Blood system changes since recognition of transfusion‐associated AIDS

T he year 2013 brought us to the close of the third decade since the discovery of human immunodeficiency virus (HIV), originally called lymphadenopathy-associated virus or human T-lymphotropic virus Type 3 (HTLV-III), as the cause of AIDS. This landmark occasions a time for reflection on the transformations of the blood system that were set in motion by recognition of transfusion-associated AIDS (TAA). While the decade of the 1980s was characterized by rapid introduction of novel strategies to address an unprecedented challenge, changes made in the 1990s, though independently significant, were also reactive, as the system tried to define and incorporate the lessons of TAA. In the latter decade, criticisms of prior decision making, coupled with new technology options, led to a broad-based initiative to enhance blood safety. In the new millennium, ongoing efforts to address blood safety have focused repeatedly on threats from known and emerging infectious diseases. However, concerns have arisen about a trend of increasing safety costs with progressively decreasing added benefits. This commentary summarizes key changes to the blood system during this 30-year period and discusses the evolving framework for blood safety decision making that is taking form.

[1]  S. Görg,et al.  Seroprevalence and incidence of hepatitis E virus infection in German blood donors , 2014, Transfusion.

[2]  R. Cable,et al.  Babesia microti real‐time polymerase chain reaction testing of Connecticut blood donors: potential implications for screening algorithms , 2013, Transfusion.

[3]  S. Kleinman,et al.  Survey of methods used to detect bacterial contamination of platelet products in the United States in 2011 , 2013, Transfusion.

[4]  S. Glynn,et al.  Emerging infectious agents and the nation's blood supply: responding to potential threats in the 21st century , 2012, Transfusion.

[5]  W. Heneine,et al.  A Multicenter Blinded Analysis Indicates No Association between Chronic Fatigue Syndrome/Myalgic Encephalomyelitis and either Xenotropic Murine Leukemia Virus-Related Virus or Polytropic Murine Leukemia Virus , 2012, mBio.

[6]  S. Montgomery,et al.  The United States Trypanosoma cruzi Infection Study: evidence for vector‐borne transmission of the parasite that causes Chagas disease among United States blood donors , 2012, Transfusion.

[7]  H. Kamel,et al.  Epidemiologic and laboratory findings from 3 years of testing United States blood donors for Trypanosoma cruzi , 2012, Transfusion.

[8]  J. Muñoz-Jordán,et al.  Dengue viremia in blood donors identified by RNA and detection of dengue transfusion transmission during the 2007 dengue outbreak in Puerto Rico , 2012, Transfusion.

[9]  W. Heneine,et al.  Failure to Confirm XMRV/MLVs in the Blood of Patients with Chronic Fatigue Syndrome: A Multi-Laboratory Study , 2011, Science.

[10]  D. Devine,et al.  Risk‐based decision‐making for blood safety: preliminary report of a consensus conference , 2011, Vox sanguinis.

[11]  L. Montagnier,et al.  HIV's leading men. , 2011, IAVI report : newsletter on international AIDS vaccine research.

[12]  R. Silverman,et al.  Xenotropic murine leukemia virus–related virus (XMRV) and blood transfusion: report of the AABB interorganizational XMRV task force , 2011, Transfusion.

[13]  M. Busch,et al.  Transfusion‐associated infections: 50 years of relentless challenges and remarkable progress , 2010, Transfusion.

[14]  J. Mikovits,et al.  Detection of an Infectious Retrovirus, XMRV, in Blood Cells of Patients with Chronic Fatigue Syndrome , 2009, Science.

[15]  A. Komaroff,et al.  Detection of MLV-related virus gene sequences in blood of patients with chronic fatigue syndrome and healthy blood donors , 2010, Proceedings of the National Academy of Sciences.

[16]  W. Heneine,et al.  Absence of evidence of Xenotropic Murine Leukemia Virus-related virus infection in persons with Chronic Fatigue Syndrome and healthy controls in the United States , 2010, Retrovirology.

[17]  S. Wessely,et al.  Comment on “Detection of an Infectious Retrovirus, XMRV, in Blood Cells of Patients with Chronic Fatigue Syndrome” , 2010, Science.

[18]  L. Montagnier 25 years after HIV discovery: prospects for cure and vaccine. , 2010, Virology.

[19]  M. Blajchman,et al.  Protecting the blood supply from emerging pathogens: the role of pathogen inactivation. , 2009, Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine.

[20]  H. Klein,et al.  The hazards of blood transfusion in historical perspective. , 2008, Blood.

[21]  L. Schonberger,et al.  Transfusion transmission of human prion diseases. , 2008, Transfusion medicine reviews.

[22]  L. Kirchhoff,et al.  Transfusion‐associated Chagas disease (American trypanosomiasis) in Mexico: implications for transfusion medicine in the United States , 2006, Transfusion.

[23]  G. Foster,et al.  West Nile Virus Among Blood Donors in the United States, 2003 and 2004 , 2005, The New England journal of medicine.

[24]  Peter Tomasulo,et al.  Screening the blood supply for West Nile virus RNA by nucleic acid amplification testing. , 2005, The New England journal of medicine.

[25]  P. Bacchetti Uncertainty due to model choice in variant Creutzfeldt–Jakob disease projections , 2005, Statistics in medicine.

[26]  P. Tomasulo,et al.  Triggers for switching from minipool testing by nucleic acid technology to individual‐donation nucleic acid testing for West Nile virus: Analysis of 2003 data to inform 2004 decision making , 2004, Transfusion.

[27]  J. Bartlett Transmission of west nile virus through blood transfusion in the United States in 2002 , 2004 .

[28]  R. Lanciotti,et al.  Transmission of West Nile virus through blood transfusion in the United States in 2002. , 2003, The New England journal of medicine.

[29]  M. Mitka As West Nile virus season heats up, blood safety testing lags behind. , 2003, JAMA.

[30]  E. Read,et al.  Trypanosoma cruzi in Los Angeles and Miami blood donors: impact of evolving donor demographics on seroprevalence and implications for transfusion transmission , 2002, Transfusion.

[31]  West Nile virus activity--United States, October 10-16, 2002, and update on West Nile virus infections in recipients of blood transfusions. , 2002, MMWR. Morbidity and mortality weekly report.

[32]  A. Valleron,et al.  Estimation of Epidemic Size and Incubation Time Based on Age Characteristics of vCJD in the United Kingdom , 2001, Science.

[33]  P. Schmidt Syphilis, a disease of direct transfusion , 2001, Transfusion.

[34]  M. Houghton,et al.  Hepatitis C Virus and eliminating post-transfusion hepatitis , 2000, Nature Medicine.

[35]  N. Restifo Flu: The Story of the Great Influenza Pandemic of 1918 and the Search for the Virus that Caused It , 2000, Nature Medicine.

[36]  G. Pugliese,et al.  Anthrax as a Biological Weapon: Medical and Public Health Management , 1999, Infection Control & Hospital Epidemiology.

[37]  Philip K. Russell,et al.  Anthrax as a biological weapon: medical and public health management. Working Group on Civilian Biodefense. , 1999, JAMA.

[38]  Philip K. Russell,et al.  Smallpox as a biological weapon: medical and public health management. Working Group on Civilian Biodefense. , 1999, JAMA.

[39]  M. Busch,et al.  The Efficiency of HIV p24 Antigen Screening of US Blood Donors: Projections versus Reality , 1998, Transfusion Medicine and Hemotherapy.

[40]  L. Leveton,et al.  HIV and the blood supply: an analysis of crisis decision making. , 1995, Transfusion.

[41]  P. Holland,et al.  Staff costs associated with the implementation of a comprehensive compliance program in a community blood center , 1995, Transfusion.

[42]  J. Ward,et al.  Risk of human immunodeficiency virus (HIV) transmission by blood transfusions before the implementation of HIV‐1 antibody screening , 1991, Transfusion.

[43]  B. Chesebro,et al.  Transmissible Spongiform Encephalopathies , 2019, Definitions.

[44]  Samuel L. Groseclose,et al.  Summary of Notifiable Diseases, United States. , 1997 .

[45]  H J Alter,et al.  An assay for circulating antibodies to a major etiologic virus of human non-A, non-B hepatitis. , 1990, Science.

[46]  R. Purcell,et al.  Detection of antibody to hepatitis C virus in prospectively followed transfusion recipients with acute and chronic non-A, non-B hepatitis. , 1989, The New England journal of medicine.

[47]  Jules L. Dienstag,et al.  An assay for circulating antibodies to a major etiologic virus of human non-A, non-B hepatitis , 1989 .

[48]  M. Houghton,et al.  Isolation of a cDNA clone derived from a blood-borne non-A, non-B viral hepatitis genome. , 1989, Science.

[49]  M. Shapiro,et al.  Determining the size of non-A, non-B hepatitis virus by filtration. , 1987, The Journal of infectious diseases.

[50]  E. Schiff,et al.  A serologic follow-up of the 1942 epidemic of post-vaccination hepatitis in the United States Army. , 1987, The New England journal of medicine.

[51]  J. Ward,et al.  Risk of human immunodeficiency virus infection from blood donors who later developed the acquired immunodeficiency syndrome. , 1987, Annals of internal medicine.

[52]  R. Purcell,et al.  Antibody to hepatitis B core antigen as a paradoxical marker for non-A, non-B hepatitis agents in donated blood. , 1986, Annals of internal medicine.

[53]  R. Kahn,et al.  Hepatitis B virus antibody in blood donors and the occurrence of non-A, non-B hepatitis in transfusion recipients. An analysis of the Transfusion-Transmitted Viruses Study. , 1984, Annals of internal medicine.

[54]  R. Purcell,et al.  Inactivation of hepatitis B virus and non-A, non-B hepatitis by chloroform , 1983, Infection and immunity.

[55]  D. Bradley,et al.  Posttransfusion Non-A, Non-B Hepatitis: Physicochemical Properties of Two Distinct Agents , 1983, The Journal of infectious diseases.

[56]  H. Goldman,et al.  Possible transfusion-associated acquired immune deficiency syndrome (AIDS) - California. , 1982, MMWR. Morbidity and mortality weekly report.

[57]  J. Elliott,et al.  Pneumocystis carinii pneumonia among persons with hemophilia A. , 1982, MMWR. Morbidity and mortality weekly report.

[58]  R. Purcell,et al.  Donor transaminase and recipient hepatitis. Impact on blood transfusion services. , 1981, JAMA.

[59]  R. Kahn,et al.  Serum alanine aminotransferase of donors in relation to the risk of non-A,non-B hepatitis in recipients: the transfusion-transmitted viruses study. , 1981, The New England journal of medicine.

[60]  R. Purcell,et al.  The chronic sequelae of non-A, non-B hepatitis. , 1979, Annals of internal medicine.

[61]  Conn Nk,et al.  Letter: Avirulent corynebacteria. , 1975 .

[62]  R. Purcell,et al.  Transfusion‐associated hepatitis not due to viral hepatitis type A or B † , 1975, The New England journal of medicine.

[63]  L. Barker,et al.  Antibody to hepatitis B core antigen. , 1974, The American journal of the medical sciences.

[64]  R. Purcell,et al.  Hepatitis A: Detection by Immune Electron Microscopy of a Viruslike Antigen Associated with Acute Illness , 1973, Science.

[65]  R. Purcell,et al.  Posttransfusion hepatitis after exclusion of commercial and hepatitis-B antigen-positive donors. , 1972, Annals of internal medicine.

[66]  W. Szmuness,et al.  Immunologic distinction between infectious and serum hepatitis. , 1970, The New England journal of medicine.

[67]  Y. Cossart,et al.  Virus-like particles in serum of patients with Australia-antigen-associated hepatitis. , 1970, Lancet.

[68]  R. Purcell,et al.  Posttransfusion hepatitis after open-heart operations. Incidence after the administration of blood from commercial and volunteer donor populations. , 1970, JAMA.

[69]  A. Sutnick,et al.  Australia antigen and acute viral hepatitis. , 1969, Annals of internal medicine.

[70]  S. Krugman,et al.  Infectious hepatitis. Evidence for two distinctive clinical, epidemiological, and immunological types of infection. , 1967, JAMA.

[71]  H. Alter,et al.  A "NEW" ANTIGEN IN LEUKEMIA SERA. , 1965, JAMA.

[72]  J. Allen,et al.  Serum hepatitis from transfusions of blood. Epidemiologic study. , 1962, JAMA.

[73]  P. Beeson JAUNDICE OCCURRING ONE TO FOUR MONTHS AFTER TRANSFUSION OF BLOOD OR PLASMA: REPORT OF SEVEN CASES , 1943 .

[74]  김성,et al.  Transmission , 1922, Sexistence.