Abstract |
Advances in the past two decades have resulted in the recognition of several tumefactive pancreatic lesions that, on histologic evaluation, show a varying combination of inflammation and fibrosis. Autoimmune pancreatitis, the prototypic tumefactive pancreatic fibroinflammatory lesion, is composed of two distinct diseases, type 1 autoimmune pancreatitis and the less common type 2 autoimmune pancreatitis. Although designated as autoimmune pancreatitis, the two diseases show little morphologic or pathogenic overlap. In type 1 disease, subsets of T lymphocytes (type 2 helper T cells, regulatory T cells, and T follicular helper 2 cells) are hypothesized to drive the inflammatory reaction. The B-cell response is characterized by an oligoclonal expansion of plasmablasts, with dominant clones that vary among patients and distinct clones that emerge at the time of relapse. Although the precise role of IgG4 in this condition remains uncertain, recent studies suggest that other IgG subclasses (eg, IgG1) may mediate the immune reactions, whereas IgG4 represents a response to dampen excessive inflammation. A recent study of type 2 autoimmune pancreatitis highlights the role of CXCL8 (alias IL-8), with duct epithelium and infiltrating T lymphocytes expressing this chemokine; the latter may contribute to the distinct form of neutrophilic inflammation in this disease. The review also highlights other forms of mass-forming chronic pancreatitis: follicular pancreatitis, groove pancreatitis, and those associated with rheumatologic diseases.
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Authors | Yoh Zen, Vikram Deshpande |
Journal | The American journal of pathology
(Am J Pathol)
Vol. 189
Issue 1
Pg. 82-93
(01 2019)
ISSN: 1525-2191 [Electronic] United States |
PMID | 30558726
(Publication Type: Journal Article, Review)
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Copyright | Copyright © 2019 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved. |
Chemical References |
- Antibodies, Neoplasm
- CXCL8 protein, human
- Immunoglobulin G
- Interleukin-8
- Neoplasm Proteins
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Topics |
- Antibodies, Neoplasm
(blood, immunology)
- Autoimmune Diseases
(blood, immunology, pathology)
- Carcinoma, Pancreatic Ductal
(blood, immunology, pathology)
- Fibrosis
- Humans
- Immunoglobulin G
(blood, immunology)
- Inflammation
(blood, immunology, pathology)
- Interleukin-8
(blood, immunology)
- Neoplasm Proteins
(blood, immunology)
- Pancreatic Neoplasms
(blood, immunology, pathology)
- Pancreatitis, Chronic
(blood, immunology, pathology)
- Plasma Cells
(immunology, metabolism, pathology)
- T-Lymphocytes, Regulatory
(immunology, metabolism, pathology)
- Th2 Cells
(immunology, metabolism, pathology)
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