Detailed Analysis of Simultaneous Renal and Liver Allografts in the Presence of DSA

Author:

O’Leary Jacqueline G.1,Farris Alton B.2,Gebel Howard M.2,Asrani Sumeet K.3,Askar Medhat3,Garcia Vanessa3,Snipes George J.4,Lo Denise J.5,Knechtle Stuart J.5,Klintmalm Goran B.3,Demetris Anthony J.6

Affiliation:

1. Department of Medicine, Dallas VA Medical Center, Dallas, TX.

2. Department of Pathology, Emory University Hospital, Atlanta, GA.

3. Annette C. & Harold C. Simmons Transplant Institute, Baylor University Medical Center, Dallas TX.

4. Department of Pathology, Baylor University Medical Center, Dallas TX.

5. Department of Surgery, Duke University, Durham, NC.

6. Department of Pathology, University of Pittsburgh, Pittsburgh, PA.

Abstract

Background. Liver allografts protect renal allografts from the same donor from some, but not all, preformed donor specific alloantibodies (DSA). However, the precise mechanisms of protection and the potential for more subtle alterations/injuries within the grafts resulting from DSA interactions require further study. Methods. We reevaluated allograft biopsies from simultaneous liver-kidney transplant recipients who had both allografts biopsied within 60 d of one another and within 30 d of DSA being positive in serum (positive: mean florescence intensity ≥5000). Routine histology, C4d staining, and specialized immunohistochemistry for Kupffer cells (KCs; CD163) and a C4d receptor immunoglobulin-like transcript-4 were carried out in 4 patients with 6 paired biopsies. Results. Overt antibody-mediated rejection was found in 3 of 4 renal and liver allografts. One patient had biopsy-confirmed renal and liver allograft antibody-mediated rejection despite serum clearance of DSA. All biopsies showed KC hypertrophy (minimal: 1; mild: 2; moderate: 1; severe: 2) and cytoplasmic C4d KC staining was easily detected in 2 biopsies from 2 patients; minimal and negative in 2 biopsies each. Implications of which are discussed. Control 1-y protocol liver allograft biopsies from DSA– recipients showed neither KC hypertrophy nor KC C4d staining (n = 6). Conclusions. Partial renal allograft protection by a liver allograft from the same donor may be partially mediated by phagocytosis/elimination of antibody and complement split products by KCs, as shown decades ago in controlled sensitized experimental animal experiments.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Transplantation

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