LETHAL GRAFT-VERSUS-HOST DISEASE AFTER SIMULTANEOUS KIDNEY-PANCREAS TRANSPLANTATION

Citation
P. Kimball et al., LETHAL GRAFT-VERSUS-HOST DISEASE AFTER SIMULTANEOUS KIDNEY-PANCREAS TRANSPLANTATION, Transplantation, 63(11), 1997, pp. 1685-1688
Citations number
10
Categorie Soggetti
Immunology,Surgery,Transplantation
Journal title
ISSN journal
00411337
Volume
63
Issue
11
Year of publication
1997
Pages
1685 - 1688
Database
ISI
SICI code
0041-1337(1997)63:11<1685:LGDASK>2.0.ZU;2-9
Abstract
Background. This case report is the first documentation of the occurre nce and potential source of lethal graft-versus-host disease (GVHD) af ter simultaneous kidney-pancreas transplantation. The patient was a 27 -year-old African-American male who received an ABO-compatible, five H LA antigen-mismatched kidney-pancreas transplant from a 17-year-old Af rican-American female donor, who died after childbirth. Methods. Preop erative crossmatches using lymphocytotoxicity and flow cytometry were negative. The patient received four blood transfusions within 10 days of transplantation. Immunosuppression consisted of OKT3 induction, and then cyclosporine, azathioprine, and corticosteroids. Results. On pos toperative day (POD) 9, the patient became febrile, and leukocytopenia and pancytopenia developed. Immunosuppression was reduced and granulo cyte colony-stimulating factor was begun. Cultures were negative, inte rleukin 6 and interleukin 8 levels were elevated, and a cutaneous rash appeared on POD 18. A skin biopsy demonstrated dermatitis with focal epidermal necrosis consistent with GVHD. In an attempt to identify the source of GVHD, variable-number tandem repeat analysis fingerprinting was performed with DNA from donor splenocytes, from the skin biopsy, as well as from the patient's buccal mucosa. The skin biopsy showed a mixed variable-number tandem repeat analysis type containing DNA fragm ents matching the recipient and donor. Blood donors were excluded as a source because they were serologically different from the organ donor . The patient developed liver abnormalities and died from multiorgan f ailure on POD 22. Conclusions. We speculate that carryover of passenge r donor lymphocytes within the transplanted organ were responsible for GVHD. Furthermore, donor traits such as sexual mismatching, African-A merican race, and alloimmune status may be important potential risk fa ctors for GVHD.