Literature DB >> 9693276

A mouse model of mosquito allergy for study of antigen-specific IgE and IgG subclass responses, lymphocyte proliferation, and IL-4 and IFN-gamma production.

Y L Chen1, F E Simons, Z Peng.   

Abstract

To date, there are no ideal animal models for study of natural sensitization leading to IgE- and lymphocyte-mediated hypersensitivities. We established such a model in which four BALB/c mice were each sensitized by exposure to at least 16 mosquito Aedes aegypti bites, twice a week for 4 weeks. Four non-exposed control mice were also studied. Mosquito A. aegypti head and thorax extract, saliva, and two recombinant salivary allergens (rAed a 1 and rAed a 2) were used in vitro as antigens. Intradermal tests were performed. Serum mosquito antigen-specific IgG, IgG1, IgG2a, and total IgE were measured by ELISA; specific IgE was measured by passive cutaneous anaphylaxis (PCA). IgE responses to each antigen in the saliva were analyzed using Western blotting. Spleen lymphocyte proliferation assays were performed to determine the cell-mediated hypersensitivity response. Antigen-induced IL-4 and IFN-gamma production in the spleen lymphocytes were evaluated using ELISA. After 4 weeks, all 4 mosquito-sensitized mice developed a positive immediate wheal 20 min after skin tests with mosquito antigens, and a positive delayed papule 24 h later, while control mice did not. Also, the sensitized mice had a positive PCA response, which correlated significantly with total IgE levels (r = 0.84, p<0.05), confirming the presence of antigen-specific IgE, while none of control mice had a positive response. Antigen-specific IgG1, but not IgG2a, was increased in the sensitized mice (p<0.01). Western blotting showed that 5 of the 8 antigens which elicited mouse IgE responses, including 2 major antigens, also elicited human IgE responses. The mean lymphocyte proliferation response to mosquito antigens also elicited human IgE responses. The mean lymphocyte proliferation response to mosquito antigens was significantly increased in the sensitized mice (p<0.05). IL-4 production was significantly increased and IFN-gamma production was decreased, further suggesting that a Th2 immune response predominates despite the development of the delayed skin reaction. This new model of natural sensitization without using an adjuvant is potentially useful for the study of other allergic disorders as well as mosquito allergy.

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Year:  1998        PMID: 9693276     DOI: 10.1159/000023955

Source DB:  PubMed          Journal:  Int Arch Allergy Immunol        ISSN: 1018-2438            Impact factor:   2.749


  16 in total

1.  Members of the salivary gland surface protein (SGS) family are major immunogenic components of mosquito saliva.

Authors:  Jonas G King; Kenneth D Vernick; Julián F Hillyer
Journal:  J Biol Chem       Date:  2011-09-29       Impact factor: 5.157

2.  Neither mosquito saliva nor immunity to saliva has a detectable effect on the infectivity of Plasmodium sporozoites injected into mice.

Authors:  Chahnaz Kebaier; Tatiana Voza; Jerome Vanderberg
Journal:  Infect Immun       Date:  2009-11-02       Impact factor: 3.441

3.  Impact of mosquito bites on asexual parasite density and gametocyte prevalence in asymptomatic chronic Plasmodium falciparum infections and correlation with IgE and IgG titers.

Authors:  Ramatoulaye Lawaly; Lassana Konate; Laurence Marrama; Ibrahima Dia; Diawo Diallo; Fatoumata Diène Sarr; Bradley S Schneider; Isabelle Casademont; Mawlouth Diallo; Paul T Brey; Anavaj Sakuntabhai; Salah Mecheri; Richard Paul
Journal:  Infect Immun       Date:  2012-03-26       Impact factor: 3.441

4.  Uninfected mosquito bites confer protection against infection with malaria parasites.

Authors:  Michael J Donovan; Andrew S Messmore; Deborah A Scrafford; David L Sacks; Shaden Kamhawi; Mary Ann McDowell
Journal:  Infect Immun       Date:  2007-03-05       Impact factor: 3.441

5.  Evaluation of inflammatory skin infiltrate following Aedes aegypti bites in sensitized and non-sensitized mice reveals saliva-dependent and immune-dependent phenotypes.

Authors:  Maressa O Henrique; Leila S Neto; Josiane B Assis; Michele S Barros; Margareth L Capurro; Ana P Lepique; Denise M Fonseca; Anderson Sá-Nunes
Journal:  Immunology       Date:  2019-09       Impact factor: 7.397

6.  Association of human immune response to Aedes aegypti salivary proteins with dengue disease severity.

Authors:  C Machain-Williams; M P Mammen; N S Zeidner; B J Beaty; J E Prenni; A Nisalak; C D Blair
Journal:  Parasite Immunol       Date:  2012-01       Impact factor: 2.280

Review 7.  The enhancement of arbovirus transmission and disease by mosquito saliva is associated with modulation of the host immune response.

Authors:  Bradley S Schneider; Stephen Higgs
Journal:  Trans R Soc Trop Med Hyg       Date:  2008-03-14       Impact factor: 2.184

8.  Aedes aegypti salivary protein "aegyptin" co-inoculation modulates dengue virus infection in the vertebrate host.

Authors:  M K McCracken; R C Christofferson; B J Grasperge; E Calvo; D M Chisenhall; C N Mores
Journal:  Virology       Date:  2014-08-28       Impact factor: 3.616

9.  Vector saliva controlled inflammatory response of the host may represent the Achilles heel during pathogen transmission.

Authors:  Claudia Demarta-Gatsi; Salah Mécheri
Journal:  J Venom Anim Toxins Incl Trop Dis       Date:  2021-05-17

10.  Immunization of mice with recombinant mosquito salivary protein D7 enhances mortality from subsequent West Nile virus infection via mosquito bite.

Authors:  Krystle L Reagan; Carlos Machain-Williams; Tian Wang; Carol D Blair
Journal:  PLoS Negl Trop Dis       Date:  2012-12-06
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