Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Review Article
  • Published:

Atypical MHC class II-expressing antigen-presenting cells: can anything replace a dendritic cell?

Key Points

  • Understanding the function of dendritic cells (DCs) forms the basis of the characterization of professional antigen-presenting cells (APCs). DCs recognize and respond to danger-associated and pathogen-associated signals; express all of the necessary antigen-processing machinery; localize to the T cell zones of secondary lymphoid organs; and express the necessary co-stimulatory molecules and cytokines to activate naive CD4+ T cells.

  • Almost all myeloid-derived cells — including neutrophils, mast cells, basophils and eosinophils — have been shown to upregulate MHC class II molecules in certain settings. There is evidence that these MHC class II-expressing cells may support ongoing T helper (TH2) cell responses but less compelling data that they can prime naive CD4+ T cells.

  • Innate lymphoid cells are a recently described population of cells that can express MHC class II molecules. Recent data conflict as to whether they drive pro-inflammatory or tolerogenic CD4+ T cell responses. As with many other atypical APCs, their function may be dependent on the anatomical site in which their activities are assessed and the specific assays that are used to measure their function.

  • Many epithelial, endothelial and stromal cell populations can express MHC class II. Expression of MHC class II molecules by these cells may contribute to CD4+ T cell tolerance.

  • Many studies that have explored the antigen-presenting functions of atypical APCs have been conducted in mice. A major limitation of the field is that there are few corroborative studies in humans.

Abstract

Dendritic cells, macrophages and B cells are regarded as the classical antigen-presenting cells of the immune system. However, in recent years, there has been a rapid increase in the number of cell types that are suggested to present antigens on MHC class II molecules to CD4+ T cells. In this Review, we describe the key characteristics that define an antigen-presenting cell by examining the functions of dendritic cells. We then examine the functions of the haematopoietic cells and non-haematopoietic cells that can express MHC class II molecules and that have been suggested to represent 'atypical' antigen-presenting cells. We consider whether any of these cell populations can prime naive CD4+ T cells and, if not, question the effects that they do have on the development of immune responses.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: Key antigen-presenting functions of professional and atypical antigen-presenting cells.
Figure 2: Epithelial cells and stromal cells express MHC class II molecules.

Similar content being viewed by others

References

  1. Lemos, M. P., Fan, L., Lo, D. & Laufer, T. M. CD8α+ and CD11b+ dendritic cell-restricted MHC class II controls Th1 CD4+ T cell immunity. J. Immunol. 171, 5077–5084 (2003).

    Article  CAS  PubMed  Google Scholar 

  2. Lemos, M. P., Esquivel, F., Scott, P. & Laufer, T. M. MHC class II expression restricted to CD8α+ and CD11b+ dendritic cells is sufficient for control of Leishmania major. J. Exp. Med. 199, 725–730 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Sokol, C. L. et al. Basophils function as antigen-presenting cells for an allergen-induced T helper type 2 response. Nature Immunol. 10, 713–720 (2009).

    Article  CAS  Google Scholar 

  4. Perrigoue, J. G. et al. MHC class II-dependent basophil-CD4+ T cell interactions promote TH2 cytokine-dependent immunity. Nature Immunol. 10, 697–705 (2009).

    Article  CAS  Google Scholar 

  5. Gregory, G. D., Robbie-Ryan, M., Secor, V. H., Sabatino, J. J. Jr & Brown, M. A. Mast cells are required for optimal autoreactive T cell responses in a murine model of multiple sclerosis. Eur. J. Immunol. 35, 3478–3486 (2005).

    Article  CAS  PubMed  Google Scholar 

  6. Maurer, M. et al. Skin mast cells control T cell-dependent host defense in Leishmania major infections. FASEB J. 20, 2460–2467 (2006).

    Article  CAS  PubMed  Google Scholar 

  7. Frandji, P. et al. Antigen-dependent stimulation by bone marrow-derived mast cells of MHC class II-restricted T cell hybridoma. J. Immunol. 151, 6318–6328 (1993).

    CAS  PubMed  Google Scholar 

  8. Fox, C. C., Jewell, S. D. & Whitacre, C. C. Rat peritoneal mast cells present antigen to a PPD-specific T cell line. Cell. Immunol. 158, 253–264 (1994).

    Article  CAS  PubMed  Google Scholar 

  9. Dimitriadou, V. et al. Expression of functional major histocompatibility complex class II molecules on HMC-1 human mast cells. J. Leukoc. Biol. 64, 791–799 (1998).

    Article  CAS  PubMed  Google Scholar 

  10. Poncet, P., Arock, M. & David, B. MHC class II-dependent activation of CD4+ T cell hybridomas by human mast cells through superantigen presentation. J. Leukoc. Biol. 66, 105–112 (1999).

    Article  CAS  PubMed  Google Scholar 

  11. Frandji, P. et al. Presentation of soluble antigens by mast cells: upregulation by interleukin-4 and granulocyte/macrophage colony-stimulating factor and downregulation by interferon-γ. Cell. Immunol. 163, 37–46 (1995).

    Article  CAS  PubMed  Google Scholar 

  12. Frandji, P. et al. Exogenous and endogenous antigens are differentially presented by mast cells to CD4+ T lymphocytes. Eur. J. Immunol. 26, 2517–2528 (1996).

    Article  CAS  PubMed  Google Scholar 

  13. Skokos, D. et al. Mast cell-derived exosomes induce phenotypic and functional maturation of dendritic cells and elicit specific immune responses in vivo. J. Immunol. 170, 3037–3045 (2003).

    Article  CAS  PubMed  Google Scholar 

  14. Tkaczyk, C. et al. In vitro and in vivo immunostimulatory potential of bone marrow-derived mast cells on B- and T-lymphocyte activation. J. Allergy Clin. Immunol. 105, 134–142 (2000).

    Article  CAS  PubMed  Google Scholar 

  15. Skokos, D. et al. Mast cell-dependent B and T lymphocyte activation is mediated by the secretion of immunologically active exosomes. J. Immunol. 166, 868–876 (2001).

    Article  CAS  PubMed  Google Scholar 

  16. Raposo, G. et al. Accumulation of major histocompatibility complex class II molecules in mast cell secretory granules and their release upon degranulation. Mol. Biol. Cell 8, 2631–2645 (1997).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Nakae, S. et al. Mast cells enhance T cell activation: importance of mast cell costimulatory molecules and secreted TNF. J. Immunol. 176, 2238–2248 (2006).

    Article  CAS  PubMed  Google Scholar 

  18. Kambayashi, T. et al. Indirect involvement of allergen-captured mast cells in antigen presentation. Blood 111, 1489–1496 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Nakano, N. et al. Notch signaling confers antigen-presenting cell functions on mast cells. J. Allergy Clin. Immunol. 123, 74–81. e1 (2009).

    Article  CAS  PubMed  Google Scholar 

  20. Kambayashi, T. et al. Inducible MHC class II expression by mast cells supports effector and regulatory T cell activation. J. Immunol. 182, 4686–4695 (2009). This study shows that MHC class II expression on mast cells is induced by TLR agonists and IFNγ, and can support the activation of effector T cells and T Reg cells but not that of naive T cells.

    Article  CAS  PubMed  Google Scholar 

  21. Razin, E. et al. Interleukin 3: A differentiation and growth factor for the mouse mast cell that contains chondroitin sulfate E proteoglycan. J. Immunol. 132, 1479–1486 (1984).

    CAS  PubMed  Google Scholar 

  22. Tkaczyk, C., Villa, I., Peronet, R., David, B. & Mecheri, S. FcεRI-mediated antigen endocytosis turns interferon-gamma-treated mouse mast cells from inefficient into potent antigen-presenting cells. Immunology 97, 333–340 (1999).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Yoshimoto, T. et al. Basophils contribute to TH2-IgE responses in vivo via IL-4 production and presentation of peptide-MHC class II complexes to CD4+ T cells. Nature Immunol. 10, 706–712 (2009). References 3, 4 and 23 show that basophils express MHC class II and present antigens to T cells to promote T H 2-type responses.

    Article  CAS  Google Scholar 

  24. Hammad, H. et al. Inflammatory dendritic cells—not basophils—are necessary and sufficient for induction of Th2 immunity to inhaled house dust mite allergen. J. Exp. Med. 207, 2097–2111 (2010). This study argues that FcεRI-expressing DCs and not basophils are responsible for antigen presentation in response to HDM allergen.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Phythian-Adams, A. T. et al. CD11c depletion severely disrupts Th2 induction and development in vivo. J. Exp. Med. 207, 2089–2096 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Gong, J. et al. The antigen presentation function of bone marrow-derived mast cells is spatiotemporally restricted to a subset expressing high levels of cell surface FcεRI and MHC II. BMC Immunol. 11, 34 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Gaudenzio, N. et al. Cell-cell cooperation at the T helper cell/mast cell immunological synapse. Blood 114, 4979–4988 (2009).

    Article  CAS  PubMed  Google Scholar 

  28. Ito, T. et al. Roles of PU.1 in monocyte- and mast cell-specific gene regulation: PU.1 transactivates CIITA pIV in cooperation with IFN-γ. Int. Immunol. 21, 803–816 (2009).

    Article  CAS  PubMed  Google Scholar 

  29. Lu, L. F. et al. Mast cells are essential intermediaries in regulatory T-cell tolerance. Nature 442, 997–1002 (2006).

    Article  CAS  PubMed  Google Scholar 

  30. Eller, K. et al. IL-9 production by regulatory T cells recruits mast cells that are essential for regulatory T cell-induced immune suppression. J Immunol. 186, 83–91 (2011).

    Article  CAS  PubMed  Google Scholar 

  31. Maurer, D. et al. Fcε receptor I on dendritic cells delivers IgE-bound multivalent antigens into a cathepsin S-dependent pathway of MHC class II presentation. J. Immunol. 161, 2731–2739 (1998).

    CAS  PubMed  Google Scholar 

  32. Shin, J. S., Shelburne, C. P., Jin, C., LeFurgey, E. A. & Abraham, S. N. Harboring of particulate allergens within secretory compartments by mast cells following IgE/FcεRI-lipid raft-mediated phagocytosis. J. Immunol. 177, 5791–5800 (2006).

    Article  CAS  PubMed  Google Scholar 

  33. Tkaczyk, C. et al. Specific antigen targeting to surface IgE and IgG on mouse bone marrow-derived mast cells enhances efficiency of antigen presentation. Immunology 94, 318–324 (1998).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Dvorak, A. M., Newball, H. H., Dvorak, H. F. & Lichtenstein, L. M. Antigen-induced IgE-mediated degranulation of human basophils. Lab Invest. 43, 126–139 (1980).

    CAS  PubMed  Google Scholar 

  35. Ishizaka, T. & Ishizaka, K. Immunological events at the surface of basophil granulocytes and mast cells which induce degranulation. Scand. J. Respir. Dis. Suppl. 98, 13–22 (1977).

    CAS  PubMed  Google Scholar 

  36. Arinobu, Y., Iwasaki, H. & Akashi, K. Origin of basophils and mast cells. Allergol Int. 58, 21–28 (2009).

    Article  CAS  PubMed  Google Scholar 

  37. Arinobu, Y. et al. Developmental checkpoints of the basophil/mast cell lineages in adult murine hematopoiesis. Proc. Natl Acad. Sci. USA 102, 18105–18110 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Voehringer, D., Shinkai, K. & Locksley, R. M. Type 2 immunity reflects orchestrated recruitment of cells committed to IL-4 production. Immunity 20, 267–277 (2004).

    Article  CAS  PubMed  Google Scholar 

  39. Min, B. et al. Basophils produce IL-4 and accumulate in tissues after infection with a Th2-inducing parasite. J. Exp. Med. 200, 507–517 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Gessner, A., Mohrs, K. & Mohrs, M. Mast cells, basophils, and eosinophils acquire constitutive IL-4 and IL-13 transcripts during lineage differentiation that are sufficient for rapid cytokine production. J. Immunol. 174, 1063–1072 (2005).

    Article  CAS  PubMed  Google Scholar 

  41. Karasuyama, H., Mukai, K., Tsujimura, Y. & Obata, K. Newly discovered roles for basophils: a neglected minority gains new respect. Nature Rev. Immunol. 9, 9–13 (2009).

    Article  CAS  Google Scholar 

  42. Sokol, C. L., Barton, G. M., Farr, A. G. & Medzhitov, R. A mechanism for the initiation of allergen-induced T helper type 2 responses. Nature Immunol. 9, 310–318 (2007).

    Article  CAS  Google Scholar 

  43. Tsujimura, Y. et al. Basophils play a pivotal role in immunoglobulin-G-mediated but not immunoglobulin-E-mediated systemic anaphylaxis. Immunity 28, 581–589 (2008).

    Article  CAS  PubMed  Google Scholar 

  44. Le Gros, G., Ben-Sasson, S. Z., Seder, R., Finkelman, F. D. & Paul, W. E. Generation of interleukin 4 (IL-4)-producing cells in vivo and in vitro: IL-2 and IL-4 are required for in vitro generation of IL-4-producing cells. J. Exp. Med. 172, 921–929 (1990).

    Article  CAS  PubMed  Google Scholar 

  45. Swain, S. L., Weinberg, A. D., English, M. & Huston, G. IL-4 directs the development of Th2-like helper effectors. J. Immunol. 145, 3796–3806 (1990).

    CAS  PubMed  Google Scholar 

  46. Else, K. J., Finkelman, F. D., Maliszewski, C. R. & Grencis, R. K. Cytokine-mediated regulation of chronic intestinal helminth infection. J. Exp. Med. 179, 347–351 (1994).

    Article  CAS  PubMed  Google Scholar 

  47. Cohn, L., Homer, R. J., Marinov, A., Rankin, J. & Bottomly, K. Induction of airway mucus production By T helper 2 (Th2) cells: a critical role for interleukin 4 in cell recruitment but not mucus production. J. Exp. Med. 186, 1737–1747 (1997).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. Min, B. Th2 immunity: a step closer to completion. Immunol. Cell Biol. 88, 235 (2010).

    Article  PubMed  Google Scholar 

  49. Hida, S., Tadachi, M., Saito, T. & Taki, S. Negative control of basophil expansion by IRF-2 critical for the regulation of Th1/Th2 balance. Blood 106, 2011–2017 (2005).

    Article  CAS  PubMed  Google Scholar 

  50. Oh, K., Shen, T., Le Gros, G. & Min, B. Induction of Th2 type immunity in a mouse system reveals a novel immunoregulatory role of basophils. Blood 109, 2921–2927 (2007).

    CAS  PubMed  Google Scholar 

  51. Allenspach, E. J., Lemos, M. P., Porrett, P. M., Turka, L. A. & Laufer, T. M. Migratory and lymphoid-resident dendritic cells cooperate to efficiently prime naive CD4 T cells. Immunity 29, 795–806 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  52. Mack, M. et al. Identification of antigen-capturing cells as basophils. J. Immunol. 174, 735–741 (2005).

    Article  CAS  PubMed  Google Scholar 

  53. Tang, H. et al. The T helper type 2 response to cysteine proteases requires dendritic cell-basophil cooperation via ROS-mediated signaling. Nature Immunol. 11, 608–617 (2010). This study argues that basophils are important for papain-induced T H 2 cell responses not for their APC function but for their effects on DCs.

    Article  CAS  Google Scholar 

  54. Merad, M. et al. Langerhans cells renew in the skin throughout life under steady-state conditions. Nature Immunol. 3, 1135–1141 (2002).

    Article  CAS  Google Scholar 

  55. Bursch, L. S. et al. Identification of a novel population of Langerin+ dendritic cells. J. Exp. Med. 204, 3147–3156 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  56. Ginhoux, F. et al. Blood-derived dermal langerin+ dendritic cells survey the skin in the steady state. J. Exp. Med. 204, 3133–3146 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  57. Poulin, L. F. et al. The dermis contains langerin+ dendritic cells that develop and function independently of epidermal Langerhans cells. J. Exp. Med. 204, 3119–3131 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  58. Ohnmacht, C. et al. Basophils orchestrate chronic allergic dermatitis and protective immunity against helminths. Immunity 33, 364–374 (2010).

    Article  CAS  PubMed  Google Scholar 

  59. Sullivan, B. M. et al. Genetic analysis of basophil function in vivo. Nature Immunol. 12, 527–535 (2011).

    Article  CAS  Google Scholar 

  60. Otsuka, A. et al. Basophils are required for the induction of Th2 immunity to haptens and peptide antigens. Nature Commun. 4, 1739 (2013).

    Article  CAS  Google Scholar 

  61. Eckl-Dorna, J. et al. Basophils are not the key antigen-presenting cells in allergic patients. Allergy 67, 601–608 (2012).

    Article  CAS  PubMed  Google Scholar 

  62. Kitzmuller, C. et al. Human blood basophils do not act as antigen-presenting cells for the major birch pollen allergen Bet v 1. Allergy 67, 593–600 (2012). References 61 and 62 were the first studies to propose that basophils might not act as APCs in the setting of human allergy.

    Article  CAS  PubMed  Google Scholar 

  63. Sharma, M. et al. Circulating human basophils lack the features of professional antigen presenting cells. Sci. Rep. 3, 1188 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  64. Charles, N., Hardwick, D., Daugas, E., Illei, G. G. & Rivera, J. Basophils and the T helper 2 environment can promote the development of lupus nephritis. Nature Med. 16, 701–707 (2010).

    Article  CAS  PubMed  Google Scholar 

  65. Voskamp, A. L., Prickett, S. R., Mackay, F., Rolland, J. M. & O'Hehir, R. E. MHC class II expression in human basophils: induction and lack of functional significance. PLoS ONE 8, e81777 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  66. Foster, P. S., Hogan, S. P., Ramsay, A. J., Matthaei, K. I. & Young, I. G. Interleukin 5 deficiency abolishes eosinophilia, airways hyperreactivity, and lung damage in a mouse asthma model. J. Exp. Med. 183, 195–201 (1996).

    Article  CAS  PubMed  Google Scholar 

  67. Collins, P. D., Marleau, S., Griffiths-Johnson, D. A., Jose, P. J. & Williams, T. J. Cooperation between interleukin-5 and the chemokine eotaxin to induce eosinophil accumulation in vivo. J. Exp. Med. 182, 1169–1174 (1995).

    Article  CAS  PubMed  Google Scholar 

  68. Hogan, S. P., Koskinen, A. & Foster, P. S. Interleukin-5 and eosinophils induce airway damage and bronchial hyperreactivity during allergic airway inflammation in BALB/c mice. Immunol. Cell Biol. 75, 284–288 (1997).

    Article  CAS  PubMed  Google Scholar 

  69. Sabin, E. A., Kopf, M. A. & Pearce, E. J. Schistosoma mansoni egg-induced early IL-4 production is dependent upon IL-5 and eosinophils. J. Exp. Med. 184, 1871–1878 (1996).

    Article  CAS  PubMed  Google Scholar 

  70. Hogan, S. P. et al. Eosinophils: biological properties and role in health and disease. Clin. Exp. Allergy 38, 709–750 (2008).

    Article  CAS  PubMed  Google Scholar 

  71. Shinkai, K., Mohrs, M. & Locksley, R. M. Helper T cells regulate type-2 innate immunity in vivo. Nature 420, 825–829 (2002).

    Article  CAS  PubMed  Google Scholar 

  72. Jacobsen, E. A. et al. Allergic pulmonary inflammation in mice is dependent on eosinophil-induced recruitment of effector T cells. J. Exp. Med. 205, 699–710 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  73. Walsh, E. R. et al. Strain-specific requirement for eosinophils in the recruitment of T cells to the lung during the development of allergic asthma. J. Exp. Med. 205, 1285–1292 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  74. Fulkerson, P. C. et al. A central regulatory role for eosinophils and the eotaxin/CCR3 axis in chronic experimental allergic airway inflammation. Proc. Natl Acad. Sci. USA 103, 16418–16423 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  75. Hansel, T. T. et al. Sputum eosinophils from asthmatics express ICAM-1 and HLA-DR. Clin. Exp. Immunol. 86, 271–277 (1991). This is the first study to show that sputum but not blood eosinophils from a large proportion of patients with asthma express HLA-DR.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  76. Mengelers, H. J. et al. Immunophenotyping of eosinophils recovered from blood and BAL of allergic asthmatics. Am. J. Respir. Crit. Care Med. 149, 345–351 (1994).

    Article  CAS  PubMed  Google Scholar 

  77. Beninati, W. et al. Pulmonary eosinophils express HLA-DR in chronic eosinophilic pneumonia. J. Allergy Clin. Immunol. 92, 442–449 (1993).

    Article  CAS  PubMed  Google Scholar 

  78. Hansel, T. T. et al. Induction and function of eosinophil intercellular adhesion molecule-1 and HLA-DR. J. Immunol. 149, 2130–2136 (1992).

    CAS  PubMed  Google Scholar 

  79. Mawhorter, S. D., Kazura, J. W. & Boom, W. H. Human eosinophils as antigen-presenting cells: relative efficiency for superantigen- and antigen-induced CD4+ T-cell proliferation. Immunology 81, 584–591 (1994).

    CAS  PubMed  PubMed Central  Google Scholar 

  80. Celestin, J. et al. IL-3 induces B7.2 (CD86) expression and costimulatory activity in human eosinophils. J. Immunol. 167, 6097–6104 (2001).

    Article  CAS  PubMed  Google Scholar 

  81. Shi, H. Z., Humbles, A., Gerard, C., Jin, Z. & Weller, P. F. Lymph node trafficking and antigen presentation by endobronchial eosinophils. J. Clin. Invest. 105, 945–953 (2000). This is the first study to show that mouse eosinophils from antigen-sensitized airways express MHC class II and can support T cell activation.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  82. Shi, H. Z. et al. Endobronchial eosinophils preferentially stimulate T helper cell type 2 responses. Allergy 59, 428–435 (2004).

    Article  CAS  PubMed  Google Scholar 

  83. Duez, C. et al. Migration and accumulation of eosinophils toward regional lymph nodes after airway allergen challenge. J. Allergy Clin. Immunol. 114, 820–825 (2004).

    Article  CAS  PubMed  Google Scholar 

  84. van Rijt, L. S. et al. Airway eosinophils accumulate in the mediastinal lymph nodes but lack antigen-presenting potential for naive T cells. J. Immunol. 171, 3372–3378 (2003).

    Article  CAS  PubMed  Google Scholar 

  85. Tamura, N. et al. Requirement of CD80 and CD86 molecules for antigen presentation by eosinophils. Scand. J. Immunol. 44, 229–238 (1996).

    Article  CAS  PubMed  Google Scholar 

  86. Del Pozo, V. et al. Eosinophil as antigen-presenting cell: activation of T cell clones and T cell hybridoma by eosinophils after antigen processing. Eur. J. Immunol. 22, 1919–1925 (1992).

    Article  CAS  PubMed  Google Scholar 

  87. Wang, H. B., Ghiran, I., Matthaei, K. & Weller, P. F. Airway eosinophils: allergic inflammation recruited professional antigen-presenting cells. J. Immunol. 179, 7585–7592 (2007).

    Article  CAS  PubMed  Google Scholar 

  88. Akuthota, P., Melo, R. C., Spencer, L. A. & Weller, P. F. M. H. C. Class II and CD9 in human eosinophils localize to detergent-resistant membrane microdomains. Am. J. Respir. Cell. Mol. Biol. 46, 188–195 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  89. Handzel, Z. T. et al. Eosinophils bind rhinovirus and activate virus-specific T cells. J. Immunol. 160, 1279–1284 (1998).

    CAS  PubMed  Google Scholar 

  90. MacKenzie, J. R., Mattes, J., Dent, L. A. & Foster, P. S. Eosinophils promote allergic disease of the lung by regulating CD4+ Th2 lymphocyte function. J. Immunol. 167, 3146–3155 (2001).

    Article  CAS  PubMed  Google Scholar 

  91. Padigel, U. M. et al. Eosinophils act as antigen-presenting cells to induce immunity to Strongyloides stercoralis in mice. J. Infect. Dis. 196, 1844–1851 (2007).

    Article  CAS  PubMed  Google Scholar 

  92. Jacobsen, E. A. et al. Eosinophil activities modulate the immune/inflammatory character of allergic respiratory responses in mice. Allergy 69, 315–327 (2014).

    Article  CAS  PubMed  Google Scholar 

  93. Denkers, E. Y., Butcher, B. A., Del Rio, L. & Bennouna, S. Neutrophils, dendritic cells and Toxoplasma. Int. J. Parasitol. 34, 411–421 (2004).

    Article  CAS  PubMed  Google Scholar 

  94. Abi Abdallah, D. S., Egan, C. E., Butcher, B. A. & Denkers, E. Y. Mouse neutrophils are professional antigen-presenting cells programmed to instruct Th1 and Th17 T-cell differentiation. Int. Immunol. 23, 317–326 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  95. Fanger, N. A. et al. Activation of human T cells by major histocompatability complex class II expressing neutrophils: proliferation in the presence of superantigen, but not tetanus toxoid. Blood 89, 4128–4135 (1997). This study shows that human neutrophils can express MHC class II after stimulation with GM-CSF and IFNγ, and can support superantigen-mediated but not peptide-mediated T cell activation.

    CAS  PubMed  Google Scholar 

  96. Yamamoto, S. et al. Cutting edge: Pseudomonas aeruginosa abolishes established lung transplant tolerance by stimulating B7 expression on neutrophils. J. Immunol. 189, 4221–4225 (2012).

    Article  CAS  PubMed  Google Scholar 

  97. Serbina, N. V., Salazar-Mather, T. P., Biron, C. A., Kuziel, W. A. & Pamer, E. G. TNF/iNOS-producing dendritic cells mediate innate immune defense against bacterial infection. Immunity 19, 59–70 (2003).

    Article  CAS  PubMed  Google Scholar 

  98. Matsushima, H. et al. Neutrophil differentiation into a unique hybrid population exhibiting dual phenotype and functionality of neutrophils and dendritic cells. Blood 121, 1677–1689 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  99. Hepworth, M. R. & Sonnenberg, G. F. Regulation of the adaptive immune system by innate lymphoid cells. Curr. Opin. Immunol. 27C, 75–82 (2014).

  100. Withers, D. R. et al. Cutting edge: lymphoid tissue inducer cells maintain memory CD4 T cells within secondary lymphoid tissue. J. Immunol. 189, 2094–2098 (2012).

    Article  CAS  PubMed  Google Scholar 

  101. Lane, P. J., Gaspal, F. M., McConnell, F. M., Withers, D. R. & Anderson, G. Lymphoid tissue inducer cells: pivotal cells in the evolution of CD4 immunity and tolerance? Front. Immunol. 3, 24 (2012).

    Article  PubMed  PubMed Central  Google Scholar 

  102. Hepworth, M. R. et al. Innate lymphoid cells regulate CD4+ T-cell responses to intestinal commensal bacteria. Nature 498, 113–117 (2013). This is the first study to suggest that ILC3s in the gut regulate CD4+ T cell responses to commensal bacteria through MHC class II expression.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  103. von Burg, N. et al. Activated group 3 innate lymphoid cells promote T-cell-mediated immune responses. Proc. Natl Acad. Sci. USA 111, 12835–12840 (2014). This study shows that ILC3s stimulated with IL-1β express MHC class II and co-stimulatory molecules, and can stimulate naive CD4+ T cell activation.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  104. Korn, L. L. et al. Conventional CD4+ T cells regulate IL-22-producing intestinal innate lymphoid cells. Mucosal Immunol. 7, 1045–1057 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  105. Neill, D. R. et al. Nuocytes represent a new innate effector leukocyte that mediates type-2 immunity. Nature 464, 1367–1370 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  106. Mirchandani, A. S. et al. Type 2 innate lymphoid cells drive CD4+ Th2 cell responses. J. Immunol. 192, 2442–2448 (2014).

    Article  CAS  PubMed  Google Scholar 

  107. Oliphant, C. J. et al. MHCII-mediated dialog between group 2 innate lymphoid cells and CD4+ T cells potentiates type 2 immunity and promotes parasitic helminth expulsion. Immunity 41, 283–295 (2014). This is the first study to show that ILC2s express MHC class II and co-stimulatory molecules, and can support peptide-mediated naive CD4+ T cell activation.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  108. Ko, H. S., Fu, S. M., Winchester, R. J., Yu, D. T. & Kunkel, H. G. Ia determinants on stimulated human T lymphocytes. Occurrence on mitogen- and antigen-activated T cells. J. Exp. Med. 150, 246–255 (1979).

    Article  CAS  PubMed  Google Scholar 

  109. Evans, R. L. et al. Peripheral human T cells sensitized in mixed leukocyte culture synthesize and express Ia-like antigens. J. Exp. Med. 148, 1440–1445 (1978).

    Article  CAS  PubMed  Google Scholar 

  110. LaSalle, J. M., Tolentino, P. J., Freeman, G. J., Nadler, L. M. & Hafler, D. A. Early signaling defects in human T cells anergized by T cell presentation of autoantigen. J. Exp. Med. 176, 177–186 (1992). This is the first study to fully characterize the potential of human CD4+ T cells to anergize other CD4+ T cells through antigen presentation.

    Article  CAS  PubMed  Google Scholar 

  111. Costantino, C. M., Spooner, E., Ploegh, H. L. & Hafler, D. A. Class, I. I. MHC self-antigen presentation in human B and T lymphocytes. PLoS ONE 7, e29805 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  112. Card, C. M., Yu, S. S. & Swartz, M. A. Emerging roles of lymphatic endothelium in regulating adaptive immunity. J. Clin. Invest. 124, 943–952 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  113. Cohen, J. N. et al. Lymph node-resident lymphatic endothelial cells mediate peripheral tolerance via Aire-independent direct antigen presentation. J. Exp. Med. 207, 681–688 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  114. Fletcher, A. L. et al. Lymph node fibroblastic reticular cells directly present peripheral tissue antigen under steady-state and inflammatory conditions. J. Exp. Med. 207, 689–697 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  115. Lee, J. W. et al. Peripheral antigen display by lymph node stroma promotes T cell tolerance to intestinal self. Nature Immunol. 8, 181–190 (2007).

    Article  CAS  Google Scholar 

  116. Tewalt, E. F. et al. Lymphatic endothelial cells induce tolerance via PD-L1 and lack of costimulation leading to high-level PD-1 expression on CD8 T cells. Blood 120, 4772–4782 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  117. Gardner, J. M. et al. Extrathymic Aire-expressing cells are a distinct bone marrow-derived population that induce functional inactivation of CD4+ T cells. Immunity 39, 560–572 (2013). This study suggests that some APCs termed LNSCs are actually a bone marrow-derived population of cells that induce T cell anergy.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  118. Malhotra, D. et al. Transcriptional profiling of stroma from inflamed and resting lymph nodes defines immunological hallmarks. Nature Immunol. 13, 499–510 (2012). This transcriptional analysis dissects which LNSCs can and do express MHC class II that is inducible by inflammatory signals.

    Article  CAS  Google Scholar 

  119. Dubrot, J. et al. Lymph node stromal cells acquire peptide-MHCII complexes from dendritic cells and induce antigen-specific CD4+ T cell tolerance. J. Exp. Med. 211, 1153–1166 (2014). This paper suggests that LNSCs express endogenous MHC class II molecules and can also acquire peptide–MHC class II complexes from DCs.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  120. Hughes, C. C., Savage, C. O. & Pober, J. S. Endothelial cells augment T cell interleukin 2 production by a contact-dependent mechanism involving CD2/LFA-3 interaction. J. Exp. Med. 171, 1453–1467 (1990).

    Article  CAS  PubMed  Google Scholar 

  121. Lechler, R. I. & Batchelor, J. R. Restoration of immunogenicity to passenger cell-depleted kidney allografts by the addition of donor strain dendritic cells. J. Exp. Med. 155, 31–41 (1982).

    Article  CAS  PubMed  Google Scholar 

  122. Lakkis, F. G., Arakelov, A., Konieczny, B. T. & Inoue, Y. Immunologic 'ignorance' of vascularized organ transplants in the absence of secondary lymphoid tissue. Nature Med. 6, 686–688 (2000).

    Article  CAS  PubMed  Google Scholar 

  123. Shiao, S. L., McNiff, J. M. & Pober, J. S. Memory T cells and their costimulators in human allograft injury. J. Immunol. 175, 4886–4896 (2005).

    Article  CAS  PubMed  Google Scholar 

  124. Shiao, S. L. et al. Human effector memory CD4+ T cells directly recognize allogeneic endothelial cells in vitro and in vivo. J. Immunol. 179, 4397–4404 (2007). References 123 and 124 are two of many articles from the Pober laboratory examining the function of MHC class II+ endothelial cells as APCs during graft acceptance or rejection. Many of the articles from this laboratory examine the mechanisms for stimulating memory but not naive CD4+ T cells.

    Article  CAS  PubMed  Google Scholar 

  125. Fan, L. et al. Antigen presentation by keratinocytes directs autoimmune skin disease. Proc. Natl Acad. Sci. USA 100, 3386–3391 (2003).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  126. Mulder, D. J. et al. Antigen presentation and MHC class II expression by human esophageal epithelial cells: role in eosinophilic esophagitis. Am. J. Pathol. 178, 744–753 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  127. Sanderson, I. R., Ouellette, A. J., Carter, E. A., Walker, W. A. & Harmatz, P. R. Differential regulation of B7 mRNA in enterocytes and lymphoid cells. Immunology 79, 434–438 (1993).

    CAS  PubMed  PubMed Central  Google Scholar 

  128. Framson, P. E., Cho, D. H., Lee, L. Y. & Hershberg, R. M. Polarized expression and function of the costimulatory molecule CD58 on human intestinal epithelial cells. Gastroenterology 116, 1054–1062 (1999).

    Article  CAS  PubMed  Google Scholar 

  129. Nakazawa, A. et al. Functional expression of costimulatory molecule CD86 on epithelial cells in the inflamed colonic mucosa. Gastroenterology 117, 536–545 (1999).

    Article  CAS  PubMed  Google Scholar 

  130. Kaiserlian, D., Vidal, K. & Revillard, J. P. Murine enterocytes can present soluble antigen to specific class II-restricted CD4+ T cells. Eur. J. Immunol. 19, 1513–1516 (1989).

    Article  CAS  PubMed  Google Scholar 

  131. Buning, J. et al. Antigen targeting to MHC class II-enriched late endosomes in colonic epithelial cells: trafficking of luminal antigens studied in vivo in Crohn's colitis patients. FASEB J. 20, 359–361 (2006).

    Article  CAS  PubMed  Google Scholar 

  132. Bland, P. W. & Warren, L. G. Antigen presentation by epithelial cells of the rat small intestine. I. Kinetics, antigen specificity and blocking by anti-Ia antisera. Immunology 58, 1–7 (1986).

    CAS  PubMed  PubMed Central  Google Scholar 

  133. Mayer, L. & Shlien, R. Evidence for function of Ia molecules on gut epithelial cells in man. J. Exp. Med. 166, 1471–1483 (1987). References 130, 132 and 133 are among the first manuscripts to demonstrate that IECs express MHC class II and present protein antigen to CD4+ T cell hybridomas.

    Article  CAS  PubMed  Google Scholar 

  134. Hershberg, R. M. et al. Intestinal epithelial cells use two distinct pathways for HLA class II antigen processing. J. Clin. Invest. 100, 204–215 (1997).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  135. Hershberg, R. M. et al. Highly polarized HLA class II antigen processing and presentation by human intestinal epithelial cells. J. Clin. Invest. 102, 792–803 (1998).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  136. Westendorf, A. M. et al. CD4+Foxp3+ regulatory T cell expansion induced by antigen-driven interaction with intestinal epithelial cells independent of local dendritic cells. Gut 58, 211–219 (2009).

    Article  CAS  PubMed  Google Scholar 

  137. Maggio-Price, L. et al. Lineage targeted MHC-II transgenic mice demonstrate the role of dendritic cells in bacterial-driven colitis. Inflamm. Bowel Dis. 19, 174–184 (2013).

    Google Scholar 

  138. Thelemann, C. et al. Interferon-γ induces expression of MHC class II on intestinal epithelial cells and protects mice from colitis. PLoS ONE 9, e86844 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  139. Cruickshank, S. M., McVay, L. D., Baumgart, D. C., Felsburg, P. J. & Carding, S. R. Colonic epithelial cell mediated suppression of CD4 T cell activation. Gut 53, 678–684 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  140. Ward, H. E. & Nicholas, T. E. Alveolar type I and type II cells. Aust. N. Z. J. Med. 14, 731–734 (1984).

    Article  CAS  PubMed  Google Scholar 

  141. Fehrenbach, H. Alveolar epithelial type II cell: defender of the alveolus revisited. Respir. Res. 2, 33–46 (2001).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  142. Strunk, R. C., Eidlen, D. M. & Mason, R. J. Pulmonary alveolar type II epithelial cells synthesize and secrete proteins of the classical and alternative complement pathways. J. Clin. Invest. 81, 1419–1426 (1988).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  143. Gereke, M., Jung, S., Buer, J. & Bruder, D. Alveolar type II epithelial cells present antigen to CD4+ T cells and induce Foxp3+ regulatory T cells. Am. J. Respir. Crit. Care Med. 179, 344–355 (2009).

    Article  PubMed  Google Scholar 

  144. Kreisel, D. et al. Cutting edge: MHC class II expression by pulmonary nonhematopoietic cells plays a critical role in controlling local inflammatory responses. J. Immunol. 185, 3809–3813 (2010).

    Article  CAS  PubMed  Google Scholar 

  145. Steinman, R. M. Dendritic cells: understanding immunogenicity. Eur. J. Immunol. 37, S53–S60 (2007).

    Article  CAS  PubMed  Google Scholar 

  146. McDevitt, H. O. & Sela, M. Genetic control of the antibody response. I. Demonstration of determinant-specific differences in response to synthetic polypeptide antigens in two strains of inbred mice. J. Exp. Med. 122, 517–531 (1965).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  147. McDevitt, H. O. et al. Genetic control of the immune response. Mapping of the IR-1 locus. J. Exp. Med. 135, 1259–1278 (1972).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  148. Grumet, F. C. & McDevitt, H. O. Genetic control of the immune response. Relationship between the immune response-1 gene(s) and individual H-2 antigenic specificities. Transplantation 13, 171–173 (1972).

    Article  CAS  PubMed  Google Scholar 

  149. Zinkernagel, R. M. & Doherty, P. C. Restriction of in vitro T cell-mediated cytotoxicity in lymphocytic choriomeningitis within a syngeneic or semiallogeneic system. Nature 248, 701–702 (1974).

    Article  CAS  PubMed  Google Scholar 

  150. Banchereau, J. & Steinman, R. M. Dendritic cells and the control of immunity. Nature 392, 245–252 (1998).

    Article  CAS  PubMed  Google Scholar 

  151. Mosier, D. E. A requirement for two cell types for antibody formation in vitro. Science 158, 1573–1575 (1967).

    Article  CAS  PubMed  Google Scholar 

  152. Steinman, R. M. & Cohn, Z. A. Identification of a novel cell type in peripheral lymphoid organs of mice. I. Morphology, quantitation, tissue distribution. J. Exp. Med. 137, 1142–1162 (1973).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  153. Steinman, R. M. & Witmer, M. D. Lymphoid dendritic cells are potent stimulators of the primary mixed leukocyte reaction in mice. Proc. Natl Acad. Sci. USA 75, 5132–5136 (1978).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  154. Blum, J. S., Wearsch, P. A. & Cresswell, P. Pathways of antigen processing. Annu. Rev. Immunol. 31, 443–473 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  155. Van Niel, G. et al. Intestinal epithelial exosomes carry MHC class II/peptides able to inform the immune system in mice. Gut 52, 1690–1697 (2003). This study suggests that IECs may generate immunologically active exosomes.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  156. Thery, C. et al. Indirect activation of naive CD4+ T cells by dendritic cell-derived exosomes. Nature Immunol. 3, 1156–1162 (2002). This is one of the first articles demonstrating that exosomes may contribute to CD4+ T cell activation.

    Article  CAS  Google Scholar 

  157. Thery, C. et al. Molecular characterization of dendritic cell-derived exosomes. Selective accumulation of the heat shock protein Hsc73. J. Cell Biol. 147, 599–610 (1999).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  158. Mallegol, J., van Niel, G. & Heyman, M. Phenotypic and functional characterization of intestinal epithelial exosomes. Blood Cells Mol. Dis. 35, 11–16 (2005).

    Article  CAS  PubMed  Google Scholar 

  159. Mallegol, J. et al. T84-intestinal epithelial exosomes bear MHC class II/peptide complexes potentiating antigen presentation by dendritic cells. Gastroenterology 132, 1866–1876 (2007).

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

Work in the laboratory of T.M.L. is supported by a VA Merit Award. Research in the laboratory of T.K. is supported by funding from the US National Institutes of Health and the American Asthma Foundation.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Terri M. Laufer.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Related links

PowerPoint slides

Glossary

Experimental autoimmune encephalomyelitis

An experimental model for the human disease multiple sclerosis. Autoimmune disease is induced in experimental animals by immunization with myelin or peptides derived from myelin. The animals develop a paralytic disease with inflammation and demyelination in the brain and spinal cord.

Mixed lymphocyte responses

A tissue-culture technique for testing T cell reactivity. The proliferation of one population of T cells — induced by exposure to inactivated MHC-mismatched stimulator cells — is determined by measuring the incorporation of 3H-thymidine into the DNA of dividing cells.

Macropinocytosis

A type of endocytosis (or phagocytosis) that occurs during the engulfment of apoptotic cells. During macropinocytosis, large droplets of fluid are trapped within the membrane protrusions (ruffles) or phagocytic arms.

Superantigens

Proteins that bind to and activate all T cells that express a particular set of Vβ T cell receptor genes.

Neutrophil extracellular traps

(NETs). A set of extracellular fibres produced by activated neutrophils to ensnare invading microorganisms. NETs enhance neutrophil killing of extracellular pathogens, while minimizing damage to host cells.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kambayashi, T., Laufer, T. Atypical MHC class II-expressing antigen-presenting cells: can anything replace a dendritic cell?. Nat Rev Immunol 14, 719–730 (2014). https://doi.org/10.1038/nri3754

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nri3754

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing