Regulatory maturation of cDC1 accelerates effector CD8 T cell contraction after severe influenza A virus infection 2267170

X Xinran Wang (School of Marine Sciences, Sun Yat-Sen University and Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai)) E Emon Hossain (Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham , Birmingham, AL,) M Michael Schultz T Troy Randall (University of Alabama at Birmingham) A Aaron Silva-Sanchez (Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham , Birmingham, AL,)

Abstract

Abstract Introduction XCR1+ dendritic cells (cDC1) initiate CD8 T cell responses against Influenza A virus (IAV) infection. In the resolution phase, sustained cytokine production by CD8 T cells prolong lung damage, however, whether cDC1 regulate effector CD8 T cells is unknown. Methods cDC1 and CD8 T cells were characterized by flow cytometry. The transcriptome of cDC1 populations was analyzed by scRNA-seq. To investigate the function of mature cDC1 we co-cultured lung cDC1 and OT-I cells, performed adoptive transfers of OT-I cells, and transplanted bone marrow (BM) into fluorescent mice. Results IAV infection triggered two rounds of cDC1 maturation. The first round during the acute infection and is followed by recruitment of effector CD8 T cells. The second round occurs in the resolution phase and is followed by contraction of antigen specific CD8 T cells. The transcriptome of mature cDC1 showed that cDC1 maturation is driven by TNFa and IFNg in naïve and infected mice respectively. In the resolution phase, mature cDC1 express genes related to efferocytosis and immunoregulation. Transplant of WT BM into fluorescent mice showed that cDC1 acquire apoptotic cells only in the resolution phase. Our in vivo and in vitro experiments showed that mature cDC1 from the resolution phase reduced T-bet and IFNg production in OT-I cells while expanding RORgt OT-I cells. Conclusion The mature cDC1 that accumulate in the lungs during the resolution phase of IAV infection regulate effector CD8 T cell responses. Funding Source R01 AI153413 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 (5)

X

Xinran Wang

School of Marine Sciences, Sun Yat-Sen University and Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai)

E

Emon Hossain

Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham , Birmingham, AL,

M

Michael Schultz

T

Troy Randall

University of Alabama at Birmingham

A

Aaron Silva-Sanchez

Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham , Birmingham, AL,