Literature DB >> 10967018

Adenoids provide a microenvironment for the generation of CD4(+), CD45RO(+), L-selectin(-), CXCR4(+), CCR5(+) T lymphocytes, a lymphocyte phenotype found in the middle ear effusion.

P S Mattila1, A Nykänen, M Eloranta, J Tarkkanen.   

Abstract

Adenoidectomy in children with otitis media with effusion reduces inflammation in the middle ear by an unknown mechanism. Potentially, the adenoids of these children may serve as a site for the differentiation of lymphocytes, which after entering blood circulation eventually extravasate in the middle ear mucosa and thereby contribute to excessive inflammation. During lymphocyte extravasation various adhesion molecules and chemokines play a crucial role. To evaluate possible connections between the adenoids and middle ear inflammation, the expression of the chemokine receptors CXCR4 and CCR5 and the lymphocyte homing receptor L-selectin were analyzed in adenoidal and middle ear lymphocytes. It was found that most CD4(+) T lymphocytes in the middle ear effusion express the memory phenotype marker CD45RO and the chemokine receptors CXCR4 and CCR5, but are negative for the lymphocyte homing receptor L-selectin. This cell phenotype was rare in peripheral blood but was found much more frequently in the adenoids. The results suggest that the adenoids provide a microenvironment for the generation for CD4(+), CD45RO(+), L-selectin(-), CXCR4(+) and CCR5(+) T lymphocytes. Further, these cells may include cells that have the capacity to home to the middle ear mucosa. As the adenoidal CD4(+) memory phenotype CD45RO(+) T cells expressed the activation antigen CD69 and included cells expressing the HIV co-receptors CXCR4 and CCR5 at a high level, they may be permissive for HIV infection.

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Year:  2000        PMID: 10967018     DOI: 10.1093/intimm/12.9.1235

Source DB:  PubMed          Journal:  Int Immunol        ISSN: 0953-8178            Impact factor:   4.823


  5 in total

Review 1.  Cellular immune response in young children accounts for recurrent acute otitis media.

Authors:  Sharad K Sharma; Michael E Pichichero
Journal:  Curr Allergy Asthma Rep       Date:  2013-10       Impact factor: 4.806

2.  Reduced memory CD4+ T-cell generation in the circulation of young children may contribute to the otitis-prone condition.

Authors:  Sharad K Sharma; Janet R Casey; Michael E Pichichero
Journal:  J Infect Dis       Date:  2011-08-15       Impact factor: 5.226

3.  HIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutants.

Authors:  Michael T Cheeseman; Hayley E Tyrer; Debbie Williams; Tertius A Hough; Paras Pathak; Maria R Romero; Helen Hilton; Sulzhan Bali; Andrew Parker; Lucie Vizor; Tom Purnell; Kate Vowell; Sara Wells; Mahmood F Bhutta; Paul K Potter; Steve D M Brown
Journal:  PLoS Genet       Date:  2011-10-20       Impact factor: 5.917

Review 4.  Prevention of otitis media caused by viral upper respiratory tract infection: vaccines, antivirals, and other approaches.

Authors:  William J Doyle; Cuneyt M Alper
Journal:  Curr Allergy Asthma Rep       Date:  2003-07       Impact factor: 4.806

5.  The Etiology, Pathophysiology, and Management of Otitis Media with Effusion.

Authors:  Christopher C. Butler; R. Gareth Williams
Journal:  Curr Infect Dis Rep       Date:  2003-06       Impact factor: 3.725

  5 in total

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