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Transcript of Hong Kong Association of Blood Transfusion & Haematology NAT and Viral Safety in Blood Transfusion...
![Page 1: Hong Kong Association of Blood Transfusion & Haematology NAT and Viral Safety in Blood Transfusion Dr. P.H. Yu Medical Officer Department of Pathology.](https://reader035.fdocuments.us/reader035/viewer/2022062407/56649d0a5503460f949dc6b6/html5/thumbnails/1.jpg)
Hong Kong Association of Blood Transfusion & Haematology
NAT and Viral Safety inBlood Transfusion
Dr. P.H. Yu
Medical Officer
Department of Pathology
Tseung Kwan O Hospital
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Viral Safety in Blood Transfusion
Public concern was heightened by the disastrous consequences of HIV epidemic in 1980s
In France, government officials and minister were charged with manslaughter for allowing HIV-contaminated blood to be used for transfusion at a time when screening test were available (1985)
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Viral Safety in Blood Transfusion
Red Cross officials in Belgium, Switzerland, Canada were also convicted for distributing contaminated blood during the same period
Public perception – blood transfusion should involve absolute no risk of transmitting viral infection
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1/100
1/1,000
1/10,000
1/100,000
1/1,000,000
Adapted from Transfusion 2000; 40:143-159
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Viral Safety in Blood Transfusion
Risk of transmitting infection to recipients has been drastically reduced in the past decades, due to
a) Improved donor selection
b) Sensitive serologic screening assays
c) Application of viral inactivation procedures during manufacturing of plasma products
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Residual Risk
In 1994, several cases of HCV infection were attributed to IVIg (Gammagard) in Europe
In 1999, an Australian schoolgirl contracted HIV via blood transfusion during surgery in Melbourne (first reported case of TT HIV in Australia since testing for HIV in 1985)
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Residual Risk
Major sources of remaining risk are:
1. Window period donation
2. Viral variants not detect by current assays
3. Immunosilent donor
4. Laboratory testing error
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Residual Risk
The greatest threat to the safety of blood supply is the donation by seronegative donors during the infectious window period
Window period donation account for 90% or more of the residual risk (Report of the Interorganization Task Force on NAT Testing of Blood Donors, 2000)
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Window Period
Period precedes the development of antibodies during the initial infection
Eclipse phase of the window period - the very initial phase after exposure when virus replication is restricted to tissue sites and there is no detectable viraemia
Infectious phase of window period is after eclipse and before seroconversion
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Window Period
Animal study in chimpanzees (Murthy KK et al, Transfusion 1999) suggested that the eclipse phase is non- infectious for HIV
Direct detection of virus by very sensitive method theoretically eliminate the infective window phase if the assay sensitive exceeds the minimum infective dose for that virus (window period closure)
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Residual Risk
Risk of acquiring a transfusion-transmitted viral infection depends not only on the length of specific window period but also on the incidence of the infection among blood donors
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Determination of Residual Risk
Study the rate of infection prospectively in transfusion recipients
Some pathogens, HIV & HCV, the risk is so low that exceeding large number of recipients & lengthy period are required for the risk to be measured accurately
Under-reporting
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Determination of Residual Risk
Incidence/Window Period Model First applied in France and US (Courouce &
Pillonel 1996; Schreiber 1996) Risk is calculated by multiplying the
incidence rate in blood donor by the length of the window period
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Determination of Residual Risk
Determine the incidence of seroconversion among donors who donate more than once (multiple time donors)
Not the prevalence rate in donor population
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USA UK Italy Australia HK
HIV 1:493,000 < 1: 2,000,000
1:408,000 1:1,200,000 1:877,147
HCV 1:103,000 < 1 : 200,000
1:230,000 1:250,000 1:86,137
HBV 1:63,000 1 : 50,000 – 170,000
1:63,400 1:160,000 1:3357
Source: (1) Muller-Breitkreutz K for the EPFA Working Group on Quality Assurance. Results of viral marker screening of unpaid donations and probability of window donations in 1997. Vox Sang 2000;78:149-157 (2) Aubuchon JP, Birkmeyer JD, Busch MP. Safety of the blood supply in the United States: opportunites and controversies. Ann Int Med 1997;127:904-909. (3) Regan FAM, Hewitt P, Barabara JAJ, Contreras M.on behalf of the current TTI Study Group Prospective investigation of transfusion in transmitted infection in recipients of over 20000 units of blood, Br Med J 2000;320:403-406. (4) Tosti ME, et al, An estimate of the current risk of transmitting blood-borne infections through blood transfusion in Itly. Br J Haemat, 2002;117:215-219.
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Residual Risk
Chung HT, Kee JS, Lok AS (Hepatology 1993 Nov;18(5):1045-9)
Among 45 HBV serology negative patients received blood of blood products during open-hear surgery in HK
3 recipients (6.7%) developed asymptomatic hepatitis B seroconversion
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What is NAT?
Nucleic Acid Technology (Nucleic Acid Amplification Testing)
A generic term that include a number of different technologies
All involve extraction or capture of nucleic acid, amplification, and detection
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What is NAT?
Commonly used systems are
I. PCR-based assays (Roche Cobas Ampliscreen)
II. Transcription mediated amplification assay (GenProbe)
III. Others, including in-house PCR preparations
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GenProbe
Recently approved by FDA (Feb 2002) for donor screening
Three main steps
1)Sample preparation & target capture
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GenProbe
1)Sample preparation & target captureRNA hybridized to target-specific oligonucleotides and then captured onto magnetic microparticles
which are separated from plasma in a magnetic field
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GenProbe
2)Transcription Mediated Amplification- single-step isothermal amplification- initial synthesis of cDNA from the target RNA followed by in-vitro transcription of cDNA into many copies of RNA amplicon
3)Detection by a chemiluminescent probe which hybridized to the amplicon
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The system includes a robotic pipettor (Tecan; Durham, NC), the Chiron Procleix target capture system, and the Procleix Leader HC+ with the Procleix system software.
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Roche Cobas Ampliscreen
Five main steps:
1) Sample preparation by ultra-centrifugation
2) Reverse transcription of target RNA to cDNA
3) Polymerase chain reaction amplification of cDNA
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Roche Cobas Ampliscreen
4) Hybridization of products to oligonucleotide peroxidase conjugated probe
5) Detection of probe-bound products by colorimetric determination
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Pooling Strategies
Short time frame for implementation and lack of high throughput automated system
The only option is to implement NAT screening in pools of aliquots form several donations (16-512 individual donations)
Sensitivity decreases as pool size increases
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Pooling Strategies
Automated pipetting system to prepare the pools
Overlapping three-dimensional pools or straight-line pools
Retesting of subpools is slow and will delays the release of final products
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Standardisation
Different units, eg. genome equivalent/ml, copies/ml, PCR detectable units/ml
WHO Collaborative Study Group has established the reference sample for HCV(1997), HIV(2001), HBV(2001), and Parvovirus B19(2002); and standardised the unit of measurement as IU/ml
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Other Technical Issues in NAT
Choice of anticoagulant Nucleic acid stability in sample during
transportation PCR inhibitors in the sample False positive result and cross-contamination Internal control Turnaround time – impact on product release
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HCV
Prolonged high-titre viraemic phase before seroconversion and elevation of ALT, 7-12 weeks after infection
Very short doubling time of 2-3 hours, therefore high viral load titres are achieved
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HCV
Very amenable to detection by pooled NAT NAT theoretically reduce the window period
by 41-60 days
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HCV
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HIV
Short doubling time of 21 hours Window period of 16 days (p24 antigen)
may be reduced to 11 days by NAT
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HIV
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HBV
HBsAg become positive 50-60 days after infection
Preceded by a prolonged phase (up to 40 days) of low-level viraemia
Long doubling time of 4 days NAT pooling will only detect a small
proportion of this pre-HBsAg window period
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HBV
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History of NAT Implementation
European Committee for Proprietary Medicinal Products required that by July 1999 all fractionated plasma products should be negative for HCV RNA by NAT technique
Required sensitivity: able to detect 100 IU/ml of HCV-RNA in the final pool (about 230 viral particles/ml)
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History of NAT Implementation
Paul Erlich Institute in Germany required all blood products should have a negative HCV NAT result before release by April 1999
Required sensitivity: able to detect 5,000 IU/ml of HCV-RNA of individual donation
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History of NAT Implementation
US blood centres implement NAT testing of blood donors for HIV and HCV in April 1999, under the Investigational New Drug applications
Studying GenProbe and Roche systems only Canadian Blood Services implemented NAT
since October 1999
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History of NAT Implementation
Australia started NAT testing of blood donors for HIV and HCV since June 2000
Japanese Red Cross Society started NAT screening for HBV, HCV, and HIV since July, 1999
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International Forum on Implementation of donor screening for infectious agents
transmitted by blood by NAT
Vox Sang 2002;82:87-111 Countries screening HBV DNA: Japan,
Germany (some plasma manufacturers) Countries screening HCV RNA: Australia,
New Zealand, Japan, USA, Canada, Germany, France, Austria, Italy, Netherlands, UK, Finland, Norway, Spain(partial), HK
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International Forum on Implementation of donor screening for infectious agents
transmitted by blood by NAT
Countries screening HIV RNA: Australia, New Zealand, Japan, USA, Canada, France, Netherlands, Spain (partial), Germany (plasma products only), HK
Still considering: Sweden, Brazil, Greece, South Africa
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International Forum on Implementation of donor screening for infectious agents
transmitted by blood by NAT
Turn Around Time: the blood products can be released within 1-2 days
Australia Red Cross: TAT is 10-26 hours In most laboratories, invalid results or false
positive are significant (2-8%); take longer time to resolve
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Yield: North America
pool sizes of 16- 24 donations GenProbe and Ampliscreen Results from the US and Canadian programs
starting from 1999 are: 113 HCV NAT-only positive donations
identified from over 29 million donations screened (1/259,000)
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Yield: North America
6 HIV NAT-reactive, p24 antigen-negative, and seronegative donations identified from 26 million donations screened (1/4,390,000)
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Yield: Germany
Institute of Transfusion Medicine and Immunohaematology, Frankfurt
From 1997-2000, tested 1,087,000 donations pool size of 96 donors Roche Amplicor for HCV In-house TaqMan PCR for HIV & HBV
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Yield: Germany
2 HCV RNA-only positive donations identified (1:543,500)
1 HIV RNA-only positive donation identified
2 HBV DNA-only positive donations identified
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Yield: Japan
Japanese Red Cross NAT Screening Research Group (Microbiol Immunol 2001;45(9):667-672)
From Feb 2000 – April 2001 Minipool of 50 donations Multiplex HBV/HCV/HIV reagent Excluded all serological positive cases
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Yield: Japan
Total donations screened: 6,805,010 HIV-RNA positive: 4 (1:1,701,253) HCV-RNA positive: 25 (1:272,200) HBV-DNA positive: 112 (1:60,759)
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USA Australia Germany Japan
HIV 1:4,390,000 0:1,440,000 1:1,087,000 1:1,701,253
HCV 1:259,000 1:360,000 1:543,500 1:272,200
HBV 1:543,500 1:60,759
Yield of NAT Screening on Blood Donors
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Will NAT Close the Window?
Ling AE, et al. JAMA 2000;284:210-214 Transmission of HIV from a blood donor to a
platelet recipient and a red blood cell recipient occurred in the window period
viral load in the implicated donation was estimated to be less than 40 copies/mL
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Will NAT Close the Window?
Current US minipool HIV NAT screening protocols fail to detect very low level viraemia
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Cost-effectiveness
NAT is a intensive process to perform, requiring specially ventilated & clean laboratory, expensive equipment and reagents
In US under the IND protocol, the cost per donation is US$8
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Cost-effectiveness
Cost per case detected is estimated at US$1.7 million
After FDA approval of GenProbe, it is estimate that the cost will reach US$15-20 a donation (America Blood Centers Newletter March 8, 2002)
How much we are willing to pay to produce further marginal improvements in safety?
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Future
Despite cost-effective issues, based on public perception and political pressure, NAT screening of the blood supply is expected to become a standard in transfusion medicine
Draft Guidance on Use of NAT to identify HIV-1 and HCV in Whole Blood and Blood components is issued by FDA in March 2002
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Future
Replacing p24 antigen More and more countries will require NAT
non-reactive results before release of blood products
Automated and high-throughput system Individual testing
![Page 58: Hong Kong Association of Blood Transfusion & Haematology NAT and Viral Safety in Blood Transfusion Dr. P.H. Yu Medical Officer Department of Pathology.](https://reader035.fdocuments.us/reader035/viewer/2022062407/56649d0a5503460f949dc6b6/html5/thumbnails/58.jpg)
Future
Screening other virus for specific blood products for specific patient group, eg. screening Parvovirus B19 for Anti-D Ig
Screening for new transfusion-transmitted viruses