Haematologica 2001; 86:E04

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Management of blood donors with a low level of exposure to variant Creutzfeld-Jacob disease
Daniela Pasqualetti,@ Alessandro Ghirardini,* Rino Bellocco,# Stefania Vaglio,@ Maria Gozzer,@ Gabriella Girelli@
@ Blood Bank, Dipartimento di Biotecnologie Cellulari ed Ematologia, University "La Sapienza", Rome, Italy (D Pasqualetti, S Vaglio, M Gozzer, G Girelli); * Laboratory of Epidemiology and Biostatistics, Istituto Superiore di Sanità Rome, Italy (A Ghirardini); #Department of Medical Epidemiology, Karolinska Institutet, Stockholm, Sweden.


Correspondence: Daniela Pasqualetti. E-mail: pasqualetti@bce.med.uniroma1.it

medline ref.
Prevention of hypothetical transmission of new variant Creutzfeldt Jacob Disease (vCJD) through blood transfusion has been the deferral from donation for those who stayed in UK or France for more than six months, and/or the adoption of leukoreduction. We suggest an approach also for people with a length of stay less than six moths, by the adoption of a protocol of multicomponent apheresis, with the donation of two red blood cells units submitted to an on-line filtration, without plasma and platelets collection. Risk of transmitting vCJD leaded several countries to modify their policies regarding blood safety. US, Canada and New Zealand deferred blood donors who lived in UK and France for more than six months during 1980-1996, as a proxy of the exposure to contaminated beef. This exclusion from donations produces an expected drop in the blood supply, from 1% to 2.5% depending on the estimates.1,2 No policy was chosen for donors with a level of exposure (less than six monhs), even if the US Red Cross has recently proposed their exclusion from donation, with an additonal drop in the blood supply. Other countries, such as Canada, France, Portugal, Ireland and Switzerland recommended and implemented universal leukoreduction,3 for removing the possible source of prion infectivity. UK also introduced leukoreduction together with the discard of plasma, which infectivity could not be affected by leukoreduction.4 An important issue in the debate on the hypothetical risk of vCJD transmission by blood5 concerns with the efficacy of leukoreduction6 in the removal of some possible sources of prion proteins, other than leukocytes, such as platelets and plasma. In fact red blood cells (RBC's) which is submitted to the standard leukoreduction process contains some amount of platelets fragments as well as plasma: for this reason it has been suggested that the currently leukoreduction techniques could not be as safe as possible to reduce the theoretical risk of vCJD transmission. This suggestion is based on some experiments7 showing that the prion protein (PrP) is expressed on leukocytes, but also in high concentration on platelets and plasma. If the rationale for the leukoreduction is the removal of cell expressing PrP (either in the normal form or in the form causing vCJD), the presence of discrete amounts of platelets and plasma in RBC's after the standard leukoreduction procedure could represent an additional risk. A way of production leukoreduced RBC's together with the removal of platelets and plasma, is represented by the multicomponent apheresis procedure with an in-line leukoreduction.8 This technique allows for the selective donation of each blood component, namely RBC's, which is produced in a standardised way and with high levels of purity. The adoption of a targeted protocol of leukoreduction applied to the "multicomponent apheresis", for people with a low level of exposure (less than 6 months in UK), could allow the flexibility to collect standardised blood components from a single donor, in one step, at the time of donation, with the availability of high quality leukoreduced RBC's, with an on-line filtration. Plasma will not be collected, eliminating any theoretical risk of infectivity for vCJD, and a frequent plasma programme by apheresis will cover this plasma deficiency. Moreover by evaluating platelets with Thoma's camera, a low level of platelets may be counted, corresponding to a 1-log estimated reduction of platelets concentration in comparison to standard leukoreduced RBC's. On the basis of the precautionary approach9 we believe the multicomponent apheresis a way of production standardised RBC's with the highest rate of purity with regard to platelets and plasma, thus further reducing the theoretical risk of vCJD transmission by blood transfusion.

References

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  2. Wilkinson SL, Mitka M. Transmissible spongiform encefalopathies and the US blood supply. JAMA 1999;282:2301-2
  3. Birchard K. Three countries to start leukocyte depletion of donated blood. Lancet 1998; 351:1112.
  4. Brown P, Cervenàkovà L L, McShane LM, Barber P, Rubenstein R, Drohan WN. Further studies of blood infectivity in an experimental model of transmissible spongiform encephalopathy, with an explanation of why blood components do not transmit Creutzfeldt-Jacob disease in humans. Transfusion 1999;39:1169-78.
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  8. PA Shi, PM Ness. Two-unit red cell apheresis and its potential advantages over traditional whole-blood donation. Transfusion 1999;39:218-225.
  9. European Commission. Communication on the precautionary principle. COM (2000)1.