Article: Characterization of Serotype-Specific Dengue Virus T-Cell Inhibition

Authors: Jinhua Xiang, James H McLinden, Qing Chang, Micaela Fosdick, Hillel Haim, Alexander Ploss, Wesley Hottel, Nirjal Bhattarai, Tomokazu Tamura, Jiayu Zhang, Jon C D Houtman, Jack T Stapleton

Journal: J Infect Dis. 2025 Nov 14;232(5):1228-1238. doi: 10.1093/infdis/jiaf241

Abstract:
Background: Dengue virus serotype 2 and 3 (DENV-2 and -3) infections are associated with more severe disease outcomes than DENV-1 and 4, though a biological explanation for this has not been identified.

Methods: DENV serotype effects on human T-cell activation were assessed by measuring T-cell receptor (TCR)-mediated interleukin 2 release following TCR stimulation. DENV envelope (env) proteins were expressed in Jurkat CD4+ T-cell lines, and regions inhibiting TCR inhibition were mapped by mutagenesis. TCR signaling pathway inhibition was characterized by total internal reflection fluorescence microscopy and immunoblot. Reverse genetics validated env mapping results.

Results: T-cell incubation with DENV-1 and -4 inhibited TCR signaling, whereas DENV-2 and -3 did not. Inhibition did not require viral replication. DENV env protein expression inhibited TCR by interfering with activation of proximal TCR signaling events. Amino acids (aa’s) 49 to 62 of DENV 1 env were sufficient to inhibit TCR signaling, with env aa’s 55 and 66 being critical. Reverse genetics confirmed that substitution of DENV-2 and -3 aa’s 55 and 66 into DENV-1 and -4 reversed TCR inhibition and that DENV-1 aa’s 55 and 66 introduced into DENV-2 and -3 enabled TCR inhibition.

Conclusions: DENV-2 and -3 are associated with more severe clinical disease than DENV-1 and -4; however, no biological explanation for this difference has been previously identified. We found that DENV-1 and -4 viral particles and env proteins blunt T-cell responses by interfering with proximal TCR signaling, while DENV-2 and -3 do not, potentially explaining DENV pathogenic outcomes in primary and secondary infection.

Link to journal online: https://pmc.ncbi.nlm.nih.gov/articles/PMC12614984/