川地163
清道夫受体
支气管肺泡灌洗
肺移植
移植
CD64
免疫学
医学
CD14型
流式细胞术
肺泡巨噬细胞
病理
肺
巨噬细胞
甘露糖受体
免疫系统
男科
生物
体外
内科学
脂蛋白
生物化学
胆固醇
作者
Mark E. Snyder,Stuart P. Weisberg,Thomas J. Connors,Luke Benvenuto,Lori Shah,Hilary Robbins,Jaime Hook,F. D’Ovidio,Joshua Sonett,Selim M. Arcasoy,Donna L. Farber
标识
DOI:10.1016/j.healun.2019.01.378
摘要
Purpose
Alveolar macrophages play vital roles in attenuating lung injury through immune modulatory effects and improving gas exchange by scavenging cellular debris within the alveoli. A recent analysis of lung biopsy specimens suggests that donor-derived macrophages persist within the allograft after lung transplantation. The phenotypic differences between donor and graft-infiltrating recipient macrophages remains unreported. Methods
Single cell suspensions obtained from bronchoalveolar lavage (BAL) of 15 lung transplant recipients at various times following transplantation were analyzed by flow cytometry. Macrophages were defined as CD45+CD3-CD19-CD64+CD14+CD11chisinglets. Cell origin (donor versus recipient) was identified by staining for human leukocyte antigen discrepancies. Paired t test was used to compare cell surface marker expression between donor and recipient macrophages. Results
The proportion of donor macrophages within the BAL was variable across patients but did not vary over the time following transplantation (p = 0.5). The median percentage of donor macrophages was 10.5% (range 1-64). Donor macrophages had increased expression of CD206 (Figure: Rep. flow cytometry plot from BAL one month following transplantation and cumulative data from 10 participants, p = 0.004), with trends in increased expression of HLADR (p = 0.07), and no difference in CD163 expression (p = 0.17). Conclusion
The scavenger function of alveolar macrophages is vital in maintaining gas exchange in the setting of severe influenza infection. Following lung transplantation, persisting donor-derived alveolar macrophages have significantly increased expression of the scavenger receptor CD206 when compared to graft-infiltrating recipient-derived macrophages. Further investigation is warranted to identify whether this has implications for graft function in the perioperative setting.
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