Takayasu's arteritis pathophysiology: Difference between revisions
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* [[Cell-mediated immunity|Cell-mediated]] mechanisms are considered as a main pathogenesis mechanism of Takayasu's arteritis and it is similar to [[giant cell arteritis]]. | * [[Cell-mediated immunity|Cell-mediated]] mechanisms are considered as a main pathogenesis mechanism of Takayasu's arteritis and it is similar to [[giant cell arteritis]]. | ||
* This [[inflammation]] leads to arterial [[stenosis]], [[thrombosis]], and [[Aneurysm|aneurysms]]. | * This [[inflammation]] leads to arterial [[stenosis]], [[thrombosis]], and [[Aneurysm|aneurysms]]. | ||
* | * Irregular [[fibrosis]] of the [[Blood vessel|blood vessels]] due to chronic [[vasculitis]] may lead to [[Tunica intima|intimal]] [[fibrosis]]. | ||
* | * There are three factors that have associated with disease susceptibility, development and progression: | ||
** Relationship to [[tuberculosis]] (TB) | ** Relationship to [[tuberculosis]] (TB) | ||
** [[Genetics|Genetic]] influences | ** [[Genetics|Genetic]] influences | ||
** [[Immunology|Immunologic]] mechanisms | ** [[Immunology|Immunologic]] mechanisms | ||
'''Relationship to tuberculosis (TB)''' | '''Relationship to tuberculosis (TB)''' | ||
* It has been suggested that Takayasu arteritis is associated with TB. Following are evidences which support this hypothesis:<ref name="pmid12655">{{cite journal |vauthors=Lupi-Herrera E, Sánchez-Torres G, Marcushamer J, Mispireta J, Horwitz S, Vela JE |title=Takayasu's arteritis. Clinical study of 107 cases |journal=Am. Heart J. |volume=93 |issue=1 |pages=94–103 |date=January 1977 |pmid=12655 |doi= |url=}}</ref> | |||
[[Granulomatous]] inflammation with the Langhans-type of [[giant cells]] in many cases of Takayasu arteritis | ** [[Granulomatous]] inflammation with the Langhans-type of [[giant cells]] in many cases of Takayasu arteritis | ||
** Intermittent coexistence of Takayasu arteritis with [[Lung|pulmonary]] and [[extrapulmonary tuberculosis]] | |||
** [[Hypersensitivity]] to the [[tuberculosis]] organism | |||
'''Genetic influences''' | '''Genetic influences''' | ||
* Geographic distribution of Takayasu arteritis, with high [[prevalence]] in Japan and Korea, suggests that [[Genetics|genetic]] factors are probably play a role in the [[pathogenesis]] of Takayasu arteritis. | |||
* Takayasu arteritis has been associated with different [[human leukocyte antigen]] ([[Human leukocyte antigen|HLA]]) [[Allele|alleles]] in different populations. In Japan and Korea, there is a clear association with the extended haplotype:<ref name="pmid10980348">{{cite journal |vauthors=Salazar M, Varela A, Ramirez LA, Uribe O, Vasquez G, Egea E, Yunis EJ, Iglesias-Gamarra A |title=Association of HLA-DRB1*1602 and DRB1*1001 with Takayasu arteritis in Colombian mestizos as markers of Amerindian ancestry |journal=Int. J. Cardiol. |volume=75 Suppl 1 |issue= |pages=S113–6 |date=August 2000 |pmid=10980348 |doi= |url=}}</ref> | |||
* Takayasu arteritis has been associated with different [[ | ** | ||
'''Immunologic mechanisms''' | '''Immunologic mechanisms''' | ||
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== Associations == | == Associations == | ||
* The most important conditions associated with Takayasu's arteritis include: | * The most important conditions associated with Takayasu's arteritis include: | ||
** [[Ankylosing spondylitis]] | ** [[Ankylosing spondylitis]] | ||
** [[Inflammatory bowel disease]](IBD) | ** [[Inflammatory bowel disease]] (IBD) | ||
** [[Behçet's disease|Behçet's syndrome]] | ** [[Behçet's disease|Behçet's syndrome]] | ||
== Gross pathology == | == Gross pathology == | ||
On gross pathology characteristic findings of Takayasu's arteritis are as follow:<ref name="pmid10980333">{{cite journal |vauthors=Gravanis MB |title=Giant cell arteritis and Takayasu aortitis: morphologic, pathogenetic and etiologic factors |journal=Int. J. Cardiol. |volume=75 Suppl 1 |issue= |pages=S21–33; discussion S35–6 |date=August 2000 |pmid=10980333 |doi= |url=}}</ref> | On gross pathology characteristic findings of Takayasu's arteritis are as follow:<ref name="pmid10980333">{{cite journal |vauthors=Gravanis MB |title=Giant cell arteritis and Takayasu aortitis: morphologic, pathogenetic and etiologic factors |journal=Int. J. Cardiol. |volume=75 Suppl 1 |issue= |pages=S21–33; discussion S35–6 |date=August 2000 |pmid=10980333 |doi= |url=}}</ref> | ||
* | * Stiff and rigid [[aorta]] on [[palpation]] | ||
* | * Gelatinous appearance of thickened [[adventitia]] | ||
* | * Enlarged [[Paraaortic lymph node|para-aortic]] [[Lymph node|lymph nodes]] in the area of [[Renal artery|renal]] and [[Subclavian artery|subclavian arteries]] | ||
* | * [[Glycosaminoglycan|<nowiki/><nowiki/>]]Sharp line of demarcation between normal and diseased segments[[Glycosaminoglycan|<nowiki/><nowiki/>]] | ||
== Microscopic pathology == | == Microscopic pathology == | ||
On microscopic histopathological analysis characteristic findings of Takayasu's arteritis are as follow:<ref name="pmid10980333" /> | On microscopic histopathological analysis characteristic findings of Takayasu's arteritis are as follow:<ref name="pmid10980333" /> | ||
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Farnaz Khalighinejad, MD [2]
Overview
The pathogenesis of Takayasu's arteritis is poorly understood. Takayasu's arteritis characterized by segmental and patchy granulomatous inflammation of the aorta and its major derivative branches.This inflammation leads to arterial stenosis, thrombosis, and aneurysms. Three factors that have been suggested to have association with susceptibility, development and progression of Takayasu's arteritis are genetic influences, immunologic mechanisms and relationship to tuberculosis.
Pathophysiology
- The pathogenesis of Takayasu's arteritis is poorly understood.[1]
- Granulomatous inflammation of the aorta and its major branches might lead to Takayasu's arteritis.
- Cell-mediated mechanisms are considered as a main pathogenesis mechanism of Takayasu's arteritis and it is similar to giant cell arteritis.
- This inflammation leads to arterial stenosis, thrombosis, and aneurysms.
- Irregular fibrosis of the blood vessels due to chronic vasculitis may lead to intimal fibrosis.
- There are three factors that have associated with disease susceptibility, development and progression:
- Relationship to tuberculosis (TB)
- Genetic influences
- Immunologic mechanisms
Relationship to tuberculosis (TB)
- It has been suggested that Takayasu arteritis is associated with TB. Following are evidences which support this hypothesis:[2]
- Granulomatous inflammation with the Langhans-type of giant cells in many cases of Takayasu arteritis
- Intermittent coexistence of Takayasu arteritis with pulmonary and extrapulmonary tuberculosis
- Hypersensitivity to the tuberculosis organism
Genetic influences
- Geographic distribution of Takayasu arteritis, with high prevalence in Japan and Korea, suggests that genetic factors are probably play a role in the pathogenesis of Takayasu arteritis.
- Takayasu arteritis has been associated with different human leukocyte antigen (HLA) alleles in different populations. In Japan and Korea, there is a clear association with the extended haplotype:[3]
Immunologic mechanisms
Because of rheumatic-type complaints in many Takayasu arteritis patients, the relationship between Takayasu arteritis and autoimmune and collagen vascular disorders has been suggested.
- Immunohistopathologic examination has shown that the infiltrating cells in aortic tissue mainly consist of killer cells, especially gamma delta T lymphocytes.
- These cells may cause vascular injury by releasing large amounts of the cytolytic compound perforin.
- Seko et al have reported that γδT cells, αβT cells (CD4 and CD8), and natural killer cells play an important role in the vascular injury.[4]
- No specific autoantigens have yet been identified.
Associations
- The most important conditions associated with Takayasu's arteritis include:
Gross pathology
On gross pathology characteristic findings of Takayasu's arteritis are as follow:[5]
- Stiff and rigid aorta on palpation
- Gelatinous appearance of thickened adventitia
- Enlarged para-aortic lymph nodes in the area of renal and subclavian arteries
- Sharp line of demarcation between normal and diseased segments
Microscopic pathology
On microscopic histopathological analysis characteristic findings of Takayasu's arteritis are as follow:[5]
- Inflammation around the vasa vasorum and at the medio-adventitial junction
- Edema of the media and adventitia
- Giant cell granulomatous reaction
- Laminar necrosis
- Fragmentation of elastic fibers
- Rapid or more severe inflammation leads to:
- Loss of smooth muscle cells
- Medial weakening
- Vascular dilatation
- Aneurysm formation
References
- ↑ Inder SJ, Bobryshev YV, Cherian SM, Wang AY, Lord RS, Masuda K, Yutani C (March 2000). "Immunophenotypic analysis of the aortic wall in Takayasu's arteritis: involvement of lymphocytes, dendritic cells and granulocytes in immuno-inflammatory reactions". Cardiovasc Surg. 8 (2): 141–8. PMID 10737351.
- ↑ Lupi-Herrera E, Sánchez-Torres G, Marcushamer J, Mispireta J, Horwitz S, Vela JE (January 1977). "Takayasu's arteritis. Clinical study of 107 cases". Am. Heart J. 93 (1): 94–103. PMID 12655.
- ↑ Salazar M, Varela A, Ramirez LA, Uribe O, Vasquez G, Egea E, Yunis EJ, Iglesias-Gamarra A (August 2000). "Association of HLA-DRB1*1602 and DRB1*1001 with Takayasu arteritis in Colombian mestizos as markers of Amerindian ancestry". Int. J. Cardiol. 75 Suppl 1: S113–6. PMID 10980348.
- ↑ Seko Y, Takahashi N, Tada Y, Yagita H, Okumura K, Nagai R (August 2000). "Restricted usage of T-cell receptor Vgamma-Vdelta genes and expression of costimulatory molecules in Takayasu's arteritis". Int. J. Cardiol. 75 Suppl 1: S77–83, discussion S85–7. PMID 10980341.
- ↑ 5.0 5.1 Gravanis MB (August 2000). "Giant cell arteritis and Takayasu aortitis: morphologic, pathogenetic and etiologic factors". Int. J. Cardiol. 75 Suppl 1: S21–33, discussion S35–6. PMID 10980333.