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魏正宗
James C. WEI, MD, PhD.
中山醫學大學附設醫院過敏免疫風濕科
Chief, Division of Allergy, Immunology and Rheumatology
Director, Chinese Medicine Clinical Trial Center
Associate professor, Institute of Medicine, Chung Shan Medical University.
Clinical Trials Experience
2010.Oct. FDA GCP SITE INSPECTION PASSED
2012.Aug. TFDA (Taiwan) GCP SITE INSPECTION PASSED
**World top one enroller in
-Norvatis RHAK study in ankylosing spondylitis.
-Pfizer Etanercept study in non-radiographic axial spondyloarthritis.
*
*Taiwan top one enroller in
-BMS abatacept study in rheumatoid arthritis
-UCB anti-IL6 in rheumatoid arthritis
-MSD Etoricoxib in ankylosing spondylitis
-TWi Biotechnology, Inc. IL-1 receptor antagonist in gouty arthritis
Pathogenesis of RA
 Traditional therapies
 Immune target therapies
 Biological agents
 Small molecules
 Summary & Take home message

Pathogenesis of RA
 Traditional therapies
 Immune target therapies
 Biological agents
 Small molecules
 Summary & Take home message

Prevalence: 0.4~1%
 A prototype of autoimmune chronic
inflammatory arthritis.
 Lifelong, progressive damage to
joints and bone.
 Market of Humira & Enbrel are top 1
and 2 in the world.

Courtesy of J. Cush, 2002.
Overview of Immunity
-Cellular
-Humoral

-Innate
Macrophage
Monocyte
Neutrophil
Eosinophil…
-Acquired
B cell
T cell
Dendritic cell…
Pathogenesis of
Rheumatoid Arthritis
Pathogenesis of RA
 Traditional therapies
 Immune target therapies
 Biological agents
 Small molecules
 Summary & Take home message

新的消炎止痛藥 --COX-2抑制劑-- 如
meloxicam (Mobic骨敏捷), celecoxib
(Celebrex希樂葆), etoricoxib (Arcoxia萬克適)
已證實效果與傳統的消炎藥相當且較不傷
胃。
 消炎藥併用止痛劑(如acetamenophen,
tramadol, ultracet及通安)及肌肉鬆弛劑,
有很好的加成效果。

1.

2.
3.
4.
5.

Hydroxyclhoroquine (Plaquenil, Genuquine)
奎寧、必賴克廔
Methotrexate (MTX) 滅殺除癌 , 治善錠
Sulfasalazine (Salazopyrin) 斯樂, 撒樂
Leflunomide (Arava, Arheuma) 亞努麻
Cyclosporin (Neoral) 環孢靈,新體睦
足夠劑量(一般每天400毫克)的奎寧
是治療紅斑狼瘡最基本的藥
 最沒有副作用的免疫調節劑
 還有降血脂、抗血栓、增加骨質、降
血糖等附帶好處。

適應症:風濕性關節炎、牛皮癬或其他自
體免疫相關疾病。亦可治療癌症。
 每周4-6顆:使用方式為每周固定一日早餐後
服用2顆,晚餐後再服2顆,隔日早餐後再
服2顆。
 副作用:口腔炎、白血球減少、血小板缺
少、噁心、肝炎
 用藥期間須特別監測血液功能。

主治:潰瘍性結腸炎,僵直性脊椎
炎,類風濕性關節炎。
 副作用:頭痛、食慾不振、腹痛、
皮膚紅疹、蕁痲疹。多於停藥後可
恢復。
 早晚各兩顆

治療類風濕性關節炎、乾癬關節炎
 用於Methotrexate治療無效,或無法忍
受Methotrexate副作用時使用。
 可能副作用:腹痛、噁心、腹瀉、影
響肝功能、貧血、白血球減少、皮膚
疹、高血壓、感染、掉髮。

Pathogenesis of RA
 Traditional therapies
 Immune target therapies
 Biological agents
 Small molecules
 Summary & Take home message





Aiming molecular target
Receptor / Ligand
Signaling pathway
Complex biotechnology
Biological agent生物製劑
Small molecule小分子藥物
Normal Interaction Neutralization of Cytokines
Inflammatory
Cytokine

Monoclonal
Antibody

Cytokine
Receptor

Soluble
Receptor

Inflammatory
Signal

No Signal

Activation of
Receptor Blockade Anti-inflammatory Pathways

Monoclonal
Antibody
Receptor
Antagonist

Antiinflammatory
Cytokine
Block signaling

No Signal

Choy EHS, Panayi GS. N Engl J Med. 2001;344:907–916.
-cept : fusion of a receptor
 -mab : a monoclonal antibody (mAb)
 -ximab: a chimeric mAb
 -zumab : a humanized mAb
 -tinib: tyrosine kinase inhibitors

Biological agents
T cell modulation
CTLA4/CD28
anti-CD2
anti-CD11a
B cell modulation
anti-CD20
anti-BAFF
Cytokines inhibition
anti-TNF
anti-IL6
anti-IL1
anti-IL12/23
anti-RANKL
Etanercept(商品名Enbrel恩博)是一種
由中國倉鼠卵巢細胞組織培養而來的對
抗腫瘤壞死因子的融合蛋白,需皮下注
射,每周兩次。
 Adalimumab(商品名Humira復邁)是一
種全人的腫瘤壞死因子的單株抗體,皮
下注射,每兩周一次。
 Golimumab(商品名Simponi辛普尼),
是一種全人的腫瘤壞死因子的單株抗體,
皮下注射每四週一次即可。

目前第一線生物製劑
 目前健保給付於嚴重頑固型之類風溼
性關節炎、僵直性脊椎炎、乾癬、乾
癬關節炎、發炎性大腸疾病。
 需事先報健保局審查。




70-90%的病患可以有明顯的進步。




發燒、倦怠、頭痛、背痛,輕微上呼吸道感染,
打針處發生皮膚疹或細菌感染。
最需要注意是可能造成肺結核的復發或擴散。發
生率大約是每100,000的病人當中24個,相當於正
常人的3倍左右。






B肝復發機率15-60%。




Baseline screening for TB
Monitor Quantiferon q6m
Close monitor or Preemptive anti-viral agents

長期使用,人體會產生對抗該藥物之抗體。
Mode of Action of Tocilizumab
[soluble IL-6 receptor (sIL-6R)]

Tocilizumab

IL-6

[membrane bound IL-6 receptor (IL-6R)]

Outer cellular

gp130
Cell membrane
Intra cellular

×
Signal transduction
個

疼痛關節數逐
漸減少

CRP, C反應蛋白

疼
痛
的
關
節
數
量
週
是一種IL-6單株抗體
 適應症為類風濕性關節炎
 靜脈輸注,每月一次。
 可以幫助60-80%的患者症狀進步及減少關
節破壞,30%以上的患者達成疾病緩解,也
能改善患者的貧血及疲倦症狀及生活品質。
 是目前唯一單一療法與合併DMARD或MTX
治療臨床療效相當生物製劑

IL-17為更專一性造成發炎的細胞
激素之ㄧ
 為學術研究的熱門主題
 每四週皮下注射一次
 目前正進行類風濕性關節炎及僵直
性脊椎炎臨床試驗。

Biological agents
T cell modulation
CTLA4/CD28
anti-CD2
anti-CD11a
B cell modulation
anti-CD20
anti-BAFF
Cytokines inhibition
anti-TNF
anti-IL6
anti-IL1
anti-IL12/23
anti-RANKL
B cell development
Antigen-independent phase

Surrogate
light chain

Stem cell

Pro-B cell

Pre-B cell

IgM

Immature
B cell

Antigen-dependent phase

IgM

IgD

Mature
B cell

IgM, IgD,
IgA, or IgE

Activated
B cell

CD19
CD20

Adapted from Sell et al. Immunology, Immunopathology, and Immunity. 6th ed. 2001; Roitt et al. Immunology. 6th ed. 2001;
Tedder et al. J Immunol 1985;135:973.

Secreted
IgG, IgA,
IgE, or IgM

Plasma
cell
Rituximab(anti-CD20) in RA
Edwards et al. Engl J Med. 2004 Jun 17;350(25):2572-81.

80
70
60
50
ACR 20
ACR 50
ACR 70

40
30
20
10
0

MTX
control

Ritux
only

Ritux + Ritux +
CTX
MTX

• 1000 mg at Day 1&15,
q6m
• Better response in RF+
or CCP+ pts
• TNF-IR RA
• Combine with MTX










是一種抗CD20單株抗体之抗B細胞療法
用來治療淋巴瘤;類風溼性關節炎,也對紅斑狼
瘡、乾燥症、血管炎等有效。
使用方法為靜脈輸注,劑量為每次 500-1000毫
克,間隔 14 天再次輸注 , 共 2 次為一個療程。
通常治療效果於靜脈注射後二個月出現,療效可
以持續6到9個月。
健保給付:限TNF抑制劑無效之類風濕性關節炎。
費用約需每年16-32萬元。
Potential use of Rituximab
• Systemic lupus
erythematosus
• Idiopathic
thrombocytopenic
purpura
• Multiple sclerosis
• Cold agglutinin disease
• Autoimmune hemolytic
anemia
• Antineutrophil
cytoplasmic antibody—
associated vasculitis
• Cryoglobulinemia

• Thrombotic
thrombocytopenic
purpura
• Sjögren's syndrome
• IgM mediated neuropathy
• Pemphigus vulgaris
• Grave's disease
• Dermatomyositis
• Neuromyelitis optica
• Idiopathic membranous
nephropathy
Infusion-related reactions
 Anaphylaxis/angioedema
 More severe
 Lymphopenia (40%)
 Neutropenia (6%)
 Leukopenia (4%)
 Hepatitis B!
 Sepsis (2%)

Belimumab, Benlysta
Human genomic science, GSK

First biologics for SLE

MoAb of soluble BLyS


是一種『B淋巴球刺激因子單株抗體』
(anti-BLyS)

已經在歐美上市,適應症是紅斑狼瘡
(SLE)
 50年來第一個核可治療紅斑狼瘡的新藥。
 另兩個類似機轉的藥正進行紅斑狼瘡臨
床試驗中。

Biological agents
T cell modulation
CTLA4/CD28
anti-CD2
anti-CD11a
B cell modulation
anti-CD20
anti-BAFF
Cytokines inhibition
anti-TNF
anti-IL6
anti-IL1
anti-IL12/23
anti-RANKL
Co-stimulatory Pathways
APC

There are several co-stimulatory
and co-inhibitory pathways; signals
through these pathways can either
upregulate or downregulate T-cell
activation

+

–

+

T cell

–
CTLA4Ig (Abatacept, Orencia)

Reduction of joint inflammation
Sustained ACR Responses Through 5 Years
Double-blind

Open-label LTE

100
% of Patients Achieving
ACR Response

90

82%
84%

80
70
54%

61%

32%

60

40%

50
40
30

20
ACR 20

10

ACR 50

ACR 70

0
0

0.5

1

1.5

2

2.5

3

3.5

4

4.5

5

Year 0.5 (n)

Year 1 (n)

Year 1.5 (n)

Year 2 (n)

Year 2.5 (n)

Year 3 (n)

Year 3.5 (n)

Year 4 (n)

Year 4.5 (n)

Year 5 (n)

ACR 20

371

373

353

337

311

303

289

288

273

268

ACR 50

373

372

348

338

314

306

289

288

274

270

ACR 70

374

374

350

340

314

309

289

288

278

270

As-observed analysis for patients initiated on ORENCIA® (abatacept) during the double-blind period.
Kremer JM, et al. EULAR 2009. Poster #FRI0263.
機轉是透過T細胞活化的抑制因子CTLA4
 適應症為類風濕性關節炎
 第一線生物製劑
 即使對TNF抑制劑無效的RA病人,此藥仍
有50%的有效率
 靜脈輸注,每月一次
 10 mg/kg

英文藥名

台灣商品名

作用機轉

適應症

Etanercept
(Enbrel)

恩博

抗腫瘤壞
死因子

類風溼性關節炎,僵直性脊椎炎, 有
乾癬,乾癬關節炎,幼年型關節炎

Adalimumab
(Humira)

復邁

抗腫瘤壞
死因子

類風溼性關節炎,僵直性脊椎炎, 有
乾癬,乾癬關節炎,潰瘍性大腸炎

Golimumab
(Simponi)

辛普尼

抗腫瘤壞
死因子

類風溼性關節炎,僵直性脊椎炎, 有
乾癬,乾癬關節炎,

Rituxtimab
(Mabthera)
Denosumab
(Prolia)
Abatacept
(Orencia)
Tocilizumab
(Actemra)

莫須瘤

類風溼性關節炎
B細胞
CD20抗原
抗RANKL 骨質疏鬆症

有

類風溼性關節炎

有

類風溼性關節炎

有

保骼麗
恩瑞舒

安挺樂

T細胞因
子CTLA4
細胞激素
IL-6

健保給付

有
Pathogenesis of immune system
 Immune target therapies
 Biological agents
 Small molecules
 Take home message

The MAPK, Syk kinase, NF-κB and JAK/STAT intracellular signalling pathways

Bonilla-Hernán M G et al. Rheumatology 2011;50:15421550
The majority of cytokine receptors use three
JAK combinations

Shown are well-studied cases where JAK usage by each cytokine receptor has been established by
genetic and biochemical studies. Exceptions shown are the G-CSFR (*) where it is currently unclear
whether both JAK1 and JAK2 are required together. Additionally, the IL-12R (†) and IL-23R (†)
require TYK2 but the requirement for JAK2 has not been definitively determined. Receptors that
use JAK2 and JAK3, JAK3 alone, TYK2 alone, or JAK3 and TYK2 have not been described.
ORAL Standard – MTX-IR RA
ORAL Standard – MTX-IR RA
ACR 50 response rates over time
Xeljanz (tofacitinib)
FDA approved on Nov. 6,
2012
5 mg twice daily
adults with moderately to
severely active rheumatoid
arthritis (RA) who have had
an inadequate response to,
or who are intolerant of,
methotrexate.
Cost: 90% of TNFi biologics


Tofacitinib
機轉是抑制細胞內訊息傳遞分子JAK-3
 用於治療類風濕性關節炎; 目前也針對中重度
乾癬及僵直性脊椎炎進行臨床試驗中




Apremilast
機轉是抑制細胞內訊息傳遞分子PDE-4
 目前正針對中重度乾癬及僵直性脊椎炎進行
臨床試驗




Fostamatinib


Syk inhibitors, phase II clinical trial
Pathogenesis of immune system
 Immune target therapies
 Biological agents
 Small molecules
 Summary & Take home message

107 ongoing Phase 2 & 3 trial in RA @
clinicaltrial.gov, 2013-Oct-12
IL6 MoAb: Sirukumab
 IL17 MoAb: Secukinumab
 B cell: BAFF, CD22
 JAKi: JNJ, VX-509 (Vertex).
 Masitinib ,a tyrosine-kinase inhibitor
 Mesenchymal Stem Cells



Small Molecules Target therapy
JAK
 SYK
 PGE4
 Tyrosine kinase inhibitor, TKI
 Histamin-4

Chronic inflammation and immune-related
diseases markets arising.
 Immune-target therapies is the trend!
 Questions to be answered


What is the most important target?
 Personalized medicine




Key to success:
Sustained efficacy
 Long-term safety
 Availability


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