In our preceding paper , we summarised current issues in relation to BSE in cattle and the possible further impact on public health. Here, we consider uncertainties in regard to the vCJD epidemic that was initiated by the consumption of food produced from BSE-infected cattle and now threatens to be extended by human-to-human transmission.
Transmission of BSE to man
Is the link between bovine BSE and human vCJD clearly established? Biological and molecular strain typing studies have demonstrated clearly that for practical purposes the BSE agent and the vCJD agent are one and the same, or at least have a similar pathogenicity for man and for macaque monkeys to which both agents have been transmitted. The association between BSE and vCJD is further supported by the epidemic curves, the presumed response to the various bans, the time-scales of the two diseases and their geographical occurrence (Fig. 1, Table I). Following a recommendation from the Southwood Working Party on BSE, from 8 Aug 1988 all cattle suspected to have BSE were removed from all food and feed chains and destroyed. Subsequently, a specified bovine offal (SBO) and finally a specified risk material (SRM) ban was introduced and controls were put in place on the use of the vertebral column and restrictions on the manufacture and sale of mechanically recovered meat (MRM) (Fig. 1). Epidemiological enquiry into vCJD has revealed no association with occupation, medicines, immunisation, gelatine, surgery (including the use of catgut derived from cattle intestine) or exposure to bovine materials or by-products by routes other than orally. Even brain consumption (as brain) has not been incriminated though this last cannot be completely ruled out because brain might have been included in processed food products before the 1989 SBO ban was in place or complete. A theoretical source that has caused great concern (to the extent that it is now completely banned from use in the EU) is mechanically recovered (or separated) meat (MRM) from ruminant animal bones. Historically, skulls were not used to prepare MRM because the teeth were destructive to the machinery. The specific risk would be from the vertebral column because it is virtually impossible to remove all vestiges of spinal cord, dorsal root ganglia (DRG) and associated autonomic and spinal nerves. Thus, there is a global restriction recommended by the OIE that from countries with a controlled or undetermined BSE risk, MRM from skulls and vertebral column from cattle >30 months old should not be traded. As European law prohibits any use or trade of ruminant MRM, any risk from this source is now eliminated completely in the EU. All of these considerations generate confidence that new exposure of humans born and resident in the EU and Switzerland is most unlikely from cattle. No new challenges for the European population are apparent from cattle even though a variant form of BSE (bovine amyloidotic spongiform encephalopathy, (BASE)) has been detected in a small number of animals in Italy . However, scrapie is presently receiving considerable attention in the EC. Although it is apparently not a risk for humans and has not been shown to be transmitted even to sheep and goats via feed, there are several plans to eradicate it. This is partly because there is no easy way to distinguish the various scrapie agents from the BSE agent in a rapid and convincing way, especially in the live animal, and partly because the presence of scrapie severely restricts international trade in sheep and goats and some of their products. One case of BSE in a goat in France has been reported .
Incubation periods for vCJD
In regard to the primary transmission from cattle to man, if the most likely period for transmission of BSE to humans was indeed 1984-89, the incubation periods for the early cases of human BSE infection (vCJD) seem to be of the order of 10 years. If the danger period is extended forward to 1996, shorter human incubation periods are a possibility. On the other hand, if the risk of human infection extended back before the 1980s, much longer incubation periods might be postulated. Since the date of exposure for no individual is known, the actual length of the incubation period is also unknown, though analysis of the epidemiological data enables a reasoned judgment to be made at least for patients with the PRNP MM polymorphism. By contrast, and in regard to secondary transmission from man to man as a result of blood transfusion, for two patients (see below) the incubation period is known with a greater degree of precision, namely 6.5 years  and 8 years . Assuming transfusion to be the cause in these cases, there would be no species barrier. Furthermore, the intravenous route of exposure is orders of magnitude more efficient than the oral route and the amount of blood transfused is likely to be greater than the amount of infected cattle product consumed at one meal. These considerations seem to be consistent with the (presently unproven) assumption that a shorter incubation period is likely in secondary (man-to-man) transfused infections than in primary transmission from cattle by the oral route (c.10 years or so). Caution should be exercised however, because we do not know the titre of infectivity in human blood from an infected donor (estimated to be 0-60 i/v ID50/g) . This is likely to be orders of magnitude less than in brain material from affected cattle (106 cattle i/c ID50/g)  or humans (estimated to be 108 i/c ID50/g ) and bearing in mind that the i/v route is about 10 times less efficient than the i/c route . Longer incubation periods could arise in patients with codon 129 MV and VV polymorphism (see below). Parallels have been drawn between vCJD and kuru, a TSE associated with endocannibalism and funeral rites in the eastern highlands of Papua New Guinea where the range of incubation periods extends from 4 to more than 40 years. Thus, it has been postulated  that some early cases of vCJD seen in the UK may have received their infections earlier than the mid-1980s and could represent infection acquired before we were even aware of BSE in cows. This is worrying, but a note of caution is justified on at least two counts. It seems that a factor, or several factors, operated when BSE transmitted to human patients. Perhaps this is related to the size of the challenge dose, or to repeated (cumulative) challenges, though evidence for the latter is unconvincing [16,21,28]. It may be that a coincident infection acted to make a victim susceptible to the BSE (vCJD) agent at a particular time (sometimes perhaps even early in childhood, in the case of teenagers who have died). Indeed, various models indicate that vCJD infection seems to be preferentially acquired by young people, and older subjects may be more resistant [11,41]. We do not yet know if they resist infection or become infected but do not develop clinical disease, either at all, or after extended incubation. In contrast to the situation with BSE in cattle , since 1996 the average age of vCJD patients has not changed significantly (median age at onset 26 and at death 28 years)  despite the fact that the major exposures from food were probably confined to a relatively short period. As noted above, teenagers and young adults might be more susceptible to infection and develop clinical signs more readily [11,41], such as may have occurred in the kuru epidemic where some young children succumbed and some adults exposed around the same time had very long incubations indeed. However, it is important to note that the agent that causes vCJD is unique among human TSE agents and is biologically indistinguishable from the BSE agent , so kuru might not be a good model to guide us. Another consideration is that, in the UK, young people may have selectively consumed food containing mechanically recovered meat (MRM) with a potentially high TSE-risk .
BSE/vCJD agent, PrP and its associated gene
Prusiner and colleagues suggested that the infectious agent in BSE, and thus in vCJD, is a prion - a small proteinaceous infectious particle that resists inactivation by procedures which modify nucleic acids and thus may be devoid of detectable DNA . To date, the prion is known to be very small, passing through small-pore filters, and to be remarkably heat-stable and resistant to a wide range of antimicrobial chemicals including formaldehyde when tested in crude mixtures of infective brain homogenates. Despite this, chemical and physical methods have been devised that are effective and widely used in hospitals, autopsy rooms and industrial suites to secure safety . The importance of thorough cleaning is stressed, with careful removal of all traces of protein from surfaces before disinfection and from surgical instruments prior to sterilization. The particle has not yet been visualized as such, but some structures called scrapie-associated fibrils and prion rods, seen by electron-microscopy after chemical extraction and treatment of infective material, may be aggregates of prions. The terminology has evolved in a confusing manner. A host-encoded glycoprotein that is a normal constituent of cell membranes in man and animals is designated PrPC. The letter C denotes the normal form of the protein expressed in many cell types and notably in the brain. The abnormal form PrPSc was so called because it was first associated with scrapie (Sc) in sheep but is commonly used to relate to any TSE. (Various other symbols are used to differentiate between the normal and abnormal forms of PrP.) Attention has been drawn to codon 129 of the gene that codes for PrPC in man, the prion protein (PRNP) gene. Homozygous individuals may have two methionine alleles (MM) or two valine (VV) alleles. Heterozygous individuals have one of each allele (MV) at codon 129. All of the patients who have died of vCJD and have been genetically investigated so far are homozygous for methionine (MM). A possible, but uncertain, exception was a heterozygous (MV) patient apparently infected by blood transfusion from a donor who subsequently developed vCJD . The heterozygote recipient developed no neurological symptoms prior to death and showed no evidence of vCJD-related neuropathology or PrPSc accumulation in the central nervous system. This case is therefore provisionally considered to be an asymptomatic vCJD infection that may (preclinical case) or may not (subclinical case) have gone on to be expressed as vCJD. Present evidence indicates that MM homozygosity at codon 129 is associated with susceptibility to vCJD. Alternatively, it may be that MM is a factor that predisposes to a shorter incubation period, whilst MV heterozygosity or VV homozygosity may be considered as factors conferring relative resistance or longer incubation periods. If this is the case, then we might expect to see another wave or waves of cases of vCJD representing infections that were incubated in MV or VV patients. Yet another worrying possibility is that the disease produced in the latter patients (if any) might differ clinically from vCJD in patients with the MM allele. These points are part of the reason for caution when the experts are pressed to predict the future course of events in this difficult field. Studies of the PrP gene of cows (which, like most other animal species, are homozygous for methionine at the equivalent codon) have revealed polymorphisms in the octa-repeat region but these show no association with disease occurrence. It is believed that cattle are uniformly susceptible to BSE. By contrast, the sheep PrP gene is polymorphic at several codons and notably at codons 136, 154 and 171. Some genotypes are highly susceptible to scrapie, others are much more resistant and some are of intermediate ‘resistance’. Use has been made of this variability by breeding rams homozygous for ‘resistance’ to increase the desirable alleles in the national flock in various European and other countries .
vCJD: Concepts and trends
The change from normal PrPC to misfolded PrPSc is post-translational. The misfolding results in the conversion of an a helix-rich protein to a form rich in b sheet, for example by a process of dimerisation in a type of chain reaction. The abnormal form is partially protease-resistant whereas PrPC is denatured by proteases and this enables a distinction to be made between the two. Results of experimental studies in rodents suggest that, in natural human infection by the oral route, it is likely that the agent is initially taken up by migrating intestinal dendritic cells. These transport it to follicular dendritic cells (FDC) resident in lymphoreticular sites in the gut and elsewhere such as in Peyer’s patches of the jejunum and ileum and lymphoid tissue of the appendix and large intestine. FDC maturation is assisted by lymphocytes, suggesting an important role for these cells in TSE, including increasing the risk of infection in chronically inflamed tissues . Accumulation and/or replication of infectivity in the FDC is a necessary prelude to neuroinvasion effected through peripheral nerves of the autonomic nervous system to the spinal cord and then the brain [1,8,38]. PrPSc accumulates in the brain, infectivity titres rise and there is progressive neurodegeneration leading to death. Patients with symptoms and signs of the disease that we now recognise as vCJD were first observed in the UK in 1995. The number of definite or probable deaths from vCJD in the UK and worldwide are given in table I and the UK data are presented graphically in figure 1. Annual numbers of deaths from vCJD rose thereafter to a peak of 28 in 2000 and have then fallen progressively (at least, up to Feb. 2006). Once again, however, a note of caution is needed. The number of onsets of vCJD (new cases each year) increased in 2004 (9 cases) compared with 2003 (5 cases). This may be a more reliable indication of the current trend and must moderate our optimism.
vCJD: The uncertain future
The ominous interpretation suggested by Collinge  is that the graph of the UK figures might include some cases of infection acquired before the overt infection in British cattle, so that an unknown number of human cases relating to infection acquired in the 1980s and later have still to be accounted for. It is tempting to draw premature but more reassuring conclusions from the shape of the graph of these mortality figures. If the patients with vCJD seen in the last decade were not attributable to infections acquired from 1984 or later (when the BSE outbreak started), they would be part of a cohort of patients who had long incubation times of 12-22 years. If such cases were going on to represent the extremes of long incubation, as in kuru, their numbers should not be so strikingly affected by the controls that were introduced from 1988-1996. Perhaps, however, there might be a strange biphasic character in their presentation, and a possible explanation could rest on the influence on incubation times of MV heterozygosity or VV homozygosity at the polymorphic codon 129. Even without this influence of host genetics on possible susceptibility, Cooper and Bird  have noted that subjects in the birth cohorts studied by them had different dietary exposure intensities to BSE that prevailed before and after significant preventive actions in 1989. Their calculations indicate that, for presently unknown reasons, significant numbers of later (primary) cases of vCJD may yet be seen in the UK in the present decade as a second wave of patients who presumably ingested the agent in cattle meat products containing or contaminated with SRM. The shape of the graph of vCJD incidence in the UK in the last decade seems to be compatible with the view that we are experiencing the effects of infection transmitted to human patients when the BSE outbreak occurred in cows in the mid-1980s or 1990s, or just a few years before this, say, in the early 1980s. In the light of the worst predictions on this premise, we have been fortunate so far. Most of these early extrapolations were based on the assumption that all of the deaths from vCJD recorded to date in the UK were attributable to infections resulting from the overt outbreak of BSE in cattle. This is a reasonable basis for prediction, though some of the earlier published estimates were alarming and present estimates are more reassuring (but see below). In the present paper, we have taken account of alternative suggestions that there may be another (later) human sequel to the bovine outbreak. We also bear in mind that BSE and cases of vCJD in other countries may have longer courses to run. Most of the literature on BSE and vCJD to date implies that vCJD in man is acquired as a primary disease from cattle. The probable (secondary) human-to-human transmission of vCJD infection via transfusion of infected blood now appears to be almost certain, but doubt remains (as noted above) about the patient originally reported by Peden et al., who may be an example of an asymptomatic infection in an MV heterozygote recipient. A death has certainly been reported in a methionine homozygote recipient who received blood from a donor who was healthy at the time but who developed and died from vCJD subsequently . The most recent report in Feb. 2006 is of another patient who is symptomatic but presently alive . There is much concern that further cases of vCJD may arise in this way. The worry extends beyond the UK to other countries across the world and it has led to major alerts and product withdrawal, with restrictions on donors of blood, organs and tissues. There are on-going urgent reviews of the safety of human blood and plasma and derived products, and similar reconsiderations of the safety of human tissues and medical and surgical instruments that may have become contaminated with the vCJD agent. In the context of transfusion, the use of leucodepletion is a recognised step to safeguard blood for transfusion, but it is not considered to be an absolute protection as tests (with blood from scrapie-infected hamsters) showed that about half of the potential infectivity may remain after the treatment .
There is another area of concern relating to the widespread distribution of PrPSc that is known to occur in lymphatic tissues of vCJD patients  when tests are done based on immunohistochemical (IHC) techniques and/or sensitive Western Blot technology [26,29]. There is evidence that, at least in the spleen and the tonsil, infectivity can also be demonstrated . A worrying development has been the finding of PrPSc in an appendix removed from an otherwise healthy patient who went on to develop vCJD 8 months later . In 2004, a report mentioned another incident where appendix tissue removed at appendicectomy was positive for PrPSc two years before the symptoms and signs of vCJD appeared and four years before death . Appendix tissue removed from a third patient at appendicectomy 10 years before vCJD was diagnosed, was negative for PrPSc . Three anonymous surveys have been done to determine the prevalence of PrPSc in appendices removed at routine appendicectomy. In the first, no positives were found in 3075 samples . In the second survey, 1 positive appendix was found out of 8318 specimens examined by IHC  and the distribution of PrPSc was similar to that found in the two preclinical samples noted above. In the third study, 3 out of 12,674 appendix samples were positive for PrPSc by IHC . The latter figure gives an estimated prevalence of 237 vCJD infections per million in the UK (95% CI 49-692 per million) . However, although the immunocytochemical method performed to detect PrPSc in this study appears to be specific, it is unlikely to be fully sensitive for all phases of the (unknown) incubation period, and this causes further uncertainty in the estimation of the numbers of vCJD infections that have occurred. Similar anonymous studies have been done on tonsils removed at tonsillectomy. In the first of these studies , all 95 tonsils examined by IHC were negative for PrPSc; and, in the second tonsil survey, no positives were found in 2,000 tonsils examined . The positive findings with appendicectomy specimens have led to the speculation that pre-clinical or sub-clinical vCJD may be present in a proportion of the population. There is an understandable call for large-scale prospective screening to provide evidence for estimations of prevalence and to increase awareness of possible secondary transmission in surgery, particularly in relation to young people who may have been exposed to BSE before it was brought under control, though the magnitude of any hidden pre/subclinical population is likely to be underestimated . All of these considerations increase the urgent need for tests that would reliably and speedily determine whether a patient may be in danger of developing vCJD, ideally by a minimally invasive procedure. Promising results are being reported, for example by Castilla, Saá and Sato  who have employed protein misfolding cyclic amplification (PMCA) technology to amplify very small amounts of PrPSc (that might be present in blood) by over 6,500 times and thus substantially increase the sensitivity of the test. A number of other potentially useful tests for detecting tiny amounts of the misfolded protein are under development and are being presented at recent and future meetings on TSE and blood. For a review of diagnostic methods in animals see Gavier-Widén et al. . Technology and research is also progressing in the elimination of TSE infectivity and decontamination and the evaluation and control of instrument- and device-borne prion infection [2,17].
Our analysis of the currently available data allows us to be optimistic in foreseeing the elimination of BSE in the EU and countries that follow the EU plan. The outlook is necessarily less assured for the control of BSE in other countries adopting less stringent remedies. In consequence, in regard to vCJD in ‘Europe’, we are content that there has been effective and virtually complete elimination of food-borne BSE from cattle to man, but we are more cautious for some countries elsewhere. The current trends in the human epidemic of vCJD in the UK are reassuring, but we note that the present reduction in numbers of these cases stems from measures adopted in the veterinary, rather than the medical field. We are presently much more uncertain about the future trends in the human epidemic that might result from a currently concealed, unknown number of infected people in the European population, due either to their PRNP genotype (MV or VV) or to existing pre-clinical or sub-clinical infection. If such concealed populations exist, are their numbers too small to permit maintenance of the epidemic, or are they already considerable and being added to by current practices? There is a need for continuing surveillance for BSE and all forms of CJD in the UK, EU and indeed globally, in view of the uncertainty of the occurrence and extent of BSE in many countries of the world, the absence of fully effective measures and their enforcement, and the uncertainty about future trends in the human epidemic of vCJD in the UK despite effective controls on BSE. The hazard of vCJD has greatly complicated the careful vetting of blood donors and there is an urgent requirement for a test that might detect infected persons. We are convinced that blood transfusion is a means of transmission of vCJD but note that the recent UK infections occurred before leucodepletion of blood was in place. Currently we know of no certain human-to-human transmissions by other routes or mechanisms, but it is probably too early to say that they will not occur. Whilst we are strongly encouraged by the actions taken to research and to reduce infectivity in blood and to determine effective ways to clean and decontaminate instruments and surfaces, we are aware that many problems remain to be solved if we are to deal effectively with this daunting challenge.
We thank Professor JW Ironside for valuable comments and much generous help with this review. We gratefully acknowledge guidance from Mr DE Bradbury on the presentation of data in the charts and Dr PW Brown for guidance on presenting vCJD case data. And we thank DEFRA, SEAC, OIE, EC, EFSA and the National CJDSU at Edinburgh for access to and regular updating of information.
1. Aguzzi A. Neuro-immune connection in spread of prions in the body? Lancet 1997; 349: 742-743. 2. Baxter HC, Campbell GA, Whittaker AG, Jones AC, Aitken A, Simpson AH, Casey M, Bountiff L, Gibbard L, Baxter RL. Elimination of transmissible spongiform encephalopathy infectivity and decontamination of surgical instruments by using radio-frequency gas-plasma treatment. J Gen Virol 2005; 86: 2393-2399. 3. Bradley R, Collee JG, Liberski PP. Variant CJD (vCJD) and bovine spongiform encephalopathy (BSE): 10 and 20 years on – part 1. Folia Neuropathol 2006; 44: 93-101. 4. Bruce ME, McConnell I, Will RG, Ironside JW. Detection of variant Creutzfeldt- Jakob disease. Infectivity in extraneural tissues. Lancet 2001; 358: 208-209. 5. Buschmann A, Groschup MH. Highly bovine spongiform encephalopathy-sensitive transgenic mice confirm the essential restriction of infectivity to the nervous system in clinically diseased cattle. J Infect Dis 2005; 192: 934-942. 6. Casalone C, Zanusso G, Acutis P, Ferrari S, Capucci L, Tagliavini F, Monaco S, Caramelli M. Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease. Proc Natl Acad Sci U S A 2004; 101: 3065-3070. 7. Castilla J, Saá P, Soto C. Detection of prions in blood. Nat Med 2005; 11: 982-985. 8. Collee JG. Transmissible Spongiform Encephalopathies. In: The Microbiological Safety and Quality of Food, Barbara M Lund, TC Baird-Parker, GW Gould eds, vol. II, Aspen, Maryland, USA 2000. Ch 57, p. 1618. 9. Collinge J. Variant Creutzfeldt-Jakob disease. Lancet 1999; 354: 317-323. 10. Communicable Disease Report Weekly. New case of transfusion-associated variant-CJD. CDR Weekly 2006; 16: 9 Feb. 2006. 11. Cooper JD, Bird SM. Predicting incidence of variant Creutzfeldt-Jakob disease from UK dietary exposure to bovine spongiform encephalopathy for the 1940 to 1969 and post-1969 birth cohorts. Int J Epidemiol 2003; 32: 784-791. 12. Dawson M, Hoinville LJ, Hosie BD, Hunter N. Guidance on the use of PrP genotyping as an aid to the control of clinical scrapie. Vet Rec 1998; 142: 623-625. 13. Department of the Environment, Food and Rural Affairs (DEFRA). BSE statistics - confirmed cases of BSE reported worldwide as at 3 Jan. 2006 Website accessed Feb. 2006. http://www.defra.gov.uk/ animalh/bse/statistics/bse/worldwide.htm 14. Department of the Environment, Food and Rural Affairs (DEFRA). Transmissible Spongiform Encephalopathies in Great Britain - A Progress Report, Dec. 2001. DEFRA, London, 2002, p. 152. 15. Det Norske Veritas. Assessment of the risk of exposure to vCJD infectivity in blood and blood products. Appendix II: Risk assessment of vCJD infectivity in blood. Report for the department of Health, Revision D. Feb. 2003. DNV Consulting London. Pp 55. Website accessed Feb. 2006. http://www.dnv.co.uk/Binaries/ AppII_tcm23-74416.pdf 16. Diringer H, Roehmel J, Beekes M. Effect of repeated oral infection of hamsters with scrapie. J Gen Virol 1998; 79: 609-612. 17. Fichet G, Comoy E, Duval C, Antloga K, Dehen C, Charbonnier A, McDonnell G, Brown P, Lasmezas CI, Deslys JP. Novel methods for disinfection of prion-contaminated medical devices. Lancet 2004; 364: 521-526. 18. Frosh A, Smith LC, Jackson CJ, Linehan JM, Brandner S, Wadsworth JD, Collinge J. Analysis of 2000 consecutive UK tonsillectomy specimens for disease-related protein. Lancet 2004; 364: 1260-1262. 19. Gavier-Widén D, Stack MJ, Baron T. Diagnosis of transmissible spongiform encephalopathies in animals: a review. J Vet Diagn Invest 2005; 17: 509-527. 20. Goldmann W, Baylis M, Chihota C, Stevenson E, Hunter N. Frequencies of PrP gene haplotypes in British sheep flocks and the implications for breeding programmes. J Appl Microbiol 2005; 98: 1294-1302. 21. Gravenor MB, Stallard N, Curnow R, McLean AR. Repeated challenge with prion disease: the risk of infection and impact on incubation period. Proc Natl Acad Sci U S A 2003; 100: 10960-10965. 22. Gregori L, McCombie N, Palmer D, Birch P, Sowemimo-Coker SO, Giulivi A, Rohwer RG. Effectiveness of leucoreduction for removal of infectivity of transmissible spongiform encephalopathies from blood. Lancet 2004; 364: 529-531. 23. Hilton DA, Fathers E, Edwards P, Ironside JW, Zajicek J. Prion immunoreactivity in appendix before clinical onset of variant Creutzfeldt-Jakob disease. Lancet 1998; 352: 703-704. 24. Hilton DA, Ghani AC, Conyers L, Edwards P, McCardle L, Penney M, Ritchie D, Ironside JW. Accumulation of prion protein in tonsil and appendix: review of tissue samples. BMJ 2002; 325: 633-634. 25. Hilton DA, Ghani AC, Conyers L, Edwards P, McCardle L, Ritchie D, Penney M, Hegazy D, Ironside JW. Prevalence of lymphoreticular prion protein accumulation in UK tissue samples. J Pathol 2004; 203: 733-739. 26. Hilton DA, Sutak J, Smith MEF, Penney M, Conyers L, Edwards P, McCardle L, Ritchie D, Head MW, Wiley CA, Ironside JW. Specificity of lymphoreticular accumulation of prion protein for variant Creutzfeldt-Jakob disease. J Clin Pathol 2004; 57: 300-302. 27. Ironside JW, Hilton DA, Ghani A, Johnston N, Conyers L, McCardle LM, Best D. Retrospective study of prion-protein accumulation in tonsil and appendix tissues. Lancet 2000; 255: 1693-1694. 28. Jacquemot C, Cuche C, Dormont D, Lazarini F. High incidence of scrapie induced by repeated injections of subinfectious prion doses. J Virol 2005; 79: 8904-8908. 29. Joiner S, Linehan J, Brandner S, Wadsworth JDF, Collinge J. Irregular presence of abnormal prion protein in appendix in variant Creutzfeldt-Jakob disease. J Neurol Neurosurg Psychiatry 2002; 73: 597-603. 30. Ligios C, Sigurdson CJ, Santucciu C, Carcassola G, Manco G, Basagni M, Maestrale C, Cancedda MG, Madau L, Aguzzi A. PrPSc in mammary glands of sheep affected by scrapie and mastitis. Nat Med 2005; 11: 1137-1138. 31. Llewelyn CA, Hewitt PE, Knight RS, Amar K, Cousens S, Mackenzie J, Will RG. Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion. Lancet 2004; 363: 417-421. 32. National CJD Surveillance Unit. Thirteenth Annual Report for 2004, 2005. Website accessed Feb. 2006. http://www.cjd.ed.ac.uk/ report13.pdf 33. National Creutzfeldt-Jakob Disease Surveillance Unit. Website accessed Feb.2006. http://www.cjd.ed.ac.uk/figures.htm 34. Office International des Epizooties (OIE). Website accessed Feb. 2006. http://www.oie.int/eng/info/en_esbru.htm 35. Office International des Epizooties (OIE). Website accessed Feb. 2006. http://www.oie.int/eng/info/en_esbmonde.htm 36. Peden AH, Head MW, Ritchie DL, Bell JE, Ironside JW. Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient. Lancet 2004; 364: 527-529. 37. Prusiner SB. Novel proteinaceous particles cause scrapie. Science 1982; 216: 136-144. 38. Shmakov AN, Ghosh S. Prion proteins and the gut: une liaison dangereuse? Gut 2001; 48: 443-447. 39. Spongiform Encephalopathy Advisory Committee (SEAC). Draft minutes of 90th meeting held on 24 November 2005. Website accessed Feb. 2006. http://www.seac.gov.uk/minutes/final90.pdf 40. Taylor DM. Resistance of TSE agents to decontamination. In: Rabenau HF, Cinatl J, Doerr HW, eds. Prions. A challenge for science, medicine and the public health system. Contrib Microb. Basel Karger 2004; 11: 136-145. 41. Valleron AJ, Boelle PY, Will RG, Cesbron JY. Estimation of epidemic size and incubation time based on age characteristics of vCJD in the United Kingdom. Science 2001; 294: 1726-1728.
Note added in Proof (June 2006)
The PRNP genotype of two of the three appendix tissue samples that tested positively for PrPSc in the large retrospective prevalence study referred to in this paper has now been determined . The genotype in both is confirmed as homozygous for the valine allele (VV) at codon 129 of the PRNP gene. There was insufficient material to test the third sample. This is the first indication that valine homozygotes may be susceptible to vCJD infection and shows now that all PRNP codon 129 genotypes may be susceptible to vCJD infection, which was not known before.
1. Ironside JW, Bishop MT, Connolly K, Hegazy D, Lowrie S, Le Grice M, Ritchie D, McCardle LM, Hilton DA. Variant Creutzfeldt-Jakob Disease: a prion protein genotype analysis of positive appendix tissue samples from a retrospective prevalence study. BMJ 2006; 332: 1186-1188. http://bmj.bmjjournals.com/cgi/content/abstract/332/7551/1186