycin may confer the benefits of rapid attainment of steady state and dissipation of effects upon drug cessation. Controlled, multicenter trials are being planned to assess the impact of these features on clinical outcomes.
ISSN:0041-1337
出版商:OVID
年代:1999
数据来源: OVID
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7. |
OUTCOME OF TRANSPLANTATION OF ORGANS PROCURED FROM BACTEREMIC DONORS1 |
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Transplantation,
Volume 68,
Issue 8,
1999,
Page 1107-1111
Richard Freeman,
Ioannis Giatras,
Mathew Falagas,
Stacey Supran,
Kevin O'Connor,
James Bradley,
David Snydman,
Francis Delmonico,
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摘要:
Background.Transplantation of organs from donors who are bacteremic is controversial. We examined the outcome of recipients of solid organs from donors with bacteremia and/or fungemia at the time of organ recovery.Methods.All organ donors from a single organ procurement organization between January 1990 and December 1996 were retrospectively analyzed. We calculated rates of transmission from bacteremic or fungemic donors to their recipients and compared the graft and patient survival rates for recipients of these organs with those for recipients of organs from nonbacteremic donors.Results.There were 95 (5.1%) bacteremic donors from a total of 1775, from whom 212 recipients received organs. Forty-six (48%) of the bacteremic donors had pathogens in their blood. Among the 101 recipients of organs from these, no evidence of transmission could be documented. (0% transmission rate, 95% CI 0-3). The remaining 49 donors had eitherStaphylococcus epidermidisor other unlikely pathogens recovered from the blood. Examination of the 111 recipients of organs from these donors also found no evidence for transmission (0% transmission rate, 95% CI 0-3). Of the 212 recipients, 193 (91%) received a mean of 3.8±2.5 days of antibiotics postoperatively. The 30-day graft and patient survival for recipients of organs from bacteremic donors was not significantly different from recipients of organs from nonbacteremic donors (P=0.695 for patient survival, andP=0.310 for graft survival).Conclusions.Organs transplanted from bacteremic donors do not transmit bacterial infection or result in poorer outcomes. Use of organs from these donors could help increase organ availability.
ISSN:0041-1337
出版商:OVID
年代:1999
数据来源: OVID
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8. |
MINIMUM GRAFT SIZE FOR SUCCESSFUL LIVING DONOR LIVER TRANSPLANTATION |
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Transplantation,
Volume 68,
Issue 8,
1999,
Page 1112-1116
Chung-Mau Lo,
Sheung-Tat Fan,
Chi-Leung Liu,
John Chan,
Banny Lam,
George Lau,
William Wei,
John Wong,
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摘要:
Background.The extension of living donor liver transplantation to adult recipients is limited by the adequacy of the size of the graft. We evaluate the effect of the graft size on the survival of the recipient in order to establish a clinical guide for the minimum requirement.Methods.The clinical records of 14 adults and 11 children (body weight 6.1-100 kg) who underwent living donor liver transplantation for chronic or acute liver failure were reviewed. The effect of the graft weight ratio (graft weight divided by standard liver weight of recipient) on graft function and survival was studied.Results.The graft weight ratio ranged from 31 to 203%. The overall graft and patient survival rates were 84% at a median follow-up of 29 months. The survival rate was 95% for recipients with a graft weight ratio >40%, and 40% only for those with a ratio ≤40% (P=0.016). It was 88% (7/8) when the ratio was >100%, 100% (5/5) when the ratio was 71 to 100%, 100% (7/7) when the ratio was 41 to 70%, and 40% (2/5) only when the ratio was ≤40%. When the graft weight ratio was ≤40%, early graft dysfunction was evident and contributed to the causes of death in three patients.Conclusions.Preoperative computed tomographic measurement of liver size of a living donor is essential. A graft that represented 40% or less of the recipient's standard liver weight should be regarded as a marginal graft with a lower success rate.
ISSN:0041-1337
出版商:OVID
年代:1999
数据来源: OVID
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9. |
EVALUATION OF PRE- AND POSTTRANSPLANT DONOR-SPECIFIC TRANSFUSION/CYCLOSPORINE A IN NON-HLA IDENTICAL LIVING DONOR KIDNEY TRANSPLANT RECIPIENTS |
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Transplantation,
Volume 68,
Issue 8,
1999,
Page 1117-1124
J. Alexander,
Jimmy Light,
Lynn Donaldson,
Francis Delmonico,
Arnold Diethelm,
Alan Wilkinson,
J. Rosenthal,
J. Thistlethwaite,
Lawrence Hunsicker,
Arthur Matas,
M. First,
Nancy Reinsmoen,
Stephen Rose,
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摘要:
Background.The beneficial effects of donor specific transfusion (DST) have become controversial in the cyclosporine era. This study was performed to evaluate the potential benefits of a new protocol for administering DSTs in the perioperative period.Methods.Non-HLA identical living donor kidney transplant recipients were randomized prospectively to control or to receive a DST 24 hr before transplant and 7-10 days posttransplant. All patients received similar immunosuppression according to protocol.Results.The protocol had 212 evaluable patients (115 transfused and 97 control). There were no differences in 1- and 2-year graft and patient survival, causes of graft failure, incidence and types of infection, repeat hospitalization, or the ability to withdraw steroids. Immunological hyporesponsiveness (by mixed lymphocyte culture) occurred more frequently in transfused patients (18%) than controls (3%) (P=0.04). Blood stored for ≥3 days was associated with fewer early rejections than blood stored ≤2 days. Overall, class II antigen mismatches were associated with more rejection episodes than class I antigen mismatches. However, transfused patients, but not control patients, with more class I antigen mismatches were more likely to have rejections.Conclusions.Administration of DSTs by the method described had no practical influence on patient or graft survival for up to 2 years. However, donor-specific hyporesponsiveness was more common in transfused patients (18 vs. 3%). Longer follow-up will be needed to determine whether DST will be associated with long-term benefit.
ISSN:0041-1337
出版商:OVID
年代:1999
数据来源: OVID
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10. |
CYTOMEGALOVIRUS PP65 ANTIGENEMIA MONITORING AS A GUIDE FOR PREEMPTIVE THERAPY: A COST EFFECTIVE STRATEGY FOR PREVENTION OF CYTOMEGALOVIRUS DISEASE IN ADULT LIVER TRANSPLANT RECIPIENTS1 |
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Transplantation,
Volume 68,
Issue 8,
1999,
Page 1125-1131
Shimon Kusne,
Paolo Grossi,
William Irish,
Kirsten St. George,
Charles Rinaldo,
Jorge Rakela,
John Fung,
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摘要:
Background.The aim of the study was to assess the incidence of cytomegalovirus (CMV) infection and disease in adult liver transplant recipients, using routine preemptive therapy guided by the pp65 antigenemia test.Methods.Antigenemia was monitored weekly after liver transplantation (OLTX) for the first 3 months, and once a month for another 3 months. CMV seronegative recipients were treated preemptively for the first positive antigenemia. Seropositive recipients were treated only when their antigenemia count reached a threshold of ≥100 positive cells per 200,000 leukocytes.Results.A total of 144 patients were included between June 1994 and April 1995, of which 137 (95%) were primary OLTX. The percentage of positive antigenemia and CMV disease was 55 and 8%, respectively. Seventy-eight (54%) patients were protocol-monitored for the entire follow-up (group 1) and received appropriate preemptive therapy, although 66 (46%) patients had protocol violation by having missed blood samples or blood drawn at unscheduled times (group 2). Using Cox's proportional hazards model, patients with a first antigenemia count of >11 leukocytes had a significantly higher rate of CMV disease compared to patients with an antigenemia count ≤11 leukocytes (RR=7.3, 95% confidence interval=2.2 to 24.5). In a multivariate Cox regression analysis, adjustments were made to control for: group 1 versus group 2, use of OKT3, and serology risk categories. This analysis showed that the relative rate of CMV disease was still significantly higher among patients with antigenemia count >11 leukocytes (adjusted RR=4.9, 95% confidence interval=1.3 to 18.1). The estimated cost of preemptive therapy was less than that of prophylaxis with i.v. (14-day course) or oral (90-day course) ganciclovir.Conclusions.Preemptive therapy guided by pp65 antigenemia is a useful and cost effective strategy for prevention of CMV disease.
ISSN:0041-1337
出版商:OVID
年代:1999
数据来源: OVID
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