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Updated: May 5, 2026

Trans-vivo Delayed Type Hypersensitivity Assay for Antigen Specific Regulation
Published on: May 2, 2013
New developments in transplant-acquired allergies
1Öner Özdemir, Division of Allergy and Immunology, Department of Pediatrics, Faculty of Medicine, Sakarya University, Research and Training Hospital of Sakarya University, Adapazarı, 54100 Sakarya, Turkey.
Transplant-acquired allergy (TAA) can develop after organ transplantation, often presenting as food allergy, particularly in children. The exact cause is unknown, but the transplanted organ and patient factors play a role, with some improvement seen after treatment adjustments.
Area of Science:
- Immunology
- Transplantation Medicine
- Allergy Research
Background:
- Transplant-acquired allergy (TAA), initially termed transplant-acquired food allergy (TAFA), is increasingly recognized following various organ transplantations.
- TAA has been observed after bone marrow, liver, heart, intestinal, lung, and renal transplantations, affecting both children and adults.
- Previous literature may have underestimated TAA prevalence and its occurrence in non-liver transplant recipients.
Purpose of the Study:
- To review and synthesize current knowledge on transplant-acquired allergy (TAA).
- To explore the prevalence, clinical presentation, and potential pathogenesis of TAA.
- To discuss management strategies and identify gaps in understanding TAA's transient nature.
Main Methods:
- Review of existing literature and case reports on transplant-acquired allergy.
- Analysis of reported prevalence, patient demographics, and clinical manifestations.
- Exploration of proposed pathogenetic mechanisms, including immune responses and immunosuppressive effects.
Main Results:
- TAA, particularly TAFA, is reported across various solid organ transplants, with prevalence estimates in children ranging widely (6%–57%).
- Children with TAFA typically develop symptoms within a year post-transplant and often exhibit allergies to multiple foods.
- The functioning transplanted organ, alongside recipient factors like age and atopy, is implicated in TAA development, not solely immunosuppression.
Conclusions:
- The pathogenesis of TAA is multifactorial, involving immune system interactions between the graft and recipient.
- Symptomatic improvement in TAA is often achieved by reducing immunosuppression and dietary modifications.
- Further research with larger patient cohorts is necessary to definitively determine if TAA is transient in solid organ transplant recipients.
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