Neutrophil deficiency increases T cell numbers at the site of tissue injury in mice
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Updated: Jun 28, 2026

Isolation, Purification and Labeling of Mouse Bone Marrow Neutrophils for Functional Studies and Adoptive Transfer Experiments
Published on: July 10, 2013
Hajnalka Halász1,2, Albert Bálint Papp3,4, Lukács Sándor Lesinszki5
1Doctoral School of Molecular Cell and Immune Biology, Faculty of Medicine, University of Debrecen, Hungary.
Abstract:
During the investigation of muscle injury and regeneration in neutrophil-deficient mice, we observed unexpected changes in the cellular composition of tissue-infiltrating inflammatory cells. Neutrophil deficiency led to reduced macrophage infiltration and a striking increase in nonconventional CD4- CD8- (double-negative) αβ and γδ T cell numbers, peaking at Day 3 postinjury. In exploring the underlying mechanisms, we identified previously unrecognized cellular and tissue alterations, including bone marrow erythroid insufficiency and compensatory extramedullary hematopoiesis accompanied by splenomegaly. Using a thioglycolate-induced peritonitis model, we further demonstrated that elevated T-cell numbers reflect a general inflammatory response in neutrophil-deficient mice. Our findings suggest that this model provides a valuable platform for investigating the properties and functions of rare nonconventional T cells in tissue injury and diverse inflammatory conditions.Impact statement Our studies demonstrate that neutrophil-deficient mice may provide a valuable model for investigating the roles and characteristics of non-conventional T cells in tissue inflammation and repair.

