Literature DB >> 8768805

Production of a monoclonal dinitrophenyl-specific rat IgE and establishment of an IgE capture ELISA for estimating the concentration of rat IgE antibodies to dinitrophenyl-Ascaris suum.

K Hanashiro1, M Nakamura, N Tamaki, T Kosugi.   

Abstract

A hybridoma producing monoclonal rat IgE antibodies of antidinitrophenyl (anti-DNP) specificity was generated by fusion of Sp2/0-Ag 14 (SP2) mouse myeloma cells and spleen cells from a DNP-Ascaris-sensitized Brown-Norway rat. Subsequently, the supernatant of the hybridoma (FE-3) was applied to an affinity column of DNP-bovine serum albumin-Sepharose 4B. The adsorbed protein fraction was pooled, concentrated, and further purified using Sephadex G-200. The molecular weight of the isolated protein was approximately 200,000 by SDS-PAGE, and the protein reacted with peroxidase (POD) mouse antirat myeloma IgE on Western blotting. Rabbit antibodies against DNP-specific rat IgE were also prepared by immunizing Japanese white rabbits with monoclonal DNP-specific rat IgE. These antibodies against DNP-specific rat IgE were applied to an affinity column of normal rat serum-Sepharose 4B and monoclonal DNP-specific rat IgG2b-Sepharose 4B to remove any other reactive substances apart from IgE contained in the serum proteins of the rat sensitized with DNP-Ascaris. On ELISA, it was found that the specificity of POD rabbit antibodies against DNP-specific rat IgE for monoclonal DNP-specific rat IgE was the same as that for rat myeloma IgE (IR 162). In addition, determinations of the monoclonal DNP-specific rat IgE revealed that the sensitivity of ELISA using POD-rabbit antibodies against DNP-specific rat IgE [POD-RA(DNP)RE] was higher than that using POD goat antibodies against rat myeloma IgE. Furthermore, an IgE capture ELISA employing the above-mentioned RA(DNP)RE was established for estimating the rat IgE antibodies to DNP-Ascaris suum. A good correlation was found between the antigen-specific IgE antibodies in the serum of Wistar rats estimated by this IgE capture ELISA and those estimated by passive cutaneous anaphylaxis.

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Year:  1996        PMID: 8768805     DOI: 10.1159/000237330

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


  4 in total

1.  Azelastine and suplatast shorten the distribution half-life of IgE in rats.

Authors:  Kazuhiko Hanashiro; Yoshihiro Tokeshi; Toshiyuki Nakasone; Masanori Sunagawa; Mariko Nakamura; Tadayoshi Kosugi
Journal:  Mediators Inflamm       Date:  2002-02       Impact factor: 4.711

2.  Analysis of IgE turnover in non-sensitized and sensitized rats.

Authors:  K Hanashiro; Y Tokeshi; T Nakasone; M Sunagawa; M Nakamura; T Kosugi
Journal:  Mediators Inflamm       Date:  2001-08       Impact factor: 4.711

3.  Modification of Cepsilon mRNA expression by EBV-encoded latent membrane protein 1.

Authors:  Kazuhiko Hanashiro; Shigeto Ohta; Masanori Sunagawa; Mariko Nakamura; Mikio Suzuki; Tadayoshi Kosugi
Journal:  Mediators Inflamm       Date:  2006       Impact factor: 4.711

4.  An immunologically relevant rodent model demonstrates safety of therapy using a tumour-specific IgE.

Authors:  D H Josephs; M Nakamura; H J Bax; T S Dodev; G Muirhead; L Saul; P Karagiannis; K M Ilieva; S Crescioli; P Gazinska; N Woodman; C Lombardelli; S Kareemaghay; C Selkirk; H Lentfer; C Barton; S Canevari; M Figini; N Downes; D Dombrowicz; C J Corrigan; F O Nestle; P S Jones; H J Gould; P J Blower; S Tsoka; J F Spicer; S N Karagiannis
Journal:  Allergy       Date:  2018-10-08       Impact factor: 14.710

  4 in total

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