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J Immunol (2022) 209 (12): 2249.

IMMUNOLOGY NOTES AND RESOURCES

J Immunol (2022) 209 (12): 2251–2259.

BRIEF REVIEWS

J Immunol (2022) 209 (12): 2261–2268.
J Immunol (2022) 209 (12): 2269–2278.

CUTTING EDGE

J Immunol (2022) 209 (12): 2281–2286.

  • CCR9 is selectively expressed on CD8+ T cells in the CMV-infected brain.

  • CCL25 is upregulated in the brain after congenital CMV infection.

  • Inhibition of CCR9/CCL25 impairs CD8+ T cell migration to the brain.

J Immunol (2022) 209 (12): 2287–2291.

  • SGK1, downstream of mTORC2 signaling, inhibits memory CD8+ T cell formation.

  • Inhibiting or deleting SGK1 promotes memory CD8+ T cells and antitumor immunity.

ALLERGY AND OTHER HYPERSENSITIVITIES

J Immunol (2022) 209 (12): 2293–2303.

  • Macrophage P2Y6 receptors selectively activate NFATC2 through Gαq/PLC.

  • NFATC2 mediates the P2Y6-potentiated IL-12 production and IFN-γ expression.

  • Macrophage P2Y6 and NFATC2 control innate and type 2 immune responses.

AUTOIMMUNITY

J Immunol (2022) 209 (12): 2304–2312.

  • The G307S mutation augmented the activating signal of DNAM-1 in CD4+ conventional T cells.

  • The G307S mutation promoted the interaction with Lck and p-Tyr322 of DNAM-1.

  • The G307S DNAM-1 mutation exacerbated CD4+ T cell–mediated autoimmune encephalomyelitis.

IMMUNOTHERAPY AND VACCINES

J Immunol (2022) 209 (12): 2313–2321.

  • CD96 mediated a costimulatory signal in both human and mouse γδ T cells.

  • CD96 on dermal γδ T cells augmented IL-17A production and exacerbated psoriasis.

  • The blockade of CD96 ameliorates psoriasis.

INNATE IMMUNITY AND INFLAMMATION

J Immunol (2022) 209 (12): 2322–2329.

  • IL-1β is key to inflammatory responses of fetal membranes at parturition.

  • IL-1β induces collagen degradation via ER-phagy in membrane mesenchymal cells.

  • IL-1β promotes removal of redundant collagen via autophagy in membrane rupture.

MOLECULAR AND STRUCTURAL IMMUNOLOGY

J Immunol (2022) 209 (12): 2330–2340.

  • The antibacterial properties of vertebrate C3a, C4a, and C5a have evolved divergently.

  • Net charge is the determining factor of the antibacterial properties.

  • Vertebrate C3a, C4a, and C5a are all resources of peptide antibiotics.

MUCOSAL IMMUNOLOGY

J Immunol (2022) 209 (12): 2341–2351.

  • LIGHT contributes to esophageal T cell infiltration and IL-13 levels in a model of EoE.

  • LIGHT regulates esophageal tissue remodeling in a model of EoE.

  • LIGHT drives esophagus fibroblast proliferation and potentiates fibroblast responses to IL-13.

SYSTEMS IMMUNOLOGY

J Immunol (2022) 209 (12): 2352–2361.

  • The Stemformatics DC atlas provides a reference tool to study human DC biology.

  • DC subsets group by tissue and remember their origin in culture.

  • In vitro–derived cDCs do not recapitulate the biology of their in vivo equivalents.

LETTERS OF RETRACTION

J Immunol (2022) 209 (12): 2362.
J Immunol (2022) 209 (12): 2363.
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