Abstract
Idiopathic pneumonia syndrome (IPS) is a life-threatening complication of hematopoietic cell transplantation, but it is not clearly described following chimeric antigen receptor (CAR) T-cell therapy. We describe a child who developed IPS after receiving tisagenlecleucel for post-hematopoietic cell transplantation relapsed acute lymphoblastic leukemia and had a remarkable improvement after treatment with corticosteroids and etanercept. We discuss the implications of cytokine signaling in IPS and immunologic considerations of allogeneic CAR T cells. We anticipate that the incidence of IPS and other allogeneic phenomena will be observed more often as allogeneic CAR T cells are employed in more varied settings with more mismatched donors.
| Original language | English |
|---|---|
| Journal | Journal of Pediatric Hematology/Oncology |
| Volume | 45 |
| Issue number | 6 |
| DOIs | |
| State | Published - 2023 |
Keywords
- hematopoietic stem cell transplant
- pneumonia
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