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The Journal of Immunology Cover Image for Volume 209, Issue 11
Volume 209, Issue 11
December 2022
ISSN 0022-1767
EISSN 1550-6606

Volume 209, Issue 11, December 2022

Top Reads

The Journal of Immunology, Volume 209, Issue 11, December 2022, Page 2071, https://doi.org/10.4049/jimmunol.2290023

Brief Revews

Kalina T Belcheva and Jayanta Chaudhuri
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2073–2081, https://doi.org/10.4049/jimmunol.2200497

Autoimmunity

Ying Lu and others
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2083–2092, https://doi.org/10.4049/jimmunol.2200439

  • CD40 supports distinct effector programs in B cells and DCs for EAE.

  • CD40 expression on DCs is required for priming pathogenic Th cells.

  • B cell CD40 is essential for class-switched MOG-specific Ab production.

Francine Lianne Emralino and others
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2093–2103, https://doi.org/10.4049/jimmunol.2200367

  • hM-R822Q Tg mice exhibit SMS-like disease phenotype.

  • Poly(I:C) injection induces lethal inflammation in female hM-R822Q Tg mice.

  • Lethal inflammation is mediated by MDA5 through MAVS, IFNAR, and JAK signaling.

Clinical and Human Immunology

Setsuko Mise-Omata and others
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2104–2113, https://doi.org/10.4049/jimmunol.2200525

  • Memory T and B cells are present for long periods with different kinetics.

  • Circulating Tfh cells correlate to the Ab production of B cells.

  • Memory T cells, but not B cells, are fully reactive to the omicron variant.

Immune Regulation

Samira Mansouri and others
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2114–2132, https://doi.org/10.4049/jimmunol.2200158

  • AQ and HAQ alleles underwent natural selection during the out-of-Africa migration.

  • Adult AQ knock-in mice are leaner than WT or HAQ mice on a chow diet.

  • The second transmembrane and TM2–TM3 linker of MPYS interacts with acyl-CoA.

William Stohl and others
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2133–2140, https://doi.org/10.4049/jimmunol.2200620

  • Numbers of CD19+ cells in B6.Baff−/− and B6.Br3−/− mice diverge as the mice age.

  • B cell subset profiles significantly differ between B6.Baff−/− and B6.Br3−/− mice.

  • CD4+Foxp3+ cells are greater in B6.Baff−/− mice than in B6.Br3−/− mice.

Immunogenetics

Gabrielle Warner Jenkins and others
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2141–2148, https://doi.org/10.4049/jimmunol.2200455

  • Bovine ultralong CDR H3s use cysteine polymorphisms to generate structural diversity.

  • Different disulfides form between germline and mutated cysteines within CDR H3.

Immunotherapy and Vaccines

Frances V Sjaastad and others
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2149–2159, https://doi.org/10.4049/jimmunol.2200324

  • Vaccine-induced T cell expansion is blunted in dirty mice compared with SPF mice.

  • XCR1+ DCs from dirty mice fail to produce IL-27p28 after vaccination.

  • Exogenous IL-27 restores T cell expansion in dirty mice.

Infectious Disease and Host Response

Eliezer Rovira-Diaz and others
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2160–2171, https://doi.org/10.4049/jimmunol.2200504

  • Helminth coinfection impairs the innate neutrophil response to T. gondii.

  • Coinfection impairs the CD8 T cell response quantitatively, but not qualitatively.

  • Helminth coinfection impairs disease tolerance during toxoplasmosis.

Femke D Hollwedel and others
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2172–2180, https://doi.org/10.4049/jimmunol.2200413

  • K. pneumoniae triggers pleuritis, bacteremia, and early mortality in old mice.

  • Nlrp3-dependent IL-1β release is increased in K. pneumoniae–infected old mice.

  • Transplantation of young bone marrow rescues old mice from fatal K. pneumoniae pneumonia.

Innate Immunity and Inflammation

Yangxiao Hou and others
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2181–2191, https://doi.org/10.4049/jimmunol.2200182

  • FABP5 in myeloid cells controls LPS-induced liver injury and M1 polarization.

  • FABP5 deletion increases unsaturated fatty acids in LPS-treated macrophages.

  • FABP5 and oleic acid master LPS-induced M1 polarization by the AMPK/NF-κB pathway.

Vanessa Moarbes and others
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2192–2202, https://doi.org/10.4049/jimmunol.2100688

  • STAT6-IP immunomodulatory peptide inhibits lung ILC2 expansion in response to IL-33.

  • Targeting innate immune cells by STAT6-IP durably reduces type 2 inflammation.

Molecular and Structural Immunology

Xiaozhen Zhu and others
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2203–2214, https://doi.org/10.4049/jimmunol.2200334

  • Carp IFN-γrel dimer is connected by two pairs of disulphide bonds.

  • Carp IFN-γrel interacts with CRFB17 and CRFB13 to induce STAT1 phosphorylation.

  • Carp IFN-γrel has a narrower spectrum of functions than IFN-γ.

Mucosal Immunology

Benjamin Garcia and others
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2215–2226, https://doi.org/10.4049/jimmunol.2200396

  • Discovery of a lymphoid structure in the nasal cavity of rainbow trout called O-NALT.

  • Trout O-NALT expresses high levels of aicda at the steady state.

  • IgM+ B cells proliferate and enter apoptosis in trout O-NALT.

Tumor Immunology

Rebecca Metzger and others
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2227–2238, https://doi.org/10.4049/jimmunol.2100867

  • CCL17 expression is increased in colitis-associated colon tumors.

  • Single-housed CCL17-deficient mice develop fewer tumors dependent on the microbiota.

  • Reduced tumor numbers coincide with increased apoptosis during tumor initiation.

Novel Immunological Methods

Shweta Mahajan and others
The Journal of Immunology, Volume 209, Issue 11, December 2022, Pages 2239–2247, https://doi.org/10.4049/jimmunol.2101122

  • Easy-to-implement in vitro amplification of specific T cells from healthy donors is described.

  • Robust amplification of viral- or tumor-specific T cells with low frequencies in blood is shown.

  • Parameters required for amplification of epitope-specific T cells are identified.

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