Depletion of polyfunctional CD26highCD8+ T cells repertoire in chronic lymphocytic leukemia

Najmeh Bozorgmehr; Mark Hnatiuk; Anthea C Peters; Shokrollah Elahi

doi:10.1186/s40164-023-00375-5

Depletion of polyfunctional CD26^highCD8⁺ T cells repertoire in chronic lymphocytic leukemia

Exp Hematol Oncol. 2023 Jan 27;12(1):13. doi: 10.1186/s40164-023-00375-5.

Authors

Najmeh Bozorgmehr¹, Mark Hnatiuk², Anthea C Peters³, Shokrollah Elahi^{4

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Affiliations

¹ School of Dentistry, Division of Foundational Sciences, University of Alberta, Edmonton, AB, T6G 2E1, Canada.
² Depatment of Medicine Division of Hematology, University of Alberta, Edmonton, AB, T6G 2E1, Canada.
³ Department of Oncology, Division of Medical Oncology, University of Alberta, Edmonton, AB, T6G 2E1, Canada.
⁴ School of Dentistry, Division of Foundational Sciences, University of Alberta, Edmonton, AB, T6G 2E1, Canada. elahi@ualberta.ca.
⁵ Department of Oncology, Division of Medical Oncology, University of Alberta, Edmonton, AB, T6G 2E1, Canada. elahi@ualberta.ca.
⁶ Li Ka Shing Institute of Virology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, T6G 2E1, Canada. elahi@ualberta.ca.

Abstract

Background: CD8⁺ T cells play an essential role against tumors but the role of human CD8⁺CD26⁺ T cell subset against tumors, in particular, haematological cancers such as chronic lymphocytic leukemia (CLL) remains unknown. Although CD4⁺CD26^high T cells are considered for adoptive cancer immunotherapy, the role of CD8⁺CD26⁺ T cells is ill-defined. Therefore, further studies are required to better determine the role of CD8⁺CD26⁺ T cells in solid tumors and haematological cancers.

Methods: We studied 55 CLL and 44 age-sex-matched healthy controls (HCs). The expression of CD26 on different T cell subsets (e.g. naïve, memory, effector, and etc.) was analyzed. Also, functional properties of CD8⁺CD26⁺ and CD8⁺CD26^- T cells were evaluated. Finally, the plasma cytokine/chemokine and Galectin-9 (Gal-9) levels were examined.

Results: CD26 expression identifies three CD8⁺ T cell subsets with distinct immunological properties. While CD26^negCD8⁺ T cells are mainly transitional, effector memory and effectors, CD26^lowCD8⁺ T cells are mainly naïve, stem cell, and central memory but CD26^high T cells are differentiated to transitional and effector memory. CD26⁺CD8⁺ T cells are significantly reduced in CLL patients versus HCs. CD26^high cells are enriched with Mucosal Associated Invariant T (MAIT) cells co-expressing CD161TVα7.2 and IL-18Rα. Also, CD26^high cells have a rich chemokine receptor profile (e.g. CCR5 and CCR6), profound cytokine (TNF-α, IFN-γ, and IL-2), and cytolytic molecules (Granzyme B, K, and perforin) expression upon stimulation. CD26^high and CD26^low T cells exhibit significantly lower frequencies of CD160, 2B4, TIGIT, ICOS, CD39, and PD-1 but higher levels of CD27, CD28, and CD73 versus CD26^neg cells. To understand the mechanism linked to CD26^high depletion, we found that malignant B cells by shedding Galectin-9 (Gal-9) contribute to the elevation of plasma Gal-9 in CLL patients. In turn, Gal-9 and the inflammatory milieu (IL-18, IL-12, and IL-15) in CLL patients contribute to increased apoptosis of CD26^high T cells.

Conclusions: Our results demonstrate that CD26⁺ T cells possess a natural polyfunctionality to traffic and exhibit effector functions and resist exhaustion. Therefore, they can be proposed for adoptive cancer immunotherapy. Finally, neutralizing and/or inhibiting Gal-9 may preserve CD26^highCD8⁺ T cells in CLL.

Keywords: Adoptive T cell therapy; Galectin-9; MAIT cells; T cells exhaustion.

Abstract

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