Acute cellular rejection grading scheme for human gastric allografts

The control of acute cellular rejection (ACR) in multivisceral transplantation improves long-term survival, but monitoring this process can be challenging because different allografts can display varying forms and degrees of rejection. Criteria for ACR of small bowel and liver have been established,...

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Veröffentlicht in:Human pathology 2004-03, Vol.35 (3), p.343-349
Hauptverfasser: Garcia, Monica, Delacruz, Victor, Ortiz, Roque, Bagni, Alberto, Weppler, Deborah, Kato, Tomoaki, Tzakis, Andreas, Ruiz, Phillip
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container_end_page 349
container_issue 3
container_start_page 343
container_title Human pathology
container_volume 35
creator Garcia, Monica
Delacruz, Victor
Ortiz, Roque
Bagni, Alberto
Weppler, Deborah
Kato, Tomoaki
Tzakis, Andreas
Ruiz, Phillip
description The control of acute cellular rejection (ACR) in multivisceral transplantation improves long-term survival, but monitoring this process can be challenging because different allografts can display varying forms and degrees of rejection. Criteria for ACR of small bowel and liver have been established, but a systematic analysis for ACR in stomach is lacking. For this reason we have developed a comprehensive grading scheme for the evaluation of gastric allograft rejection. The grading scheme was designed to individually grade a variety of changes in the surface epithelium, lamina propria, and glandular structures. The individual values are cumulated, and the final score determines assignment of the rejection grade. The ACR grades range from no evidence of acute cellular rejection to severe rejection. We performed a retrospective study based on 70 gastric allograft biopsies from 20 patients who received multivisceral transplantation from 1995 to 2001. We found that the scoring system showed no significant interobserver variability and allowed for an accurate designation of the ACR grade to the gastric allografts. We found with this grading system that neither clinical symptoms nor gastric endoscopic findings could serve as specific indicators of gastric ACR. Our results also showed that there were differences in the occurrence and intensity of acute rejection between the stomach and other transplanted organs, suggesting that ACR can occur independently among different allografts of the same host. In conclusion, we find that this scheme for grading ACR in gastric transplants is objective and reproducible. This grading system will likely allow for improved correlation between gastric ACR grade and clinical symptoms, as well as improve interobserver uniformity within and between institutions.
doi_str_mv 10.1016/j.humpath.2003.10.011
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Criteria for ACR of small bowel and liver have been established, but a systematic analysis for ACR in stomach is lacking. For this reason we have developed a comprehensive grading scheme for the evaluation of gastric allograft rejection. The grading scheme was designed to individually grade a variety of changes in the surface epithelium, lamina propria, and glandular structures. The individual values are cumulated, and the final score determines assignment of the rejection grade. The ACR grades range from no evidence of acute cellular rejection to severe rejection. We performed a retrospective study based on 70 gastric allograft biopsies from 20 patients who received multivisceral transplantation from 1995 to 2001. We found that the scoring system showed no significant interobserver variability and allowed for an accurate designation of the ACR grade to the gastric allografts. We found with this grading system that neither clinical symptoms nor gastric endoscopic findings could serve as specific indicators of gastric ACR. Our results also showed that there were differences in the occurrence and intensity of acute rejection between the stomach and other transplanted organs, suggesting that ACR can occur independently among different allografts of the same host. In conclusion, we find that this scheme for grading ACR in gastric transplants is objective and reproducible. 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We found with this grading system that neither clinical symptoms nor gastric endoscopic findings could serve as specific indicators of gastric ACR. Our results also showed that there were differences in the occurrence and intensity of acute rejection between the stomach and other transplanted organs, suggesting that ACR can occur independently among different allografts of the same host. In conclusion, we find that this scheme for grading ACR in gastric transplants is objective and reproducible. 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subjects Acute Disease
Adolescent
Adult
Architecture
Biological and medical sciences
Child
Child, Preschool
Female
gastric rejection
gastric transplant
Gastrointestinal diseases
Graft Rejection - classification
Graft Rejection - mortality
Graft Rejection - pathology
Humans
Infant
Investigative techniques, diagnostic techniques (general aspects)
Liver
Male
Medical sciences
Middle Aged
Observer Variation
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Respiratory distress syndrome
Stomach - pathology
Stomach - transplantation
Studies
Survival Rate
Transplantation, Homologous
Transplants & implants
title Acute cellular rejection grading scheme for human gastric allografts
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