Skip to main content
Erschienen in: Current Allergy and Asthma Reports 1/2014

01.01.2014 | IMMUNE DEFICIENCY AND DYSREGULATION (DP HUSTON, SECTION EDITOR)

Emerging Role of Human Basophil Biology in Health and Disease

verfasst von: Jessica L. Cromheecke, Kathleen T. Nguyen, David P. Huston

Erschienen in: Current Allergy and Asthma Reports | Ausgabe 1/2014

Einloggen, um Zugang zu erhalten

Abstract

Basophils have emerged in recent years as a small but potent subpopulation of leukocytes capable of bridging innate and adaptive immunity. They can be activated through IgE-dependent and IgE-independent mechanisms to release preformed mediators and to produce Th2 cytokines. In addition to their role in protective immunity to helminths, basophils are major participants in allergic reactions as diverse as anaphylaxis and immediate hypersensitivity reactions, late-phase hypersensitivity reactions, and delayed hypersensitivity reactions. Additionally, basophils have been implicated in the pathophysiology of autoimmune diseases such as lupus nephritis and rheumatoid arthritis, and the modulation of immune responses to bacterial infections, as well as being a feature of myelogenous leukemias. Distinct signals for activation, degranulation, transendothelial migration, and immune regulation are being defined, and demonstrate the important role of basophils in promoting a Th2 microenvironment. These mechanistic insights are driving innovative approaches for diagnostic testing and therapeutic targeting of basophils.
Literatur
1.
Zurück zum Zitat Chirumbolo S. State-of-the-art review about basophil research in immunology and allergy: is the time right to treat these cells with the respect they deserve? Blood Transfus. 2012;10:148–64.PubMedCentralPubMed Chirumbolo S. State-of-the-art review about basophil research in immunology and allergy: is the time right to treat these cells with the respect they deserve? Blood Transfus. 2012;10:148–64.PubMedCentralPubMed
2.
Zurück zum Zitat Durrani SR, Montville DJ, Pratt AS, et al. Innate immune responses to rhinovirus are reduced by the high-affinity IgE receptor in allergic asthmatic children. J Allergy Clin Immunol. 2012;130(2):489–95.PubMedCentralPubMedCrossRef Durrani SR, Montville DJ, Pratt AS, et al. Innate immune responses to rhinovirus are reduced by the high-affinity IgE receptor in allergic asthmatic children. J Allergy Clin Immunol. 2012;130(2):489–95.PubMedCentralPubMedCrossRef
3.
Zurück zum Zitat Siracusa MC, Artis D. Basophil functions during type 2 inflammation: initiators, regulators and effectors. Open Allergy J. 2010;3:46–51.CrossRef Siracusa MC, Artis D. Basophil functions during type 2 inflammation: initiators, regulators and effectors. Open Allergy J. 2010;3:46–51.CrossRef
4.
Zurück zum Zitat Wang H, Fang Y, Barrenas F, et al. Allergen challenge of peripheral blood mononuclear cells from patients with seasonal allergic rhinitis increases IL-17RB, which regulates basophil apoptosis and degranulation Clinical & Experimental Allergy. Clin Et Exp Allergy. 2010;40:1194–202.CrossRef Wang H, Fang Y, Barrenas F, et al. Allergen challenge of peripheral blood mononuclear cells from patients with seasonal allergic rhinitis increases IL-17RB, which regulates basophil apoptosis and degranulation Clinical & Experimental Allergy. Clin Et Exp Allergy. 2010;40:1194–202.CrossRef
5.
Zurück zum Zitat Leung DYM, Boguniewicz M, Howell MD, et al. New insights into atopic dermatitis. J Clin Invest. 2004;113:651–7.PubMedCentralPubMed Leung DYM, Boguniewicz M, Howell MD, et al. New insights into atopic dermatitis. J Clin Invest. 2004;113:651–7.PubMedCentralPubMed
6.
Zurück zum Zitat Dvorak HF, Hammond ME, Colvin RB, et al. Systemic expression of cutaneous basophil hypersensitivity. J Immunol. 1977;118:1549–57.PubMed Dvorak HF, Hammond ME, Colvin RB, et al. Systemic expression of cutaneous basophil hypersensitivity. J Immunol. 1977;118:1549–57.PubMed
7.
Zurück zum Zitat Dvorak AM, Mihm MC, Dvorak HF. Degranulation of basophilic leukocytes in allergic contact dermatitis reactions in man. J Immunol. 1976;116:687–95.PubMed Dvorak AM, Mihm MC, Dvorak HF. Degranulation of basophilic leukocytes in allergic contact dermatitis reactions in man. J Immunol. 1976;116:687–95.PubMed
9.
Zurück zum Zitat Sabato V, Verweij MM, Bridts CH, et al. CD300a is expressed on human basophils and seems to inhibit IgE/FcεRI-dependent anaphylactic degranulation. Clin Cytom. 2012;82B:132–8.CrossRef Sabato V, Verweij MM, Bridts CH, et al. CD300a is expressed on human basophils and seems to inhibit IgE/FcεRI-dependent anaphylactic degranulation. Clin Cytom. 2012;82B:132–8.CrossRef
10.•
Zurück zum Zitat Sokol CL, Medzhitov R. Emerging functions of basophils in protective and allergic immune responses. Mucosal Immunol. 2010;3(2):129–37. This review explained the role of basophils in promoting Th2 immune responses.PubMedCrossRef Sokol CL, Medzhitov R. Emerging functions of basophils in protective and allergic immune responses. Mucosal Immunol. 2010;3(2):129–37. This review explained the role of basophils in promoting Th2 immune responses.PubMedCrossRef
11.
Zurück zum Zitat Siracusa MC, Saenz SA, Hill DA, et al. TSLP promotes IL-3-independent basophils hematopoiesis and type 2 inflammation. Nature. 2012;477:229–33.CrossRef Siracusa MC, Saenz SA, Hill DA, et al. TSLP promotes IL-3-independent basophils hematopoiesis and type 2 inflammation. Nature. 2012;477:229–33.CrossRef
12.
Zurück zum Zitat Saenz SA, Noti M, Artis D. Innate immune cell populations function as initiators and effectors in Th2 cytokine responses. Trends Immunol. 2010;31(11):407–13.PubMedCrossRef Saenz SA, Noti M, Artis D. Innate immune cell populations function as initiators and effectors in Th2 cytokine responses. Trends Immunol. 2010;31(11):407–13.PubMedCrossRef
13.
Zurück zum Zitat Gibbs BF, Haas H, Falcone FH, et al. Purified human peripheral blood release interleukin-13 and preformed interleukin-4 following immunological activation. Eur J Immunol. 1996;26:2493–8.PubMedCrossRef Gibbs BF, Haas H, Falcone FH, et al. Purified human peripheral blood release interleukin-13 and preformed interleukin-4 following immunological activation. Eur J Immunol. 1996;26:2493–8.PubMedCrossRef
14.
Zurück zum Zitat MacGlashan Jr DW, White JM, Huang SK, et al. Secretion of interleukin-4 from basophils; the relationship between IL-4 mRNA and protein in resting and stimulated basophils. J Immunol. 1994;152:3006–16.PubMed MacGlashan Jr DW, White JM, Huang SK, et al. Secretion of interleukin-4 from basophils; the relationship between IL-4 mRNA and protein in resting and stimulated basophils. J Immunol. 1994;152:3006–16.PubMed
15.
Zurück zum Zitat Min B, Prout M, Hu-Li J, et al. Basophils produce IL-4 and accumulate in tissues after infection with a Th2-inducing parasite. J Exp Med. 2004;200:507–17.PubMedCentralPubMedCrossRef Min B, Prout M, Hu-Li J, et al. Basophils produce IL-4 and accumulate in tissues after infection with a Th2-inducing parasite. J Exp Med. 2004;200:507–17.PubMedCentralPubMedCrossRef
16.
Zurück zum Zitat Schroeder JT, MacGlashan Jr DW, Lichtenstein LM. Human basophils: mediator release and cytokine production. Adv Immunol. 2001;77:93–122.PubMedCrossRef Schroeder JT, MacGlashan Jr DW, Lichtenstein LM. Human basophils: mediator release and cytokine production. Adv Immunol. 2001;77:93–122.PubMedCrossRef
17.
Zurück zum Zitat Kim S, Shen T, Min B. Basophils can directly present or cross-present antigen to CD8 lymphocytes and alter CD8 T cell differentiation into IL-10-producing phenotypes. J Immunol. 2009;183:3033–9.PubMedCrossRef Kim S, Shen T, Min B. Basophils can directly present or cross-present antigen to CD8 lymphocytes and alter CD8 T cell differentiation into IL-10-producing phenotypes. J Immunol. 2009;183:3033–9.PubMedCrossRef
18.
Zurück zum Zitat Perrigoue JG, Saenz SA, Siracusa MC, et al. MHC class II-dependent basophil-CD4+ T cell interactions promote T(H)2 cytokine-dependent immunity. Nat Immunol. 2009;10:697–705.PubMedCentralPubMedCrossRef Perrigoue JG, Saenz SA, Siracusa MC, et al. MHC class II-dependent basophil-CD4+ T cell interactions promote T(H)2 cytokine-dependent immunity. Nat Immunol. 2009;10:697–705.PubMedCentralPubMedCrossRef
19.
Zurück zum Zitat Yoshimoto T, Yasuda K, Tanaka H, 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. Nat Immunol. 2009;10:706–12.PubMedCrossRef Yoshimoto T, Yasuda K, Tanaka H, 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. Nat Immunol. 2009;10:706–12.PubMedCrossRef
20.
Zurück zum Zitat Sokol CL, Chu NQ, Yu S, et al. Basophils function as antigen-presenting cells an allergen-induced T helper type 2 response. Nat Immunol. 2009;10:713–20.PubMedCentralPubMedCrossRef Sokol CL, Chu NQ, Yu S, et al. Basophils function as antigen-presenting cells an allergen-induced T helper type 2 response. Nat Immunol. 2009;10:713–20.PubMedCentralPubMedCrossRef
21.
22.
Zurück zum Zitat Kim S, Prout M, Ramshaw H, et al. Cutting edge: basophils are transiently recruited into the draining lymph nodes during helminth infection via IL-3, but infection-induced Th2 immunity can develop without basophil lymph node recruitment or IL-3. J Immunol. 2010;184:1143–7.PubMedCentralPubMedCrossRef Kim S, Prout M, Ramshaw H, et al. Cutting edge: basophils are transiently recruited into the draining lymph nodes during helminth infection via IL-3, but infection-induced Th2 immunity can develop without basophil lymph node recruitment or IL-3. J Immunol. 2010;184:1143–7.PubMedCentralPubMedCrossRef
24.
Zurück zum Zitat Voehringer D, Shinkai K, Locksley RM. Type 2 immunity reflects orchestrated recruitment of cells committed to IL-4 production. Immunity. 2004;20:267–77.PubMedCrossRef Voehringer D, Shinkai K, Locksley RM. Type 2 immunity reflects orchestrated recruitment of cells committed to IL-4 production. Immunity. 2004;20:267–77.PubMedCrossRef
25.
Zurück zum Zitat Min B. Basophils: what they ‘can do’ versus what they ‘actually do’. Nat Immunol. 2008;9:1333–9.PubMedCrossRef Min B. Basophils: what they ‘can do’ versus what they ‘actually do’. Nat Immunol. 2008;9:1333–9.PubMedCrossRef
26.
27.
Zurück zum Zitat Sokol CL, Barton GM, Farr AG, Medzhitov R. A mechanism for the initiation of allergen-induced T helper type 2 responses. Nat Immunol. 2007;9:310–8.CrossRef Sokol CL, Barton GM, Farr AG, Medzhitov R. A mechanism for the initiation of allergen-induced T helper type 2 responses. Nat Immunol. 2007;9:310–8.CrossRef
28.
Zurück zum Zitat Chen K, Xu W, Wilson M, et al. Immunoglobulin D enhances immune surveillance by activating antimicrobial, proinflammatory and B cell–stimulating programs in basophils. Nat Immunol. 2009;10:889–98.PubMedCentralPubMedCrossRef Chen K, Xu W, Wilson M, et al. Immunoglobulin D enhances immune surveillance by activating antimicrobial, proinflammatory and B cell–stimulating programs in basophils. Nat Immunol. 2009;10:889–98.PubMedCentralPubMedCrossRef
29.•
Zurück zum Zitat Charles N, Hardwick D, Daugas E, et al. Basophils and the T helper 2 environment can promote the development of lupus nephritis. Nat Med. 2010;16(6):701–7. This was the first report potentially linking basophils to the pathogenesis of autoimmune lupus nephritis.PubMedCentralPubMedCrossRef Charles N, Hardwick D, Daugas E, et al. Basophils and the T helper 2 environment can promote the development of lupus nephritis. Nat Med. 2010;16(6):701–7. This was the first report potentially linking basophils to the pathogenesis of autoimmune lupus nephritis.PubMedCentralPubMedCrossRef
30.
Zurück zum Zitat Warde N. Activated basophils exacerbate lupus nephritis by amplifying production of autoreactive IgE. Nat Rev Rheumatol. 2010;6(8):438.PubMedCrossRef Warde N. Activated basophils exacerbate lupus nephritis by amplifying production of autoreactive IgE. Nat Rev Rheumatol. 2010;6(8):438.PubMedCrossRef
31.•
Zurück zum Zitat Schuerwegh JM, Ioan-Facsinay A, Dorjee AL, et al. Evidence for a functional role of IgE anticitrullinated protein antibodies in rheumatoid arthritis. PNAS. 2010;107:2586–91. This article provides the first evidence for the potential role of basophils in rheumatoid arthritis.PubMedCrossRef Schuerwegh JM, Ioan-Facsinay A, Dorjee AL, et al. Evidence for a functional role of IgE anticitrullinated protein antibodies in rheumatoid arthritis. PNAS. 2010;107:2586–91. This article provides the first evidence for the potential role of basophils in rheumatoid arthritis.PubMedCrossRef
32.
Zurück zum Zitat Anyan WK, Kumagi T, Shimogawara RF, et al. Schistosome eggs have a direct role in the induction of basophils capable of a high level of IL-4 production: comparative study of single- and bisexual infection of Schistosoma mansoni in vivo. Trop Med Health. 2010;38(1):13–22.CrossRef Anyan WK, Kumagi T, Shimogawara RF, et al. Schistosome eggs have a direct role in the induction of basophils capable of a high level of IL-4 production: comparative study of single- and bisexual infection of Schistosoma mansoni in vivo. Trop Med Health. 2010;38(1):13–22.CrossRef
33.
Zurück zum Zitat Pelleau S, Diop S, Dia Badiane M, et al. Enhanced basophil reactivities during severe malaria and their relationship with the plasmodial histamine releasing factor PfTCTP. Infect Immune. 2012;80(8):2963–70.CrossRef Pelleau S, Diop S, Dia Badiane M, et al. Enhanced basophil reactivities during severe malaria and their relationship with the plasmodial histamine releasing factor PfTCTP. Infect Immune. 2012;80(8):2963–70.CrossRef
34.
Zurück zum Zitat Cerny-Reiterer S, Ghanim V, Hoermann G, et al. Identification of basophils as a major source of hepatocyte growth factor in chronic myeloid leukemia: a novel mechanism of BCR-ABL1 – independent disease progression. Neoplasia. 2012;14(7):572–84. Cerny-Reiterer S, Ghanim V, Hoermann G, et al. Identification of basophils as a major source of hepatocyte growth factor in chronic myeloid leukemia: a novel mechanism of BCR-ABL1 – independent disease progression. Neoplasia. 2012;14(7):572–84.
35.
Zurück zum Zitat Yasuda H, Aritaka N, Ando J, et al. Chronic myelogenous leukemia with mild basophilia as the predominant manifestation at presentation. Intern Med. 2011;50:501–2.PubMedCrossRef Yasuda H, Aritaka N, Ando J, et al. Chronic myelogenous leukemia with mild basophilia as the predominant manifestation at presentation. Intern Med. 2011;50:501–2.PubMedCrossRef
36.
Zurück zum Zitat Bain BJ, Heller M. Dysplastic basophils in the accelerated phase of chronic myelogenous leukemia. Am J Hematol. 2011;86:949.PubMedCrossRef Bain BJ, Heller M. Dysplastic basophils in the accelerated phase of chronic myelogenous leukemia. Am J Hematol. 2011;86:949.PubMedCrossRef
37.
Zurück zum Zitat Stacchini A, Demurtas A, Godio L. Flow cytometric detection of degranulated basophils in chronic myeloid leukemia in accelerated phase. Clin Cytom. 2011;80B:122–4.CrossRef Stacchini A, Demurtas A, Godio L. Flow cytometric detection of degranulated basophils in chronic myeloid leukemia in accelerated phase. Clin Cytom. 2011;80B:122–4.CrossRef
38.
Zurück zum Zitat Wimazal F, Germing U, Kundi M, et al. Evaluation of the prognostic significance of eosinophilia and basophilia in a larger cohort of patients with myelodysplastic syndromes. Cancer. 2010;116:2372–81.PubMed Wimazal F, Germing U, Kundi M, et al. Evaluation of the prognostic significance of eosinophilia and basophilia in a larger cohort of patients with myelodysplastic syndromes. Cancer. 2010;116:2372–81.PubMed
39.
Zurück zum Zitat Rudman SM, Josephs DH, Cambrook H, et al. Harnessing engineered antibodies of the IgE class to combat malignancy: initial assessment of FcєRI-mediated basophil activation by a tumour- specific IgE antibody to evaluate the risk of type I hypersensitivity. Clin Exp Allergy. 2011;41:1400–13.PubMedCrossRef Rudman SM, Josephs DH, Cambrook H, et al. Harnessing engineered antibodies of the IgE class to combat malignancy: initial assessment of FcєRI-mediated basophil activation by a tumour- specific IgE antibody to evaluate the risk of type I hypersensitivity. Clin Exp Allergy. 2011;41:1400–13.PubMedCrossRef
40.•
42.
43.
Zurück zum Zitat Hida S, Tadachi M, Saito T, et al. Negative control of basophil expansion by IRF-2 critical for the regulation of Th1 / Th2 balance. Blood. 2005;106(6):2011–7.PubMedCrossRef Hida S, Tadachi M, Saito T, et al. Negative control of basophil expansion by IRF-2 critical for the regulation of Th1 / Th2 balance. Blood. 2005;106(6):2011–7.PubMedCrossRef
44.
Zurück zum Zitat Wakahara K, Baba N, Van VQ, et al. Human basophils interact with memory T cells to augment Th17 responses. Blood. 2012;120:4761–71.PubMedCrossRef Wakahara K, Baba N, Van VQ, et al. Human basophils interact with memory T cells to augment Th17 responses. Blood. 2012;120:4761–71.PubMedCrossRef
45.
Zurück zum Zitat Wada T, Ishiwata K, Koseki H, et al. Selective ablation of basophils in mice reveals their nonredundant role in acquired immunity against ticks. J Clin Invest. 2010;120:2867–75.PubMedCentralPubMedCrossRef Wada T, Ishiwata K, Koseki H, et al. Selective ablation of basophils in mice reveals their nonredundant role in acquired immunity against ticks. J Clin Invest. 2010;120:2867–75.PubMedCentralPubMedCrossRef
46.
Zurück zum Zitat Valent P, Schmidt G, Mayer P, et al. Interleukin-3 is a differentiation factor for human basophils. Blood. 1989;73(7):1763–9.PubMed Valent P, Schmidt G, Mayer P, et al. Interleukin-3 is a differentiation factor for human basophils. Blood. 1989;73(7):1763–9.PubMed
47.
Zurück zum Zitat Conti P, Kempuraj D, Di Gioaccino M, et al. Interleukin-6 and mast cells. Allergy Asthma Proc. 2002;23(5):331–5.PubMed Conti P, Kempuraj D, Di Gioaccino M, et al. Interleukin-6 and mast cells. Allergy Asthma Proc. 2002;23(5):331–5.PubMed
48.
Zurück zum Zitat Schneider E, Thieblemont N, De Moraes ML, Dy M. Basophils: new players in the cytokine network. Eur Cytokine Netw. 2010;21(3):142–53.PubMed Schneider E, Thieblemont N, De Moraes ML, Dy M. Basophils: new players in the cytokine network. Eur Cytokine Netw. 2010;21(3):142–53.PubMed
49.•
Zurück zum Zitat Siracusa MC, Tait Wojno ED, Artis D. Functional heterogeneity in the basophil cell lineage. Adv Immunol. 2012;115:141–59. This article provides insight into potential heterogeneity in basophil development.PubMedCentralPubMedCrossRef Siracusa MC, Tait Wojno ED, Artis D. Functional heterogeneity in the basophil cell lineage. Adv Immunol. 2012;115:141–59. This article provides insight into potential heterogeneity in basophil development.PubMedCentralPubMedCrossRef
51.
Zurück zum Zitat Charles N, Dema B, Rivera J. Reply to: basophils from humans with systemic lupus erythematosus do not express MHC-II. Nat Med. 2012;18:489–90.CrossRef Charles N, Dema B, Rivera J. Reply to: basophils from humans with systemic lupus erythematosus do not express MHC-II. Nat Med. 2012;18:489–90.CrossRef
52.
Zurück zum Zitat Ford LS, Bloom KA, Nowak-Wegrzyn AH, et al. Basophil reactivity, wheal size, and immunoglobulin levels distinguish degrees of cow’s milk tolerance. J Allergy Clin Immunol. 2013;131:180–6.PubMedCentralPubMedCrossRef Ford LS, Bloom KA, Nowak-Wegrzyn AH, et al. Basophil reactivity, wheal size, and immunoglobulin levels distinguish degrees of cow’s milk tolerance. J Allergy Clin Immunol. 2013;131:180–6.PubMedCentralPubMedCrossRef
53.
Zurück zum Zitat MacGlashan Jr D. Expression of CD203c and CD63 in human basophils: relationship to differential regulation of piecemeal and anaphylactic degranulation processes. Clin Exp Allergy. 2010;40:1365–77.PubMedCentralPubMedCrossRef MacGlashan Jr D. Expression of CD203c and CD63 in human basophils: relationship to differential regulation of piecemeal and anaphylactic degranulation processes. Clin Exp Allergy. 2010;40:1365–77.PubMedCentralPubMedCrossRef
54.
Zurück zum Zitat Crivellato E, Beatrice N, Ribatti D. The history of the controversial relationship between mast cells and basophils. Immunol Lett. 2011;141(1):10–7.PubMedCrossRef Crivellato E, Beatrice N, Ribatti D. The history of the controversial relationship between mast cells and basophils. Immunol Lett. 2011;141(1):10–7.PubMedCrossRef
55.
Zurück zum Zitat Kleine-Tebbe J, Erdmann S, Knol EF, et al. Diagnostic tests based on human basophils: potentials, pitfalls and perspectives. Int Arch Allergy Immunol. 2006;141:79–90.PubMedCrossRef Kleine-Tebbe J, Erdmann S, Knol EF, et al. Diagnostic tests based on human basophils: potentials, pitfalls and perspectives. Int Arch Allergy Immunol. 2006;141:79–90.PubMedCrossRef
56.
Zurück zum Zitat Bieneman AP, Chichester KL, Chen YH, Schroeder JT. Toll-like receptor 2 ligands activate human basophils for both IgE-dependent and IgE-independent secretion. J Allergy Clin Immunol. 2005;115:295–301.PubMedCrossRef Bieneman AP, Chichester KL, Chen YH, Schroeder JT. Toll-like receptor 2 ligands activate human basophils for both IgE-dependent and IgE-independent secretion. J Allergy Clin Immunol. 2005;115:295–301.PubMedCrossRef
57.
Zurück zum Zitat Yamada T, Sun Q, Zeibecoglou K, et al. IL-3, IL-5, granulocyte-macrophage colony-stimulating factor receptor alpha-subunit, and common beta-subunit expression by peripheral leukocytes and blood dendritic cells. J Allergy Clin Immunol. 1998;101:677–82.PubMedCrossRef Yamada T, Sun Q, Zeibecoglou K, et al. IL-3, IL-5, granulocyte-macrophage colony-stimulating factor receptor alpha-subunit, and common beta-subunit expression by peripheral leukocytes and blood dendritic cells. J Allergy Clin Immunol. 1998;101:677–82.PubMedCrossRef
58.
Zurück zum Zitat Uguccioni M, Mackay C, Ochensberger B, et al. High expression of the chemokine receptor CCR3 in human blood basophils. Role in activation by eotaxin, MCP-4, and other chemokines. J Clin Invest. 1997;100:1137–43.PubMedCentralPubMedCrossRef Uguccioni M, Mackay C, Ochensberger B, et al. High expression of the chemokine receptor CCR3 in human blood basophils. Role in activation by eotaxin, MCP-4, and other chemokines. J Clin Invest. 1997;100:1137–43.PubMedCentralPubMedCrossRef
59.
Zurück zum Zitat Siraganian RP, Hook WA. Mechanism of histamine release by formyl methionine-containing peptides. J Immunol. 1977;119:2078–83.PubMed Siraganian RP, Hook WA. Mechanism of histamine release by formyl methionine-containing peptides. J Immunol. 1977;119:2078–83.PubMed
60.
Zurück zum Zitat Tedeschi A, Salmaso C, Di Donato M, et al. Granulocyte-macrophage colony-stimulating factor and interleukin-3 cause basophil histamine release by a common pathway: downregulation by sodium. Immunology. 1999;96:164–70.PubMedCrossRef Tedeschi A, Salmaso C, Di Donato M, et al. Granulocyte-macrophage colony-stimulating factor and interleukin-3 cause basophil histamine release by a common pathway: downregulation by sodium. Immunology. 1999;96:164–70.PubMedCrossRef
61.
Zurück zum Zitat Bischoff SC, Brunner T, De Weck AL, Dahinden C. Interleukin 5 modifies histamine release and leukotriene generation by human basophils in response to diverse agonists. J Exp Med. 1990;172:1577–82.PubMedCrossRef Bischoff SC, Brunner T, De Weck AL, Dahinden C. Interleukin 5 modifies histamine release and leukotriene generation by human basophils in response to diverse agonists. J Exp Med. 1990;172:1577–82.PubMedCrossRef
62.
Zurück zum Zitat Jürgensen H, Braam U, Kownatzki E, et al. Human C5a induces a substantial histamine release in human basophils but not in tissue mast cells. Int Arch Allergy Appl Immunol. 1988;85(4):487–8.PubMedCrossRef Jürgensen H, Braam U, Kownatzki E, et al. Human C5a induces a substantial histamine release in human basophils but not in tissue mast cells. Int Arch Allergy Appl Immunol. 1988;85(4):487–8.PubMedCrossRef
63.
Zurück zum Zitat Komiya A, Nagase H, Okugawa S, et al. Expression and function of toll-like receptors in human basophils. Allergy Immunol. 2006;140 suppl 1:23–7.CrossRef Komiya A, Nagase H, Okugawa S, et al. Expression and function of toll-like receptors in human basophils. Allergy Immunol. 2006;140 suppl 1:23–7.CrossRef
64.
Zurück zum Zitat Smithgall MD, Comeau MR, Yoon B, et al. IL-33 amplifies both Th1- and Th2-type responses through its activity on human basophils, allergen-reactive Th2 cells, iNKT and NK Cells. Int Immunol. 2008;20(8):1019–30.PubMedCrossRef Smithgall MD, Comeau MR, Yoon B, et al. IL-33 amplifies both Th1- and Th2-type responses through its activity on human basophils, allergen-reactive Th2 cells, iNKT and NK Cells. Int Immunol. 2008;20(8):1019–30.PubMedCrossRef
65.
Zurück zum Zitat Watanabe T, Yamashita K, Sakurai T, et al. Toll-like receptor activation in basophils contributes to the development of IgG4-related disease. J Gastroenterol. 2012;48(2):247–53.PubMedCrossRef Watanabe T, Yamashita K, Sakurai T, et al. Toll-like receptor activation in basophils contributes to the development of IgG4-related disease. J Gastroenterol. 2012;48(2):247–53.PubMedCrossRef
66.
Zurück zum Zitat Mochizuki A, Mceuen AR, Buckley MG, et al. The release of basogranulin in response to IgE-dependent and IgE-independent stimuli: validity of basogranulin measurement as an indicator of basophil activation. J Allergy Clin Immunol. 1995;12(1):102–8. Mochizuki A, Mceuen AR, Buckley MG, et al. The release of basogranulin in response to IgE-dependent and IgE-independent stimuli: validity of basogranulin measurement as an indicator of basophil activation. J Allergy Clin Immunol. 1995;12(1):102–8.
67.
Zurück zum Zitat Lantz CS, Min B, Tsai M, et al. IL-3 is required for increases in blood basophils in nematode infection in mice and can enhance IgE-dependent IL-4 production by basophils in vitro. Lab Investig. 2008;88:1134–42.PubMedCentralPubMedCrossRef Lantz CS, Min B, Tsai M, et al. IL-3 is required for increases in blood basophils in nematode infection in mice and can enhance IgE-dependent IL-4 production by basophils in vitro. Lab Investig. 2008;88:1134–42.PubMedCentralPubMedCrossRef
68.
Zurück zum Zitat Takao K, Tanimoto Y, Fujii M, et al. In vitro expansion of human basophils by interleukin-3 from granulocyte colony-stimulating factor-mobilized peripheral blood stem cells. Clin Exp Allergy. 2003;33:1561–7.PubMedCrossRef Takao K, Tanimoto Y, Fujii M, et al. In vitro expansion of human basophils by interleukin-3 from granulocyte colony-stimulating factor-mobilized peripheral blood stem cells. Clin Exp Allergy. 2003;33:1561–7.PubMedCrossRef
69.
Zurück zum Zitat Iikura M, Yamaguchi M, Fujisawa T, et al. Secretory IgA induces degranulation of IL-3-primed basophils. J Immunol. 1998;161:1510–5.PubMed Iikura M, Yamaguchi M, Fujisawa T, et al. Secretory IgA induces degranulation of IL-3-primed basophils. J Immunol. 1998;161:1510–5.PubMed
70.
Zurück zum Zitat Verweij MM, Sabato V, Nullens S, et al. STAT5 in human basophils: IL-3 is required for its FcεRI-mediated phosphorylation. Clin Cytom. 2012;82B:101–6.CrossRef Verweij MM, Sabato V, Nullens S, et al. STAT5 in human basophils: IL-3 is required for its FcεRI-mediated phosphorylation. Clin Cytom. 2012;82B:101–6.CrossRef
71.
Zurück zum Zitat Pecaric-Petkovic T, Didichenko SA, Kaempfer S, et al. Human basophils and eosinophils are the direct target leukocytes of the novel IL-1 family member IL-33. Blood. 2009;113:1526–34.PubMedCrossRef Pecaric-Petkovic T, Didichenko SA, Kaempfer S, et al. Human basophils and eosinophils are the direct target leukocytes of the novel IL-1 family member IL-33. Blood. 2009;113:1526–34.PubMedCrossRef
72.
Zurück zum Zitat Cady CT, Powell MS, Harbeck RJ, et al. IgG antibodies produced during subcutaneous allergen immunotherapy mediate inhibition of basophil activation via a mechanism involving both FcγRIIA and FcγRIIB. Immunol Lett. 2010;130:57–65.PubMedCentralPubMedCrossRef Cady CT, Powell MS, Harbeck RJ, et al. IgG antibodies produced during subcutaneous allergen immunotherapy mediate inhibition of basophil activation via a mechanism involving both FcγRIIA and FcγRIIB. Immunol Lett. 2010;130:57–65.PubMedCentralPubMedCrossRef
73.
Zurück zum Zitat Patella V, Florio G, Petraroli, Marone G. HIV-1 gp120 induces IL-4 and IL-13 release from human Fc epsilon RI+ cells through interaction with the VH3 region of IgE. J Immunol. 2000;164:589–95.PubMed Patella V, Florio G, Petraroli, Marone G. HIV-1 gp120 induces IL-4 and IL-13 release from human Fc epsilon RI+ cells through interaction with the VH3 region of IgE. J Immunol. 2000;164:589–95.PubMed
75.
Zurück zum Zitat Kroeger KM, Sullivan BM, Locksley RM. IL-18 and IL-33 elicit Th2 cytokines from basophils via a MyD88- and p38alpha-dependent pathway. J Leuko Biol. 2009;86:769–78.PubMedCrossRef Kroeger KM, Sullivan BM, Locksley RM. IL-18 and IL-33 elicit Th2 cytokines from basophils via a MyD88- and p38alpha-dependent pathway. J Leuko Biol. 2009;86:769–78.PubMedCrossRef
76.•
Zurück zum Zitat Seok J, Shaw Warren H, Cuenca AG, et al. Genomic responses in mouse models poorly mimic human inflammatory diseases. PNAS. 2013;110:3507–12. Evidence was presented that the current mouse model for inflammatory diseases may not be appropriate for translation to understanding human disease.PubMedCrossRef Seok J, Shaw Warren H, Cuenca AG, et al. Genomic responses in mouse models poorly mimic human inflammatory diseases. PNAS. 2013;110:3507–12. Evidence was presented that the current mouse model for inflammatory diseases may not be appropriate for translation to understanding human disease.PubMedCrossRef
77.
Zurück zum Zitat Suzukawa M, Hirai K, Iikura M, et al. IgE- and FcєRI-mediated migration of human basophils. Int Immunol. 2005;17:1249–55.PubMedCrossRef Suzukawa M, Hirai K, Iikura M, et al. IgE- and FcєRI-mediated migration of human basophils. Int Immunol. 2005;17:1249–55.PubMedCrossRef
78.
Zurück zum Zitat Bochner BS, McKelvey AA, Sterbinsky SA, et al. IL-3 augments adhesiveness for endothelium and CD11b expression in human basophils but not neutrophils. J Immunol. 1990;145(6):1832–7.PubMed Bochner BS, McKelvey AA, Sterbinsky SA, et al. IL-3 augments adhesiveness for endothelium and CD11b expression in human basophils but not neutrophils. J Immunol. 1990;145(6):1832–7.PubMed
79.
Zurück zum Zitat Iikura M, Ebisawa M, Yamaguchi M, et al. Transendothelial migration of human basophils. J Immunol. 2004;173:5189–95.PubMed Iikura M, Ebisawa M, Yamaguchi M, et al. Transendothelial migration of human basophils. J Immunol. 2004;173:5189–95.PubMed
80.
Zurück zum Zitat Lie WJ, Homburg E, Kuijers TW, et al. Regulation and kinetics of platelet-activating factor and leukotriene C4 synthesis by activated human basophils. Clin Exp Allergy. 2003;33:1125–34.PubMedCrossRef Lie WJ, Homburg E, Kuijers TW, et al. Regulation and kinetics of platelet-activating factor and leukotriene C4 synthesis by activated human basophils. Clin Exp Allergy. 2003;33:1125–34.PubMedCrossRef
81.
Zurück zum Zitat Tsujimura Y, Obata K, Mukai K, et al. Basophils play a pivotal role in immunoglobulin-G-mediated but not immunoglobulin-E-mediated systemic anaphylaxis. Immunity. 2008;2:581–9.CrossRef Tsujimura Y, Obata K, Mukai K, et al. Basophils play a pivotal role in immunoglobulin-G-mediated but not immunoglobulin-E-mediated systemic anaphylaxis. Immunity. 2008;2:581–9.CrossRef
82.
Zurück zum Zitat Steiner M, Harrer A, Lang R, et al. Basophil activation test for investigation of IgE-mediated mechanisms in drug hypersensitivity. J Visualized Exp. 2011;55:1–6. Steiner M, Harrer A, Lang R, et al. Basophil activation test for investigation of IgE-mediated mechanisms in drug hypersensitivity. J Visualized Exp. 2011;55:1–6.
83.
Zurück zum Zitat Chirumbolo S. Basophil activation test to optimize the diagnosis of adverse effects following immunization to vaccines. Iran J Asthma Immunol. 2013;12:196–202. Chirumbolo S. Basophil activation test to optimize the diagnosis of adverse effects following immunization to vaccines. Iran J Asthma Immunol. 2013;12:196–202.
84.•
Zurück zum Zitat Macglashan Jr DW. Basophil activation testing. J Allergy Immunol. 2013;132(4):777–87. This review discusses the potential of BAT to assess functional changes in basophils.CrossRef Macglashan Jr DW. Basophil activation testing. J Allergy Immunol. 2013;132(4):777–87. This review discusses the potential of BAT to assess functional changes in basophils.CrossRef
85.
Zurück zum Zitat De Weck AL, Sanz ML, Gamboa PM, et al. Diagnostic tests based on human basophils: more potentials and perspectives than pitfalls. Int Allergy Immunol. 2008;146:177–89.CrossRef De Weck AL, Sanz ML, Gamboa PM, et al. Diagnostic tests based on human basophils: more potentials and perspectives than pitfalls. Int Allergy Immunol. 2008;146:177–89.CrossRef
86.
Zurück zum Zitat Khan FM, Ueno-Yamanouchi A, Serushago B, et al. Basophil activation test compared to skin prick test and fluorescence enzyme immunoassay for aeroallergen-specific Immunoglobulin-E. Allergy Clin Immunol. 2012;8:1–13. Khan FM, Ueno-Yamanouchi A, Serushago B, et al. Basophil activation test compared to skin prick test and fluorescence enzyme immunoassay for aeroallergen-specific Immunoglobulin-E. Allergy Clin Immunol. 2012;8:1–13.
87.•
Zurück zum Zitat Savage JH, Courneya JP, Sterba PM, et al. Kinetics of mast cell, basophil, and oral food challenge responses in omalizumab-treated adults with peanut allergy. J Allergy Clin Immunol. 2012;130:1123–9. Provided here is the application of omalizumab and its effects in modulating immune response to allergy challenge.PubMedCrossRef Savage JH, Courneya JP, Sterba PM, et al. Kinetics of mast cell, basophil, and oral food challenge responses in omalizumab-treated adults with peanut allergy. J Allergy Clin Immunol. 2012;130:1123–9. Provided here is the application of omalizumab and its effects in modulating immune response to allergy challenge.PubMedCrossRef
88.
Zurück zum Zitat Blank S. Components and mechanisms in diagnosis and therapy of hymenoptera venom allergy. University Dissertation - Hamburg. 2009;1–70. Blank S. Components and mechanisms in diagnosis and therapy of hymenoptera venom allergy. University Dissertation - Hamburg. 2009;1–70.
89.•
Zurück zum Zitat Konstantinou GN, Asero R, Ferrer M, et al. EAACI taskforce position paper: evidence for autoimmune urticaria and proposal for defining diagnostic criteria. Allergy. 2013;68:27–36. Urticaria as an autoimmune disorder involving basophils is discussed.PubMedCrossRef Konstantinou GN, Asero R, Ferrer M, et al. EAACI taskforce position paper: evidence for autoimmune urticaria and proposal for defining diagnostic criteria. Allergy. 2013;68:27–36. Urticaria as an autoimmune disorder involving basophils is discussed.PubMedCrossRef
90.
Zurück zum Zitat Gentinetta T, Pecaric-Petkovic T, Wan D, et al. Individual IL-3 priming is crucial for consistent in vitro activation of donor basophils in patients with chronic urticaria. J Allergy Clin Immunol. 2011;128:1227–34.PubMedCrossRef Gentinetta T, Pecaric-Petkovic T, Wan D, et al. Individual IL-3 priming is crucial for consistent in vitro activation of donor basophils in patients with chronic urticaria. J Allergy Clin Immunol. 2011;128:1227–34.PubMedCrossRef
91.
Zurück zum Zitat Imoto Y, Tokunaga T, Matsumoto Y, et al. Cystatin SN upregulation in patients with seasonal allergic rhinitis. PLOS One. 2013;8(8):1–8.CrossRef Imoto Y, Tokunaga T, Matsumoto Y, et al. Cystatin SN upregulation in patients with seasonal allergic rhinitis. PLOS One. 2013;8(8):1–8.CrossRef
92.
Zurück zum Zitat Zeiger S, Heller S. Development of nasal basophilic cells and nasal eosinophils from age 4 months through 4 years in children of atopic parents. J Allergy Clin Immunol. 1993;91(3):723–34.PubMedCrossRef Zeiger S, Heller S. Development of nasal basophilic cells and nasal eosinophils from age 4 months through 4 years in children of atopic parents. J Allergy Clin Immunol. 1993;91(3):723–34.PubMedCrossRef
93.
Zurück zum Zitat Kepley CL, McFeeley PJ, Oliver JM, Lipscomb MF. Immunohistochemical detection of human basophils in postmortem cases of fatal asthma. Am J Resp Crit Care Med. 2011;164:1053–8.CrossRef Kepley CL, McFeeley PJ, Oliver JM, Lipscomb MF. Immunohistochemical detection of human basophils in postmortem cases of fatal asthma. Am J Resp Crit Care Med. 2011;164:1053–8.CrossRef
94.•
Zurück zum Zitat Siracusa MC, Kim BS, Spergel JM, Artis D. Basophils and allergic inflammation. J Allergy Clin Immunol. 2013;132:789–801. This review encapsulates many functions of basophils in allergy but is skewed to mouse biology.PubMedCrossRef Siracusa MC, Kim BS, Spergel JM, Artis D. Basophils and allergic inflammation. J Allergy Clin Immunol. 2013;132:789–801. This review encapsulates many functions of basophils in allergy but is skewed to mouse biology.PubMedCrossRef
95.
Zurück zum Zitat Botturi K, Langelot M, Lair D, et al. Preventing asthma exacerbations: what are the targets? Pharmacol Ther. 2011;131(1):114–29.PubMedCrossRef Botturi K, Langelot M, Lair D, et al. Preventing asthma exacerbations: what are the targets? Pharmacol Ther. 2011;131(1):114–29.PubMedCrossRef
96.
Zurück zum Zitat Shelley WB, Resnik SS. Basophil degranulation induced by oral poison ivy antigen. Arch Dermatol. 1965;92:147–50.CrossRef Shelley WB, Resnik SS. Basophil degranulation induced by oral poison ivy antigen. Arch Dermatol. 1965;92:147–50.CrossRef
97.
Zurück zum Zitat Brandt EB, Sivaprasad U. Th2 cytokines and atopic dermatitis. J Clin Cell Immunol. 2011;2(3):1–25.CrossRef Brandt EB, Sivaprasad U. Th2 cytokines and atopic dermatitis. J Clin Cell Immunol. 2011;2(3):1–25.CrossRef
98.
Zurück zum Zitat Sabroe I, Jones EC, Usher LR, et al. Toll-like receptor (TLR)2 and TLR4 in human peripheral blood granulocytes: a critical role for monocytes in leukocyte lipopolysaccharide responses. J Immunol. 2002;168:4701–10.PubMed Sabroe I, Jones EC, Usher LR, et al. Toll-like receptor (TLR)2 and TLR4 in human peripheral blood granulocytes: a critical role for monocytes in leukocyte lipopolysaccharide responses. J Immunol. 2002;168:4701–10.PubMed
99.
Zurück zum Zitat Wong S, McLaughlin J, Cheng D, et al. IL-3 receptor signaling is dispensable for BCR-ABL-induced myeloproliferative disease. Proc Natl Acad Sci U S A. 2003;100(20):11630–5.PubMedCentralPubMedCrossRef Wong S, McLaughlin J, Cheng D, et al. IL-3 receptor signaling is dispensable for BCR-ABL-induced myeloproliferative disease. Proc Natl Acad Sci U S A. 2003;100(20):11630–5.PubMedCentralPubMedCrossRef
100.
Zurück zum Zitat Noti M, Tait Wojno ED, Kim BS, et al. Thymic stromal lymphopoietin-elicited basophil responses promote eosinophilic esophagitis. Nat Med. 2013;19:1005–13.PubMedCrossRef Noti M, Tait Wojno ED, Kim BS, et al. Thymic stromal lymphopoietin-elicited basophil responses promote eosinophilic esophagitis. Nat Med. 2013;19:1005–13.PubMedCrossRef
101.
Zurück zum Zitat Roan F, Bell BD, Stoklasek TA, et al. The multiple facets of thymic thromal lymphopoietin (TSLP) during allergic inflammation and beyond. J Leukoc Biol. 2012;91(6):1–10. Roan F, Bell BD, Stoklasek TA, et al. The multiple facets of thymic thromal lymphopoietin (TSLP) during allergic inflammation and beyond. J Leukoc Biol. 2012;91(6):1–10.
102.
Zurück zum Zitat Bogiatzi SI, Guillot-Delost M, Cappuccio A, et al. Multiple-checkpoint inhibition of thymic stromal lymphopoietin – induced TH2 response by TH17-related cytokines. J Allergy Clin Immunol. 2012;1:233–40.CrossRef Bogiatzi SI, Guillot-Delost M, Cappuccio A, et al. Multiple-checkpoint inhibition of thymic stromal lymphopoietin – induced TH2 response by TH17-related cytokines. J Allergy Clin Immunol. 2012;1:233–40.CrossRef
Metadaten
Titel
Emerging Role of Human Basophil Biology in Health and Disease
verfasst von
Jessica L. Cromheecke
Kathleen T. Nguyen
David P. Huston
Publikationsdatum
01.01.2014
Verlag
Springer US
Erschienen in
Current Allergy and Asthma Reports / Ausgabe 1/2014
Print ISSN: 1529-7322
Elektronische ISSN: 1534-6315
DOI
https://doi.org/10.1007/s11882-013-0408-2

Weitere Artikel der Ausgabe 1/2014

Current Allergy and Asthma Reports 1/2014 Zur Ausgabe

AUTOIMMUNITY (TK TARRANT, SECTION EDITOR)

Noninfectious Immune-Mediated Uveitis and Ocular Inflammation

OCCUPATIONAL ALLERGIES (JA POOLE, SECTION EDITOR)

Irritant-Induced Asthma in the Workplace

Update HNO

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert – ganz bequem per eMail.