Literature DB >> 15848576

Reversal of acute cellular rejection after renal transplantation with Campath-1H.

A Basu1, M Ramkumar, H P Tan, A Khan, J McCauley, A Marcos, J J Fung, T E Starzl, R Shapiro.   

Abstract

Between September 2002 and February 2004, 40 kidney transplant (27 from deceased and 13 from living donors) recipients (25 male and 15 female, aged 50.3 +/- 15.1 years) were treated with Campath 1H (C 1H; 30 mg/dose IV) for biopsy-proven steroid-resistant rejection (SRR) or rejections equal to or worse than Banff 1B. All transplantations occurred between August 2001 and May 2003. All patients had received antibody preconditioning (RATG 5 mg/kg, n = 34; C 1H 60 mg, n = 4; C 1H 30 mg, n = 2) preoperatively and were treated with Tacrolimus monotherapy (target level 10 ng/ml) postoperatively and subsequent spaced weaning. Elevated creatinine levels at follow-up were evaluated by renal transplant biopsy. Rejection was treated with steroids, reversal of weaning, addition of sirolimus, and/or antibody treatment, depending on grade of rejection. The mean duration of follow-up was 453 +/- 163 days after C 1H administration. Twenty-nine patients received C 1H for SRR and 11 patients for Banff 1B or worse rejections; 26 patients received more than 1 dose of C 1H. Graft survival was 62.5% (25 patients); 6 of the 15 allografts (40%) that failed had presented with rejections because of noncompliance. Graft survival in compliant patients with SRR or rejections equal to or worse than Banff 1B was 73.5% (25 of 34). Fourteen patients (35%) had infectious complications, of whom 2 patients (5%) died. C 1H is an effective agent for SRR and Banff 1B or worse rejections, with 95% patient survival and 73.5% graft survival (in compliant patients). The number of doses of 30 mg C 1H should be restricted to two, as there is a high incidence of potentially fatal infectious complications.

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Year:  2005        PMID: 15848576     DOI: 10.1016/j.transproceed.2004.12.019

Source DB:  PubMed          Journal:  Transplant Proc        ISSN: 0041-1345            Impact factor:   1.066


  8 in total

Review 1.  Immunosuppressive preconditioning or induction regimens : evidence to date.

Authors:  Henkie P Tan; Marc C Smaldone; Ron Shapiro
Journal:  Drugs       Date:  2006       Impact factor: 9.546

2.  Living donor renal transplantation using alemtuzumab induction and tacrolimus monotherapy.

Authors:  H P Tan; D J Kaczorowski; A Basu; M Unruh; J McCauley; C Wu; J Donaldson; I Dvorchik; L Kayler; A Marcos; P Randhawa; C Smetanka; T E Starzl; R Shapiro
Journal:  Am J Transplant       Date:  2006-08-04       Impact factor: 8.086

Review 3.  Antibody immunosuppressive therapy in solid-organ transplant: Part I.

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4.  Regulation of human T cell responses by dNP2-ctCTLA-4 inhibits human skin and microvessel graft rejection.

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6.  Review of the Clinical Pharmacokinetics and Pharmacodynamics of Alemtuzumab and Its Use in Kidney Transplantation.

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7.  Comparison of Alemtuzumab and Anti-thymocyte Globulin Treatment for Acute Kidney Allograft Rejection.

Authors:  Marieke van der Zwan; Marian C Clahsen-Van Groningen; Martijn W F van den Hoogen; Marcia M L Kho; Joke I Roodnat; Katya A L Mauff; Dave L Roelen; Madelon van Agteren; Carla C Baan; Dennis A Hesselink
Journal:  Front Immunol       Date:  2020-07-03       Impact factor: 7.561

8.  Alemtuzumab as Antirejection Therapy: T Cell Repopulation and Cytokine Responsiveness.

Authors:  Anne P Bouvy; Mariska Klepper; Michiel G H Betjes; Willem Weimar; Dennis A Hesselink; Carla C Baan
Journal:  Transplant Direct       Date:  2016-05-25
  8 in total

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