Authors
Sebastian Kobold
Published in
Cancer immunology research. Pages OF1-OF2. Oct 30, 2026. Epub Oct 30, 2026.
Abstract
Chimeric antigen receptor (CAR) T cells can provide cures to patients affected by certain hematologic malignancies. Cytokine release syndrome (CRS) is a major side effect of this treatment, yet its pathophysiology remains incompletely understood and selective therapeutic options are limited. In this issue, Li and colleagues identify the CCR1-CCR2 axis as a key mediator of inflammatory macrophage recruitment to sites of CAR T-cell activation, thereby contributing to CRS. In preclinical models, blockade of this axis prevented macrophage recruitment and substantially diminished CRS severity. This discovery could open a new avenue for targeted intervention against CRS, although further validation of the role of the CCR1/CCR2 axis, particularly in clinically relevant settings, is required. See related article by Li and colleagues et al., p. XX.
PMID:
42961088
Bibliographic data and abstract were imported from PubMed on 30 Oct 2026.
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