Towards a crucial role for DC-SIGN in tuberculosis and beyond

Trends in Microbiology

Volumn 14, Issue 9, 2006, Pages 383-387

  Neyrolles, Olivier ^a   Gicquel, Brigitte ^a   Quintana Murci, Lluís ^a  

^a INSTITUT PASTEUR   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CD209 ANTIGEN; LECTIN; PATTERN RECOGNITION RECEPTOR;

ARTICLE; BACTERIAL COLONIZATION; DENDRITIC CELL; GENE; GENE EXPRESSION; GENE FREQUENCY; GENETIC CODE; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENETICS; HOST PATHOGEN INTERACTION; HUMAN; IMMUNITY; MYCOBACTERIUM; MYCOBACTERIUM TUBERCULOSIS; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN STRUCTURE; TUBERCULOSIS;

CELL ADHESION MOLECULES; EVOLUTION, MOLECULAR; GENE EXPRESSION; GENETIC PREDISPOSITION TO DISEASE; GEOGRAPHY; HUMANS; LECTINS, C-TYPE; PROMOTER REGIONS (GENETICS); RECEPTORS, CELL SURFACE; TUBERCULOSIS;

EID: 33747179633     PISSN: 0966842X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tim.2006.07.007     Document Type: Article

References (51)

1. Gordon S. Pattern recognition receptors: doubling up for the innate immune response. Cell 111 (2002) 927-930
2. Mogensen T.H., and Paludan S.R. Reading the viral signature by Toll-like receptors and other pattern recognition receptors. J. Mol. Med. 83 (2005) 180-192
3. Kaufmann S.H. How can immunology contribute to the control of tuberculosis?. Nat. Rev. Immunol. 1 (2001) 20-30
4. Ernst J.D. Macrophage receptors for Mycobacterium tuberculosis. Infect. Immun. 66 (1998) 1277-1281
5. Quesniaux V., et al. Toll-like receptor pathways in the immune responses to mycobacteria. Microbes Infect. 6 (2004) 946-959
6. Curtis B.M., et al. Sequence and expression of a membrane-associated C-type lectin that exhibits CD4-independent binding of human immunodeficiency virus envelope glycoprotein gp120. Proc. Natl. Acad. Sci. U. S. A. 89 (1992) 8356-8360
7. Geijtenbeek T.B., et al. DC-SIGN, a dendritic cell-specific HIV-1-binding protein that enhances trans-infection of T cells. Cell 100 (2000) 587-597
8. Geijtenbeek T.B., et al. Identification of DC-SIGN, a novel dendritic cell-specific ICAM-3 receptor that supports primary immune responses. Cell 100 (2000) 575-585
9. Cambi A., et al. How C-type lectins detect pathogens. Cell. Microbiol. 7 (2005) 481-488
10. Geijtenbeek T., et al. Mycobacteria target DC-SIGN to suppress dendritic cell function. J. Exp. Med. 197 (2003) 7-17
11. Koppel E.A., et al. Identification of the mycobacterial carbohydrate structure that binds the C-type lectins DC-SIGN, L-SIGN and SIGNR1. Immunobiology 209 (2004) 117-127
12. Maeda N., et al. The cell surface receptor DC-SIGN discriminates between Mycobacterium species through selective recognition of the mannose caps on lipoarabinomannan. J. Biol. Chem. 278 (2002) 5513-5516
13. Pitarque S., et al. Deciphering the molecular bases of Mycobacterium tuberculosis binding to the lectin DC-SIGN reveals an underestimated complexity. Biochem. J. 392 (2005) 615-624
14. Tailleux L., et al. DC-SIGN is the major Mycobacterium tuberculosis receptor on human dendritic cells. J. Exp. Med. 197 (2003) 121-127
15. Casanova J.L., and Abel L. Inborn errors of immunity to infection: the rule rather than the exception. J. Exp. Med. 202 (2005) 197-201
16. Frodsham A.J., and Hill A.V. Genetics of infectious diseases. Hum. Mol. Genet. 13 Spec. No. 2 (2004) R187-R194
17. Lienhardt C. From exposure to disease: the role of environmental factors in susceptibility to and development of tuberculosis. Epidemiol. Rev. 23 (2001) 288-301
18. Cooke G.S., and Hill A.V. Genetics of susceptibility to human infectious disease. Nat. Rev. Genet. 2 (2001) 967-977
19. Casanova J.L., and Abel L. The human model: a genetic dissection of immunity to infection in natural conditions. Nat. Rev. Immunol. 4 (2004) 55-66
20. Casanova J.L., and Abel L. Genetic dissection of immunity to mycobacteria: the human model. Annu. Rev. Immunol. 20 (2002) 581-620
21. Barreiro L.B., et al. Promoter variation in the DC-SIGN-encoding gene CD209 is associated with tuberculosis. PLoS Med 3 (2006) e20
22. Munch Z., et al. Tuberculosis transmission patterns in a high-incidence area: a spatial analysis. Int. J. Tuberc. Lung Dis. 7 (2003) 271-277
23. Martin M.P., et al. Association of DC-SIGN promoter polymorphism with increased risk for parenteral, but not mucosal, acquisition of human immunodeficiency virus type 1 infection. J. Virol. 78 (2004) 14053-14056
24. Sakuntabhai A., et al. A variant in the CD209 promoter is associated with severity of dengue disease. Nat. Genet. 37 (2005) 507-513
25. Tailleux L., et al. DC-SIGN induction in alveolar macrophages defines privileged target host cells for mycobacteria in patients with tuberculosis. PLoS Med 2 (2005) e381
26. Hirsch C.S., et al. Complement receptor-mediated uptake and tumor necrosis factor-α-mediated growth inhibition of Mycobacterium tuberculosis by human alveolar macrophages. J. Immunol. 152 (1994) 743-753
27. Tailleux L., et al. Constrained intracellular survival of Mycobacterium tuberculosis in human dendritic cells. J. Immunol. 170 (2003) 1939-1948
28. Caparros E., et al. DC-SIGN ligation on dendritic cells results in ERK and PI3K activation and modulates cytokine production. Blood 107 (2006) 3950-3958
29. Geijtenbeek T.B., and van Kooyk Y. Pathogens target DC-SIGN to influence their fate DC-SIGN functions as a pathogen receptor with broad specificity. APMIS 111 (2003) 698-714
30. Bamshad M., and Wooding S.P. Signatures of natural selection in the human genome. Nat. Rev. Genet. 4 (2003) 99-111
31. Akey J.M., et al. Population history and natural selection shape patterns of genetic variation in 132 genes. PLoS Biol. 2 (2004) e286
32. Haldane J.B.S. Disease and evolution. Ric. Sci. 19 (1949) 68-76
33. Vallender E.J., and Lahn B.T. Positive selection on the human genome. Hum. Mol. Genet. 13 Spec. No. 2 (2004) R245-R254
34. Ohta T. Role of diversifying selection and gene conversion in evolution of major histocompatibility complex loci. Proc. Natl. Acad. Sci. U. S. A. 88 (1991) 6716-6720
35. Harding R.M., et al. A gene tree for β-globin sequences from Melanesia. J. Mol. Evol. 44 Suppl. 1 (1997) S133-S138
36. Sabeti P.C., et al. Detecting recent positive selection in the human genome from haplotype structure. Nature 419 (2002) 832-837
37. Bamshad M.J., et al. A strong signature of balancing selection in the 5′ cis-regulatory region of CCR5. Proc. Natl. Acad. Sci. U. S. A. 99 (2002) 10539-10544
38. Barreiro L.B., et al. The heritage of pathogen pressures and ancient demography in the human innate-immunity CD209/CD209L region. Am. J. Hum. Genet. 77 (2005) 869-886
39. Feinberg H., et al. Extended neck regions stabilize tetramers of the receptors DC-SIGN and DC-SIGNR. J. Biol. Chem. 280 (2005) 1327-1335
40. Park C.G., et al. Five mouse homologues of the human dendritic cell C-type lectin, DC-SIGN. Int. Immunol. 13 (2001) 1283-1290
41. Powlesland A.S., et al. Widely divergent biochemical properties of the complete set of mouse DC-SIGN-related proteins. J. Biol. Chem. 281 (2006) 20440-20449
42. Smits H.H., et al. Selective probiotic bacteria induce IL-10-producing regulatory T cells in vitro by modulating dendritic cell function through dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin. J. Allergy Clin. Immunol. 115 (2005) 1260-1267
43. van Gisbergen K.P., et al. Neutrophils mediate immune modulation of dendritic cells through glycosylation-dependent interactions between Mac-1 and DC-SIGN. J. Exp. Med. 201 (2005) 1281-1292
44. Geijtenbeek T.B., et al. DC-SIGN-ICAM-2 interaction mediates dendritic cell trafficking. Nat. Immunol. 1 (2000) 353-357
45. Muramatsu T. Developmentally regulated expression of cell surface carbohydrates during mouse embryogenesis. J. Cell. Biochem. 36 (1988) 1-14
46. Thorpe S.J., et al. Developmental patterning of carbohydrate antigens during early embryogenesis of the chick: expression of antigens of the poly-N-acetyllactosamine series. Development 102 (1988) 193-210
47. Fenderson B.A., et al. Glycoconjugate expression during embryogenesis and its biological significance. Bioessays 12 (1990) 173-179
48. Masteller E.L., et al. Chicken B cells undergo discrete developmental changes in surface carbohydrate structure that appear to play a role in directing lymphocyte migration during embryogenesis. Development 121 (1995) 1657-1667
49. van Die I., et al. The dendritic cell-specific C-type lectin DC-SIGN is a receptor for Schistosoma mansoni egg antigens and recognizes the glycan antigen Lewis x. Glycobiology 13 (2003) 471-478
50. Muramatsu T., and Muramatsu H. Carbohydrate antigens expressed on stem cells and early embryonic cells. Glycoconj. J. 21 (2004) 41-45
51. Soilleux E.J., et al. Constitutive and induced expression of DC-SIGN on dendritic cell and macrophage subpopulations in situ and in vitro. J. Leukoc. Biol. 71 (2002) 445-457