Peri-weaning, diet-induced activation of an IFNγ-mediated regulatory circuit promotes cDC1 maturation and CD8+ T cell differentiation

D Doğuş Altunöz R Ramin Shakiba (Institute for Immunology, Biomedical Center Munich, Faculty of Medicine, Ludwig-Maximilians-Universität in Munich) K Kaushikk Ravi Rengarajan (Institute for Immunology, Biomedical Center Munich, Faculty of Medicine, Ludwig-Maximilians-Universität in Munich) H Hamsa Narasimhan (Institute for Immunology, Biomedical Center Munich, Faculty of Medicine, Ludwig-Maximilians-Universität in Munich) N Nikos E. Papaioannou (Biomedical Center, Institute of Cardiovascular Physiology and Pathophysiology, Faculty of Medicine, Ludwig-Maximilians-Universität in Munich) S Sadiq Nasrah J Jessica Vetters M Maria L. Richter (Biomedical Center, Physiological Chemistry, Faculty of Medicine, Ludwig-Maximilians-Universität in Munich) M María Parra Reyes N Nadine Nuschele D Denise Messerer S Sabine Schwamberger A Andreas Goschin D Dimitrios Starfas M Melanie Schmid T Tobias Straub (Core Facility Bioinformatics, Biomedical Center, Faculty of Medicine, LMU) M Michele Proietti K Katrin Böttcher M Maria Colomé-Tatché D Dirk Haller J Jan P. Böttcher S Stephanie C. Ganal-Vonarburg S Sophie Janssens C Christian Schulz A Anne B. Krug (Institute for Immunology, Biomedical Center, Faculty of Medicine, LMU) B Barbara U. Schraml (Institute for Immunology, Biomedical Center Munich, Faculty of Medicine, Ludwig-Maximilians-Universität in Munich)

Abstract

Abstract Maintaining a balanced immunity between pathogen defense and tolerance to environmental antigens in neonates is essential for survival and the establishment of life-long immune homeostasis. Instructed by environmental signals, type 1 conventional dendritic cells (cDC1) contribute to both processes but how the balance may be achieved is unclear. Here, we uncover an interferon (IFN)γ-driven regulatory circuit in early life that relays dietary cues to spleen cDC1. IFNγ-mediated STAT1-signaling induces an immunogenic maturation program in spleen cDC1 that enables them to shape the effector differentiation of antigen-experienced effector memory CD8⁺ T cells. This cDC1 program emerges during the transition from breastfeeding to solid food at weaning, occurs in germ-free mice, and remains operative to dietary intervention in adult mice. At weaning, this IFNγ signal enables spleen cDC1 to shape the effector phenotype of food-antigen-specific CD8 + T cells in a feedforward manner, thereby recalibrating the developing T cell pool. Our findings identify diet as a modifiable cue that can tune systemic cDC1-mediated immunity, opening new opportunities to steer immune responses during early life and beyond.

Article Details

Volume / Issue Vol. 17, Issue 1
Published August 04, 2026
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (26)

D

Doğuş Altunöz

R

Ramin Shakiba

Institute for Immunology, Biomedical Center Munich, Faculty of Medicine, Ludwig-Maximilians-Universität in Munich

K

Kaushikk Ravi Rengarajan

Institute for Immunology, Biomedical Center Munich, Faculty of Medicine, Ludwig-Maximilians-Universität in Munich

H

Hamsa Narasimhan

Institute for Immunology, Biomedical Center Munich, Faculty of Medicine, Ludwig-Maximilians-Universität in Munich

N

Nikos E. Papaioannou

Biomedical Center, Institute of Cardiovascular Physiology and Pathophysiology, Faculty of Medicine, Ludwig-Maximilians-Universität in Munich

S

Sadiq Nasrah

J

Jessica Vetters

M

Maria L. Richter

Biomedical Center, Physiological Chemistry, Faculty of Medicine, Ludwig-Maximilians-Universität in Munich

M

María Parra Reyes

N

Nadine Nuschele

D

Denise Messerer

S

Sabine Schwamberger

A

Andreas Goschin

D

Dimitrios Starfas

M

Melanie Schmid

T

Tobias Straub

Core Facility Bioinformatics, Biomedical Center, Faculty of Medicine, LMU

M

Michele Proietti

K

Katrin Böttcher

M

Maria Colomé-Tatché

D

Dirk Haller

J

Jan P. Böttcher

S

Stephanie C. Ganal-Vonarburg

S

Sophie Janssens

C

Christian Schulz

A

Anne B. Krug

Institute for Immunology, Biomedical Center, Faculty of Medicine, LMU

B

Barbara U. Schraml

Institute for Immunology, Biomedical Center Munich, Faculty of Medicine, Ludwig-Maximilians-Universität in Munich