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Life in the allogeneic environment after lung transplantation
I Paradis1, H Rabinowich, A Zeevi
1Department of Medicine, University of Pittsburgh, Pennsylvania 15261.
Lung
|January 1, 1990
Summary
Lung transplant recipients show impaired antimicrobial functions in alveolar macrophages, increasing infection risk. However, their macrophages retain functions crucial for transplant immunity, suggesting a role in allograft rejection.
Area of Science:
- Immunology
- Transplantation Biology
- Pulmonary Medicine
Background:
- Lung transplantation is susceptible to infection and rejection.
- Alveolar macrophages are vital for lung defense and may influence transplant outcomes.
- Understanding alveolar macrophage function is key to improving lung allograft survival.
Purpose of the Study:
- To assess key functions of alveolar macrophages in lung transplant recipients.
- To evaluate both antimicrobial and transplant-related immune functions.
- To determine the role of alveolar macrophages in post-transplant complications.
Main Methods:
- Collection and functional assessment of alveolar macrophages and blood monocytes from lung recipients and normal subjects.
- Chemotaxis, phagocytosis, and intracellular killing assays for antimicrobial function.
- Mitogen and antigen presentation assays, primed lymphocyte test, and mixed lymphocyte reaction for transplant immunity.
Main Results:
- Impaired chemotaxis, phagocytosis, and intracellular killing in alveolar macrophages from lung recipients.
- Reduced ability of alveolar macrophages and blood monocytes to support mitogen and antigen presentation.
- Preserved lymphocyte proliferation support by alveolar macrophages in response to donor or allogeneic antigens, unlike blood monocytes.
Conclusions:
- Impaired antimicrobial functions of alveolar macrophages may explain increased infection susceptibility in lung allografts.
- Preserved functions in transplant immunity suggest alveolar macrophages contribute to lung allograft rejection.
- Alveolar macrophage dysfunction impacts both infection defense and immune response post-lung transplantation.