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Printable Handouts
Navigable Slide Index
- Introduction
- Sjögren's syndrome - Autoimmune Epithelitis
- Sjögren’s syndrome
- Autoimmune rheumatic diseases
- Immunopathology
- Autoantibodies to cellular autoantigens
- Autoantibodies & clinical associations (1)
- Autoantibodies & clinical associations (2)
- High heterogeneity (1)
- Clinical manifestations (1)
- Clinical manifestations (2)
- Wide clinical spectrum - autoimmune epithelitis
- Autoimmune lesion
- Autoimmune lesion: cytokines
- Antigen-driven autoimmune response
- The salivary glands and autoantibody production
- Central role of epithelial cells - main findings
- Clinical manifestations (3)
- Peri-epithelial vs extra-epithelial
- High heterogeneity (2)
- Autoimmune MSG lesions (1)
- Autoimmune MSG lesions (2)
- Germinal centers
- B cell disturbances
- Heterogeneous B-cell population
- High heterogeneity (3)
- Outcome
- Wide clinical spectrum
- Mortality in SS with or without lymphoma
- Malignant lymphoma
- Clinical characteristics of lymphoma
- MALT lymphoma - extranodal involvement
- Clinical risk factors
- Serological / hematological markers
- Histological markers: minor salivary glands (1)
- Histological markers: minor salivary glands (2)
- Predictors of lymphoma development in SS
- Adverse prognostic factors
- High heterogeneity (4)
- Biologic treatments
- Targeted treatments (1)
- Targeted treatments (2)
- Studies: failure to conclude
- Definition
- Mission
- Biomarkers (1)
- microRNAs (miRNAs)
- miR200b miRNAs
- miR200b-5p expression in MSGs (1)
- miR200b-5p expression in MSGs (2)
- Biomarkers (2)
- We might be more efficient if…
- HarmonicSS
- The consortium
- Harmonization process
- A conceptual step-wise categorization
- From biomarkers to precision medicine
- Acknowledgements
Topics Covered
- Introduction to Sjögren's syndrome
- Humoral and cellular autoimmune responses in Sjögren's syndrome
- Description of heterogenic clinical features of disease
- Pathogenetic/immunopathologic aspects and associations with clinical phenotypes
- The need for precise therapeutic approaches
- Development and features of lymphoma in Sjögren's syndrome
- Risk factors for development of severe disease
- Biomarkers for disease severity, outcome and lymphoma
Links
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Therapeutic Areas:
Talk Citation
Tzioufas, A.G. (2018, November 29). Sjögren's syndrome: current knowledge and future prospects [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 21, 2024, from https://doi.org/10.69645/UTHJ4820.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Athanasios G. Tzioufas has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Sjögren's syndrome: current knowledge and future prospects
Published on November 29, 2018
44 min
A selection of talks on Immunology
Transcript
Please wait while the transcript is being prepared...
0:00
My name is Athanasios Tzioufas.
I'm Professor of Medicine and Rheumatology in
the department of Pathophysiology in the School of Medicine in Athens.
My mission today is to present
our current knowledge and future prospects on Sjogren's syndrome.
0:16
Sjogren's syndrome or also called autoimmune epithelitis is
a common disease since it affects 0.5 to one percent of adult females.
As you see, there are nine females
versus one male that they are affected from the disease.
As you will see in the next slides,
it has a wide clinical spectrum including
organ-specific disease affecting only the excrete glands.
It can be in the form of systemic disease,
and finally some patients,
around five percent, may end by developing non-Hodgkin's B-cell lymphoma.
Sjogren's syndrome has an easy lesion to be studied that is the minor salivary glands.
It can be taken without significant morbidity from patients.
By studying this lesion,
it can also share as a paradigm for other autoimmune disorders.
1:17
Sjogren's syndrome is a disease that affects ladies,
as I told you previously,
particularly in the middle ages.
You see in the slide that with the red dot line,
the disease is appear usually in the middle ages,
I told you, the peak around the middle age of 50's,
but the onset of the disease come several years earlier.
There are also some clinical forms of the disease,
as you see here,
that is normal individuals that they may
have autoantibodies of Sjogren's syndrome before the disease develop.
So, between the onset of symptoms at diagnosis,
they are usually seven years elapsed.