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CD4 T cells promote tissue inflammation via CD40 signaling without de novo activation in a murine model of liver ischemia/reperfusion injury by Xiuda Shen; Yue Wang; Feng Gao; Feng Ren; Ronald W. Busuttil; Jerzy W. Kupiec-Weglinski; Yuan Zhai is a Medicine article available to read on EtoBox.

What is CD4 T cells promote tissue inflammation via CD40 signaling without de novo activation in a murine model of liver ischemia/reperfusion injury about?

Although the role of CD4 T cells in tissue inflammation and organ injury resulting from ischemia and reperfusion injury (IRI) has been well documented, it remains unclear how CD4 T cells are activated and function in the absence of a specific antigen (Ag). We used a murine liver warm IRI model to determine first whether de novo Ag-specific CD4 T cell activation was required and then what its functional mechanism was. The critical role of CD4 T cells in liver immune activation against ischemia and reperfusion (IR) was confirmed in CD4 knockout mice and CD4 depleted wild-type mice. Interestingly, the inhibition of CD4 T cell activation without target cell depletion failed to protect livers against IRI, and this suggested that T cells function in liver IRI without Ag-specific de novo activation. To dissect the T cell functional mechanism, we found that CD154 blockade, but not interferon ␥ (IFN-␥) neutralization, inhibited local immune activation and protected livers from IRI. Furthermore, agonist anti-CD40 antibodies restored liver IRI in otherwise protected CD4-deficient hosts. Finally, fluorescence-activated cell sorting analysis of liver CD4 T cells revealed the selective infiltrat

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It is typically read by researchers, students, and practitioners in Medicine.

Author
Xiuda Shen; Yue Wang; Feng Gao; Feng Ren; Ronald W. Busuttil; Jerzy W. Kupiec-Weglinski; Yuan Zhai
Publisher
Ovid Technologies (Wolters Kluwer Health)
Published
2009
Language
EN
Field
Medicine (Health Sciences)

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