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Mixed donor chimerism following simultaneous pancreas-kidney transplant
Objectives: Graft-versus-host disease after solid-organ transplant is exceedingly rare. Although the precise pathogenetic mechanisms are unknown, a progressive increase in donor chimerism is a requirement for its development. The incidence of mixed donor chimerism and its timeline after simultaneous...
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Published in: | Experimental and clinical transplantation 2018-06, Vol.16 (3), p.307-313 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | Objectives: Graft-versus-host disease after solid-organ
transplant is exceedingly rare. Although the precise
pathogenetic mechanisms are unknown, a progressive
increase in donor chimerism is a requirement
for its development. The incidence of mixed donor
chimerism and its timeline after simultaneous
pancreas-kidney transplant is unknown.
Materials and Methods: After encountering 2 cases of
graft-versus-host disease after simultaneous pancreaskidney
transplant at our institution over a period of
< 2 years, a collaborative pilot study was conducted by
the bone marrow transplant, nephrology, and
abdominal transplant surgery teams. We enrolled all
consecutive patients undergoing sex-mismatched
simultaneous pancreas-kidney transplant over 1 year
and longitudinally monitored donor chimerism using
fluorescence in situ hybridization for sex chro mosomes.
Results:We found no evidence for chimerism in our 7
patients. In a comprehensive literature review, we
found a total of 25 previously reported cases of graftversus-
host disease after kidney, pancreas, and
simultaneous pancreas-kidney transplants. The
median onset of graft-versus-host disease was ap -
proximately 5 weeks after transplant, with a median of
about 2 weeks of delay between first presentation and
diagnosis. Skin, gut, and bone marrow were almost
equally affected at initial presentation, and fever of
unknown origin occurred in more than half of patients.
The median survival measured from the first mani -
festation of graft-versus-host disease was only 48 days.
Conclusions: Within the limitations related to small
sample size, our results argue against an unusually
high risk of graft-versus-host disease after simulta -
neous pancreas-kidney transplant. Collaboration
between solid-organ and stem cell transplant
investigators can be fruitful and can improve our
understanding of the complications that are shared between the 2 fields. |
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ISSN: | 1304-0855 2146-8427 |
DOI: | 10.6002/ect.2016.0299 |