Targeting CD4+ T cells for the treatment of sarcoidosis: a promising strategy?

被引:0
|
作者
Celada, Lindsay J. [1 ]
Drake, Wonder P. [1 ,2 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Med, Div Infect Dis, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Pathol Microbiol & Immunol, Sch Med, Nashville, TN 37232 USA
关键词
anti-CD20; therapy; corticosteroids; granuloma; sarcoidosis; T helper cells; TNF-alpha antagonists; ACTIVE PULMONARY SARCOIDOSIS; INTERFERON-GAMMA PRODUCTION; NECROSIS-FACTOR-ALPHA; MYCOBACTERIAL CATALASE-PEROXIDASE; ADAPTIVE IMMUNE-RESPONSE; BLOOD MONONUCLEAR-CELLS; LUNG LYMPHOCYTES-T; SYSTEMIC SARCOIDOSIS; INFLIXIMAB THERAPY; PERIPHERAL-BLOOD;
D O I
10.2217/IMT.14.103
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Sarcoidois is an inflammatory disease of unknown origin characterized by the abnormal accumulation of noncaseating granulomas at sites of disease activity in multiple organs throughout the body with a predilection for the lungs. Because the exact trigger that leads to disease activity is still under investigation, current treatment options are contingent on the organ or organs affected. Corticosteroids are the therapy of choice, but antimalarials and TNF-alpha antagonists are also commonly prescribed. Recent findings provide evidence for the use of CD20 B-cell-depleting therapy as an alternative method of choice. However, because sarcoidosis is predominantly a T-helper cell-driven disorder, an overwhelming amount of compelling evidence exists for the use of CD4(+) T-cell targeted therapy.
引用
收藏
页码:57 / 66
页数:10
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