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Invest in ME have written to the
NHS Blood and Transfusion Service regarding two points -
1/ Why in the recent NHS press
release there was no mention the Lo et al. paper from the NIH/FDA [http://www.pnas.org/content/107/36/15874.abstract?sid=30cc5eaa-5902-4097-b2ba-f436ae4eae7b]
published by PNAS in May 25, 2010 ?
We indicated that
the Impact Factor rating, which is
used as a guide to the relative importance of a journal within its
field, would have been higher for the PNAS paper than the
publications that published the negative studies and to which the
press release did refer. We believed it would be appropriate to
reference the important Lo et al. paper from the two big US federal
agencies in this context and not just the negative study from the
CDC.
We asked if the blood service were not at all concerned about the possible
contamination of the blood banks with a new gamma retrovirus that
has been associated with ME/CFS by two very high impact
publications, The Science Magazine and PNAS?
The reason for banning ME(CFS) patients from donating blood in New
Zealand, Australia and Canada (and the recommendation in USA) is due
to the risk of contamination of the blood supply with a retrovirus.
2/Would NHSBT comment on whether
the ban applies to people with ME from donating organs?
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Reply from UK
NHS Blood and Transplant
Service
The UK Blood Services have a Joint
Professional Advisory Committee (JPAC) which collates advice from standing
committees of experts on blood transfusion medicine and practice. The committee
members are employed by the UK
and Irish blood services, the Health Protection Agency (HPA), and universities
and hospitals throughout the
UK. JPAC
commissions risk assessments and makes recommendations on exclusion and deferral
criteria for blood donors in the light of the advice of these committees.
In November 2009 the UK Blood Services Standing Advisory
Committee on Transfusion Transmitted Infections (SACTTI) submitted a risk
assessment to JPAC regarding XMRV. A list of the research which informed that
risk assessment is shown at the end of this e-mail. Whilst there was not
considered to be any evidence to change donor selection criteria in the UK on
patient safety grounds, the committee agreed to continue monitoring and
reviewing new evidence.
Since the submission of that risk assessment a number of new
pieces of research on murine related viruses (MLV) and XMRV have been reviewed
by SACTTI. In October 2010 the committee examined the paper you referenced,
Detection of MLV-related
virus gene sequences in blood of patients with chronic fatigue syndrome and
healthy blood donors
(Lo et al, 2010) which reported
evidence of MLV-related virus gene sequences in 86% of
myalgic encephalomyelitis/chronic
fatigue syndrome (ME/CFS) patients compared to 6% of healthy controls; as well
as two other papers that failed to show evidence of XMRV in ME/CFS patients in
the USA and China. The Lo et al paper specifically commented that the MLV-related
virus gene sequences which they detected were not XMRV, and represented a
broader group of MLV-related viruses than just XMRV. The committee noted that
currently there are more published papers with negative than positive
associations between XMRV/MLVs and ME/CFS, and none using
UK samples. However, relevant new research will
continue to be reviewed.
The Department of
Health's independent Advisory Committee on the Safety of Blood, Tissues and
Organs (SaBTO) and the National Expert Panel on New and Emerging Infections (NEPNEI)
also monitor developments which are relevant to blood safety, both nationally
and internationally, in conjunction with the UK Blood Services and the HPA.
An
expert subgroup of NEPNEI met in May 2010, and considered all available data
about XMRV. The
subgroup concluded that XMRV can infect humans but there is currently no
evidence that it causes human disease, and that on the evidence before the group
no public health action is required at this time. On the
basis of current evidence SaBTO also does not recommend further measures at
present, but wishes to continue monitoring the situation.
With regard to your question about organ donation, at present
people with ME/CFS can be considered as potential organ donors. This policy will
also be kept under review in the context of new evidence.
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References for risk assessment submitted by SACCTI to JPAC, November
2009 |
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D'Arcy F, R.
Foley, A. Perry, L. Marignol, M. Lawler, E. Gaffney, R.G.W.
Watson, J.M. Fitzpatrick, T.H. Lynch.
No evidence of XMRV in Irish prostate cancer patients with the
R462Q mutation. European Urology
Supplements, 7 (3): 271, March 2008,
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Dong
B, Kim S, Hong S, Das Gupta J, Malathi K, Klein EA, Ganem D, Derisi
JL, Chow SA, Silverman RH.
An infectious retrovirus susceptible to an IFN antiviral pathway
from human prostate tumors.
Proc
Natl Acad Sci U S A.
2007 Jan 30;104(5):1655-60.
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Fischer
N, Hellwinkel O, Schulz C, Chun FK, Huland H, Aepfelbacher M,
Schlomm T.
Prevalence of human gammaretrovirus XMRV in sporadic prostate
cancer. J Clin Virol.
2008
Nov;43(3):277-83.
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Furuta
RA, Miyazawa T, Sugiyama T, Kimura T, Hirayama F, Tani Y, Shibata H.
The Prevalence of Xenotropic Murine Leukemia
Virus-Related Virus in Healthy Blood Donors in Japan.
In
Abstracts of papers presented at the 2009 meeting on
Retroviruses, May 18 - May 23, 2009 Cold Spring Harbour Laboratory.
pp. 100; 2009:100.
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Hohn O,
Krause H, Barbarotto P, Niederstadt L, Beimforde N, Denner J, Miller
K, Kurth R, Bannert N.
Lack of evidence for xenotropic murine leukemia virus-related virus
(XMRV) in German prostate cancer patients.Retrovirology.
2009 Oct 16;6(1):92
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Lombardi VC, Ruscetti FW, Das Gupta J, Pfost MA, Hagen KS, Peterson
DL, Ruscetti SK, Bagni RK, Petrow-Sadowski C, Gold B, Dean M,
Silverman RH, Mikovits JA.
Detection of an Infectious Retrovirus, XMRV, in Blood Cells of
Patients with Chronic Fatigue Syndrome.
Science. 2009 Oct 8
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McCormick AL, Brown RH Jr, Cudkowicz ME, Al-Chalabi A, Garson JA.
Quantification of reverse transcriptase in ALS and elimination of a
novel retroviral candidate.Neurology.
2008 Jan 22;70(4):278-83.
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Schlaberg R, Choe DJ, Brown KR, Thaker HM, Singh IR.
XMRV is present in malignant prostatic epithelium and is associated
with prostate cancer, especially high-grade tumors.
Proc Natl Acad Sci U S A.
2009 Sep 22;106(38):16351-6.
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Urisman A, Molinaro RJ, Fischer N, Plummer SJ, Casey G, Klein EA,
Malathi K, Magi-Galluzzi C, Tubbs RR, Ganem D, Silverman RH, DeRisi
JL.
Identification of a novel Gammaretrovirus in prostate tumors of
patients homozygous for R462Q RNASEL variant.
PLoS Pathog. 2006 Mar;2(3):e25. |
Last Updated:
04/11/2010

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