Literature DB >> 7657805

Transfer of allergic airway responses with antigen-primed CD4+ but not CD8+ T cells in brown Norway rats.

A Watanabe1, H Mishima, P M Renzi, L J Xu, Q Hamid, J G Martin.   

Abstract

Activated CD4+ helper T cells have been demonstrated in asthmatic airways and postulated to play a central role in eliciting allergic inflammation; direct evidence of their involvement seems to be lacking. We hypothesized that CD4+ T cells have the potential to induce allergic responses to antigen challenge, and tested this hypothesis in a model of allergic bronchoconstriction, the Brown Norway rat, using the approach of adoptive transfer. Animals were actively sensitized to either ovalbumin (OVA) or BSA and were used as donors of T cells. W3/25(CD4)+ or OX8(CD8)+ T cells were isolated from the cervical lymph nodes of sensitized donors and transferred to naive BN rats. 2 d after adoptive transfer recipient rats were challenged by OVA inhalation, and changes in lung resistance (RL), bronchoalveolar lavage (BAL) cells, and serum levels of antigen-specific IgE were studied. After OVA challenge recipients of OVA-primed W3/25+ T cells exhibited sustained increases in RL throughout the entire 8-h observation period and had significant bronchoalveolar lavage eosinophilia, which was detected by immunocytochemistry using an antimajor basic protein mAb. Recipients of BSA-primed W3/25+ T cells or OVA-primed OX8+ T cells failed to respond to inhaled OVA. OVA-specific immunoglobulin E was undetectable by ELISA or skin testing in any of the recipient rats after adoptive transfer. In conclusion, antigen-induced airway bronchoconstriction and eosinophilia were successfully transferred by antigen-specific W3/25+ T cells in Brown Norway rats. These responses were dependent on antigen-primed W3/25+ T cells and appeared to be independent of IgE-mediated mast cell activation. This study provides clear evidence for T cell mediated immune mechanisms in allergic airway responses in this experimental model.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7657805      PMCID: PMC185752          DOI: 10.1172/JCI118165

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  39 in total

1.  Immunoenzymatic labeling of monoclonal antibodies using immune complexes of alkaline phosphatase and monoclonal anti-alkaline phosphatase (APAAP complexes).

Authors:  J L Cordell; B Falini; W N Erber; A K Ghosh; Z Abdulaziz; S MacDonald; K A Pulford; H Stein; D Y Mason
Journal:  J Histochem Cytochem       Date:  1984-02       Impact factor: 2.479

2.  Antigen and antibody detection by in vivo methods; a reevaluation of passive cutaneous anaphylactic reactions.

Authors:  N Watanabe; Z Ovary
Journal:  J Immunol Methods       Date:  1977       Impact factor: 2.303

3.  Late bronchial obstructive reaction to experimental inhalation of house dust extract.

Authors:  H Booij-Noord; K de Vries; H J Sluiter; N G Orie
Journal:  Clin Allergy       Date:  1972-03

4.  Bronchoalveolar eosinophilia during allergen-induced late asthmatic reactions.

Authors:  J G De Monchy; H F Kauffman; P Venge; G H Koëter; H M Jansen; H J Sluiter; K De Vries
Journal:  Am Rev Respir Dis       Date:  1985-03

5.  T cell lines mediating experimental autoimmune uveoretinitis (EAU) in the rat.

Authors:  R R Caspi; F G Roberge; C G McAllister; M el-Saied; T Kuwabara; I Gery; E Hanna; R B Nussenblatt
Journal:  J Immunol       Date:  1986-02-01       Impact factor: 5.422

6.  The recirculating lymphocyte pool of the rat: a systematic description of the migratory behaviour of recirculating lymphocytes.

Authors:  M E Smith; W L Ford
Journal:  Immunology       Date:  1983-05       Impact factor: 7.397

7.  Correlation between the myotropic activity of leukotriene A4 on guinea-pig lung, trachea and ileum and its biotransformation in situ.

Authors:  P Sirois; Y Brousseau; H Salari; P Borgeat
Journal:  Prostaglandins       Date:  1985-07

8.  The requirement for polymorphonuclear leukocytes in the late asthmatic response and heightened airways reactivity in an animal model.

Authors:  K R Murphy; M C Wilson; C G Irvin; L S Glezen; W R Marsh; C Haslett; P M Henson; G L Larsen
Journal:  Am Rev Respir Dis       Date:  1986-07

9.  Transfer of experimental autoimmune thyroiditis with T cell clones.

Authors:  C G Romball; W O Weigle
Journal:  J Immunol       Date:  1987-02-15       Impact factor: 5.422

10.  T cell subsets in allergic respiratory disease using monoclonal antibodies.

Authors:  P Engel; J Huguet; J Sanosa; P Sierra; N Cols; P A García-Calderón
Journal:  Ann Allergy       Date:  1984-10
View more
  22 in total

1.  Adoptive transfer of allergen-specific CD4+ T cells induces airway inflammation and hyperresponsiveness in brown-Norway rats.

Authors:  A Haczku; P Macary; T J Huang; H Tsukagoshi; P J Barnes; A B Kay; D M Kemeny; K F Chung; R Moqbel
Journal:  Immunology       Date:  1997-06       Impact factor: 7.397

2.  Expression of Th-2 cytokines interleukin-4 and -5 and of Th-1 cytokine interferon-gamma in ovalbumin-exposed sensitized Brown-Norway rats.

Authors:  A Haczku; P Macary; E B Haddad; T J Huang; D M Kemeny; R Moqbel; K F Chung
Journal:  Immunology       Date:  1996-06       Impact factor: 7.397

Review 3.  The role of the T follicular helper cells in allergic disease.

Authors:  D M Kemeny
Journal:  Cell Mol Immunol       Date:  2012-08-20       Impact factor: 11.530

4.  Inhibitory effects of endogenous and exogenous interferon-gamma on bronchial hyperresponsiveness, allergic inflammation and T-helper 2 cytokines in Brown-Norway rats.

Authors:  T J Huang; P A MacAry; T Wilke; D M Kemeny; K F Chung
Journal:  Immunology       Date:  1999-10       Impact factor: 7.397

5.  Systemic mycobacterial infection inhibits antigen-specific immunoglobulin E production, bronchial mucus production and eosinophilic inflammation induced by allergen.

Authors:  X Yang; S Wang; Y Fan; L Zhu
Journal:  Immunology       Date:  1999-11       Impact factor: 7.397

6.  Construction of a Der p2-transgenic plant for the alleviation of airway inflammation.

Authors:  C C Lee; H Ho; K T Lee; S T Jeng; B L Chiang
Journal:  Cell Mol Immunol       Date:  2011-05-23       Impact factor: 11.530

7.  Antigen-specific CD4+ T cells drive airway smooth muscle remodeling in experimental asthma.

Authors:  David Ramos-Barbón; John F Presley; Qutayba A Hamid; Elizabeth D Fixman; James G Martin
Journal:  J Clin Invest       Date:  2005-05-02       Impact factor: 14.808

8.  Effect of CD8+ T-cell depletion on bronchial hyper-responsiveness and inflammation in sensitized and allergen-exposed Brown-Norway rats.

Authors:  T J Huang; P A MacAry; D M Kemeny; K F Chung
Journal:  Immunology       Date:  1999-03       Impact factor: 7.397

Review 9.  Airway remodeling: lessons from animal models.

Authors:  David Ramos-Barbón; Mara S Ludwig; James G Martin
Journal:  Clin Rev Allergy Immunol       Date:  2004-08       Impact factor: 8.667

10.  Requirements for allergen-induced airway hyperreactivity in T and B cell-deficient mice.

Authors:  D B Corry; G Grünig; H Hadeiba; V P Kurup; M L Warnock; D Sheppard; D M Rennick; R M Locksley
Journal:  Mol Med       Date:  1998-05       Impact factor: 6.354

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.