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Long-Term persistence of human donor alveolar macrophages in lung transplant recipients

Eguíluz-Gracia, Ibon (author)
Oslo university hospital,University of Oslo
Schultz, Hans Henrik Lawaetz (author)
Copenhagen University Hospital
Sikkeland, Liv I B (author)
Oslo university hospital,University of Oslo
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Danilova, Elena (author)
Oslo university hospital,University of Oslo
Holm, Are M. (author)
Oslo university hospital,University of Oslo
Pronk, Cornelis J H (author)
Lund University
Agace, William W. (author)
Lund University,Lunds universitet,Slemhinnans immunologi,Forskargrupper vid Lunds universitet,Mucosal Immunology,Lund University Research Groups
Iversen, Martin (author)
Copenhagen University Hospital
Andersen, Claus (author)
University of Copenhagen,Copenhagen University Hospital
Jahnsen, Frode L. (author)
Oslo university hospital,University of Oslo
Baekkevold, Espen S. (author)
University of Oslo,Oslo university hospital
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 (creator_code:org_t)
2016-06-21
2016
English 6 s.
In: Thorax. - : BMJ. - 0040-6376 .- 1468-3296. ; 71:11, s. 1006-1011
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background Alveolar macrophages (AMFs) are critical regulators of lung function, and may participate in graft rejection following lung transplantation. Recent studies in experimental animals suggest that most AMFs are self-maintaining cells of embryonic origin, but knowledge about the ontogeny and life span of human AMFs is scarce. Methods To follow the origin and longevity of AMFs in patients with lung transplantation for more than 100â €..weeks, we obtained transbronchial biopsies from 10 gender-mismatched patients with lung transplantation. These were subjected to combined in situ hybridisation for X/Y chromosomes and immunofluorescence staining for macrophage markers. Moreover, development of AMFs in humanised mice reconstituted with CD34+ umbilical cord-derived cells was assessed. Results The number of donor-derived AMFs was unchanged during the 2â €..year post-Transplantation period. A fraction of the AMFs proliferated locally, demonstrating that at least a subset of human AMFs have the capacity to self-renew. Lungs of humanised mice were found to abundantly contain populations of human AMFs expressing markers compatible with a monocyte origin. Moreover, in patients with lung transplantation we found that recipient monocytes seeded the alveoli early after transplantation, and showed subsequent phenotypical changes consistent with differentiation into proliferating mature AMFs. This resulted in a stable mixed chimerism between donor and recipient AMFs throughout the 2-year period. Conclusions The finding that human AMFs are maintained in the lung parenchyma for several years indicates that pulmonary macrophage transplantation can be a feasible therapeutic option for patients with diseases caused by dysfunctional AMFs. Moreover, in a lung transplantation setting, long-Term persistence of donor AMFs may be important for the development of chronic graft rejection.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Lungmedicin och allergi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Respiratory Medicine and Allergy (hsv//eng)

Keyword

Lung Transplantation
Macrophage Biology
Pulmonary alveolar proteinosis

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art (subject category)
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