AI Article Synopsis

  • Donor lymphocyte infusion (DLI) is a treatment for hematologic cancers that can lead to complications like graft-versus-host disease, but noninfectious pulmonary complications (NIPCs) after DLI are less commonly reported.
  • A case study described a 55-year-old woman with acute myeloid leukemia who developed NIPC eight weeks after DLI, characterized by respiratory symptoms and imaging findings, and she was successfully treated with prednisolone.
  • Analysis of her bronchoalveolar lavage fluid showed recipient-derived immune cells, and a rise in specific cytokines was noted, indicating that recipient cells were primarily responsible for the NIPCs, not a response from the donor cells.

Article Abstract

Background: Donor lymphocyte infusion (DLI) is used for treatment of hematologic malignancy relapse or mixed chimerism after allogeneic hematopoietic stem cell transplantation. Although graft-versus-host disease is well recognized as one of the adverse effects of DLI, there are limited reports on noninfectious pulmonary complications (NIPCs) after DLI.

Case Report: A 55-year-old woman with acute myeloid leukemia received DLI for conversion from recipient predominant to complete donor chimerism on Day +193 after allogeneic HSCT. Eight weeks later, she complained of dyspnea with fever; chest computed tomography revealed diffuse, bilateral, ground glass opacity and reticular appearance. She was diagnosed as having NIPC based on serum and bronchoalveolar lavage fluid (BALF) findings. She was successfully treated with prednisolone (PSL) and completely recovered.

Discussion: We analyzed the cell profile from the BALF and 27 cytokines and chemokines in the serum using the Bio-Plex platform. The cells consisted of recipient predominant macrophages and T cells. The serum cytokine and chemokine profile showed significant elevation of interleukin (IL)-1β, IL-6, IL-8, tumor necrosis factor-α, macrophage inflammatory protein (MIP)-1α, and MIP-1β, which declined with the improvement of symptoms after initiation of PSL treatment.

Conclusion: Inflammatory effectors by recipient cells, rather than allogeneic responses by donor cells, played an important role in the pathogenesis of NIPCs after DLI in the present case.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7169758PMC
http://dx.doi.org/10.1111/trf.13283DOI Listing

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