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Set Up for Failure: Pre-Existing Autoantibodies in Lung Transplant

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FRONTIERS IN IMMUNOLOGY
卷 12, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.711102

关键词

lung transplant; complement; Autoantibodies; primary graft dysfunction; chronic lung allograft dysfunction; glycans

资金

  1. NIH [NHLBI R1R01HL 140470-01A1, NHLBI 3RO1HL140470-03S1, NIAID U01 AI132894-01, TL1 TR001451, U01CA242096, NHLBI K24-HL115354, NHLBI R01HL087115, NHLBI U01-HL145435]

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Patients undergoing lung transplantation have the lowest long-term survival rates among solid organ transplant recipients, largely due to complications like primary graft dysfunction and chronic lung allograft dysfunction. Recent studies suggest that lung-specific autoantibodies, recognizing non-HLA antigens, may play a role in graft injury both before and after transplantation.
Lung transplant patients have the lowest long-term survival rates compared to other solid organ transplants. The complications after lung transplantation such as primary graft dysfunction (PGD) and ultimately chronic lung allograft dysfunction (CLAD) are the main reasons for this limited survival. In recent years, lung-specific autoantibodies that recognize non-HLA antigens have been hypothesized to contribute to graft injury and have been correlated with PGD, CLAD, and survival. Mounting evidence suggests that autoantibodies can develop during pulmonary disease progression before lung transplant, termed pre-existing autoantibodies, and may participate in allograft injury after transplantation. In this review, we summarize what is known about pulmonary disease autoantibodies, the relationship between pre-existing autoantibodies and lung transplantation, and potential mechanisms through which pre-existing autoantibodies contribute to graft injury and rejection.

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