Immunopathology & Immunotherapy
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Immunopathology & Immunotherapy
Latest advances in immunopathology diagnosis and treatment
Curated by Alfredo Corell
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New strategies in improve mucosal vaccines against tuberculosis

New strategies in improve mucosal vaccines against tuberculosis | Immunopathology & Immunotherapy | Scoop.it

Mucosal Immunology advance online publication 9 January 2013; doi: 10.1038/mi.2012.135

Interleukin-17-dependent CXCL13 mediates mucosal vaccine–induced immunity against tuberculosis

R Gopal1, J Rangel-Moreno2, S Slight1, Y Lin1, H F Nawar3, B A Fallert Junecko4, T A Reinhart4, J Kolls5, T D Randall2,6, T D Connell3 and S A Khader1

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Mucosal immunology: Infection induces friendly fire | Nature 04 October

Mucosal immunology: Infection induces friendly fire | Nature 04 October | Immunopathology & Immunotherapy | Scoop.it

David Masopust & Vaiva Vezys

Nature 490,41–43 (04 October 2012) doi:10.1038/490041a

 

Our immune system usually ignores 'friendly' gut bacteria. But when infection with a pathogen damages the intestine's mucosal lining, the resident microbes can invade the body, inducing immune responses directed at themselves.

 

More on: http://www.nature.com/nature/journal/v490/n7418/full/490041a.html

 

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The intestinal B-cell response in celiac disease | Frontiers in Mucosal Immunity

The intestinal B-cell response in celiac disease | Frontiers in Mucosal Immunity | Immunopathology & Immunotherapy | Scoop.it

Mesin L, Sollid LM and Di Niro R (2012) The intestinal B-cell response in celiac disease. Front. Immun. 3:313. doi: 10.3389/fimmu.2012.00313

 

The function of intestinal immunity is to provide protection toward pathogens while preserving the composition of the microflora and tolerance to orally fed nutrients. This is achieved via a number of tightly regulated mechanisms including production of IgA antibodies by intestinal plasma cells. Celiac disease is a common gut disorder caused by a dysfunctional immune regulation as signified, among other features, by a massive intestinal IgA autoantibody response. Here we review the current knowledge of this B-cell response and how it is induced, and we discuss key questions to be addressed in future research....

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Topographical distribution and characterization of epithelial cells and intraepithelial lymphocytes in the human ocular mucosa. [Mucosal Immunol. 2012] - PubMed - NCBI

Topographical distribution and characterization of epithelial cells and intraepithelial lymphocytes in the human ocular mucosa. [Mucosal Immunol. 2012] - PubMed - NCBI | Immunopathology & Immunotherapy | Scoop.it

The conjunctiva plays a key role in the protection of the ocular surface by initiating and regulating immune responses. In this study, we analyze the relative proportion of intraepithelial lymphocytes (IELs), apoptotic cells, and proliferative state in three different topographical regions of the normal human conjunctiva. Superior tarsal, superior bulbar, and inferior tarsal-bulbar-fornical conjunctival cells were collected by brush cytology from 63 healthy donors. Flow cytometry analysis showed higher levels of CD3⁺ and CD8⁺ IELs in both upper tarsal and bulbar conjunctiva than in the inferior tarsal-bulbar-fornix, where the CD19⁺ B cells were increased. For all zones two different cell populations (by cell size and complexity) were present in the apoptosis assay. The more complex cells were reduced within the inferior tarsal-bulbar-fornix when compared with the superior bulbar and tarsal areas. Less complex cells were more predominant in the inferior conjunctiva and were mainly alive. The mean proliferation index of the conjunctival epithelium was significantly lower in the superior bulbar conjunctiva than in superior tarsal and inferior fornical conjunctivas. These findings suggest that each topographical zone from normal human conjunctiva has a unique profile of immunophenotype, viability, and proliferative state that could be related to a differentiated regional functionality.

 

Complete article at Mucosal Immunology Site:

http://www.nature.com/mi/journal/v5/n4/full/mi201227a.html

 

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