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Published 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

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

Published in: Current Allergy and Asthma Reports | Issue 1/2014

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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.
Literature
1.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
6.
go back to reference 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.
go back to reference 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.
go back to reference 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.•
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.•
go back to reference 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.
go back to reference 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.•
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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
43.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.•
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.•
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.•
go back to reference 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.
go back to reference 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.
go back to reference 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.•
go back to reference 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.
go back to reference 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.•
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.•
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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.
go back to reference 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
Metadata
Title
Emerging Role of Human Basophil Biology in Health and Disease
Authors
Jessica L. Cromheecke
Kathleen T. Nguyen
David P. Huston
Publication date
01-01-2014
Publisher
Springer US
Published in
Current Allergy and Asthma Reports / Issue 1/2014
Print ISSN: 1529-7322
Electronic ISSN: 1534-6315
DOI
https://doi.org/10.1007/s11882-013-0408-2

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