mTOR Inhibitors Prevent CMV Infection through the Restoration of Functional αβ and γδ T cells in Kidney Transplantation

J Am Soc Nephrol. 2022 Jan;33(1):121-137. doi: 10.1681/ASN.2020121753. Epub 2021 Nov 1.

Abstract

Background: The reported association of mTOR-inhibitor (mTORi) treatment with a lower incidence of cytomegalovirus (CMV) infection in kidney transplant recipients (KTR) who are CMV seropositive (R+) remains unexplained.

Methods: The incidence of CMV infection and T-cell profile was compared between KTRs treated with mTORis and mycophenolic acid (MPA), and in vitro mTORi effects on T-cell phenotype and functions were analyzed.

Results: In KTRs who were R+ and treated with MPA, both αβ and γδ T cells displayed a more dysfunctional phenotype (PD-1+, CD85j+) at day 0 of transplantation in the 16 KTRs with severe CMV infection, as compared with the 17 KTRs without or with spontaneously resolving CMV infection. In patients treated with mTORis (n=27), the proportion of PD-1+ and CD85j+ αβ and γδ T cells decreased, when compared with patients treated with MPA (n=44), as did the frequency and severity of CMV infections. mTORi treatment also led to higher proportions of late-differentiated and cytotoxic γδ T cells and IFNγ-producing and cytotoxic αβ T cells. In vitro, mTORis increased proliferation, viability, and CMV-induced IFNγ production of T cells and decreased PD-1 and CD85j expression in T cells, which shifted the T cells to a more efficient EOMESlow Hobithigh profile. In γδ T cells, the mTORi effect was related to increased TCR signaling.

Conclusion: Severe CMV replication is associated with a dysfunctional T-cell profile and mTORis improve T-cell fitness along with better control of CMV. A dysfunctional T-cell phenotype could serve as a new biomarker to predict post-transplantation infection and to stratify patients who should benefit from mTORi treatment.

Clinical trial registry name and registration number: Proportion of CMV Seropositive Kidney Transplant Recipients Who Will Develop a CMV Infection When Treated With an Immunosuppressive Regimen Including Everolimus and Reduced Dose of Cyclosporine Versus an Immunosuppressive Regimen With Mycophenolic Acid and Standard Dose of Cyclosporine A (EVERCMV), NCT02328963.

Keywords: CMV; CMV-specific immunity; kidney transplantation; mTOR inhibitors.

Publication types

  • Clinical Trial, Phase IV
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Anti-Bacterial Agents / therapeutic use
  • Antigens, CD / metabolism
  • Cell Culture Techniques
  • Cytomegalovirus Infections / epidemiology
  • Cytomegalovirus Infections / pathology
  • Cytomegalovirus Infections / prevention & control*
  • Female
  • Humans
  • Kidney Transplantation / adverse effects*
  • Leukocyte Immunoglobulin-like Receptor B1 / metabolism
  • MTOR Inhibitors / therapeutic use*
  • Male
  • Middle Aged
  • Mycophenolic Acid / therapeutic use
  • Programmed Cell Death 1 Receptor / metabolism
  • T-Lymphocyte Subsets / drug effects*
  • T-Lymphocyte Subsets / metabolism

Substances

  • Anti-Bacterial Agents
  • Antigens, CD
  • LILRB1 protein, human
  • Leukocyte Immunoglobulin-like Receptor B1
  • MTOR Inhibitors
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
  • Mycophenolic Acid

Associated data

  • ClinicalTrials.gov/NCT02328963