Infliximab treatment for refractory kawasaki disease

Post on 24-Dec-2014

871 views 2 download

Tags:

description

Infliximab treatment for refractory kawasaki disease Presented by Theerapan Songnuy, MD. April26, 2013

transcript

INFLIXIMAB TREATMENT FOR

REFRACTORY KAWASAKI DISEASE

Theerapan Songnuy M.D.

Overview

Kawasaki disease Standard Treatment Refractory Kawasaki Disease New Treatment : Infliximab - Mechanism - Efficacy - Side effects Conclusion

Kawasaki Disease

Acute febrile illness in children Classical symptoms: - Persistent high fever - Polymorphous rash - Conjunctival congestion - Lip cracking/ strawberry tongue - Cervical lymphadenopathy - Indurative edema of extremities

Inflammatory Process

Inflammatory markers: - TNF-alpha - IL-2R - IL-6 - etc.

Clin Immunol Immunopathol 1990; 56:29-36

Aim

To examine the role of TNF-alpha in the immune response leading to vascular damage in the coronary arteritis mice model of Kawasaki disease

Materials & Methods

Mice : - Wild-type C57BL/6, TNFRI-/- &

TNFRII-/- - From Charles River Lab & The

Jackson Lab - Housed under pathogen-free

condition at U. of Toronto

Materials & Methods Lactobacillus casei cell wall extract - MRS broth ( Difco, Detroit, MI) - Cytoplasmic membrane disrupted by detergent lysis with 4%

sodium dodecyl sulfate for 1night at room temp.

- Washing cell wall-associated materials - Incubated with DNase, RNase, trypsin to remove cytoplasmic

material - Cell wall-materials were sonicated 2 hr by W-375 sonicator &

cooling by a dry ice-ethanol bath

- Centrifuged for 1 hr at 20,000 /min - Suspended in phosphase buffed saline before use to induce coronary arteritis

Materials & Methods Quantitative real time RT-PCR - Mice 4-5 wk old were injected intra-peritoneally with 0.5 ml PBS or 1 ml of LCWE - After sacrificed, heart & spleen were processed for RNA isolation - cDNA was synthesized & amplified by real time PCR - Relative quantity of PCR products were determined (TNF-alpha) compared to GAPDH - Also can be used for ICAM-1, VCAM-1, E-Selectin et

al

Materials & Methods Confocal immunomicroscopy - Serial 6-um heart& spleen cryo-section, fixed in acetone - Incubation in PBS plus 0.1% saponin & 2% BSA - Stained with purified rat antimouse TNF- alpha mAb or isotype control - Followed by biotinylated goat anti-rat IgG - Mounted in DAKO anti-fade fluoresent mounting medium - View under a confocal microscope

Materials & Methods

Cardiac histology & histological evaluation

- Tissue embedded in compound ( Tissue- Tek)

snap-frozen in liquid nitrogen, stored at -80 c

- Coronary artery: 6-um-thick serial section of

left coronary artery - Stained with H&E or elastin van Giesen - Assess arteritis & elastin breakdown

Materials & Methods

Treatment of mice with TNF antagonist Etanerept

- After disease induced, Etanercept was induced

IP at 8-10 mg/kg twice weekly - Mice were sacrificed 28 & 42 d later - Cardiac tissue prepared for histology

Conclusion TNF-alpha plays a key role of coronary artery damage

in a murine model After disease induction, TNF-alpha rose in the

peripheral immune system & localized at coronary artery

Lead to lymphocyte recruitment Lead to elastin degradation, vessel wall damage,

coronary artery aneurysm

Blocking TNF-alpha activity ( Etanercept & abolish signal via TNFRI) result in decrease inflammation & elastin breakdown

Standard Treatments

-If left untreated, coronary aneurysm 15-25%-IVIG treatment reduced coronary complication to only 3-5 %

Refractory Kawasaki Disease

Refractoriness to IVIG defined as: - Persisting or re-emerging fever

> 38 C - Positive fractional changes of

CRP - Leukocytosis / increased

neutrophils After IVIG therapy for 48 hr

Therapy for IVIG-resistance Kawasaki Disease

Additional doses of IVIG Intravenous methyl prednisolone Oral corticosteroids Cyclophosphamide Cyclosporin Methotrexate Plasma exchange Infliximab, a tumor necrosis factor-

alpha blocker Pediatrics 2004; 114: 1708-33.

Infliximab ( Tumor Necrotic Factor-alpha

Antagonist)

Paper infliximab

Aim

To study the efficacy of infliximab for suppressing the progression of coronary artery lesions in cases of refractory to extensive IVIG therapy

Materials & Methods

Patients aged 2-10 years Fulfilled criteria diagnosis as

Kawasaki disease* Primarily treated with IVIG 2-4 g/kg

Materials & Methods Refractoriness to IVIG defined as: - Persisting or re-emerging fever > 38

C - Positive fractional changes of CRP - Leukocytosis / increased neutrophilsAfter IVIG therapy for 48 hr : Then infliximab would be started within

10 days of disease onset

J Rheumatol 2012;39:864-867

Materials & Methods Exclusion criteria: - TB lung - Recent therapy with corticosteroids or biologic response modifiers - Vaccination with BCG within 6 mo before disease onset - Low cardiac function - Liver/renal dysfunction J Rheumatol 2012;39:864-867

Infliximab Administration Dose : 5 mg/kg in 100 ml saline Route : intravenous In case of refractory to infliximab, plasma pheresis was performed with 5% albumin for 3 consecutive

days Evaluation : - At 48 hr. after infliximab (fever & inflammatory markers ) -At 30 days ( intact coronary artery by echocardio- graphy) J Rheumatol 2012;39:864-867

Day after infliximab

J Rheumatol 2012;39:864-867

Day after infliximab

J Rheumatol 2012;39:864-867

J Rheumatol 2012;39:864-867

Results

One patient showed coronary artery lesion at

30 d of follow up but complete regression 1 y later

No adverse reactions ( anaphylactoid reaction, heart failure, or severe infectious)

Aim

Efficacy and safety of infliximab compared to re-treated IVIG for treating IVIG-resistant Kawasaki disease patients

Materials & Methods A two-center retrospective study From Jan 2000-March 2008 Inclusion criteria: - Fever > 4 d & 4 from 5 principal symptoms - Fever > 4 d & < 4 from 5 principal

symptoms & coronary artery abnormality - Received at least one re-treatment for recurrent or persistent fever > 38 c beyond 36 h after completion of initial IVIG ( 2 g/k)

Exclusion criteria - Initial treatment at other centers - Initial treatment with others than IVIG

& aspirin - Re-treatment for coronary artery

changes in the absence of fever - First re-treatment > 10 d after initial

IVIG or infliximab

Materials & Methods

Results

Primary IVIG

Met Inclusion criteria

Re-treated IVIG

Re-treatedInfliximab

Center 1Boston

243 41 (17%)

41 0

Center 2San Diego

398 65(16%) 45 20

J Pediatr 2011; 158: 644-9

(continued)

J Pediatr 2011; 158: 644-9

J Pediatr 2011; 158: 644-9

J Pediatr 2011; 158: 644-9

Conclusion

Infliximab as the first re-treatment : - Fewer days of fever - Fewer length of stay - Not improve coronary artery outcomes - No adverse effects were noted Need a prospective trials for IVIG-

resistance Kawasaki disease patients

Thank You Very Much