Literature DB >> 34424753

The Reaction of Innate Lymphoid Cells in the Mouse Female Genital Tract to Chlamydial Infection.

Svenja Barth1, Susanne Kirschnek1, Noemi Ortmann1, Yakup Tanriver1, Georg Häcker1,2.   

Abstract

Innate lymphoid cells (ILCs) comprise five distinct subsets. ILCs are found at mucosal barriers and may fight invading pathogens. Chlamydia is an intracellular bacterium that infects the mucosa of the genital tract and can cause severe tissue damage. Here, we used a mouse infection model with Chlamydia muridarum to measure the reaction of genital tract ILCs to the infection. Tissue-resident natural killer (NK) cells were the largest group in the uninfected female genital tract, and their number did not substantially change. Conventional NK cells were present in the greatest numbers during acute infection, while ILC1s continuously increased to high numbers. ILC2 and ILC3s were found at lower numbers that oscillated by a factor of 2 to 4. The majority of ILC3s transdifferentiated into ILC1s. NK cells and ILC1s produced gamma interferon (IFN-γ) and, rarely, tumor necrosis factor (TNF), but only early in the infection. Lack of B and T cells increased ILC numbers, while the loss of myeloid cells decreased them. ILCs accumulated to a high density in the oviduct, a main site of tissue destruction. ILC subsets are part of the inflammatory and immune reaction during infection with C. muridarum and may contribute to tissue damage during chlamydial infection.

Entities:  

Keywords:  Chlamydia; genital infection; innate lymphoid cells; tissue damage

Mesh:

Substances:

Year:  2021        PMID: 34424753      PMCID: PMC8519299          DOI: 10.1128/IAI.00800-20

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  46 in total

1.  MyD88 deficiency leads to decreased NK cell gamma interferon production and T cell recruitment during Chlamydia muridarum genital tract infection, but a predominant Th1 response and enhanced monocytic inflammation are associated with infection resolution.

Authors:  Uma M Nagarajan; James Sikes; Daniel Prantner; Charles W Andrews; Lauren Frazer; Anna Goodwin; Jessica N Snowden; Toni Darville
Journal:  Infect Immun       Date:  2010-11-15       Impact factor: 3.441

2.  Constitutive Bcl-2 expression throughout the hematopoietic compartment affects multiple lineages and enhances progenitor cell survival.

Authors:  S Ogilvy; D Metcalf; C G Print; M L Bath; A W Harris; J M Adams
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-21       Impact factor: 11.205

3.  Apoptosis Modulation in the Immune System Reveals a Role of Neutrophils in Tissue Damage in a Murine Model of Chlamydial Genital Infection.

Authors:  Tom Zortel; Annette Schmitt-Graeff; Susanne Kirschnek; Georg Häcker
Journal:  J Infect Dis       Date:  2018-05-05       Impact factor: 5.226

4.  Tumor Necrosis Factor (TNF) Receptor Superfamily Member 1b on CD8+ T Cells and TNF Receptor Superfamily Member 1a on Non-CD8+ T Cells Contribute Significantly to Upper Genital Tract Pathology Following Chlamydial Infection.

Authors:  Srikanth Manam; Joshua D Thomas; Weidang Li; Allison Maladore; Justin H Schripsema; Kyle H Ramsey; Ashlesh K Murthy
Journal:  J Infect Dis       Date:  2014-12-30       Impact factor: 5.226

5.  VACCINES. A mucosal vaccine against Chlamydia trachomatis generates two waves of protective memory T cells.

Authors:  Georg Stary; Andrew Olive; Aleksandar F Radovic-Moreno; David Gondek; David Alvarez; Pamela A Basto; Mario Perro; Vladimir D Vrbanac; Andrew M Tager; Jinjun Shi; Jeremy A Yethon; Omid C Farokhzad; Robert Langer; Michael N Starnbach; Ulrich H von Andrian
Journal:  Science       Date:  2015-06-19       Impact factor: 47.728

6.  Repeated Chlamydia trachomatis infections are associated with lower bacterial loads.

Authors:  K Gupta; R K Bakshi; B Van Der Pol; G Daniel; L Brown; C G Press; R Gorwitz; J Papp; J Y Lee; W M Geisler
Journal:  Epidemiol Infect       Date:  2018-10-04       Impact factor: 2.451

7.  Thymic origin of intestinal alphabeta T cells revealed by fate mapping of RORgammat+ cells.

Authors:  Gérard Eberl; Dan R Littman
Journal:  Science       Date:  2004-07-09       Impact factor: 47.728

8.  A T-bet gradient controls the fate and function of CCR6-RORγt+ innate lymphoid cells.

Authors:  Christoph S N Klose; Elina A Kiss; Vera Schwierzeck; Karolina Ebert; Thomas Hoyler; Yannick d'Hargues; Nathalie Göppert; Andrew L Croxford; Ari Waisman; Yakup Tanriver; Andreas Diefenbach
Journal:  Nature       Date:  2013-01-16       Impact factor: 49.962

9.  Interleukin-15 and natural killer and NKT cells play a critical role in innate protection against genital herpes simplex virus type 2 infection.

Authors:  Ali A Ashkar; Kenneth L Rosenthal
Journal:  J Virol       Date:  2003-09       Impact factor: 5.103

10.  Interleukin-33-dependent innate lymphoid cells mediate hepatic fibrosis.

Authors:  Tamar McHedlidze; Maximilian Waldner; Steffen Zopf; Jennifer Walker; Andrew L Rankin; Marcus Schuchmann; David Voehringer; Andrew N J McKenzie; Markus F Neurath; Stefan Pflanz; Stefan Wirtz
Journal:  Immunity       Date:  2013-08-15       Impact factor: 31.745

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  2 in total

Review 1.  Innate Lymphoid Cells in Response to Intracellular Pathogens: Protection Versus Immunopathology.

Authors:  Anna A Korchagina; Ekaterina Koroleva; Alexei V Tumanov
Journal:  Front Cell Infect Microbiol       Date:  2021-12-06       Impact factor: 5.293

Review 2.  Immunosuppressive Mechanisms in Brucellosis in Light of Chronic Bacterial Diseases.

Authors:  Joaquin Miguel Pellegrini; Jean-Pierre Gorvel; Sylvie Mémet
Journal:  Microorganisms       Date:  2022-06-21
  2 in total

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