Impact of Thymus Removal in Altering CD8 T Cell Properties 2260157

Y Yi-Chung Huang (Univ. of Cincinnati Col. of Med) K Koichi Araki (Emory Vaccine Center, Emory University School of Medicine) C Charles Perkins (Cincinnati Children’s Hospital Medical Center) Y Yamato Sajiki (Cincinnati Children’s Hospital Medical Center)

Abstract

Abstract Introduction The thymus supplies naïve T cells to sustain T cell populations, but it gradually shrinks with age, leading to a decline in thymic output. Consequently, cessation of thymic output reduces naïve T cell numbers, raising the question of whether the remaining cells adapt to maintain immune competence. Methods Here, we examined the quantity and quality of antigen-specific CD8 T cells in mice after thymectomy. Results Our experiments showed that thymectomy reduced the number of antigen-specific CD8 T cells. Interestingly, following acute lymphocytic choriomeningitis virus (LCMV) infection, antigen-specific CD8 T cells derived from thymectomized mice exhibited greater expansion and generated more memory cells than those from controls. To explore why CD8 T cells from thymectomized mice possess such augmented expansion capacity, we analyzed these CD8 T cells prior to infection and found significant phenotypic remodeling after thymectomy, thereby altering their subset composition. Virtual memory (VM) cells, which exhibits memory phenotypes yet remain antigen inexperienced, increased within the antigen-specific CD8 T cell pool after thymectomy. In addition, thymectomy altered the phenotypes of antigen-specific naïve CD8 T cells, greatly enriching the IL-18Rα+ CD73+ CXCR3+ subset. Importantly, this subset contributed to the enhanced expansion of antigen-specific CD8 T cells after LCMV infection. Conclusion Together, our findings suggest that upon loss of thymic output during thymic involution or thymectomy, antigen-inexperienced CD8 T cells undergo qualitative remodeling, compensating for reduced cell numbers by increasing functionally potent subsets that help preserve antiviral immunity. Funding Source n/a Topic Categories Viral Immunology (VIR)

Article Details

Volume / Issue Vol. 215, Issue Supplement_1
Published August 01, 2026
ISSN 0022-1767
Publisher American Association of Immunologists

Authors (4)

Y

Yi-Chung Huang

Univ. of Cincinnati Col. of Med

K

Koichi Araki

Emory Vaccine Center, Emory University School of Medicine

C

Charles Perkins

Cincinnati Children’s Hospital Medical Center

Y

Yamato Sajiki

Cincinnati Children’s Hospital Medical Center