Immune hallmarks of rheumatoid arthritis management: A brief review

被引:7
|
作者
Peixoto, Rephany Fonseca [1 ]
Rodrigues, Carlos Ewerton Maia [2 ,3 ]
Palmeira, Pedro Henrique de Sousa [1 ]
dos Santos, Fernando Cezar Comberlang Queiroz Davis [1 ]
Lima, Tatjana Keesen de Souza [1 ]
Braz, Alessandra de Sousa [4 ]
机构
[1] Univ Fed Paraiba, Dept Cellular & Mol Biol, Lab Immunol Infect Dis, BR-58051900 Joao Pessoa, PB, Brazil
[2] Univ Fortaleza Unifor, Med Sch, Postgrad Program Med Sci, Fortaleza, Brazil
[3] Univ Fed Ceara, Dept Internal Med, Fortaleza, Brazil
[4] Univ Fed Paraiba, Med Sci Ctr, BR-58051900 Joao Pessoa, PB, Brazil
关键词
Autoimmunity; Rheumatoid arthritis; Autoantibodies; Inflammation; Therapeutic drugs; Immunomodulation; T-CELLS; B-CELLS; TNF-ALPHA; THERAPY; RITUXIMAB; SUPPRESSION; ABATACEPT; IL-6; IMMUNOPATHOGENESIS; SUBSETS;
D O I
10.1016/j.cyto.2022.156007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The purpose of this review was to examine current evidence on immunomodulation mediated by conventional drugs and the use of novel biological agents for the treatment of rheumatoid arthritis (RA). Currently, treatment is focused on maximizing quality of life through sustained clinical remission and/or attenuating disease activity. To do so, disease-modifying antirheumatic drugs, especially methotrexate, are used alone or in combination with other drugs, including leflunomide, biological disease-modifying antirheumatic drugs (bDMARDs) and targeted synthetic disease-modifying antirheumatic drugs (tsDMARDs). The most recent strategies modulate the immune response of the individual RA patient using tsDMARDs such as JAK inhibitors and bDMARDs such as ig-CTLA-4, anti-IL6R, anti-TNF-alpha and anti-CD20. To better understand current immunopharmacological interventions, we also looked at documented mechanisms of RA-mediated immunomodulation, highlighting perspectives poten-tially boosting RA treatment.
引用
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页数:10
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