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 (US) |
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Pages (from-to) | E775-E780 |
Journal | Journal of Pediatric Hematology/Oncology |
Volume | 45 |
Issue number | 6 |
DOIs | |
State | Published - Aug 1 2023 |
Keywords
- ALL
- CAR T cells
- IPS
- acute lymphoblastic leukemia
- hematopoietic cell transplantation
- idiopathic pneumonia syndrome
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Hematology
- Oncology