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In Vitro and In Vivo Assessment of T, B and Myeloid Cells Suppressive Activity and Humoral Responses from Transplant Recipients
Published on: August 12, 2017
The combined organ effect: protection against rejection?
Abbas Rana1, Susanne Robles, Mark J Russo
1Division of Transplant Surgery, Department of Surgery, Columbia University College of Physicians and Surgeons, New York, New York 10032, USA. aar2107@columbia.edu
Combined organ transplants involving heart, liver, and kidney allografts show reduced rejection rates, suggesting organs protect each other. This immunoprotection requires shared antigenic identity or increased antigen load, particularly in double-organ transplants.
Area of Science:
- Transplantation immunology
- Organ allograft research
- Immunoprotection in combined transplants
Background:
- Liver allografts are traditionally considered immunoprotective for co-transplanted donor-specific allografts.
- Emerging evidence suggests this protective property extends to other organ types.
Purpose of the Study:
- To compare rejection-free survival and 1-year rejection rates in various combined organ transplants.
- To elucidate the immunoprotective effects of one allograft on another in simultaneous transplantation.
Main Methods:
- Analysis of a large cohort (n=133,416) from the United Network of Organ Sharing database.
- Inclusion criteria: recipients aged 18+, primary transplants (excluding intestinal), between 1994-2005.
- Exclusion criteria: previous transplants, live donors, insufficient follow-up.
Main Results:
- Co-transplanted liver, kidney, and heart allografts showed significantly lower rejection rates compared to single transplants.
- Intestinal or pancreatic allografts did not confer similar protective effects.
- Reduced rejection observed in interval kidney-heart transplants with partial antigenic identity and in double-organ transplants of the same type.
Conclusions:
- Simultaneous heart, liver, and kidney allografts are protected from rejection and offer protection to co-transplanted organs.
- Immunoprotection in interval heart-kidney transplants necessitates partial antigenic identity.
- Increased antigen load from identical antigens, as in double-lung or double-kidney transplants, also provides immunologic protection.
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