Hostname: page-component-586b7cd67f-tf8b9 Total loading time: 0 Render date: 2024-11-22T08:29:07.714Z Has data issue: false hasContentIssue false

The role of dendritic cells in shaping the immune response

Published online by Cambridge University Press:  28 February 2007

C. J. Howard*
Affiliation:
Institute for Animal Health, Compton, Newbury, Berkshire RG20 7NN, UK
B. Charleston
Affiliation:
Institute for Animal Health, Compton, Newbury, Berkshire RG20 7NN, UK
S. A. Stephens
Affiliation:
Institute for Animal Health, Compton, Newbury, Berkshire RG20 7NN, UK
P. Sopp
Affiliation:
Institute for Animal Health, Compton, Newbury, Berkshire RG20 7NN, UK
J. C. Hope
Affiliation:
Institute for Animal Health, Compton, Newbury, Berkshire RG20 7NN, UK

Abstract

Dendritic cells are central to the initiation of primary immune responses. They are the only antigen-presenting cell capable of stimulating naive T cells, and hence they are pivotal in the generation of adaptive immunity. Dendritic cells also interact with and influence the response of cells of the innate immune system. The manner in which dendritic cells influence the responses in cells of both the innate and adaptive immune systems has consequences for the bias of the adaptive response that mediates immunity to infection after vaccination or infection. It also provides an opportunity to intervene and to influence the response, allowing ways of developing appropriate vaccination strategies. Mouse and human studies have identified myeloid, lymphoid and plasmacytoid dendritic cells. Studies in domesticated animals with agents of specific infectious diseases have confirmed the applicability of certain of the generic models developed from mice or from in vitro studies on human cells. In vivo and ex vivo studies in cattle have demonstrated the existence of a number of subpopulations of myeloid dendritic cells. These cells differ in their ability to stimulate T cells and in the cytokines that they produce, observations clearly having important implications for the bias of the T-cell response. Dendritic cells also interact with the innate immune system, inducing responses that potentially bias the subsequent adaptive response.

Type
Research Article
Copyright
Copyright © CAB International 2004

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Brooke, GP, Parsons, KR and Howard, CJ (1998). Cloning of two members of the SIRP alpha family of protein tyrosine phosphatase binding proteins in cattle that are expressed on monocytes and a subpopulation of dendritic cells and which mediate binding to CD4 T cells. European Journal of Immunology 28: 111.Google Scholar
Cella, M, Jarrossay, D, Facchetti, F, Alebardi, O, Nakajima, H, Lanzavecchia, A and Colonna, M (1999). Plasmacytoid monocytes migrate to inflamed lymph nodes and produce large amounts of type I interferon. Nature Medicine 5: 919923.CrossRefGoogle ScholarPubMed
Cella, M, Facchetti, F, Lanzavecchia, A and Colonna, M (2000). Plasmacytoid dendritic cells activated by influenza virus and CD40L drive a potent TH1 polarization. Nature Immunology 1: 305310.CrossRefGoogle ScholarPubMed
Colonna, M, Krug, A and Cella, M (2002). Interferon-producing cells: on the front line in immune responses against pathogens. Current Opinion in Immunology 14: 373379.CrossRefGoogle ScholarPubMed
Gliddon, DR and Howard, CJ (2002). CD26 is expressed on a restricted subpopulation of dendritic cells in vivo. European Journal of Immunology 32: 14721481.3.0.CO;2-Q>CrossRefGoogle ScholarPubMed
Haig, DM, Hopkins, J and Miller, HR (1999). Local immune responses in afferent and efferent lymph. Immunology 96: 155163.CrossRefGoogle ScholarPubMed
Hawiger, D, Inaba, K, Dorsett, Y, Guo, M, Mahnke, K, Rivera, M, Ravetch, JV, Steinman, RM and Nussenzweig, M (2001). Dendritic cells induce peripheral T cell unresponsiveness under steady state conditions in vivo. Journal of Experimental Medicine 194: 769779.CrossRefGoogle ScholarPubMed
Hein, WR and Griebel, PJ (2003). A road less travelled: large animal models in immunological research. Nature reviews. Immunology 3: 7984.CrossRefGoogle ScholarPubMed
Hope, JC, Kwong, LS, Sopp, P, Collins, RA and Howard, CJ (2000). Dendritic cells induce CD4+ and CD8+ T-cell responses to Mycobacterium bovis and M. avium antigens in Bacille Calmette Guerin vaccinated and nonvaccinated cattle. Scandinavian Journal of Immunology 52: 285291.CrossRefGoogle Scholar
Hope, JC, Sopp, P, Collins, RA and Howard, CJ (2001). Differences in the induction of CD8+ T cell responses by subpopulations of dendritic cells from afferent lymph are related to IL-1 alpha secretion. Journal of Leukocyte Biology 69: 271279.CrossRefGoogle ScholarPubMed
Hope, JC, Sopp, P and Howard, CJ (2002). NK-like CD8(+) cells in immunologically naive neonatal calves that respond to dendritic cells infected with Mycobacterium bovis BCG. Journal of Leukocyte Biology 71: 184194.CrossRefGoogle ScholarPubMed
Howard, CJ and Hope, JC (2000). Dendritic cells, implications on function from studies of the afferent lymph veiled cell. Veterinary Immunology and Immunopathology 77: 113.CrossRefGoogle ScholarPubMed
Howard, CJ, Sopp, P, Brownlie, J, Kwong, LS, Parsons, KR and Taylor, G (1997). Identification of two distinct populations of dendritic cells in afferent lymph that vary in their ability to stimulate T cells. Journal of Immunology 159: 53725382.CrossRefGoogle ScholarPubMed
Howard, CJ, Hope, JC, Stephens, SA, Gliddon, DR and Brooke, GP (2002). Co-stimulation and modulation of the ensuing immune response. Veterinary Immunology and Immunopathology 87: 123130.CrossRefGoogle ScholarPubMed
Huang, FP and MacPherson, GG (2001). Continuing education of the immune system–dendritic cells, immune recognition and tolerance. Current Molecular Medicine 1: 247468.CrossRefGoogle Scholar
Huang, FP, Platt, N, Wykes, M, Major, JR, Powell, TJ, Jenkins, CD and MacPherson, GG (2000). A discrete subpopulation of dendritic cells transports apoptotic intestinal epithelial cells to T cell areas of mesenteric lymph nodes. Journal of Experimental Medicine 191: 435443.CrossRefGoogle Scholar
Iwasaki, A and Kelsall, BL (1999). Freshly isolated Peyer's patch, but not spleen, dendritic cells produce interleukin 10 and induce the differentiation of T helper type 2 cells. Journal of Experimental Medicine 190: 229239.CrossRefGoogle Scholar
Jonuleit, H, Schmitt, E, Schuler, G, Knop, J and Enk, AH (2000). Induction of interleukin 10-producing, nonproliferating CD4+ T cells with regulatory properties by repetitive stimulation with allogeneic immature human dendritic cells. Journal of Experimental Medicine 192: 12131222.CrossRefGoogle ScholarPubMed
Le Bon, A and Tough, DF (2002). Links between innate and adaptive immunity via type I interferon. Current Opinion in Immunology 14: 432436.CrossRefGoogle ScholarPubMed
Lertmemongkolchai, G, Cai, G, Hunter, CA and Bancroft, GJ (2001). Bystander activation of CD8+ T cells contributes to the rapid production of IFN-gamma in response to bacterial pathogens. Journal of Immunology 166: 10971105.CrossRefGoogle Scholar
Maldonado-Lopez, R, De Smedt, T, Michel, P, Godfroid, J, Pajak, B, Heirman, C, Thielemans, K, Leo, O, Urbain, J and Moser, M (1999). CD8alpha+ and CD8alpha- subclasses of dendritic cells direct the development of distinct T helper cells in vivo. Journal of Experimental Medicine 189: 587592.CrossRefGoogle ScholarPubMed
Manickasingham, SP, Edwards, AD, Schulz, O and Reis e Sousa, C (2003). The ability of murine dendritic cell subsets to direct T helper cell differentiation is dependent on microbial signals. European Journal of Immunology 33: 101107.CrossRefGoogle ScholarPubMed
Matzinger, P and Guerder, S (1989). Does T-cell tolerance require a dedicated antigen presenting cell? Nature 338: 7476.CrossRefGoogle ScholarPubMed
McKeever, DJ, MacHugh, ND, Goddeeris, BM, Awino, E and Morrison, WI (1991). Bovine afferent lymph veiled cells differ from blood monocytes in phenotype and accessory function. Journal of Immunology 147: 37033709.CrossRefGoogle ScholarPubMed
Palucka, K and Banchereau, J (2002). How dendritic cells and microbes interact to elicit or subvert protective immune responses. Current Opinion in Immunology 14: 420431.CrossRefGoogle ScholarPubMed
Patel, V, Smith, RE, Serra, A, Brooke, G, Howard, CJ and Rigley, KP (2002). MyD-1 (SIRPalpha) regulates T cell function in the absence of exogenous danger signals, via a TNFalpha-dependent pathway. European Journal of Immunology 32: 18651872.3.0.CO;2-F>CrossRefGoogle Scholar
Riffault, S, Eloranta, ML, Carrat, C, Sandberg, K, Charley, B and Alm, G (1996). Herpes simplex virus induces appearance of interferon-alpha/beta-producing cells and partially interferon-alpha/beta-dependent accumulation of leukocytes in murine regional lymph nodes. Journal of Interferon and Cytokine Research 16: 10071014.CrossRefGoogle ScholarPubMed
Riffault, S, Carrat, C, van Reeth, K, Pensaert, M and Charley, B (2001). Interferon-alpha-producing cells are localized in gut-associated lymphoid tissues in transmissible gastroenteritis virus (TGEV) infected piglets. Veterinary Research 32: 7179.CrossRefGoogle ScholarPubMed
Smith, RE, Patel, V, Seatter, SD, Deehan, MR, Brown, MH, Brooke, GP, Goodridge, HS, Howard, CJ, Rigley, KP, Harnett, W and Harnett, MM (2003). A novel MyD-1 (SIRP{alpha}) signalling pathway that inhibits LPS induced TNF{alpha} production by monocytes. Blood 102: 25322540.CrossRefGoogle Scholar
Steinman, RM and Pope, M (2002). Exploiting dendritic cells to improve vaccine efficacy. Journal of Clinical Investigation 109: 15191526.CrossRefGoogle ScholarPubMed
Steinman, RM, Hawiger, D and Nussenzweig, MC (2003). Tolerogenic dendritic cells. Annual Review of Immunology 21: 685711.CrossRefGoogle ScholarPubMed
Stephens, SA, Charleston, B, Brownlie, J and Howard, CJ (2003). Differences in cytokine synthesis by the sub-populations of dendritic cells from afferent lymph. Immunology 110: 4857.CrossRefGoogle ScholarPubMed
Stumbles, PA, Thomas, JA, Pimm, CL, Lee, PT, Venaille, TJ, Proksch, S and Holt, PG (1998). Resting respiratory tract dendritic cells preferentially stimulate T helper cell type 2 (Th2) responses and require obligatory cytokine signals for induction of Th1 immunity. Journal of Experimental Medicine 188: 20192031.CrossRefGoogle ScholarPubMed