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Issues

EDITORIAL

J Immunol (2021) 206 (2): 241–242.

TOP READS

J Immunol (2021) 206 (2): 243.

PILLARS OF IMMUNOLOGY

J Immunol (2021) 206 (2): 245–247.

BRIEF REVIEWS

J Immunol (2021) 206 (2): 249–256.
J Immunol (2021) 206 (2): 257–263.
J Immunol (2021) 206 (2): 264–272.
J Immunol (2021) 206 (2): 273–281.
J Immunol (2021) 206 (2): 282–291.
J Immunol (2021) 206 (2): 292–301.
J Immunol (2021) 206 (2): 302–309.
J Immunol (2021) 206 (2): 310–320.

CUTTING EDGE

J Immunol (2021) 206 (2): 323–328.

  • NOX2 deficiency promotes systemic L. monocytogenes infection in a type I IFN–dependent manner.

  • NOX2 limits ISG expression in response to type I IFN.

J Immunol (2021) 206 (2): 329–334.

  • Systemic lipidomic changes distinguish COVID-19 disease severity in humans.

  • Lipidomic changes correspond to different levels of immune lipid mediators.

  • Lipid mediator differences correlate with BMI, hypertension, and heart disease.

AUTOIMMUNITY

J Immunol (2021) 206 (2): 335–344.

  • GrB-induced intracellular cleavage and phosphorylation events do not need perforin.

  • These cleavages and phosphorylations require GrB enzyme activity.

  • DDR and IRF-3 phosphorylation are some of the functional results of these events.

CLINICAL AND HUMAN IMMUNOLOGY

J Immunol (2021) 206 (2): 345–354.

  • Only a small subset of flagellin-induced CD40LhiCD4 cells express cytokines.

  • This CD40LhiCD4 cytokine production is restricted to T effector memory cells.

IMMUNE REGULATION

J Immunol (2021) 206 (2): 355–365.

  • IL-17A is produced mainly by γδ T cells in hypersensitivity pneumonitis (HP).

  • The IL-17A/chemokines/CD11b+ alveolar macrophage axis underlies development of HP.

  • Memory responses of γδ T cells are involved in sensitization and development of HP.

J Immunol (2021) 206 (2): 366–375.

  • Arf1 and Arf6 are dispensable for cytokine secretion in T cells.

  • Arf1 and Arf6 redundantly protect activated naive T cells from apoptosis.

  • Loss of Arf1 and Arf6 in T cells alleviates autoimmune diseases.

INFECTIOUS DISEASE AND HOST RESPONSE

J Immunol (2021) 206 (2): 376–385.

  • Antiviral activity of the c-di-GMP cyclase AdrA is STING dependent.

  • An optimal AdrA-induced response requires synergistic action of type I IFN and TNF-α.

J Immunol (2021) 206 (2): 386–397.

  • In vivo priming with OCH does not curb subsequent iNKT cell responses to α-GalCer.

  • Sequential treatment with OCH and α-GalCer reduces CLP-induced mortality.

  • α-GalCer treatment of OCH-primed septic mice restores their immunocompetence.

J Immunol (2021) 206 (2): 398–409.

  • IRF3 contributes to sepsis in a mouse model incorporating antibiotics and fluids.

  • IRF3 acts in stromal cells (nonleukocytes) to mediate this effect.

  • IRF3 indirectly alters macrophage behavior and the inflammatory network in sepsis.

INNATE IMMUNITY AND INFLAMMATION

J Immunol (2021) 206 (2): 410–421.

  • Suppression of leaky Ad gene expression in the liver attenuated acute hepatotoxicity.

  • IL-6 enhanced leaky Ad gene expression and Ad vector–induced cytotoxicity.

  • Acute hepatotoxicity and leaky Ad gene expression were reduced in IL-6 KO mice.

SYSTEMS IMMUNOLOGY

J Immunol (2021) 206 (2): 422–431.

  • BET inhibitor JQ1 downregulated BRD2/BRD4 superenhancer genes in RA-FLS.

  • JQ1 inhibited key inflammatory pathways in activated RA-FLS.

  • JQ1 altered the chromatin occupancy of proinflammatory transcription factors.

NOVEL IMMUNOLOGICAL METHODS

J Immunol (2021) 206 (2): 432–445.

  • HoxB8 progenitor–derived neutrophils can repopulate irradiated mice.

  • HoxB8 chimeras are useful for the in vivo analysis of neutrophil functions.

J Immunol (2021) 206 (2): 446–451.

  • MSRE-qPCR is an accurate and rapid method to determine TSDR methylation status.

  • MSRE-qPCR produces similar results to previously described orthogonal methods.

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