» Articles » PMID: 17675510

IFN-gamma-producing Dendritic Cells Are Important for Priming of Gut Intraepithelial Lymphocyte Response Against Intracellular Parasitic Infection

Overview
Journal J Immunol
Date 2007 Aug 7
PMID 17675510
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

The importance of intraepithelial lymphocytes (IEL) in immunoprotection against orally acquired pathogens is being increasingly recognized. Recent studies have demonstrated that Ag-specific IEL can be generated and can provide an important first line of defense against pathogens acquired via oral route. However, the mechanism involved in priming of IEL remains elusive. Our current study, using a microsporidial model of infection, demonstrates that priming of IEL is dependent on IFN-gamma-producing dendritic cells (DC) from mucosal sites. DC from mice lacking the IFN-gamma gene are unable to prime IEL, resulting in failure of these cells to proliferate and lyse pathogen-infected targets. Also, treatment of wild-type DC from Peyer's patches with Ab to IFN-gamma abrogates their ability to prime an IEL response against Encephalitozoon cuniculi in vitro. Moreover, when incubated with activated DC from IFN-gamma knockout mice, splenic CD8(+) T cells are not primed efficiently and exhibit reduced ability to home to the gut compartment. These data strongly suggest that IFN-gamma-producing DC from mucosal sites play an important role in the generation of an Ag-specific IEL response in the small intestine. To our knowledge, this report is the first demonstrating a role for IFN-gamma-producing DC from Peyer's patches in the development of Ag-specific IEL population and their trafficking to the gut epithelium.

Citing Articles

Immune Response to Microsporidia.

Moretto M, Khan I Exp Suppl. 2022; 114:373-388.

PMID: 35544009 DOI: 10.1007/978-3-030-93306-7_13.


Phagocytosis Is the Sole Arm of Known Host Defenses That Provides Some Protection Against Microsporidia Infection.

Caravello G, Franchet A, Niehus S, Ferrandon D Front Immunol. 2022; 13:858360.

PMID: 35493511 PMC: 9043853. DOI: 10.3389/fimmu.2022.858360.


Generating Bovine Monocyte-Derived Dendritic Cells for Experimental and Clinical Applications Using Commercially Available Serum-Free Medium.

Guinan J, Lopez B Front Immunol. 2020; 11:591185.

PMID: 33178224 PMC: 7596353. DOI: 10.3389/fimmu.2020.591185.


Production of IFN-γ by splenic dendritic cells during innate immune responses against Francisella tularensis LVS depends on MyD88, but not TLR2, TLR4, or TLR9.

De Pascalis R, Rossi A, Mittereder L, Takeda K, Akue A, Kurtz S PLoS One. 2020; 15(8):e0237034.

PMID: 32745117 PMC: 7398525. DOI: 10.1371/journal.pone.0237034.


Innate and Adaptive Immune Responses Against Microsporidia Infection in Mammals.

Han Y, Gao H, Xu J, Luo J, Han B, Bao J Front Microbiol. 2020; 11:1468.

PMID: 32670257 PMC: 7332555. DOI: 10.3389/fmicb.2020.01468.


References
1.
Iwasaki A, Kelsall B . Localization of distinct Peyer's patch dendritic cell subsets and their recruitment by chemokines macrophage inflammatory protein (MIP)-3alpha, MIP-3beta, and secondary lymphoid organ chemokine. J Exp Med. 2000; 191(8):1381-94. PMC: 2193144. DOI: 10.1084/jem.191.8.1381. View

2.
Fan Z, Zhang Q . Molecular mechanisms of lymphocyte-mediated cytotoxicity. Cell Mol Immunol. 2005; 2(4):259-64. View

3.
Banchereau J, Briere F, Caux C, Davoust J, Lebecque S, Liu Y . Immunobiology of dendritic cells. Annu Rev Immunol. 2000; 18:767-811. DOI: 10.1146/annurev.immunol.18.1.767. View

4.
Moretto M, Casciotti L, Durell B, Khan I . Lack of CD4(+) T cells does not affect induction of CD8(+) T-cell immunity against Encephalitozoon cuniculi infection. Infect Immun. 2000; 68(11):6223-32. PMC: 97703. DOI: 10.1128/IAI.68.11.6223-6232.2000. View

5.
Suzuki K, Oida T, Hamada H, Hitotsumatsu O, Watanabe M, Hibi T . Gut cryptopatches: direct evidence of extrathymic anatomical sites for intestinal T lymphopoiesis. Immunity. 2000; 13(5):691-702. DOI: 10.1016/s1074-7613(00)00068-6. View