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Heme disposal inside heart transplants: a trigger for rejection?
Fuyi Liao, Andrew E. Gelman
Fuyi Liao, Andrew E. Gelman
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Commentary

Heme disposal inside heart transplants: a trigger for rejection?

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Abstract

Cardiac allograft vasculopathy (CAV) is a fibroproliferative form of transplant rejection with limited treatment options other than retransplantation. In this issue, See and colleagues examined human explanted allografts with CAV. They found that a high proportion of intragraft plasma cells produce antibodies that recognize the heme catabolic end product, bilirubin. Clonotypic profiling revealed that bilirubin-reactive antibody-producing plasma cells develop from graft-infiltrating innate-like B cells, a subset often characterized by their rapid production of polyreactive natural antibodies as an early defense against infection. CAV but not nonrejecting graft tissue contained bilirubin deposits along with macrophages that expressed genes involved in heme catabolism. These findings raise the intriguing possibility that graft-derived bilirubin-specific antibodies target local heme catabolism to promote CAV.

Authors

Fuyi Liao, Andrew E. Gelman

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Figure 1

Schematic of intragraft heme catabolism and bilirubin-specific antibody production during CAV pathogenesis.

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Schematic of intragraft heme catabolism and bilirubin-specific antibody ...
See et al. demonstrated that intragraft plasma cells are derived locally from graft-infiltrating innate-like B cell clones that recognize bilirubin (6). Heme catabolism also likely occurs within allograft tissue, as evidenced by bilirubin and iron deposits in the tunica media of the coronary artery and macrophages, upregulating genes that drive heme degradation, such as HMOX1 (encoding HO-1). CO, carbon monoxide.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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