The formation of eosinophil and neutrophil chemotactic activity during a pollen season and after allergen challenge
Heat-stable (HS) and heat-labile (HL) neutrophil chemotactic activities (NCAs) have been demonstrated in serum after allergen challenge of subjects with asthma. In this investigation, we have studied the possible occurrence of similar activities in 20 atopic individuals on natural exposure to allerg...
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Published in | Journal of allergy and clinical immunology Vol. 83; no. 5; pp. 933 - 939 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
New York, NY
Mosby, Inc
01.05.1989
Elsevier |
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Abstract | Heat-stable (HS) and heat-labile (HL) neutrophil chemotactic activities (NCAs) have been demonstrated in serum after allergen challenge of subjects with asthma. In this investigation, we have studied the possible occurrence of similar activities in 20 atopic individuals on natural exposure to allergen, that is, during the birch-pollen season. Since eosinophil accumulation is a hallmark of an ongoing allergic inflammation in the respiratory tract also, the possible production of eosinophil chemotactic activity (ECA) was examined in serum after allergen challenge and at natural exposure to pollen. Both HL-NCA and HL-ECA were produced to a significant extent (
p < 0.001) during the season, with the peak of activities occurring simultaneously with the peak pollen count. HL-ECA was produced after allergen challenge of subjects with asthma in the laboratory, as has been demonstrated for NCA previously. The activity of the HS-NCA was unaltered during season. Gel-filtration studies of the major HL-NCA and HL-ECA indicated a molecular weight for both activities of 100 to 150,000, and the activities produced during season cocromatographed with the HL-NCA and HL-ECA produced after allergen challenge in the laboratory, suggesting that all these activities are due to one and the same molecule. The results suggest that the heat-labile chemotactic activity found in serum of atopic subjects and subjects with asthma after allergen exposure may be involved in the attraction of eosinophils and neutrophils to the site of allergic inflammation. |
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AbstractList | Heat-stable (HS) and heat-labile (HL) neutrophil chemotactic activities (NCAs) have been demonstrated in serum after allergen challenge of subjects with asthma. In this investigation, we have studied the possible occurrence of similar activities in 20 atopic individuals on natural exposure to allergen, that is, during the birch-pollen season. Since eosinophil accumulation is a hallmark of an ongoing allergic inflammation in the respiratory tract also, the possible production of eosinophil chemotactic activity (ECA) was examined in serum after allergen challenge and at natural exposure to pollen. Both HL-NCA and HL-ECA were produced to a significant extent (p less than 0.001) during the season, with the peak of activities occurring simultaneously with the peak pollen count. HL-ECA was produced after allergen challenge of subjects with asthma in the laboratory, as has been demonstrated for NCA previously. The activity of the HS-NCA was unaltered during season. Gel-filtration studies of the major HL-NCA and HL-ECA indicated a molecular weight for both activities of 100 to 150,000, and the activities produced during season cochromatographed with the HL-NCA and HL-ECA produced after allergen challenge in the laboratory, suggesting that all these activities are due to one and the same molecule. The results suggest that the heat-labile chemotactic activity found in serum of atopic subjects and subjects with asthma after allergen exposure may be involved in the attraction of eosinophils and neutrophils to the site of allergic inflammation.Heat-stable (HS) and heat-labile (HL) neutrophil chemotactic activities (NCAs) have been demonstrated in serum after allergen challenge of subjects with asthma. In this investigation, we have studied the possible occurrence of similar activities in 20 atopic individuals on natural exposure to allergen, that is, during the birch-pollen season. Since eosinophil accumulation is a hallmark of an ongoing allergic inflammation in the respiratory tract also, the possible production of eosinophil chemotactic activity (ECA) was examined in serum after allergen challenge and at natural exposure to pollen. Both HL-NCA and HL-ECA were produced to a significant extent (p less than 0.001) during the season, with the peak of activities occurring simultaneously with the peak pollen count. HL-ECA was produced after allergen challenge of subjects with asthma in the laboratory, as has been demonstrated for NCA previously. The activity of the HS-NCA was unaltered during season. Gel-filtration studies of the major HL-NCA and HL-ECA indicated a molecular weight for both activities of 100 to 150,000, and the activities produced during season cochromatographed with the HL-NCA and HL-ECA produced after allergen challenge in the laboratory, suggesting that all these activities are due to one and the same molecule. The results suggest that the heat-labile chemotactic activity found in serum of atopic subjects and subjects with asthma after allergen exposure may be involved in the attraction of eosinophils and neutrophils to the site of allergic inflammation. Heat-stable (HS) and heat-labile (HL) neutrophil chemotactic activities (NCAs) have been demonstrated in serum after allergen challenge of subjects with asthma. In this investigation, we have studied the possible occurrence of similar activities in 20 atopic individuals on natural exposure to allergen, that is, during the birch-pollen season. Since eosinophil accumulation is a hallmark of an ongoing allergic inflammation in the respiratory tract also, the possible production of eosinophil chemotactic activity (ECA) was examined in serum after allergen challenge and at natural exposure to pollen. Both HL-NCA and HL-ECA were produced to a significant extent ( p < 0.001) during the season, with the peak of activities occurring simultaneously with the peak pollen count. HL-ECA was produced after allergen challenge of subjects with asthma in the laboratory, as has been demonstrated for NCA previously. The activity of the HS-NCA was unaltered during season. Gel-filtration studies of the major HL-NCA and HL-ECA indicated a molecular weight for both activities of 100 to 150,000, and the activities produced during season cocromatographed with the HL-NCA and HL-ECA produced after allergen challenge in the laboratory, suggesting that all these activities are due to one and the same molecule. The results suggest that the heat-labile chemotactic activity found in serum of atopic subjects and subjects with asthma after allergen exposure may be involved in the attraction of eosinophils and neutrophils to the site of allergic inflammation. Heat-stable (HS) and heat-labile (HL) neutrophil chemotactic activities (NCAs) have been demonstrated in serum after allergen challenge of subjects with asthma. In this investigation, the authors have studied the possible occurrence of similar activities in 20 atopic individuals on natural exposure to allergen, that is, during the birch-pollen season. Since eosinophil accumulation is a hallmark of an ongoing allergic inflammation in the respiratory tract also, the possible production of eosinophil chemotactic activity (ECA) was examined in serum after allergen challenge and at natural exposure to pollen. The results suggest that the heat-labile chemotactic activity found in serum of atopic subjects and subjects with asthma after allergen exposure may be involved in the attraction of eosinophils and neutrophils to the site of allergic inflammation. Heat-stable (HS) and heat-labile (HL) neutrophil chemotactic activities (NCAs) have been demonstrated in serum after allergen challenge of subjects with asthma. In this investigation, we have studied the possible occurrence of similar activities in 20 atopic individuals on natural exposure to allergen, that is, during the birch-pollen season. Since eosinophil accumulation is a hallmark of an ongoing allergic inflammation in the respiratory tract also, the possible production of eosinophil chemotactic activity (ECA) was examined in serum after allergen challenge and at natural exposure to pollen. Both HL-NCA and HL-ECA were produced to a significant extent (p less than 0.001) during the season, with the peak of activities occurring simultaneously with the peak pollen count. HL-ECA was produced after allergen challenge of subjects with asthma in the laboratory, as has been demonstrated for NCA previously. The activity of the HS-NCA was unaltered during season. Gel-filtration studies of the major HL-NCA and HL-ECA indicated a molecular weight for both activities of 100 to 150,000, and the activities produced during season cochromatographed with the HL-NCA and HL-ECA produced after allergen challenge in the laboratory, suggesting that all these activities are due to one and the same molecule. The results suggest that the heat-labile chemotactic activity found in serum of atopic subjects and subjects with asthma after allergen exposure may be involved in the attraction of eosinophils and neutrophils to the site of allergic inflammation. |
Author | Venge, Per Håkansson, Lena Rak, Sabina Dahl, Ronald |
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Keywords | HL-NCA ECA NCA IAR HL-ECA LAR ECA CV NCA HS-NCA Human Allergy Immunopathology Lung function Rhinitis Immunological investigation Neutrophile ENT disease Pollen Inhalation test Chemotaxis Eosinophil |
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References | Håkansson, Westerlund, Venge (BIB8) 1987; 42 Atkins, Norman, Weiner, Zweiman (BIB1) 1977; 86 Kay (BIB13) 1970; 7 Durham, Lee, Cromwell, Shaw, Merrett, Cooper, Kay (BIB7) 1984; 74 Metzger, Richerson, Wasserman (BIB9) 1986; 78 Lee, Nagy, Nagakura, Walport, Kay (BIB5) 1982; 69 Rak S, Håkansson L, Venge P. Immunotherapy abrogates the generation of eosinophil and neutrophil chemotactic activity during pollen season [submitted]. . Tannous, Cavender-Zylich, Ginsberg (BIB16) 1981; 98 Venge, Dahl, Håkansson (BIB4) 1987; 80 Wasserman, Austen, Soter (BIB14) 1982; 47 Wilkinson (BIB12) 1974 Håkansson, Venge (BIB11) 1980; 11 Venge, Dahl, Håkansson, Peterson (BIB3) 1982; 37 Venge, Håkansson, Peterson (BIB17) 1987; 82 Wardlaw, Kay (BIB18) 1987; 42 Rak, Löwhagen, Venge (BIB10) 1988; 82 Nagy, Lee, Goetzl, Pickett, Kay (BIB2) 1982; 306 Venge P, Dahl R, Henriksen J, Håkansson L. Generation of neutrophil chemotactic activity in blood after exercise of asthmatics: effects of asthma medication [submitted]. |
References_xml | – volume: 42 start-page: 689 year: 1987 ident: BIB8 article-title: A new method for the measurement of eosinophil migration publication-title: J Leukocyte Biol – volume: 86 start-page: 415 year: 1977 ident: BIB1 article-title: Release of neutrophil chemotactic activity during immediate hypersensitivity reactions in humans publication-title: Ann Intern Med – year: 1974 ident: BIB12 article-title: Chemotaxis and inflammation – volume: 306 start-page: 497 year: 1982 ident: BIB2 article-title: Neutrophil chemotactic activity in antigen-induced late asthmatic reactions publication-title: N Engl J Med – volume: 82 start-page: 333 year: 1987 ident: BIB17 article-title: Eosinophil activation in allergic disease publication-title: Int Arch Allergy Appl Immunol – reference: Venge P, Dahl R, Henriksen J, Håkansson L. Generation of neutrophil chemotactic activity in blood after exercise of asthmatics: effects of asthma medication [submitted]. – volume: 80 start-page: 679 year: 1987 ident: BIB4 article-title: Heat-labile neutrophil chemotactic activity in subjects with asthma after allergen inhalation: relation to the late asthmatic reaction and effects of asthma medication publication-title: J Allergy Clin Immunol – volume: 11 start-page: 271 year: 1980 ident: BIB11 article-title: The influence of serum on random migration and chemotaxis of polymorphonuclear leukocytes: methodological evaluation using sera from infectio-prone patients and normals publication-title: Scand J Immunol – volume: 69 start-page: 889 year: 1982 ident: BIB5 article-title: Identification and partial characterization of an exercise-nduced neutrophil chemotactic factor in bronchial asthma publication-title: J Clin Invest – volume: 78 start-page: 282 year: 1986 ident: BIB9 article-title: Generation and partial characterization of eosinophil chemotactic activity and neutrophil chemotactic activity during early and late-phase asthmatic response publication-title: J Allergy Clin Immunol – volume: 47 start-page: 570 year: 1982 ident: BIB14 article-title: The functional and physicochemical characterization of three eosinophilotactic activities released into the circulation by cold challenge of patients with cold urticaria publication-title: Clin Exp Immunol – volume: 42 start-page: 321 year: 1987 ident: BIB18 article-title: The role of the eosinophil in the pathogenesis of asthma publication-title: Allergy – volume: 74 start-page: 49 year: 1984 ident: BIB7 article-title: Immunologic studies in allergen-induced late-phase reactions publication-title: J Allergy Clin Immunol – reference: Rak S, Håkansson L, Venge P. Immunotherapy abrogates the generation of eosinophil and neutrophil chemotactic activity during pollen season [submitted]. – volume: 37 start-page: 55 year: 1982 ident: BIB3 article-title: Generation of heat-labile chemotactic activity in blood after inhalation challenge and its relationship to neutrophil and monocyte/macrophage turnover and activity publication-title: Allergy – volume: 98 start-page: 238 year: 1981 ident: BIB16 article-title: The role of chemotactic factor inactivation in neutrophil chemotaxis publication-title: J Lab Clin Med – volume: 7 start-page: 723 year: 1970 ident: BIB13 article-title: Studies on eosinophil leukocyte migration publication-title: Clin Exp Immunol – volume: 82 start-page: 470 year: 1988 end-page: 480 ident: BIB10 article-title: The effect of immunotherapy on bronchial hyperresponsiveness and eosinophil cationic protein in pollen-allergic patients publication-title: J Allergy Clin Immunol – reference: . |
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SubjectTerms | Allergic diseases Asthma - immunology Biological and medical sciences Chemotactic Factors - biosynthesis Chemotactic Factors - blood Chemotactic Factors, Eosinophil - biosynthesis Chemotactic Factors, Eosinophil - blood Chemotaxis, Leukocyte Chromatography, Gel Eosinophils - physiology Humans Immunopathology Interleukin-8 Medical sciences Neutrophils - physiology Pollen - immunology Respiratory and ent allergic diseases |
Title | The formation of eosinophil and neutrophil chemotactic activity during a pollen season and after allergen challenge |
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