Viral Inactivation of Blood Products inactivation.pdf · 2009. 10. 27. · Human and animal Blood...
Transcript of Viral Inactivation of Blood Products inactivation.pdf · 2009. 10. 27. · Human and animal Blood...
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Viral Inactivation of Blood Products
Soheir Adam, MD, MSc., MRCPathAsst. Professor & Consultant H t l i tHematologist
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Human and animal Blood derived medicinal products & related in vitro diagnostic devices
Animal- derived sera Anti-rabiesA ti ( k / i )
Human blood derived productsBlood components (red cells, Anti-venoms (snake/scorpion)
Anti-tetanus toxinsAnti-diphteria toxins
p ( ,platelets, plasma) Blood Coagulation FactorsImmunoglobulins
A i h i i B Anti-botulism toxinsAnti-hepatitis BAnti-rabiesAnti-tetanusAnti-rhesus (anti-D)
Fibrin sealantAlbumin
Other related products
Anticoagulant & fibrinolysis Albumin
In vitro diagnostic devices for the control of q alit and safet of blood
Anticoagulant & fibrinolysis biological therapeutic products
In vitro diagnostic devices for the control of quality and safety of blood derived medicinal products including in vitro diagnostic devices
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Th i CThe main Concern:
encouragement of
voluntary & unpaid bloodvoluntary & unpaid blood donationsdonations
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Quality and Safety: Q y yBiological Products
Blood collection & Blood collection & Plasma quality & safetyPlasma quality & safetyStarting materialStarting material
FractionationFractionation
q y yq y y
Fractionation Fractionation Technology/ Viral Technology/ Viral inactivation /Removal inactivation /Removal
Production Production ProcessProcess
ProceduresProceduresProcessProcess
Product characteristics:Product characteristics:Bulk &Bulk & Formulated Formulated ProductProduct
Final product Final product consistencyconsistency
Product Product
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Transfusion TransmissibleTransfusion Transmissible Diseases
Hepatitis BHepatitis CHepatitis CHIV 1&2HTLV 1&11HTLV 1&11SyphilisCMVCMVBacterial contaminationvCJDWest Nile VirusParasites
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Residual risks of major TTIs*
1993-1996 2000-2002WPWP Serology WP NATdays days
HIV 22 1: 3 000 000 11 1: 5 000 000HIV 22 1: 3 000 000 11 1: 5 000 000HCV 70 1: 500 000 10 1: 5 000 000HBV 68 1: 135 000 45 1: 250 000**
* Schreiber et al NEJM 1996 ;334:1685-90 ** serology
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Transfusion Safety
Careful selection of donorsTestingViral inactivation /recombinant productsAppropriate blood useAppropriate blood useHaemovigilance
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Why Viral Inactivation
The growing list of blood- Borne th i t i bilit t d ipathogens is outpacing ability to devise
and implement new screening tests
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Plasma
Platelets & leucocytesPlatelets & leucocytes
Red Cells
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PlateletsPlatelets
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Platelet Production
2nd ti i2nd separation in an extractor
Leucoreduction by filtration
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D S iDonor Screening
Donor TestingDonor Testing
Viral removal/ inactivation
Quarantine
P d t lProduct release
Prinicples of Collection and Manufacturing Process
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Pl T tiPlasma Testing
Plasma tested for HBsAg
Plasma pools tested forHBsAg
Anti- HCVAnti HIV
tested forHBsAgAnti- HCVAnti-HIV
ALTPCR for HCV
Anti- HCVAnti-HIVPCR for HCVPCR for HCV,
HBV, HIV, Parvovirus B19
PCR for HCV, HBV, HIV, Parvovirus B19
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Nucleic Amplification TestingNucleic Amplification Testing(NAT)
HCV NAT SNBTS Nov 99HIV NAT Sept 01Approx 950 000 screened ppNo HCV RNA, anti-HCV neg detectedNo HIV RNA anti HIV neg detectedNo HIV RNA, anti-HIV neg detected
UK 3: 3,500,000 HCV RNA pos
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Product Safety
Full Traceability From Donor To Final ProductNotification System For Advising Of Post DonationNotification System For Advising Of Post Donation InfectionsValidated Virus Elimination Step(s)Validated Virus Elimination Step(s)Control Of Process To Prevent Re-contamination After Virus Elimination SteppClinical Trial DataPost Marketing Surveillanceg
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Vi l S f tViral SafetyResearch into effective methods for inactivation or removal of viruses from blood products
Chemical Inactivation Inactivation by heatRemoval by virus filter (nanofiltration)Removal by alcohol precipitationRemoval by alcohol precipitation
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Vir s Inacti ation and Remo alVirus Inactivation and RemovalD i th d th t ill l ti l i ti t d/• Devise methods that will selectively inactivate and/or remove viruses without undue product damage/loss.
St d l t t t i i l d d• Study relevant test viruses in scaled-down process.
• Ensure that method is capable of giving the degree of virus inacti ation/remo al req iredinactivation/removal required.
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Common Virus ClearanceCommon Virus Clearance Methods
Virus inactivation: Virus removal
Chemical:organic solvents; pH extremes;
Precipitation:ammonium sulfate etc; p ;
solvent detergent; alcoholPhysical: Heat treatment (dry heat or
ammonium sulfate etc.Chromatography: ion exchange; gel filtration; (dry heat or
pasteurization) affinity; reverse phaseMembrane filtration:Omega, Planova, DV50Omega, Planova, DV50
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Criteria for An Effective VirusCriteria for An Effective Virus Clearance Step
Si ifi t i l killSignificant viral killReproducible and controllable at process
l d d l bl t th l b tscale and model-able at the laboratory scaleSh ld h i i l i t d tShould have minimal impact on product yield and activityN t t ti l t iNot generate neo-antigens or leave toxic residues
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Vi S f tVirus Safety
Cold ethanol fractionationH4/ i i i ti tipH4/pepsin virus inactivation
effective against enveloped viruses e.g. HIV, Hep B and Cand non-enveloped viruses e.g. Hep A
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Red Blood Cells
Hb has phostoabsorptive effects.Light – independent compounds have been devised.S- 303, PEN110 have no adverse effects.
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Fresh Frozen Plasma
PsoralenRiboflavinSolvent – detergent plasmag p
Large pools : 250,000 donors/ batchThrombotic complicationsThrombotic complications
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Platelets
No approved method of viral i ti ti f l t l tinactivationof plateletsS- 59 is effective but less effective clinically than untreated platelets.
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Pooled screened human p lasma
C ld th l f ti ti t i ldCold ethanol fractionation to yieldfraction II
Remove process ethanolRemove process ethanol
pH4/pepsin VI step
Sterilisa tion, aseptic dispensing
Product returned to a neutral pH
and freeze drying
SNBTS Intravenous Immunoglobulin
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ConclusionConclusion
Manufacturing processes for blood g pderived products should contain two effective steps for premoval/inactivation of viruses
At least one step should be effective against non-enveloped virusesagainst non-enveloped viruses
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ConclusionConclusion(cont.)
At least one stage in a production processAt least one stage in a production process must inactivate rather than remove viruses
A single step having a large effect gives more f i l f t th l tassurance of viral safety than several steps
having the same overall effect