Batf3-Dependent Dendritic Cells in the Renal Lymph Node Induce Tolerance against Circulating Antigens

Although the spleen is a major site where immune tolerance to circulating innocuous antigens occurs, the kidney also contributes. Circulating antigens smaller than albumin are constitutively filtered and concentrated in the kidney and reach the renal lymph node by lymphatic drainage, where resident...

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Veröffentlicht in:Journal of the American Society of Nephrology 2013-04, Vol.24 (4), p.543-549
Hauptverfasser: GOTTSCHALK, Catherine, DAMUZZO, Vera, GOTOT, Janine, KROCZEK, Richard A, YAGITA, Hideo, MURPHY, Kenneth M, KNOLLE, Percy A, LUDWIG-PORTUGALL, Isis, KURTS, Christian
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container_end_page 549
container_issue 4
container_start_page 543
container_title Journal of the American Society of Nephrology
container_volume 24
creator GOTTSCHALK, Catherine
DAMUZZO, Vera
GOTOT, Janine
KROCZEK, Richard A
YAGITA, Hideo
MURPHY, Kenneth M
KNOLLE, Percy A
LUDWIG-PORTUGALL, Isis
KURTS, Christian
description Although the spleen is a major site where immune tolerance to circulating innocuous antigens occurs, the kidney also contributes. Circulating antigens smaller than albumin are constitutively filtered and concentrated in the kidney and reach the renal lymph node by lymphatic drainage, where resident dendritic cells (DCs) capture them and induce tolerance of specific cytotoxic T cells through unknown mechanisms. Here, we found that the coinhibitory cell surface receptor programmed death 1 (PD-1) on cytotoxic T cells mediates to their tolerance. Renal lymph node DCs of the CD8(+) XCR1(+) subset, which depend on the transcription factor Batf3, expressed the PD-1 cognate ligand PD-L1. Batf3-dependent DCs in the renal lymph node presented antigen that had been concentrated in the kidney and used PD-L1 to induce apoptosis of cytotoxic T cells. In contrast, T cell tolerance in the spleen was independent of PD-1, PD-L1, and Batf3. In summary, these results clarify how the kidney/renal lymph node system tolerizes the immune system against circulating innocuous antigens.
doi_str_mv 10.1681/ASN.2012101022
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Circulating antigens smaller than albumin are constitutively filtered and concentrated in the kidney and reach the renal lymph node by lymphatic drainage, where resident dendritic cells (DCs) capture them and induce tolerance of specific cytotoxic T cells through unknown mechanisms. Here, we found that the coinhibitory cell surface receptor programmed death 1 (PD-1) on cytotoxic T cells mediates to their tolerance. Renal lymph node DCs of the CD8(+) XCR1(+) subset, which depend on the transcription factor Batf3, expressed the PD-1 cognate ligand PD-L1. Batf3-dependent DCs in the renal lymph node presented antigen that had been concentrated in the kidney and used PD-L1 to induce apoptosis of cytotoxic T cells. In contrast, T cell tolerance in the spleen was independent of PD-1, PD-L1, and Batf3. 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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Animals
Antigens - blood
Antigens - immunology
Basic-Leucine Zipper Transcription Factors - genetics
Basic-Leucine Zipper Transcription Factors - metabolism
Biological and medical sciences
Brief Communications
Dendritic Cells - immunology
Dendritic Cells - metabolism
Immune Tolerance - immunology
Kidney - immunology
Kidney - metabolism
Lymph Nodes - immunology
Lymph Nodes - metabolism
Medical sciences
Mice
Mice, Mutant Strains
Nephrology. Urinary tract diseases
Programmed Cell Death 1 Receptor - immunology
Programmed Cell Death 1 Receptor - metabolism
Repressor Proteins - genetics
Repressor Proteins - metabolism
T-Lymphocytes, Cytotoxic - immunology
T-Lymphocytes, Cytotoxic - metabolism
title Batf3-Dependent Dendritic Cells in the Renal Lymph Node Induce Tolerance against Circulating Antigens
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