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DOI 10.1681/asn.2020121753

Медицинская библиотека · Journal of the American Society of Nephrology : JASN · 2021

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

Kaminski Hannah, Marseres Gabriel, Yared Nathalie, Nokin Marie-Julie, Pitard Vincent, Zouine Atika, Garrigue Isabelle, Loizon Séverine, Capone Myriam, Gauthereau Xavier, Mamani-Matsuda Maria, Coueron Roxane, Durán Raúl V, Pinson Benoît, Pellegrin Isabelle, Thiébaut Rodolphe, Couzi Lionel, Merville Pierre, Déchanet-Merville Julie

Клиническое исследование IV фазыСтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

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.

Для цитирования: Kaminski Hannah, Marseres Gabriel, Yared Nathalie, Nokin Marie-Julie, Pitard Vincent, Zouine Atika, Garrigue Isabelle, Loizon Séverine, Capone Myriam, Gauthereau Xavier, Mamani-Matsuda Maria, Coueron Roxane, Durán Raúl V, Pinson Benoît, Pellegrin Isabelle, Thiébaut Rodolphe, Couzi Lionel, Merville Pierre, Déchanet-Merville Julie. mTOR Inhibitors Prevent CMV Infection through the Restoration of Functional αβ and γδ T cells in Kidney Transplantation.. Journal of the American Society of Nephrology : JASN. 2021. DOI: 10.1681/asn.2020121753.

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