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21. |
IMPAIRMENT OF FIBRINOLYTIC POTENTIAL IN LONG-TERM STEROID TREATMENT AFTER HEART TRANSPLANTATION1 |
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Transplantation,
Volume 64,
Issue 11,
1997,
Page 1610-1614
Patrassi2,3 Giovanni,
Sartori2 Maria,
Livi4 Ugolino,
Casonato2 Alessandra,
Danesin2 Cristina,
Vettore2 Silvia,
Girolami2 Antonio,
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摘要:
Thrombotic complications constitute an important risk in transplant recipients, in whom a hypercoagulable state and hypofibrinolysis have been associated with immunosuppressive treatment, especially with cyclosporine. In no case have clotting and fibrinolytic abnormalities been correlated with steroid immunosuppression, even though steroids were always administered. Previous studies found a relationship between hypercorticism and hypofibrinolysis both in Cushing's disease and after renal transplantation. The aim of this investigation was to compare fibrinolytic potential using the venous occlusion test in two similar groups of heart transplant patients treated with or without steroids. Euglobulin lysis time, tissue-type plasminogen activator and plasminogen activator inhibitor-1 (PAI-1) activities, and antigens were determined before and after the venous occlusion test. A reduced fibrinolytic potential (significant prolongation of lysis time) due to a significant increase in PAI-1 activity and antigen levels was found in heart transplant patients treated with steroids, as compared with patients without steroid treatment and control subjects. The prevalence of reduced fibrinolytic potential was 69.2% (18 cases) in the steroid-treated group and 34.8% (8 cases) in the non-steroid-treated group. In every case, the impaired fibrinolytic potential was due to high basal PAI-1 levels. Our results are compatible with the presence of a hypofibrinolytic state secondary to long-term steroid treatment. In heart transplant recipients, steroid-induced hypofibrinolysis may constitute a further risk factor for thrombotic disease.
ISSN:0041-1337
出版商:OVID
年代:1997
数据来源: OVID
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22. |
LONG-TERM GANCICLOVIR PROPHYLAXIS FOR SUCCESSFUL PREVENTION OF PRIMARY CYTOMEGALOVIRUS (CMV) DISEASE IN CMV-SERONEGATIVE LIVER TRANSPLANT RECIPIENTS WITH CMV-SEROPOSITIVE DONORS1 |
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Transplantation,
Volume 64,
Issue 11,
1997,
Page 1614-1617
Seu2 Philip,
Winston3,4 Drew,
Holt2 Curtis,
Kaldas2 Fady,
Busuttil2 Ronald,
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摘要:
Background.We conducted a trial of long-term ganciclovir prophylaxis for prevention of primary cytomegalovirus (CMV) disease in CMV-seronegative liver transplant recipients with CMV-seropositive donors.Methods.Patients received intravenous ganciclovir at a dose of 6 mg/kg once a day from day 1 to day 30 after transplant, and then at a dose of 6 mg/kg once a day, Monday through Friday, until day 100. Fortyseven consecutive patients were evaluated. Due to the primary physician's decision or administrative error, 10 patients received less than 7 weeks of ganciclovir(mean duration, 3 weeks).Results.Four of the 10 (40%) patients who received less than 7 weeks of ganciclovir developed CMV disease (hepatitis). In contrast, none of the 37 patients given 100 days of prophylactic ganciclovir developed CMV disease while receiving ganciclovir. Two patients (5.4%) subsequently developed CMV disease (hepatitis) 21 and 88 days, respectively, after completing their ganciclovir prophylaxis. Reversible neutropenia in three patients (8.1%) was the only side effect associated with long-term ganciclovir. Complications from central intravenous catheters did not occur.Conclusions.These results reaffirm the efficacy and safety of long-term ganciclovir prophylaxis for prevention of primary CMV disease in a large number of high-risk CMV-seronegative liver transplant recipients with CMV-seropositive donors.
ISSN:0041-1337
出版商:OVID
年代:1997
数据来源: OVID
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23. |
HLA ANTIBODY SCREENINGComparison of a Solid Phase Enzyme-Linked Immunoassay with Antiglobulin-Augmented Lymphocytotoxicity |
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Transplantation,
Volume 64,
Issue 11,
1997,
Page 1617-1620
Moore1 Breanndan,
Ploeger Nancy,
DeGoey Steven,
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摘要:
Background.IgG antibodies to HLA class I antigens can cause hyperacute rejection of renal allografts. Screening of sera from such transplant candidates is laborious, time-consuming, and expensive when performed by sensitive antihuman globulin-augmented lymphocytotoxicity (AHG-CDC).Methods.Because 60-70% of our transplant screens are negative, we evaluated a solid phase enzyme-linked method (EIA) as a potential prescreen by parallel testing 215 sera by AHG-CDC and by EIA. This EIA method is designed to detect only IgG antibodies, and all positive AHG-CDC sera were retested after dithiothreitol treatment.Results.There was 96.2% concordance between the tests for IgG antibodies. Seven sera (3.25%) were positive by EIA alone, and one (0.46%) was negative by EIA alone. The EIA method was also less costly ($15.00 versus $105.00) and less time consuming (hours versus days) than AHG-CDC panel testing for large numbers of sera.Conclusions.We conclude that this EIA method is simple, sensitive, objective, and cost effective as a prescreen for HLA class I antibodies.
ISSN:0041-1337
出版商:OVID
年代:1997
数据来源: OVID
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24. |
ADMINISTRATION OF OKT3 AS A TWO-HOUR INFUSION ATTENUATES FIRST-DOSE SIDE EFFECTS1 |
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Transplantation,
Volume 64,
Issue 11,
1997,
Page 1620-1623
Buysmann2,3 Saskia,
Hack4 C.,
van Diepen3 Frank,
Surachno2 Janto,
ten Berge2,3,5 Ineke,
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摘要:
Background.Use of the murine CD3 monoclonal antibody OKT3 is limited by first-dose side effects, which are thought to be caused by the release of inflammatory mediators. Because these processes might be influenced by the speed of administration, we compared a 2-hr OKT3 infusion with the bolus infusion usually applied nowadays.Methods.Eighteen renal allograft recipients were prophylactically treated with OKT3 and randomized to receive the first dose either as a 2-hr infusion or as an intravenous bolus infusion. Clinical side effects score and the occurrence of complement activation, cytokine release, and activation of neutrophils were determined.Results.Two-hour infusion of OKT3 completely prevented the occurrence of dyspnea, reduced the incidence of other side effects, and attenuated complement activation. Cytokine release and depletion of peripheral blood lymphocytes were similar in both groups.Conclusions.Thus, complement activation seems to play an additional role in the development of side effects after the first OKT3 dose.
ISSN:0041-1337
出版商:OVID
年代:1997
数据来源: OVID
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25. |
EFFICACY AND SAFETY OF LAMIVUDINE ON REPLICATION OF RECURRENT HEPATITIS B AFTER CADAVERIC RENAL TRANSPLANTATION |
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Transplantation,
Volume 64,
Issue 11,
1997,
Page 1624-1627
Rostaing1,2 Lionel,
Henry3 Sabine,
Cisterne1 Jean-Marc,
Duffaut4 Michel,
Icart3 Josette,
Durand1 Dominique,
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摘要:
Background.The aim of this pilot study was to evaluate the efficacy and the safety of lamivudine therapy in hepatitis B virus (HBV)-positive/DNA-positive renal transplant recipients.Methods.Six HBV DNA-positive cadaveric renal transplant recipients ranging in age from 49±6 years were administered lamivudine, at 100 mg/day for a period of at least 6 months, on a compassionate-use basis. Lamivudine is the(-) enantiomer of 3′-thiacytidine, which is known to be a potent inhibitor of HBV replication. All of the patients but one were on cyclosporine-based immunosuppression.Results.The mean serum creatinine was 134±44 μmol/L. The mean duration of HBV infection was 230±54 months (156-288). All of the patients but one had high serum alanine aminotransferase levels (122±52 IU/L; range, 45-243). Histological evaluation showed the presence of either chronic active hepatitis (n=4) or cirrhosis (n=2). All of the patients but one were hepatitis B e antigen negative/hepatitis B e antibody positive, but none were coinfected with either hepatitis C virus or hepatitis D virus.Conclusions.Lamivudine therapy was associated with (i) a normalization of alanine aminotransferase levels in four of five patients when these levels were increased at the beginning (n=5); (ii) a rapid disappearance of HBV DNA from the serum (detected by hybridization) in all of the patients; (iii) the negativity of HBV DNA by polymerase chain reaction in four patients; and (iv) no change in renal function and in proteinuria when present (one patient). Finally, no adverse effects were noted. When lamivudine therapy was stopped for four patients after 6 months, it was associated with a biochemical and virological relapse within the weeks that followed. Lamivudine therapy was therefore resumed for these patients.
ISSN:0041-1337
出版商:OVID
年代:1997
数据来源: OVID
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26. |
LIMITED T-CELL REPERTOIRE IN RENAL ALLOGRAFT AND ALLOGENEIC MELANOMA TRANSMITTED BY THE GRAFT1 |
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Transplantation,
Volume 64,
Issue 11,
1997,
Page 1627-1630
Barth2,3 Claudia,
Stachowski2 Jozef,
von Menges2 Albrecht,
Rodermann2 Ernst,
Pollok2 Manfred,
Smola4 Hans,
Krieg4 Thomas,
Baldamus2 Conrad,
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摘要:
In a patient with metastatic melanoma transmitted by the renal allograft, HLA serves as an alloantigen per se and is associated with tumor antigens at the same time. The influence of this antigeneic pattern on the Vβ T-cell repertoire in an allogeneic melanoma, allograft, and peripheral blood mononuclear cells (PBMC) was assessed by polymerase chain reaction. Vβ13.1 and 19 were found in both the melanoma and the graft. Vβ14 was detected only in the melanoma and Vβ6 was detected only in the kidney. PBMC revealed an unrestricted Vβ pattern. Markers for cytotoxic activity of T cells-granzyme B and perforin-were not expressed during immunosuppressive therapy as clinically reflected in a nonrejecting allograft and in a progressing melanoma. In vitro PBMC proliferated to recombinant interleukin-2, whereas recombinant interferon-γ did not augment this response. Initiation of immune therapy, in addition to discontinuation of immunosuppression, might support the rejection of the allogeneic tumor by dominant Vβ T cells.
ISSN:0041-1337
出版商:OVID
年代:1997
数据来源: OVID
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27. |
ANNOUNCEMENTS |
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Transplantation,
Volume 64,
Issue 11,
1997,
Page 1634-1636
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ISSN:0041-1337
出版商:OVID
年代:1997
数据来源: OVID
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28. |
ERRATUM |
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Transplantation,
Volume 64,
Issue 11,
1997,
Page 1636-1636
&NA;,
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ISSN:0041-1337
出版商:OVID
年代:1997
数据来源: OVID
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29. |
ALOPECIA AS A CONSEQUENCE OF TACROLIMUS THERAPY IN RENAL TRANSPLANTATION? |
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Transplantation,
Volume 64,
Issue 11,
1997,
Page 16311632-16311632
Talbot1 David,
Rix David,
Abusin Kamal,
Mirza Darius,
Manas Derek,
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ISSN:0041-1337
出版商:OVID
年代:1997
数据来源: OVID
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30. |
APOPTOSIS IS THE MAIN MECHANISM OF CARDIOMYOCYTE DEATH IN THE HYPERACUTE REJECTION OF HEART XENO- AND ALLOGRAFTS |
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Transplantation,
Volume 64,
Issue 11,
1997,
Page 16321633-16321633
Beranek1 Jiri,
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ISSN:0041-1337
出版商:OVID
年代:1997
数据来源: OVID
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