4.5 Article

TIGIT blockade enhances NK cell activity against autologous HIV-1-infected CD4+ T cells

期刊

CLINICAL & TRANSLATIONAL IMMUNOLOGY
卷 10, 期 10, 页码 -

出版社

WILEY
DOI: 10.1002/cti2.1348

关键词

ADCC; checkpoint inhibitor; CMV; HIV-1; NK cells; PVR; TIGIT

资金

  1. Canadian Institutes of Health Research (CIHR) [PJT 361426]
  2. CIHR doctoral fellowship

向作者/读者索取更多资源

This study investigates the role of TIGIT in individuals living with HIV, revealing its expression on CD4(+) T cells, CD8(+) T cells, and NK cells, and its association with HIV-1 disease progression. Therapeutic targeting of TIGIT may enhance NK cell antibody-dependent cytotoxicity against HIV-1.
Objectives. During chronic human immunodeficiency virus (HIV)-1 infection, inhibitory molecules upregulated on lymphocytes contribute to effector cell dysfunction and immune exhaustion. People living with HIV (PLWH) are at greater risk for age-related morbidities, an issue magnified by human cytomegalovirus (CMV) coinfection. As CMV infection modifies natural killer (NK) cell properties and NK cells contribute to protection against HIV-1 infection, we considered the role of T-cell immunoreceptor with immunoglobulin and intracellular tyrosine inhibitory motif domains (TIGIT) in NK cell-based HIV-1 immunotherapy and elimination strategies. Methods. We measured TIGIT expression on immune cell subsets of 95 PLWH and assessed its impact on NK cell function, including elimination of autologous CD4(+) T cells infected through reactivation of endogenous HIV-1. Results. TIGIT was expressed on CD4(+) T cells, CD8(+) T cells and NK cells from PLWH. Although TIGIT levels on T cells correlated with HIV-1 disease progression, the extent of TIGIT expression on NK cells more closely paralleled adaptation to CMV. TIGIT interacts with its predominant ligand, poliovirus receptor (PVR), to inhibit effector cell functions. Circulating CD4(+) T cells from PLWH more frequently expressed PVR than HIV-seronegative controls, and PVR expression was enriched in CD4(+) T cells replicating HIV-1 ex vivo. Treatment with anti-TIGIT monoclonal antibodies increased NK cell HIV-1-specific antibody-dependent cytotoxicity in vitro and ex vivo. Conclusion. Blocking TIGIT may be an effective strategy to invigorate antibody-dependent NK cell activity against HIV-1 activated in cellular reservoirs for cure or treatment strategies.

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