Literature DB >> 3885772

Quantitative and qualitative changes in the humoral response of dogs through the course of infection with Dirofilaria immitis.

W K Tamashiro, K G Powers, D A Levy, A L Scott.   

Abstract

The present study compared the humoral response of dogs which developed microfilaremic or occult forms of dirofilariasis following experimental infection with Dirofilaria immitis L3 larvae. Quantitative analysis by ELISA revealed that antibody levels to adult somatic (AS), excretory-secretory (ES), and microfilarial (MF) antigens were highest during the patent phase of infection in dogs with either form of dirofilariasis. Patent sera from dogs destined for occult infections contained anti-AS and anti-MF antibody concentrations of 1,572 and 1,004 micrograms/ml, respectively, while microfilaremic-bound dogs contained 1,044 and 906 micrograms/ml, respectively. Chronic sera (430 days post infection) from occult dogs contained anti-AS and anti-MF antibody levels of 982 and 600 micrograms/ml, respectively, which were higher than in microfilaremic dogs. The antibody response to ES antigen was generally 10-fold less in absolute antibody concentrations at all time points tested. Immunoperoxidase staining of antigens transferred to nitrocellulose revealed the presence of several antigenic proteins which were recognized by occult, and to a lesser extent or not at all, by microfilaremic dogs. Sera drawn from occult-bound dogs 280 days post-infection, a time corresponding to microfilarial clearance (transition phase), contained higher antibody activity to microfilarial proteins weighing 47.5, 42.0, 34.2, and 22.4 kilodaltons compared to the microfilaremic dogs. This difference in antigen recognition became more apparent during the chronic phase of infection.

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Year:  1985        PMID: 3885772     DOI: 10.4269/ajtmh.1985.34.292

Source DB:  PubMed          Journal:  Am J Trop Med Hyg        ISSN: 0002-9637            Impact factor:   2.345


  7 in total

1.  Are transient pulmonary solitary nodules a common event in human dirofilariosis?

Authors:  M Cordero; A Muro; F Simón; J I Tapia; E Espinoza
Journal:  Clin Investig       Date:  1992-05

2.  Differential recognition of a protective filarial antigen by antibodies from humans with bancroftian filariasis.

Authors:  J W Kazura; H Cicirello; K Forsyth
Journal:  J Clin Invest       Date:  1986-06       Impact factor: 14.808

3.  Antibody and cellular immune responses to microfilarial antigens in ferrets experimentally infected with Brugia malayi.

Authors:  J P Thompson; R B Crandall; T J Doyle; S A Hines; C A Crandall
Journal:  Z Parasitenkd       Date:  1986

4.  Coxsackievirus induced myocarditis in mice: cardiac myosin autoantibodies do not cross-react with the virus.

Authors:  N Neu; S W Craig; N R Rose; F Alvarez; K W Beisel
Journal:  Clin Exp Immunol       Date:  1987-09       Impact factor: 4.330

Review 5.  Human and animal dirofilariasis: the emergence of a zoonotic mosaic.

Authors:  Fernando Simón; Mar Siles-Lucas; Rodrigo Morchón; Javier González-Miguel; Isabel Mellado; Elena Carretón; Jose Alberto Montoya-Alonso
Journal:  Clin Microbiol Rev       Date:  2012-07       Impact factor: 26.132

6.  Molecular cloning of a serine proteinase inhibitor from Brugia malayi.

Authors:  P Yenbutr; A L Scott
Journal:  Infect Immun       Date:  1995-05       Impact factor: 3.441

7.  Inflammatory mediators and modulators released in organ culture from rabbit skin lesions produced in vivo by sulfur mustard. III. Electrophoretic protein fractions, trypsin-inhibitory capacity, alpha 1-proteinase inhibitor, and alpha 1- and alpha 2-macroglobulin proteinase inhibitors of culture fluids and serum.

Authors:  S Harada; A M Dannenberg; R F Vogt; J E Myrick; F Tanaka; L C Redding; R M Merkhofer; P J Pula; A L Scott
Journal:  Am J Pathol       Date:  1987-01       Impact factor: 4.307

  7 in total

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