Interferon-alpha drives T cell-mediated immunopathology in the intestine
Interferon-alpha drives T cell-mediated immunopathology in the intestine
The ability of interferon (IFN)-alpha to induce autoimmunity and exacerbate Th1 diseases is well known. We have recently described enhanced expression of IFN-alpha in the mucosa of patients with celiac disease (CD), a gluten-sensitive Th1-mediated enteropathy, characterized by villous atrophy and crypt cell hyperplasia. Previous studies from this laboratory have shown that T cell activation in explant cultures of human fetal gut can also result in villous atrophy and crypt cell hyperplasia. We have, therefore, examined changes that take place in explant cultures of human fetal gut after activation of T cells with anti-CD3 and/or IFN-alpha. We show that activation of T cells with anti-CD3 alone elicits a small IFN-gamma and TNF-alpha response with no tissue injury. Similarly, no changes are seen in explants cultured with IFN-alpha alone. However, addition of IFN-alpha with anti-CD3 results in enhanced Th1 response and crypt cell hyperplasia. This is associated with enhanced phosphorylation of STAT1, STAT3, and Fyn, a Src homology tyrosine kinase, which interacts with both TCR and IFN-alpha signal components. Together these data indicate that IFN-alpha can facilitate activation of Th1-reactive cells in the gut and drive immunopathology.
IFN-?, STAT, celiac disease
2247-2255
Monteleone, Giovanni
a289342b-54b5-414a-9e06-aa6b052f91b2
Pender, Sylvia L. F.
62528b03-ec42-41bb-80fe-48454c2c5242
Wathen, Neville C.
352e9a51-ce7a-42e4-9a2a-f3ff270f96b8
MacDonald, Thomas T.
a6bde8a9-acc4-4128-851f-dd5dbfe28816
2001
Monteleone, Giovanni
a289342b-54b5-414a-9e06-aa6b052f91b2
Pender, Sylvia L. F.
62528b03-ec42-41bb-80fe-48454c2c5242
Wathen, Neville C.
352e9a51-ce7a-42e4-9a2a-f3ff270f96b8
MacDonald, Thomas T.
a6bde8a9-acc4-4128-851f-dd5dbfe28816
Abstract
The ability of interferon (IFN)-alpha to induce autoimmunity and exacerbate Th1 diseases is well known. We have recently described enhanced expression of IFN-alpha in the mucosa of patients with celiac disease (CD), a gluten-sensitive Th1-mediated enteropathy, characterized by villous atrophy and crypt cell hyperplasia. Previous studies from this laboratory have shown that T cell activation in explant cultures of human fetal gut can also result in villous atrophy and crypt cell hyperplasia. We have, therefore, examined changes that take place in explant cultures of human fetal gut after activation of T cells with anti-CD3 and/or IFN-alpha. We show that activation of T cells with anti-CD3 alone elicits a small IFN-gamma and TNF-alpha response with no tissue injury. Similarly, no changes are seen in explants cultured with IFN-alpha alone. However, addition of IFN-alpha with anti-CD3 results in enhanced Th1 response and crypt cell hyperplasia. This is associated with enhanced phosphorylation of STAT1, STAT3, and Fyn, a Src homology tyrosine kinase, which interacts with both TCR and IFN-alpha signal components. Together these data indicate that IFN-alpha can facilitate activation of Th1-reactive cells in the gut and drive immunopathology.
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Published date: 2001
Keywords:
IFN-?, STAT, celiac disease
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Local EPrints ID: 27275
URI: http://eprints.soton.ac.uk/id/eprint/27275
ISSN: 0014-2980
PURE UUID: 96415d18-541f-40e5-ae87-ff6aa8c2d5a4
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Date deposited: 27 Apr 2006
Last modified: 16 Mar 2024 03:19
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Author:
Giovanni Monteleone
Author:
Neville C. Wathen
Author:
Thomas T. MacDonald
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