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Delineating the short- and long-term impact of ionizing radiation on antigen-inexperienced CD8+ T cell subsets
Mohammad Heidarian, Shravan K. Kannan, Whitney Swanson, Thomas S. Griffith, John T. Harty, Vladimir P. Badovinac
Mohammad Heidarian, Shravan K. Kannan, Whitney Swanson, Thomas S. Griffith, John T. Harty, Vladimir P. Badovinac
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Research Article Immunology Inflammation

Delineating the short- and long-term impact of ionizing radiation on antigen-inexperienced CD8+ T cell subsets

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Abstract

Radiation-induced lymphopenia (RIL) remains a challenging side effect of radiation therapy that is often associated with poor prognosis and reduced overall survival. Although CD8+ T cells are highly radiosensitive, the dynamics of quantitative and qualitative changes to the CD8+ T cell pool following exposure to high doses of ionizing radiation (IR) remain understudied. Herein, we sought to determine the long-term impact of sublethal whole body irradiation (WBI) on the antigen-inexperienced (Ag-inexperienced) CD8+ T cell pool, comprising naive (TN) and virtual memory (TVM) CD8+ T cells. We show that although both TN and TVM cells gradually regenerated after WBI-induced loss, TN recovery occurred only through de novo thymic production. Despite the numerical restoration, the subset and phenotypic composition of postrecovery Ag-inexperienced CD8+ T cells did not qualitatively recapitulate the pre-WBI state. Specifically, the frequency of TVM cells is increased, especially during the early stages of recovery. Within the TN subset, a lasting overrepresentation of Ly6C+CD122+ cells and an altered TCR clonotype diversity are also observed. Overall, our data highlight the dynamic changes to the Ag-inexperienced CD8+ T cell pool upon recovery from RIL

Authors

Mohammad Heidarian, Shravan K. Kannan, Whitney Swanson, Thomas S. Griffith, John T. Harty, Vladimir P. Badovinac

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Figure 3

Thymus is required for naive CD8+ T cell numerical recovery.

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Thymus is required for naive CD8+ T cell numerical recovery.
(A) Experim...
(A) Experimental design: thymectomized and euthymic SPF mice were subjected to 0 Gy, 2 Gy, or 5 Gy dose of WBI and cellular analysis was performed in PBL longitudinally. (B) Number of naive (TN) CD8+ T cells in blood of euthymic (left) and athymic mice (right) at indicated time points. (C) Number of CD19+ B cells in blood of euthymic (left) and athymic mice (right) at indicated time points. Number of TN cells (D) and B cells (E) at each indicated time point was divided to the pre-WBI (D-1) number from the same mouse, and the mean of this ratio was plotted for 2 Gy (left) and 5 Gy (right) euthymic and athymic mice. Data in A–E are representative of 2 independent experiments with n = 2–5 mice per group in each experiment. Statistical significance was determined by 2-way ANOVA with Bonferroni’s multiple comparisons post hoc test. Graphs in B and C show the mean ± SEM, with each symbol representing 1 mouse. Graphs in D and E show the mean ± SD. Individual P values are noted on respective graphs or are summarized as follows: *P < 0.05, **P < 0.01, ***P < 0.001.

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