Expression and immunological characterization a heat shock cognate-70 protein allergen, rAed a 8, from the mosquito species Aedes aegypti

Background: Aedes aegypti is the source of saliva as well as somatic allergens. An IgE-binding Heat shock cognate-70 protein (Aed a 8) from this mosquito, has been described as a somatic allergen. Its biological and immunological properties have been scarcely studied. Objective: To perform the immu...

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Main Authors: José Fernando Cantillo, Leonardo Puerta, Enrique Fernández-Caldas, José Luis Subiza, Irene Soria, Sylvie Lafosse-Marin, Barbara Bohle
Format: Article
Language:English
Published: Colegio Mexicano de Inmunología Clínica y Alergia, A.C. 2018-06-01
Series:Revista Alergia México
Subjects:
Online Access:http://revistaalergia.mx/ojs/index.php/ram/article/view/491
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author José Fernando Cantillo
Leonardo Puerta
Enrique Fernández-Caldas
José Luis Subiza
Irene Soria
Sylvie Lafosse-Marin
Barbara Bohle
author_facet José Fernando Cantillo
Leonardo Puerta
Enrique Fernández-Caldas
José Luis Subiza
Irene Soria
Sylvie Lafosse-Marin
Barbara Bohle
author_sort José Fernando Cantillo
collection DOAJ
description Background: Aedes aegypti is the source of saliva as well as somatic allergens. An IgE-binding Heat shock cognate-70 protein (Aed a 8) from this mosquito, has been described as a somatic allergen. Its biological and immunological properties have been scarcely studied. Objective: To perform the immunological characterization of the recombinant allergen, rAed a 8. Methods: Recombinant Aed a 8 was expressed in Escherichia coli, purified and its IgE-binding capacity was evaluated by ELISA and immunoblotting using the sera from 14 individuals residing on the tropical island of Martinique, with positive skin test against Aedes communis whole body extract. The allergenicity of rAed a 8 was studied by the Basophil Activation Test and ELISA competition. For the Basophil Activation Test, stripped basophils re-sensitized with IgE from a rAed a 8 sensitized patient were used. These cells were incubated with rAed a 8 and CD63 up-regulation was assessed by flow cytometry. BALB/c mice were immunized with rAed a 8, or PBS, and specific IgE, IgG1, IgG2a and IgG3 were measured. For detection of IgG1, IgG2a and IgG3 sera were diluted 1:500; and for IgE 1:12. Murine IgG1 binding of the whole extract was verified by ELISA. T-cell activation was studied in splenocytes stimulated with rAed a 8. Results: rAed a 8 was expressed as a 74 kDa protein linked to a His-tag. The recombinant was purified by affinity, reacted with specific-IgE in 6 out of 14 (43 %) allergic individuals and induced the activation of basophils, suggesting that is an important allergen that could be considered in diagnostic tests and in specific-immunotherapy for mosquito allergy. When the Aedes aegypti extract was on the solid phase, rAed a 8 produced 40 % of inhibition of the IgE reactivity at the highest concentration. When rAed a 8 was on the solid phase, the extract produced a similar degree of inhibition. rAed a 8 induced the production of specific IgE, IgG1, IgG2a and IgG3 antibodies. At the same dilution of the mice sera, the levels of IgG2a were higher than the levels of the other IgG subclasses. Murine IgG1 showed reactivity with the mosquito extract in ELISA. rAed a 8 induced proliferation of mice splenocytes. Conclusions: rAed a 8 was expressed as a biological active protein. The allergen induced a mixed antibody response characterized by the production of Th1 and Th2 related antibodies. Further studies in well-defined allergic populations are needed to define whether Aed a 8 is a major or minor allergen.
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spelling doaj.art-1d4991c808e74d349a21b2ff8cd72d892023-09-02T12:05:12ZengColegio Mexicano de Inmunología Clínica y Alergia, A.C.Revista Alergia México0002-51512448-91902018-06-0165 suppl 1117118331Expression and immunological characterization a heat shock cognate-70 protein allergen, rAed a 8, from the mosquito species Aedes aegyptiJosé Fernando Cantillo0Leonardo Puerta1Enrique Fernández-Caldas2José Luis Subiza3Irene Soria4Sylvie Lafosse-Marin5Barbara Bohle6Inmunotek S.L., Alcalá de HenaresUniversidad de Cartagena, Instituto para la Investigación Inmunológica, CartagenaInmunotek S.L., Alcalá de HenaresInmunotek S.L., Alcalá de HenaresInmunotek S.L., Alcalá de HenaresUniversidad de Cartagena, Instituto para la Investigación Inmunológica, CartagenaMedical University of Vienna, Department of Pathophysiology and Allergy Research, ViennaBackground: Aedes aegypti is the source of saliva as well as somatic allergens. An IgE-binding Heat shock cognate-70 protein (Aed a 8) from this mosquito, has been described as a somatic allergen. Its biological and immunological properties have been scarcely studied. Objective: To perform the immunological characterization of the recombinant allergen, rAed a 8. Methods: Recombinant Aed a 8 was expressed in Escherichia coli, purified and its IgE-binding capacity was evaluated by ELISA and immunoblotting using the sera from 14 individuals residing on the tropical island of Martinique, with positive skin test against Aedes communis whole body extract. The allergenicity of rAed a 8 was studied by the Basophil Activation Test and ELISA competition. For the Basophil Activation Test, stripped basophils re-sensitized with IgE from a rAed a 8 sensitized patient were used. These cells were incubated with rAed a 8 and CD63 up-regulation was assessed by flow cytometry. BALB/c mice were immunized with rAed a 8, or PBS, and specific IgE, IgG1, IgG2a and IgG3 were measured. For detection of IgG1, IgG2a and IgG3 sera were diluted 1:500; and for IgE 1:12. Murine IgG1 binding of the whole extract was verified by ELISA. T-cell activation was studied in splenocytes stimulated with rAed a 8. Results: rAed a 8 was expressed as a 74 kDa protein linked to a His-tag. The recombinant was purified by affinity, reacted with specific-IgE in 6 out of 14 (43 %) allergic individuals and induced the activation of basophils, suggesting that is an important allergen that could be considered in diagnostic tests and in specific-immunotherapy for mosquito allergy. When the Aedes aegypti extract was on the solid phase, rAed a 8 produced 40 % of inhibition of the IgE reactivity at the highest concentration. When rAed a 8 was on the solid phase, the extract produced a similar degree of inhibition. rAed a 8 induced the production of specific IgE, IgG1, IgG2a and IgG3 antibodies. At the same dilution of the mice sera, the levels of IgG2a were higher than the levels of the other IgG subclasses. Murine IgG1 showed reactivity with the mosquito extract in ELISA. rAed a 8 induced proliferation of mice splenocytes. Conclusions: rAed a 8 was expressed as a biological active protein. The allergen induced a mixed antibody response characterized by the production of Th1 and Th2 related antibodies. Further studies in well-defined allergic populations are needed to define whether Aed a 8 is a major or minor allergen.http://revistaalergia.mx/ojs/index.php/ram/article/view/491aedes aegyptirecombinant allergen
spellingShingle José Fernando Cantillo
Leonardo Puerta
Enrique Fernández-Caldas
José Luis Subiza
Irene Soria
Sylvie Lafosse-Marin
Barbara Bohle
Expression and immunological characterization a heat shock cognate-70 protein allergen, rAed a 8, from the mosquito species Aedes aegypti
Revista Alergia México
aedes aegypti
recombinant allergen
title Expression and immunological characterization a heat shock cognate-70 protein allergen, rAed a 8, from the mosquito species Aedes aegypti
title_full Expression and immunological characterization a heat shock cognate-70 protein allergen, rAed a 8, from the mosquito species Aedes aegypti
title_fullStr Expression and immunological characterization a heat shock cognate-70 protein allergen, rAed a 8, from the mosquito species Aedes aegypti
title_full_unstemmed Expression and immunological characterization a heat shock cognate-70 protein allergen, rAed a 8, from the mosquito species Aedes aegypti
title_short Expression and immunological characterization a heat shock cognate-70 protein allergen, rAed a 8, from the mosquito species Aedes aegypti
title_sort expression and immunological characterization a heat shock cognate 70 protein allergen raed a 8 from the mosquito species aedes aegypti
topic aedes aegypti
recombinant allergen
url http://revistaalergia.mx/ojs/index.php/ram/article/view/491
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