Literature DB >> 12138061

Upregulated eotaxin expression and T cell infiltration in the basal and papillary epithelium in cows' milk associated reflux oesophagitis.

A M Butt1, S H Murch, C-L Ng, P Kitching, S M Montgomery, A D Phillips, J A Walker-Smith, M A Thomson.   

Abstract

BACKGROUND: Cows' milk sensitive reflux oesophagitis is an emerging clinical entity in children, normally indistinguishable from primary gastro-oesophageal reflux (GOR) apart from the response to dietary antigen exclusion. It is conjectural whether a tendency towards mucosal eosinophilia distinguishes this group from primary GOR. AIMS: To determine whether there may be differences in the mucosal lesion within the oesophagus in those children with reflux in association with cows' milk induced small bowel pathology, particularly in relation to the eosinophil chemokine eotaxin.
METHODS: A total of 29 children underwent endoscopic assessment, including nine with cows' milk sensitive enteropathy (CMSE) and associated GOR, seven histologically normal controls, six with primary GOR, and seven disease controls. Oesophageal biopsy specimens were examined immunohistochemically for the chemokines eotaxin and MCP-2, and T cell lineage and activation markers.
RESULTS: Strong upregulation of eotaxin expression, limited to basal and papillary epithelium, occurred in all CMSE patients. By contrast, weak expression was seen in a minority of controls and in 50% of primary GOR patients. Infiltration of CD3, CD4, and CD8 lymphocytes occurred in similar distribution in CMSE patients, significantly increased above controls. Significant upregulation of activation markers (CD25, HLA-DR) was also seen in the CMSE group within basal and papillary epithelium compared to controls and primary GOR.
CONCLUSION: Basal and papillary epithelial eotaxin expression, with focal lymphocyte activation, was seen in infants with CMSE associated GOR. This preliminary study provides early evidence to suggest a pathogenesis distinct from primary GOR, in which specific recruitment of T cells and eosinophils may contribute to oesophageal dysmotility.

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Year:  2002        PMID: 12138061      PMCID: PMC1719188          DOI: 10.1136/adc.87.2.124

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  29 in total

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2.  A pathological function for eotaxin and eosinophils in eosinophilic gastrointestinal inflammation.

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4.  Functional expression of the eotaxin receptor CCR3 in T lymphocytes co-localizing with eosinophils.

Authors:  B O Gerber; M P Zanni; M Uguccioni; M Loetscher; C R Mackay; W J Pichler; N Yawalkar; M Baggiolini; B Moser
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5.  Evaluation of T-lymphocytes in esophageal mucosal biopsies.

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7.  Eosinophilic esophagitis attributed to gastroesophageal reflux: improvement with an amino acid-based formula.

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8.  Intraepithelial eosinophils: a new diagnostic criterion for reflux esophagitis.

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9.  Th2-induced eotaxin expression and eosinophilia coexist with Th1 responses at the effector stage of lung inflammation.

Authors:  L Li; Y Xia; A Nguyen; L Feng; D Lo
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Authors:  P D Ponath; S Qin; D J Ringler; I Clark-Lewis; J Wang; N Kassam; H Smith; X Shi; J A Gonzalo; W Newman; J C Gutierrez-Ramos; C R Mackay
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1.  Eosinophilia in the upper gastrointestinal tract is not a characteristic feature in cow's milk sensitive gastro-oesophageal reflux disease. Measurement by two methodologies.

Authors:  R G Nielsen; C Fenger; C Bindslev-Jensen; S Husby
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3.  Low reproducibility of 2 x 24-hour continuous esophageal pH monitoring in infants and children: a limiting factor for interventional studies.

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Review 4.  Chemokines in eosinophil-associated gastrointestinal disorders.

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Journal:  Curr Allergy Asthma Rep       Date:  2004-01       Impact factor: 4.919

Review 5.  Lymphocytic esophagitis: Still an enigma a decade later.

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