Immunity against a Chlamydia infection and disease may be determined by a balance of IL-17 signaling. (Q37845255)

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3 March 2020

title

Immunity against a Chlamydia infection and disease may be determined by a balance of IL-17 signaling (English)

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3 March 2020

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5

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3 March 2020

Connor P O'Meara

1

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3 March 2020

Charles W. Armitage

2

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3 March 2020

Ken Beagley

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3 March 2020

3

Marina C G Harvie

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3 March 2020

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Nils Y Lycke

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3 March 2020

author name string

Dean W Andrew

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3 March 2020

publication date

24 December 2013

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Immunology & Cell Biology

3 March 2020

published in

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3 March 2020

volume

92

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3 March 2020

issue

3

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3 March 2020

page(s)

287-297

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Evaluation of rapid diagnostic tests: chlamydia and gonorrhoea

3 March 2020

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Protective immunity against mouse upper genital tract pathology correlates with high IFNγ but low IL-17 T cell and anti-secretion protein antibody responses induced by replicating chlamydial organisms in the airway

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Transcutaneous immunization with combined cholera toxin and CpG adjuvant protects against Chlamydia muridarum genital tract infection

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CD4+ T cells and antibody are required for optimal major outer membrane protein vaccine-induced immunity to Chlamydia muridarum genital infection

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The effect of doxycycline treatment on the development of protective immunity in a murine model of chlamydial genital infection

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OT-1 mice display minimal upper genital tract pathology following primary intravaginal Chlamydia muridarum infection

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Tumor necrosis factor alpha production from CD8+ T cells mediates oviduct pathological sequelae following primary genital Chlamydia muridarum infection

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Chlamydia muridarum T-cell antigens formulated with the adjuvant DDA/TDB induce immunity against infection that correlates with a high frequency of gamma interferon (IFN-gamma)/tumor necrosis factor alpha and IFN-gamma/interleukin-17 double-positive

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Protection against Chlamydia promoted by a subunit vaccine (CTH1) compared with a primary intranasal infection in a mouse genital challenge model

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Monitoring the T cell response to genital tract infection

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Immunization with a MOMP-based vaccine protects mice against a pulmonary Chlamydia challenge and identifies a disconnection between infection and pathology

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Progression of armed CTL from draining lymph node to spleen shortly after localized infection with herpes simplex virus 1.

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Protective immunity to chlamydial genital infection: evidence from animal studies

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The infecting dose of Chlamydia muridarum modulates the innate immune response and ascending infection

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A chlamydial type III-secreted effector protein (Tarp) is predominantly recognized by antibodies from humans infected with Chlamydia trachomatis and induces protective immunity against upper genital tract pathologies in mice

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Prevention of Chlamydia-induced infertility by inhibition of local caspase activity.

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Significant role of IL-1 signaling, but limited role of inflammasome activation, in oviduct pathology during Chlamydia muridarum genital infection

21 January 2018

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Critical role for interleukin-1beta (IL-1beta) during Chlamydia muridarum genital infection and bacterial replication-independent secretion of IL-1beta in mouse macrophages

21 January 2018

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A MyD88-dependent early IL-17 production protects mice against airway infection with the obligate intracellular pathogen Chlamydia muridarum

21 January 2018

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The duration of Chlamydia muridarum genital tract infection and associated chronic pathological changes are reduced in IL-17 knockout mice but protection is not increased further by immunization.

21 January 2018

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Interleukin-17 contributes to generation of Th1 immunity and neutrophil recruitment during Chlamydia muridarum genital tract infection but is not required for macrophage influx or normal resolution of infection

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7 January 2021

CpG oligonucleotides induce the differentiation of CD4(+)Th17 cells by triggering plasmacytoid dendritic cells in adoptively cell transfer immunotherapy

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7 January 2021

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7 January 2021

Identifiers

DOI

10.1038/ICB.2013.92

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24366518%20AND%20SRC:MED&resulttype=core&format=json

3 March 2020

1 reference