Erratum: NLRP10 is a NOD-like receptor essential to initiate adaptive immunity by dendritic cells (Nature (2012) 484 (510-513) DOI:10.1038/nature11012);NLRP10 is a NOD-like receptor essential to initiate adaptive immunity by dendritic cells

Nature

Volumn 484, Issue 7395, 2012, Pages 510-513

  Eisenbarth, Stephanie C ^a   Williams, Adam ^a   Colegio, Oscar R ^a   Meng, Hailong ^a   Strowig, Till ^a   Rongvaux, Anthony ^a   Henao Mejia, Jorge ^a   Thaiss, Christoph A ^a   Joly, Sophie ^b   Gonzalez, David G ^a   Xu, Lan ^a   Zenewicz, Lauren A ^a   Haberman, Ann M ^a   Elinav, Eran ^a   Kleinstein, Steven H ^a   Sutterwala, Fayyaz S ^b,c   Flavell, Richard A ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF IOWA   (United States)

^c VETERANS AFFAIRS MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALUMINUM HYDROXIDE; CHEMOKINE RECEPTOR CCR7; CHEMOKINE RECEPTOR CXCR4; INFLAMMASOME; LIPOPOLYSACCHARIDE; MACROPHAGE INFLAMMATORY PROTEIN 3BETA; NOD LIKE RECEPTOR P10; NUCLEOTIDE BINDING OLIGOMERIZATION DOMAIN LIKE RECEPTOR; OVALBUMIN; SECONDARY LYMPHOID TISSUE CHEMOKINE; UNCLASSIFIED DRUG;

ADAPTATION; CHEMICAL BINDING; CYTOLOGY; IMMUNE RESPONSE; LIGAND;

ADAPTIVE IMMUNITY; ALLERGIC ENCEPHALOMYELITIS; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIGEN FUNCTION; ARTICLE; ASTHMA; CD4+ T LYMPHOCYTE; CELL MATURATION; CELL MIGRATION; CHEMOTAXIS; CONTROLLED STUDY; DENDRITIC CELL; EMBRYONIC STEM CELL; HELPER CELL; IMMUNOSTIMULATION; IN VITRO STUDY; IN VIVO STUDY; LIGAND BINDING; LUNG LAVAGE; LYMPH NODE; LYMPHOCYTE PROLIFERATION; MACROPHAGE; MOUSE; MYCOBACTERIUM TUBERCULOSIS; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; SPLEEN; SPLEEN CELL;

MUS;

EID: 84860233490     PISSN: 00280836     EISSN: 14764687     Source Type: Journal    
DOI: 10.1038/nature16074     Document Type: Erratum

References (36)

1. Takeuchi, O. & Akira, S. Pattern recognition receptors and inflammation. Cell 140, 805-820 (2010).
2. Williams, A., Flavell, R. A. & Eisenbarth, S. C. The role of NOD-like receptors in shaping adaptive immunity. Curr. Opin. Immunol. 22, 34-40 (2010).
3. Medzhitov, R. & Janeway, C. A. Jr. Innate immune induction of the adaptive immune response. Cold Spring Harb. Symp. Quant. Biol. 64, 429-436 (1999).
4. Imamura, R. et al. Anti-inflammatory activity of PYNOD and its mechanism in humans and mice. J. Immunol. 184, 5874-5884 (2010).
5. Inohara, N. & Nunez, G. NODs: intracellular proteins involved in inflammation and apoptosis. Nature Rev. Immunol. 3, 371-382 (2003).
6. Wang, Y. et al. PYNOD, a novel Apaf-1/CED4-like protein is an inhibitor of ASC and caspase-1. Int. Immunol. 16, 777-786 (2004).
7. Eisenbarth, S. C., Colegio, O. R., O'Connor, W., Sutterwala, F. S. & Flavell, R. A. Crucial role for the Nalp3 inflammasome in the immunostimulatory properties of aluminium adjuvants. Nature 453, 1122-1126 (2008).
8. Li, H., Willingham, S. B., Ting, J. P. & Re, F. Cutting edge: inflammasome activation by alum and alum's adjuvant effect are mediated by NLRP3. J. Immunol. 181, 17-21 (2008).
9. Gris, D. et al. NLRP3 plays a critical role in the development of experimental autoimmune encephalomyelitis by mediating Th1 and Th17 responses. J. Immunol. 185, 974-981 (2010).
10. Eisenbarth, S. C. et al. Lipopolysaccharide-enhanced, toll-like receptor 4-dependent T helper cell type 2 responses to inhaled antigen. J. Exp. Med. 196, 1645-1651 (2002).
11. Bachmann, M. F., Hengartner, H. & Zinkernagel, R. M. T helper cell-independent neutralizing B cell response against vesicular stomatitis virus: role of antigen patterns in B cell induction? Eur. J. Immunol. 25, 3445-3451 (1995).
12. Palm, N. W. & Medzhitov, R. Immunostimulatory activity of haptenated proteins. Proc. Natl Acad. Sci. USA 106, 4782-4787 (2009).
13. Banchereau, J. & Steinman, R. M. Dendritic cells and the control of immunity. Nature 392, 245-252 (1998).
14. Ohl, L. et al. CCR7 governs skin dendritic cell migration under inflammatory and steady-state conditions. Immunity 21, 279-288 (2004).
15. Martin-Fontecha, A. et al. Regulation of dendritic cell migration to the draining lymph node: impact on T lymphocyte traffic and priming. J. Exp. Med. 198, 615-621 (2003).
16. Saeki, H., Moore, A. M., Brown, M. J. & Hwang, S. T. Cutting edge: secondary lymphoid-tissue chemokine (SLC) and CC chemokine receptor 7 (CCR7) participate in the emigration pathway of mature dendritic cells from the skin to regional lymph nodes. J. Immunol. 162, 2472-2475 (1999).
17. Itano, A. A. et al. Distinct dendritic cell populations sequentially present antigen to CD4 T cells and stimulate different aspects of cell-mediated immunity. Immunity 19, 47-57 (2003).
18. Jakubzick, C. et al. Lymph-migrating, tissue-derived dendritic cells are minor constituentswithinsteady-state lymphnodes. J. Exp.Med. 205,2839-2850(2008).
19. Edelson, B. T. et al. Peripheral CD1031 dendritic cells form a unified subset developmentally related to CD8a1 conventional dendritic cells. J. Exp. Med. 207, 823-836 (2010).
20. Ginhoux, F. et al. The origin and development of nonlymphoid tissueCD1031 DCs. J. Exp. Med. 206, 3115-3130 (2009).
21. Plantinga, M., Hammad, H. & Lambrecht, B. N. Origin and functional specializations of DC subsets in the lung. Eur. J. Immunol. 40, 2112-2118 (2010).
22. Cyster, J. G. Chemokines, sphingosine-1-phosphate, and cell migration in secondary lymphoid organs. Annu. Rev. Immunol. 23, 127-159 (2005).
23. Czeloth, N., Bernhardt, G., Hofmann, F., Genth, H. & Forster, R. Sphingosine-1-phosphate mediates migration of mature dendritic cells. J. Immunol. 175, 2960-2967 (2005).
24. Dieu, M. C. et al. Selective recruitment of immature and mature dendritic cells by distinct chemokines expressed in different anatomic sites. J. Exp. Med. 188, 373-386 (1998).
25. Gunn, M. D. et al. Mice lacking expressionof secondary lymphoid organ chemokine have defects in lymphocyte homing and dendritic cell localization. J. Exp. Med. 189, 451-460 (1999).
26. Sallusto, F. et al. Rapid and coordinated switch in chemokine receptor expression during dendritic cell maturation. Eur. J. Immunol. 28, 2760-2769 (1998).
27. Noben-Trauth, N. et al. An interleukin 4 (IL-4)-independent pathway for CD41 T cell IL-4 production is revealed in IL-4 receptor-deficient mice. Proc. Natl Acad. Sci. USA 94, 10838-10843 (1997).
28. Zheng, B., Berrie, C. P., Corda, D. & Farquhar, M. G. GDE1/MIR16 is a glycerophosphoinositol phosphodiesterase regulated by stimulation of G proteincoupled receptors. Proc. Natl Acad. Sci. USA 100, 1745-1750 (2003).
29. Arthur, J. C. et al. Cutting edge: NLRP12 controls dendritic and myeloid cell migration to affect contact hypersensitivity. J. Immunol. 185, 4515-4519 (2010).
30. Ippagunta, S. K. et al. The inflammasome adaptor ASC regulates the function of adaptive immune cells by controlling Dock2-mediated Rac activation and actin polymerization. Nature Immunol. 12, 1010-1016 (2011).
31. Sutterwala, F. S. et al. Critical role for NALP3/CIAS1/cryopyrin in innate and adaptive immunity through its regulation of caspase-1. Immunity 24, 317-327 (2006).
32. Cohn, L., Homer, R. J., Niu, N. & Bottomly, K. T helper 1 cells and interferon c regulate allergic airway inflammation and mucus production. J. Exp. Med. 190, 1309-1318 (1999).
33. Laouar, Y. et al. TGF-b signaling in dendritic cells is a prerequisite for the control of autoimmune encephalomyelitis. Proc. Natl Acad. Sci. USA 105, 10865-10870 (2008).
34. Lutz, M. B. et al. An advanced culture method for generating large quantities of highly pure dendritic cells from mouse bone marrow. J. Immunol. Methods 223, 77-92 (1999).
35. Jakubzick, C., Helft, J., Kaplan, T. J. & Randolph, G. J. Optimization of methods to study pulmonary dendritic cell migration reveals distinct capacities of DC subsets to acquire soluble versus particulate antigen. J. Immunol. Methods 337, 121-131 (2008).
36. Edgar, R., Domrachev, M. & Lash, A. E. Gene Expression Omnibus: NCBI gene expression and hybridization array data repository. Nucleic Acids Res. 30, 207-210 (2002).