Investigational Testing for Zika Virus among US Blood Donors

被引:53
作者
Saa, Paula [1 ]
Proctor, Melanie [1 ]
Foster, Gregory [1 ]
Krysztof, David [1 ]
Winton, Colleen [1 ]
Linnen, Jeffrey M. [2 ]
Gao, Kui [2 ]
Brodsky, Jaye P. [3 ]
Limberger, Ronald J. [4 ]
Dodd, Roger Y. [1 ]
Stramer, Susan L. [1 ]
机构
[1] Amer Red Cross, Sci Affairs, Gaithersburg, MD 20877 USA
[2] Grifols Diagnost Solut, San Diego, CA USA
[3] Qual Analyt, Riverwoods, IL USA
[4] New York State Dept Hlth, Wadsworth Ctr, Albany, NY USA
关键词
TRANSMISSION; INFECTION; STATES;
D O I
10.1056/NEJMoa1714977
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Because of the potential severe clinical consequences of Zika virus (ZIKV) infection, the large numbers of asymptomatic travelers returning from ZIKV-active areas, the detection of ZIKV nucleic acid in blood, and reports of transmission of ZIKV through transfusion, in 2016 the Food and Drug Administration released recommendations for individual-unit nucleic acid testing to minimize the risk of transmission of ZIKV through blood transfusions. METHODS The American Red Cross implemented investigational screening of donated blood for ZIKV RNA by means of transcription-mediated amplification (TMA). Confirmatory testing of reactive donations involved repeat TMA, TMA testing in exploratory mini-pools, real-time reverse-transcriptase polymerase chain reaction, IgM serologic testing, and red-cell TMA. Viral loads in plasma and red cells were estimated by means of end-point TMA. The costs of interdicting a donation that was confirmed to be positive were calculated for the 15-month period between June 2016 and September 2017. RESULTS Of the 4,325,889 donations that were screened, 393,713 (9%) were initially tested in 24,611 minipools, and no reactive donations were found. Of the 3,932,176 donations that were subsequently tested individually, 160 were initially reactive and 9 were confirmed positive (a 1:480,654 confirmed-positive rate overall; positive predictive value, 5.6%; specificity, 99.997%). Six (67%) of the confirmed-positive donations were reactive on repeat TMA, of which 4 were IgM-negative; of these 4, all 3 that could be tested were reactive on minipool TMA. Two confirmed-positive donors had infections that had been transmitted locally (in Florida), 6 had traveled to ZIKV-active areas, and 1 had received an experimental ZIKV vaccine. ZIKV RNA levels in red cells ranged from 40 to 800,000 copies per milliliter and were detected up to 154 days after donation, as compared with 80 days of detection in plasma at levels of 12 to 20,000 copies per milliliter. On the basis of industry-reported costs of testing and the yield of the tests in our study, the cost of identifying 8 mosquito-borne ZIKV infections through individual-unit nucleic acid testing was $5.3 million per ZIKV RNA-positive donation. CONCLUSIONS Screening of U.S. blood donations for ZIKV by individual-donation TMA was costly and had a low yield. Among the 9 confirmed ZIKV-positive donations, only 4 were IgM-negative; of these donations, all 3 that were tested were reactive on minipool TMA.
引用
收藏
页码:1778 / 1788
页数:11
相关论文
共 40 条
[1]   Probable transfusion-transmitted Zika virus in Brazil [J].
Barjas-Castro, Maria L. ;
Angerami, Rodrigo N. ;
Cunha, Mariana S. ;
Suzuki, Akemi ;
Nogueira, Juliana S. ;
Rocco, Iray M. ;
Maeda, Adriana Y. ;
Vasami, Fernanda G. S. ;
Katz, Gizelda ;
Boin, Ilka F. S. F. ;
Stucchi, Raquel S. B. ;
Resende, Mariangela R. ;
Esposito, Danillo L. A. ;
de Souza, Renato P. ;
da Fonseca, Benedito A. ;
Addas-Carvalho, Marcelo .
TRANSFUSION, 2016, 56 (07) :1684-1688
[2]   Evidence of perinatal transmission of Zika virus, French Polynesia, December 2013 and February 2014 [J].
Besnard, M. ;
Lastere, S. ;
Teissier, A. ;
Cao-Lormeau, V. M. ;
Musso, D. .
EUROSURVEILLANCE, 2014, 19 (13) :13-16
[3]   Detection and sequencing of Zika virus from amniotic fluid of fetuses with microcephaly in Brazil: a case study [J].
Calvet, Guilherme ;
Aguiar, Renato S. ;
Melo, Adriana S. O. ;
Sampaio, Simone A. ;
de Filippis, Ivano ;
Fabri, Allison ;
Araujo, Eliane S. M. ;
de Sequeira, Patricia C. ;
de Mendonca, Marcos C. L. ;
de Oliveira, Louisi ;
Tschoeke, Diogo A. ;
Schrago, Carlos G. ;
Thompson, Fabiano L. ;
Brasil, Patricia ;
dos Santos, Flavia B. ;
Nogueira, Rita M. R. ;
Tanurit, Amilcar ;
de Filippis, Ana M. B. .
LANCET INFECTIOUS DISEASES, 2016, 16 (06) :653-660
[4]   Guillain-Barre Syndrome outbreak associated with Zika virus infection in French Polynesia: a case-control study [J].
Cao-Lormeau, Van-Mai ;
Blake, Alexandre ;
Mons, Sandrine ;
Lastere, Stephane ;
Roche, Claudine ;
Vanhomwegen, Jessica ;
Dub, Timothee ;
Baudouin, Laure ;
Teissier, Anita ;
Larre, Philippe ;
Vial, Anne-Laure ;
Decam, Christophe ;
Choumet, Valerie ;
Halstead, Susan K. ;
Willison, Hugh J. ;
Musset, Lucile ;
Manuguerra, Jean-Claude ;
Despres, Philippe ;
Fournier, Emmanuel ;
Mallet, Henri-Pierre ;
Musso, Didier ;
Fontanet, Arnaud ;
Neil, Jean ;
Ghawche, Frederic .
LANCET, 2016, 387 (10027) :1531-1539
[5]  
Cao-Lormeau VM, 2014, EMERG INFECT DIS, V20, P1085, DOI [10.3201/eid2006.140138, 10.3201/eid2011.141380]
[6]   Zika Virus Associated with Meningoencephalitis [J].
Carteaux, Guillaume ;
Maquart, Marianne ;
Bedet, Alexandre ;
Contou, Damien ;
Brugieres, Pierre ;
Fourati, Slim ;
de Langavant, Laurent Cleret ;
de Broucker, Thomas ;
Brun-Buisson, Christian ;
Leparc-Goffart, Isabelle ;
Dessap, Armand Mekontso .
NEW ENGLAND JOURNAL OF MEDICINE, 2016, 374 (16) :1595-1597
[7]  
Centers forDisease Control Prevention (CDC), 2017, ZIK MAC ELISA
[8]   Use of Blood Donor Screening Data to Estimate Zika Virus Incidence, Puerto Rico, April-August 2016 [J].
Chevalier, Michelle S. ;
Biggerstaff, Brad J. ;
Basavaraju, Sridhar V. ;
Ocfemia, M. Cheryl Banez ;
Alsina, Jose O. ;
Climent-Peris, Consuelo ;
Moseley, Robin R. ;
Chung, Koo-Whang ;
Rivera-Garcia, Brenda ;
Bello-Pagan, Melissa ;
Pate, Lisa L. ;
Galel, Susan A. ;
Williamson, Phillip ;
Kuehnert, Matthew J. .
EMERGING INFECTIOUS DISEASES, 2017, 23 (05) :790-795
[9]  
Davidson A, 2016, MMWR-MORBID MORTAL W, V65, P716, DOI 10.15585/mmwr.mm6528e2
[10]  
de Oliveira WK, 2016, MMWR-MORBID MORTAL W, V65