4-1BB signal stimulates the activation, expansion, and effector functions of γδ T cells in mice and humans
- Resource Type
- Authors
- Yu I. Kim; Sun H. Hwang; Byoung S. Kwon; Dass S. Vinay; In S. Han; Young Ho Kim; Seung Jin Lee
- Source
- European Journal of Immunology. 43:1839-1848
- Subject
- Cell division
medicine.medical_treatment
Immunology
Regulator
Stimulation
Biology
medicine.disease_cause
Cell biology
Interleukin 21
Cytokine
Listeria monocytogenes
medicine
Immunology and Allergy
Cytotoxic T cell
Ligation
- Language
- ISSN
- 0014-2980
We show here that the expression of 4-1BB is rapidly induced in γδ T cells following antigenic stimulation in both mice and humans, and ligation of the newly acquired 4-1BB with an agonistic anti-4-1BB augments cell division and cytokine production. We further demonstrate that γδ rather than αβ T cells protect mice from Listeria monocytogenes (LM) infection and 4-1BB stimulation enhances the γδ T-cell activities in the acute phase of LM infection. IFN-γ produced from γδ T cells was the major soluble factor regulating LM infection. Vγ1(+) T cells were expanded in LM-infected mice and 4-1BB signal triggered an exclusive expansion of Vγ1(+) T cells and induced IFN-γ in these Vγ1(+) T cells. Similarly, 4-1BB was induced on human γδ T cells and shown to be fully functional. Combination treatment with human γδ T cells and anti-hu4-1BB effectively protected against LM infection in human γδ T cell-transferred NOD-SCID mice. Taken together, these data provide evidence that the 4-1BB signal is an important regulator of γδ T cells and induces robust host defense against LM infection.