This application, consisting of two projects, is a joint effort of 44 centers of the NAPRTCS and its two core laboratories of Cornell and Harvard Universities. Project I is entitled """"""""Steroid withdrawal (SW) post- transplantation (PT)"""""""" and has 4 specific aims. We will conduct a randomized trial (ratio 2:1) of 600 primary transplant recipients to test the 1st hypothesis, that patients randomized to RAD, cyclosporine (CSA) and prednisone (P) (test arm) will have significantly less acute rejections in the first six months than the control arm of mycophenolate mofetal (MMF), CSA and P. To test the 2nd hypothesis, that test arm patients who are rejection free by histology (H) and molecular (M) studies can be weaned off P, whereas patients with a H clean biopsy but M evidence of rejection will fail SW, we will perform a protocol biopsy on all clinically rejection free test arm patients six months. PT and randomize (1:1) those who are clear to continue P or to undergo SW. We will perform RT-PCR on the protocol biopsy tissues to quantify mRNA encoding granzyme B, perforin and Fas ligand (CTL), and cytokines IL-10, TNFalpha and TGF- beta1. To test the 3rd hypothesis, that peripheral blood and urine can serve as surrogate markers for intragraft events, we will quantify gene expression for CTL and cytokines in blood and urine obtained at the time of protocol and rejection biopsies following SW. To test the 4th hypothesis, that a high TGF-beta1/low TNFalpha and low IL-10 genotype, is a surrogate marker for steroid withdrawal-permissive donor- specific hyporesponsiveness we will study the individual genotype for these cytokines in all patients in the SW trial using ARMS PCR. Project II is entitled """"""""Pilot study of anti-CD40L mAb in repeat cadaver donor transplants,"""""""" and has two specific aims. To test the 1st hypothesis, that treatment using a co-stimulatory blockade without calcineurin inhibition will enable us to achieve on-year graft survival comparable to that seen in primary transplants (85%), we will perform an open label trial using the Biogen antibody hu5c8 with steroids and MMF in 66 cadaver donor repeat transplants. To test the 2nd hypothesis, that the interruption of the CD40/CD40L pathway will result in the absence or reduced expression of CTL molecules and cytokines IL-2, IFNgamma, IL-10, IL-12 and up- regulation of IL-4 in surveillance biopsies (RB), we will perform an SB on all patients on day 12 and an RB with each episode. The biopsy tissue will be studied by PCR and by immunohistology.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01AI046134-02
Application #
6170822
Study Section
Special Emphasis Panel (ZAI1-MCH-I (S2))
Program Officer
Rose, Stephen M
Project Start
1999-09-30
Project End
2003-08-30
Budget Start
2000-09-01
Budget End
2001-08-31
Support Year
2
Fiscal Year
2000
Total Cost
$1,105,776
Indirect Cost
Name
New York Medical College
Department
Pediatrics
Type
Schools of Medicine
DUNS #
City
Valhalla
State
NY
Country
United States
Zip Code
10595
Toyoda, Mieko; Ge, Shili; Pao, Andy et al. (2010) Cellular allo reactivity against paternal HLA antigens in normal multiparous females as detected by intracellular cytokine flow cytometry remains elevated over years despite diminution of anti-HLA antibody levels. Transpl Immunol 23:133-40
Toyoda, Mieko; Pao, Andy; Vo, Ashley et al. (2010) Intracellular IFNgamma production in CD3 negative cells exposed to allo-antigens is an indicator of prior sensitization. Transpl Immunol 22:121-7
Schachter, Asher D; Benfield, Mark R; Wyatt, Robert J et al. (2006) Sirolimus pharmacokinetics in pediatric renal transplant recipients receiving calcineurin inhibitor co-therapy. Pediatr Transplant 10:914-9
Toyoda, Mieko; Puliyanda, Dechu P; Amet, Nurmamet et al. (2005) Co-infection of polyomavirus-BK and cytomegalovirus in renal transplant recipients. Transplantation 80:198-205
Avihingsanon, Yingyos; Ma, Naili; Pavlakis, Martha et al. (2005) On the intraoperative molecular status of renal allografts after vascular reperfusion and clinical outcomes. J Am Soc Nephrol 16:1542-8
Avihingsanon, Yingyos; Ma, Naili; Csizmadia, Eva et al. (2002) Expression of protective genes in human renal allografts: a regulatory response to injury associated with graft rejection. Transplantation 73:1079-85