Nature Immunology, ranked first out of more than 100 primary immunology research journals, brings together the most significant immunology research from every discipline. Nature Immunology’s scope is broad, covering all areas of immunology, including (but not limited to) innate immunity and inflammation, development, immune receptors, signaling and apoptosis, antigen presentation, gene regulation and recombination, cellular and systemic immunity, vaccines, immune tolerance, autoimmunity and tumor immunology, microbial immunopathology and transplantation. By presenting research that provides fundamental insight into the working of the immune system, Nature Immunology communicates the most significant and influential advances to a broad audience. http://feeds.nature.com/ni/rss/current Nature Publishing Group en © 2025 Macmillan Publishers Limited, part of Springer Nature. All rights reserved. Nature Immunology © 2025 Macmillan Publishers Limited, part of Springer Nature. All rights reserved. [email protected]

https://www.nature.com/uploads/product/ni/rss.gif http://feeds.nature.com/ni/rss/current https://www.nature.com/articles/s41590-025-02260-1 Nature Immunology, Published online: 04 August 2025; doi:10.1038/s41590-025-02260-1Author Correction: LARP4-mediated hypertranslation drives T cell dysfunction in tumors]]> Yi LiuHaochen NiJie LiJing YangIvann SekielykBryan E. SnowZihao ZhangFeifan ZhangMichael St. PaulJinyi HanMeghan KatesShaofeng LiuYawei ZhangZurui HuangYin XuSamuel D. SaibilTak W. MakDali HanMeng Michelle Xu doi:10.1038/s41590-025-02260-1 Nature Immunology, Published online: 2025-08-04; | doi:10.1038/s41590-025-02260-1 2025-08-04 Nature Immunology 10.1038/s41590-025-02260-1 https://www.nature.com/articles/s41590-025-02260-1 https://www.nature.com/articles/s41590-025-02249-w Nature Immunology, Published online: 29 July 2025; doi:10.1038/s41590-025-02249-wCarboxylation switch]]> Ioana Staicu doi:10.1038/s41590-025-02249-w Nature Immunology, Published online: 2025-07-29; | doi:10.1038/s41590-025-02249-w 2025-07-29 Nature Immunology 10.1038/s41590-025-02249-w https://www.nature.com/articles/s41590-025-02249-w https://www.nature.com/articles/s41590-025-02251-2 Nature Immunology, Published online: 29 July 2025; doi:10.1038/s41590-025-02251-2TLRs are blind to pseudouridine RNA]]> Paula Jauregui doi:10.1038/s41590-025-02251-2 Nature Immunology, Published online: 2025-07-29; | doi:10.1038/s41590-025-02251-2 2025-07-29 Nature Immunology 10.1038/s41590-025-02251-2 https://www.nature.com/articles/s41590-025-02251-2 https://www.nature.com/articles/s41590-025-02248-x Nature Immunology, Published online: 29 July 2025; doi:10.1038/s41590-025-02248-xTargeting CAFs]]> Nicholas J. Bernard doi:10.1038/s41590-025-02248-x Nature Immunology, Published online: 2025-07-29; | doi:10.1038/s41590-025-02248-x 2025-07-29 Nature Immunology 10.1038/s41590-025-02248-x https://www.nature.com/articles/s41590-025-02248-x https://www.nature.com/articles/s41590-025-02250-3 Nature Immunology, Published online: 29 July 2025; doi:10.1038/s41590-025-02250-3Restoring balanced HSC youth]]> Laurie A. Dempsey doi:10.1038/s41590-025-02250-3 Nature Immunology, Published online: 2025-07-29; | doi:10.1038/s41590-025-02250-3 2025-07-29 Nature Immunology 10.1038/s41590-025-02250-3 https://www.nature.com/articles/s41590-025-02250-3 https://www.nature.com/articles/s41590-025-02201-y Nature Immunology, Published online: 29 July 2025; doi:10.1038/s41590-025-02201-yTGFβ-mediated signals enable CD8+ T cells to establish tissue-residence. IL-4 and PD-1 are each connected to TGFβ signaling to regulate the formation of CD8+ T cell tissue residence in skin.]]> Quinn PetersMartin Prlic doi:10.1038/s41590-025-02201-y Nature Immunology, Published online: 2025-07-29; | doi:10.1038/s41590-025-02201-y 2025-07-29 Nature Immunology 10.1038/s41590-025-02201-y https://www.nature.com/articles/s41590-025-02201-y https://www.nature.com/articles/s41590-025-02221-8 Nature Immunology, Published online: 29 July 2025; doi:10.1038/s41590-025-02221-8During late gestation, unconventional intraepithelial αβ T cells migrate from the gut to the mammary gland to remodel the tissue for lactation and enhance its mucosal barrier state.]]> Amanpreet Singh ChawlaMahima Swamy doi:10.1038/s41590-025-02221-8 Nature Immunology, Published online: 2025-07-29; | doi:10.1038/s41590-025-02221-8 2025-07-29 Nature Immunology 10.1038/s41590-025-02221-8 https://www.nature.com/articles/s41590-025-02221-8 https://www.nature.com/articles/s41590-025-02224-5 Nature Immunology, Published online: 29 July 2025; doi:10.1038/s41590-025-02224-5Tumor-infiltrating CD8+ T cells acquire HOBIT expression and features of tissue-resident memory cells. This TGFβ-driven process is dispensable for tumor control by immune checkpoint blockade, but disrupting TGFβ signaling in HOBIT-expressing tumor-infiltrating lymphocytes enhances anti-tumor immunity.]]> Dongmei ZhaoHai-Hui Xue doi:10.1038/s41590-025-02224-5 Nature Immunology, Published online: 2025-07-29; | doi:10.1038/s41590-025-02224-5 2025-07-29 Nature Immunology 10.1038/s41590-025-02224-5 https://www.nature.com/articles/s41590-025-02224-5