The management of axial spondyloarthritis with cutting-edge therapies: advancements and innovations
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作者:
Lopalco, Giuseppe
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Univ Bari Aldo Moro, Dept Precis Regenerat Med & Ionian Area DiMePRe J, Piazza G Cesare 11, I-70124 Bari, ItalyUniv Bari Aldo Moro, Dept Precis Regenerat Med & Ionian Area DiMePRe J, Piazza G Cesare 11, I-70124 Bari, Italy
Lopalco, Giuseppe
[1
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Cito, Andrea
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Univ Bari Aldo Moro, Dept Precis Regenerat Med & Ionian Area DiMePRe J, Piazza G Cesare 11, I-70124 Bari, ItalyUniv Bari Aldo Moro, Dept Precis Regenerat Med & Ionian Area DiMePRe J, Piazza G Cesare 11, I-70124 Bari, Italy
Cito, Andrea
[1
]
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Venerito, Vincenzo
[1
]
Iannone, Florenzo
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Univ Bari Aldo Moro, Dept Precis Regenerat Med & Ionian Area DiMePRe J, Piazza G Cesare 11, I-70124 Bari, ItalyUniv Bari Aldo Moro, Dept Precis Regenerat Med & Ionian Area DiMePRe J, Piazza G Cesare 11, I-70124 Bari, Italy
Iannone, Florenzo
[1
]
Proft, Fabian
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Charite Univ Med Berlin, Dept Gastroenterol Infectiol & Rheumatol Including, Berlin, Germany
Free Univ Berlin, Berlin, Germany
Humboldt Univ, Berlin, GermanyUniv Bari Aldo Moro, Dept Precis Regenerat Med & Ionian Area DiMePRe J, Piazza G Cesare 11, I-70124 Bari, Italy
Proft, Fabian
[2
,3
,4
]
机构:
[1] Univ Bari Aldo Moro, Dept Precis Regenerat Med & Ionian Area DiMePRe J, Piazza G Cesare 11, I-70124 Bari, Italy
Axial spondyloarthritis;
TNFa inhibitors;
IL-17;
inhibitors;
small molecules;
precision medicine;
ACTIVE ANKYLOSING-SPONDYLITIS;
NECROSIS-FACTOR INHIBITORS;
ANTI-IL17RA MONOCLONAL-ANTIBODY;
INFLAMMATORY-BOWEL-DISEASE;
PLACEBO-CONTROLLED TRIAL;
SEVERE PLAQUE PSORIASIS;
INNATE LYMPHOID-CELLS;
ACTIVITY SCORE ASDAS;
C-REACTIVE PROTEIN;
NF-KAPPA-B;
D O I:
10.1080/14712598.2024.2389987
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
IntroductionAxial involvement in spondyloarthritis has significantly evolved from the original 1984 New York criteria for ankylosing spondylitis, leading to an improved understanding of axial spondyloarthritis (axSpA) as a disease continuum encompassing non- radiographic axSpA (nr-axSpA) and radiographic axSpA (r-axSpA). A clear definition for early axSpA has been established, underscoring the need for early intervention with biological and targeted synthetic drugs to mitigate pain, reduce functional impairment, and prevent radiographic progression.Areas coveredThis review explores therapeutic strategies in axSpA management, focusing on biological and targeted synthetic therapies and recent advancements. Biologics targeting TNF alpha or IL-17 and targeted synthetic disease-modifying antirheumatic drugs (DMARDs) are primary treatment options. These therapies significantly impact clinical outcomes, radiographic progression, and patient-reported functional improvement.Expert opinionAxSpA treatment has evolved significantly, offering various therapeutic options. Biological DMARDs, particularly TNF alpha inhibitors, have transformed treatment, significantly enhancing patient outcomes. However, challenges persist for patients unresponsive or intolerant to existing therapies. Emerging therapeutic targets promise to address these challenges. Comprehensive management strategies and personalized approaches, considering extra-articular manifestations and individual patient factors, are crucial for achieving optimal outcomes in axSpA management.
机构:
Vilnius Gediminas Tech Univ, Dept Foreign Languages, Fac Creat Ind, Vilnius, LithuaniaVilnius Gediminas Tech Univ, Dept Foreign Languages, Fac Creat Ind, Vilnius, Lithuania