Coronavirus Disease 2019: Coronaviruses and Blood Safety
Identifieur interne : 001409 ( Pmc/Corpus ); précédent : 001408; suivant : 001410Coronavirus Disease 2019: Coronaviruses and Blood Safety
Auteurs : Le Chang ; Ying Yan ; Lunan WangSource :
- Transfusion Medicine Reviews [ 0887-7963 ] ; 2020.
Abstract
With the outbreak of unknown pneumonia in Wuhan, China, in December 2019, a new coronavirus,
Url:
DOI: 10.1016/j.tmrv.2020.02.003
PubMed: 32107119
PubMed Central: 7135848
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PMC:7135848Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Coronavirus Disease 2019: Coronaviruses and Blood Safety</title>
<author><name sortKey="Chang, Le" sort="Chang, Le" uniqKey="Chang L" first="Le" last="Chang">Le Chang</name>
<affiliation><nlm:aff id="af0005">National Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology; Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, PR China</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="af0010">Beijing Engineering Research Center of Laboratory Medicine, Beijing Hospital, PR China</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Yan, Ying" sort="Yan, Ying" uniqKey="Yan Y" first="Ying" last="Yan">Ying Yan</name>
<affiliation><nlm:aff id="af0005">National Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology; Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, PR China</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="af0010">Beijing Engineering Research Center of Laboratory Medicine, Beijing Hospital, PR China</nlm:aff>
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<author><name sortKey="Wang, Lunan" sort="Wang, Lunan" uniqKey="Wang L" first="Lunan" last="Wang">Lunan Wang</name>
<affiliation><nlm:aff id="af0005">National Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology; Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, PR China</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="af0010">Beijing Engineering Research Center of Laboratory Medicine, Beijing Hospital, PR China</nlm:aff>
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<affiliation><nlm:aff id="af0015">Graduate School, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, PR China</nlm:aff>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Coronavirus Disease 2019: Coronaviruses and Blood Safety</title>
<author><name sortKey="Chang, Le" sort="Chang, Le" uniqKey="Chang L" first="Le" last="Chang">Le Chang</name>
<affiliation><nlm:aff id="af0005">National Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology; Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, PR China</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="af0010">Beijing Engineering Research Center of Laboratory Medicine, Beijing Hospital, PR China</nlm:aff>
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<author><name sortKey="Yan, Ying" sort="Yan, Ying" uniqKey="Yan Y" first="Ying" last="Yan">Ying Yan</name>
<affiliation><nlm:aff id="af0005">National Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology; Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, PR China</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="af0010">Beijing Engineering Research Center of Laboratory Medicine, Beijing Hospital, PR China</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Wang, Lunan" sort="Wang, Lunan" uniqKey="Wang L" first="Lunan" last="Wang">Lunan Wang</name>
<affiliation><nlm:aff id="af0005">National Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology; Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, PR China</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="af0010">Beijing Engineering Research Center of Laboratory Medicine, Beijing Hospital, PR China</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="af0015">Graduate School, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, PR China</nlm:aff>
</affiliation>
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<series><title level="j">Transfusion Medicine Reviews</title>
<idno type="ISSN">0887-7963</idno>
<idno type="eISSN">1532-9496</idno>
<imprint><date when="2020">2020</date>
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<front><div type="abstract" xml:lang="en"><p>With the outbreak of unknown pneumonia in Wuhan, China, in December 2019, a new coronavirus, <italic>Severe Acute Respiratory Syndrome Coronavirus 2</italic>
(SARS-CoV-2), aroused the attention of the entire world. The current outbreak of infections with SARS-CoV-2 is termed <italic>Coronavirus Disease 2019</italic>
(COVID-19). The World Health Organization declared COVID-19 in China as a Public Health Emergency of International Concern. Two other coronavirus infections—SARS in 2002-2003 and Middle East Respiratory Syndrome (MERS) in 2012—both caused severe respiratory syndrome in humans. All 3 of these emerging infectious diseases leading to a global spread are caused by <italic>β</italic>
-coronaviruses. Although coronaviruses usually infect the upper or lower respiratory tract, viral shedding in plasma or serum is common. Therefore, there is still a theoretical risk of transmission of coronaviruses through the transfusion of labile blood products. Because more and more asymptomatic infections are being found among COVID-19 cases, considerations of blood safety and coronaviruses have arisen especially in endemic areas. In this review, we detail current evidence and understanding of the transmission of SARS-CoV, MERS–CoV, and SARS-CoV-2 through blood products as of February 10, 2020, and also discuss pathogen inactivation methods on coronaviruses.</p>
</div>
</front>
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</TEI>
<pmc article-type="review-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Transfus Med Rev</journal-id>
<journal-id journal-id-type="iso-abbrev">Transfus Med Rev</journal-id>
<journal-title-group><journal-title>Transfusion Medicine Reviews</journal-title>
</journal-title-group>
<issn pub-type="ppub">0887-7963</issn>
<issn pub-type="epub">1532-9496</issn>
<publisher><publisher-name>Elsevier Inc.</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">32107119</article-id>
<article-id pub-id-type="pmc">7135848</article-id>
<article-id pub-id-type="publisher-id">S0887-7963(20)30014-6</article-id>
<article-id pub-id-type="doi">10.1016/j.tmrv.2020.02.003</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Coronavirus Disease 2019: Coronaviruses and Blood Safety</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" id="au0005"><name><surname>Chang</surname>
<given-names>Le</given-names>
</name>
<xref rid="af0005" ref-type="aff">a</xref>
<xref rid="af0010" ref-type="aff">b</xref>
</contrib>
<contrib contrib-type="author" id="au0010"><name><surname>Yan</surname>
<given-names>Ying</given-names>
</name>
<xref rid="af0005" ref-type="aff">a</xref>
<xref rid="af0010" ref-type="aff">b</xref>
</contrib>
<contrib contrib-type="author" id="au0015"><name><surname>Wang</surname>
<given-names>Lunan</given-names>
</name>
<email>lunan99@163.com</email>
<xref rid="af0005" ref-type="aff">a</xref>
<xref rid="af0010" ref-type="aff">b</xref>
<xref rid="af0015" ref-type="aff">c</xref>
<xref rid="cr0005" ref-type="corresp">⁎</xref>
</contrib>
</contrib-group>
<aff id="af0005"><label>a</label>
National Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology; Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, PR China</aff>
<aff id="af0010"><label>b</label>
Beijing Engineering Research Center of Laboratory Medicine, Beijing Hospital, PR China</aff>
<aff id="af0015"><label>c</label>
Graduate School, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, PR China</aff>
<author-notes><corresp id="cr0005"><label>⁎</label>
Corresponding author at: Lunan Wang, No. 1 Dahua Rd, Beijing 100730, PR China. <email>lunan99@163.com</email>
</corresp>
</author-notes>
<pub-date pub-type="pmc-release"><day>21</day>
<month>2</month>
<year>2020</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="epub"><day>21</day>
<month>2</month>
<year>2020</year>
</pub-date>
<elocation-id></elocation-id>
<permissions><copyright-statement>© 2020 Elsevier Inc. All rights reserved.</copyright-statement>
<copyright-year>2020</copyright-year>
<copyright-holder>Elsevier Inc.</copyright-holder>
<license><license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p>
</license>
</permissions>
<abstract id="ab0005"><p>With the outbreak of unknown pneumonia in Wuhan, China, in December 2019, a new coronavirus, <italic>Severe Acute Respiratory Syndrome Coronavirus 2</italic>
(SARS-CoV-2), aroused the attention of the entire world. The current outbreak of infections with SARS-CoV-2 is termed <italic>Coronavirus Disease 2019</italic>
(COVID-19). The World Health Organization declared COVID-19 in China as a Public Health Emergency of International Concern. Two other coronavirus infections—SARS in 2002-2003 and Middle East Respiratory Syndrome (MERS) in 2012—both caused severe respiratory syndrome in humans. All 3 of these emerging infectious diseases leading to a global spread are caused by <italic>β</italic>
-coronaviruses. Although coronaviruses usually infect the upper or lower respiratory tract, viral shedding in plasma or serum is common. Therefore, there is still a theoretical risk of transmission of coronaviruses through the transfusion of labile blood products. Because more and more asymptomatic infections are being found among COVID-19 cases, considerations of blood safety and coronaviruses have arisen especially in endemic areas. In this review, we detail current evidence and understanding of the transmission of SARS-CoV, MERS–CoV, and SARS-CoV-2 through blood products as of February 10, 2020, and also discuss pathogen inactivation methods on coronaviruses.</p>
</abstract>
<abstract abstract-type="author-highlights" id="ab0010"><title>Highlights</title>
<p><list list-type="simple" id="l0005"><list-item id="li0005"><label>•</label>
<p id="p0005">Review current information and understanding (as of February 10, 2020) of the potential for transmission of SARS-CoV, MERS-CoV, and SARS-CoV-2 (2019-nCoV) through blood products.</p>
</list-item>
<list-item id="li0010"><label>•</label>
<p id="p0010">Summarize current understanding of pathogen inactivation methods on coronaviruses.</p>
</list-item>
<list-item id="li0015"><label>•</label>
<p id="p0015">Review measures that Chinese blood banks are taking during the outbreak of COVID-19.</p>
</list-item>
</list>
</p>
</abstract>
<kwd-group id="ks0005"><title>Keywords</title>
<kwd>Coronavirus</kwd>
<kwd>Blood safety</kwd>
<kwd>SARS</kwd>
<kwd>MERS</kwd>
<kwd>2019-nCoV</kwd>
<kwd>COVID-19</kwd>
<kwd>SARS-CoV-2</kwd>
<kwd>Pathogen inactivation technology</kwd>
</kwd-group>
</article-meta>
</front>
<body><p id="p0020">Since a cluster of unknown pneumonia patients was found in December 2019 in Wuhan, China, a new coronavirus (CoV), which was temporarily named <italic>2019 novel coronavirus</italic>
(2019-nCoV) by the World Health Organization (WHO) on January 7, 2020, suddenly came into our sight <xref rid="bb0005" ref-type="bibr">[1]</xref>
. The virus was subsequently renamed <italic>Severe Acute Respiratory Syndrome Coronavirus 2</italic>
(SARS-CoV-2), and the disease it causes was named <italic>Coronavirus Disease 2019</italic>
(COVID-19). As of February 10, 2020, there have been more than 43,000 patients confirmed positive by nucleic acid testing in China and 23 other countries, and it has caused 1017 deaths due to acute respiratory failure or other related complications. In addition, more than 21,000 suspected infected people were isolated and are waiting to be tested. On January 31, WHO announced the outbreak of COVID-19 in China as a Public Health Emergency of International Concern.</p>
<p id="p0025">In 2002-2003, more than 8000 patients suffered from Severe Acute Respiratory Syndrome (SARS) due to a coronavirus, with 774 virus-related deaths reported to WHO. Since September 2012, there were 2494 laboratory-confirmed cases of infection with Middle East Respiratory Syndrome Coronavirus (MERS-CoV), with 858 virus-related deaths reported to WHO <xref rid="bb0010" ref-type="bibr">[2]</xref>
, <xref rid="bb0015" ref-type="bibr">[3]</xref>
. All 3 of these emerging infectious diseases leading to a global spread are caused by <italic>β</italic>
-coronaviruses.</p>
<p id="p0030">In China, prior outbreaks of emerging infections have had an unfavorable impact on the blood supply. <xref rid="bb0020" ref-type="bibr">[4]</xref>
. However, consideration must also be given to the safety of the transfusion recipient even if the emerging infection is a respiratory disease. Previous studies indicated that viral RNA could be detected from plasma or serum of patients infected with SARS-CoV <xref rid="bb0025" ref-type="bibr">[5]</xref>
, <xref rid="bb0030" ref-type="bibr">[6]</xref>
, <xref rid="bb0035" ref-type="bibr">[7]</xref>
, <xref rid="bb0040" ref-type="bibr">[8]</xref>
, MERS-CoV <xref rid="bb0045" ref-type="bibr">[9]</xref>
, or SARS-CoV-2 <xref rid="bb0005" ref-type="bibr">[1]</xref>
during different periods after the onset of symptoms. However, the detection of viral RNA by polymerase chain reaction (PCR) is not equivalent to the detection of intact infectious virus. Although WHO noted in 2003 that no cases of SARS-CoV have been reported due to transfusion of blood products, there was still a theoretical risk of transmission of SARS-CoV through transfusion <xref rid="bb0050" ref-type="bibr">[10]</xref>
. With more and more asymptomatic infections being found among COVID-19 cases, blood safety is worthy of consideration. In this review, we detail current evidence and understanding of the transmission of SARS-CoV, MERS-CoV, and SARS-CoV-2 via transfusion as of February 10, 2020, and discuss pathogen inactivation methods on coronaviruses.</p>
<sec id="s0005"><label>1</label>
<title>Diversity of Coronaviruses</title>
<p id="p0035">As the largest known RNA viruses, CoVs are further divided into four genera: <italic>α</italic>
-CoVs, <italic>β</italic>
-CoVs, <italic>γ</italic>
-CoVs, and <italic>δ</italic>
-CoVs <xref rid="bb0055" ref-type="bibr">[11]</xref>
, among which <italic>α</italic>
- and <italic>β</italic>
-CoVs are able to infect mammals, whereas the other two genera can infect birds and could also infect mammals <xref rid="bb0060" ref-type="bibr">[12]</xref>
. So far, seven coronaviruses have been found to infect humans and cause respiratory diseases. Four of seven are common human CoVs (HCoVs) usually leading to common self-limited upper respiratory disease: HCoV-229E, HCoV-OC43, HCoV-NL63, and HCoV-HKU1. These viruses can occasionally cause more serious disease in young, elderly, or immunocompromised individuals.</p>
<p id="p0040">The first two HCoVs, HCoV-229E and HCoV-OC43, have been known since the 1960s. With the emergence of SARS in 2002, a novel <italic>β</italic>
-coronavirus came to attention; and subsequently, HCoV-NL63 and HCoV-HKU1 were identified in 2004 and 2005, respectively <xref rid="bb0065" ref-type="bibr">[13]</xref>
. MERS-CoV, which was isolated in 2012, is similar to SARS-CoV—both can infect the lower respiratory tract and usually cause a severe respiratory syndrome in humans <xref rid="bb0070" ref-type="bibr">[14]</xref>
with a case fatality rate of 35.5% and 10%, respectively <xref rid="bb0075" ref-type="bibr">[15]</xref>
. SARS-CoV-2 was recently isolated from human airway epithelial cells, characterized by next-generation sequencing in January 2020, and identified to be a new member of <italic>β</italic>
-CoVs <xref rid="bb0080" ref-type="bibr">[16]</xref>
. SARS-CoV-2 can also infect the lower respiratory tract, but the clinical symptoms are milder than SARS and MERS according to current limited evidence and reports <xref rid="bb0005" ref-type="bibr">[1]</xref>
.</p>
</sec>
<sec id="s0010"><label>2</label>
<title>SARS-CoV</title>
<p id="p0045">Atypical pneumonia putatively caused by SARS-CoV was first identified following an outbreak in Guangdong Province, China, in November 2002. The infection quickly spread to Beijing, Hong Kong, Vietnam, Singapore, and Canada in March 2003. This disease proved to be highly infectious with respiratory droplets as the main route of transmission. Infected feces also played an important role in some cluster outbreak cases <xref rid="bb0085" ref-type="bibr">[17]</xref>
, <xref rid="bb0090" ref-type="bibr">[18]</xref>
. Fortunately, it has been proved that SARS patients are not infectious during the period of incubation (within 16 days of infection, usually 3-5 days).</p>
<p id="p0050">Many studies found that SARS-CoV RNA could be detected in the plasma of SARS patients even though it is a respiratory disease. The first report published on April 10, 2003 <xref rid="bb0025" ref-type="bibr">[5]</xref>
, indicated that extremely low concentrations of viral RNA existed in plasma of a SARS patient during the acute phase of illness, at 9 days after the onset of symptoms. The viral content of plasma was low. Researchers could only detect SARS-CoV RNA using a nested PCR assay established in-house, and the viral load was 190 copies/mL performed after ultracentrifugation of 2 mL of plasma. They could not detect viral RNA in the plasma collected from two close contacts, although the sputum of one was positive by 3 of 4 different PCR assays and the viral load in sputum was as high as 6.3×10<sup>4</sup>
copies/mL. Based on this study and other information, WHO <xref rid="bb0050" ref-type="bibr">[10]</xref>
and the US Food and Drug Administration (FDA) <xref rid="bb0095" ref-type="bibr">[19]</xref>
drafted recommendations on blood safety and pointed out a theoretical risk of transmission of the SARS virus through transfusion of blood products. They also recommended some precautionary principles regarding the deferral of blood donation by individuals from areas with recent local transmission. In addition, blood donors should report to collection agencies if they were diagnosed as suspected or confirmed SARS patients within 1 month following their donation; and in such instances, efforts would be made to trace recipients or recall any blood products not transfused. Later, two studies focused on new PCR methods for detection of SARS-CoV RNA. One study was based on serial analysis of plasma viral RNA concentrations in adult SARS patients by quantitative reverse-transcription PCR with a limit of detection of 74 copies/mL. The study found that, on the first day of fever onset, 50% (6/12) of confirmed patients had detectable viral RNA in plasma and that, by day 14, the proportion fell to 25% (3/12). Overall, 78% of patients had detectable viral RNA in the first week of their illness <xref rid="bb0035" ref-type="bibr">[7]</xref>
. Similar to the first study, the average viral concentration was low at 140 copies/mL in patients who had relatively mild symptoms and did not require intensive care unit admission in hospital. In pediatric patients, 87.5% (7/8) of children had viremia, and the median concentration of plasma was 357 copies/mL based on the same PCR method used with adult SARS patients above <xref rid="bb0040" ref-type="bibr">[8]</xref>
. Finally, Grant et al <xref rid="bb0030" ref-type="bibr">[6]</xref>
reported that within 3 days after fever onset, 79% (19/24) of patients had detectable SARS-CoV RNA in plasma. The viral load level rose fast, and the maximal viral load was at around day 4 or day 5 after the onset of fever, after which the viral load quickly decreased. Their findings showed viral shedding in plasma was common when people were clinically ill with SARS virus and that plasma may be a better sample compared with nasal and throat swabs. The detection sensitivity of plasma was equivalent to that of nasopharyngeal aspirates within the first 3 days after the onset of fever.</p>
<p id="p0055">In addition, researchers found that lymphocytes have a much higher concentration of SARS-CoV RNA than plasma whether tested in the acute phase or convalescent phase <xref rid="bb0100" ref-type="bibr">[20]</xref>
, although plasma viral RNA from only 5 patients in acute phase and 5 in convalescent phase was detected. It was subsequently shown that SARS-CoV could not only infect lymphocytes but also replicate in them in a self-limited manner <xref rid="bb0105" ref-type="bibr">[21]</xref>
, <xref rid="bb0110" ref-type="bibr">[22]</xref>
, <xref rid="bb0115" ref-type="bibr">[23]</xref>
. These findings provided evidence that lymphocytes might be one of targets for SARS-CoV and indicated the potential for a transmission risk by blood products with high concentrations of donor lymphocytes (peripheral blood stem cells, bone marrow, granulocyte concentrates, etc).</p>
<p id="p0060">Although these findings provided some evidence that SARS-CoV indeed existed in plasma or lymphocytes of SARS patients, no nation including those with local transmission of SARS and no organizations including WHO <xref rid="bb0050" ref-type="bibr">[10]</xref>
and the American Association of Blood Banks (AABB) recommended screening donors for SARS-CoV RNA or related antibodies based on the following facts: (1) SARS patients are not infectious in the period of incubation time and the incubation time is relatively short; (2) almost all SARS-CoV–infected people have severe symptoms, and few asymptomatic carriers were found; (3) data showed that the viral load from plasma of SARS patients was low <xref rid="bb0085" ref-type="bibr">[17]</xref>
, <xref rid="bb0120" ref-type="bibr">[24]</xref>
, <xref rid="bb0125" ref-type="bibr">[25]</xref>
; (4) no transfusion transmission cases have been reported so far <xref rid="bb0050" ref-type="bibr">[10]</xref>
, and studies that screened blood donations for SARS-CoV RNA in 2003 failed to identify any positives <xref rid="bb0130" ref-type="bibr">[26]</xref>
.</p>
<p id="p0065">However, an alternative view was expressed in 2004. Researchers in Hong Kong <xref rid="bb0135" ref-type="bibr">[27]</xref>
found that tests of the plasma from 3 of 400 healthy blood donors and 1 of 131 nonpneumonic pediatric inpatients collected during the outbreak of SARS tested positive for IgG antibody to SARS-CoV. The results were confirmed by two Western blot assays. The presence of antibody does not imply infectious material. Nevertheless, because Hong Kong was among the worst-hit regions in the world during the 2002-2003 outbreak of SARS, they concluded that, in Hong Kong, subclinical or nonpneumonic SARS-CoV infections existed, indicating a potential transmission risk of SARS virus via blood products. Soon afterward, four different groups raised questions and objections to the Hong Kong study focusing on the specificity of the assays and the representativeness of the population <xref rid="bb0140" ref-type="bibr">[28]</xref>
, <xref rid="bb0145" ref-type="bibr">[29]</xref>
, <xref rid="bb0150" ref-type="bibr">[30]</xref>
, <xref rid="bb0155" ref-type="bibr">[31]</xref>
. To provide additional information, the theoretical the risk of SARS-CoV transmission through blood transfusion was estimated in Shenzhen, Guangdong Province, in China. The estimate used data from Shenzhen, Hong Kong, and Taiwan in 2003 and calculated that the mean risk was 14.11 (95% confidence interval [CI]: 11.00-17.22) per million and the maximum risk was 23.57 (95% CI: 6.83-47.69) per million on April 2, 2003 <xref rid="bb0160" ref-type="bibr">[32]</xref>
.</p>
</sec>
<sec id="s0015"><label>3</label>
<title>MERS-CoV</title>
<p id="p0070">In 2012, the MERS virus was first identified from a 60-year-old man who had acute pneumonia and renal failure with a fatal outcome in Saudi Arabia <xref rid="bb0165" ref-type="bibr">[33]</xref>
. At that time, MERS-CoV was the sixth human coronavirus identified. MERS is a highly lethal respiratory disease and had a higher case fatality rate than SARS <xref rid="bb0015" ref-type="bibr">[3]</xref>
. It caused large nosocomial outbreaks in Jeddah, Kingdom of Saudi Arabia, in 2014 and the Republic of Korea in 2015 <xref rid="bb0170" ref-type="bibr">[34]</xref>
.</p>
<p id="p0075">In a study on the viral load in different samples among 37 MERS patients, investigators found that nearly half of serum samples tested yielded a viral RNA signal during the first week after diagnosis and that the viral load ranged from about 2.1×10<sup>2</sup>
to 2.51×10<sup>5</sup>
copies/mL. However, they failed to isolate virus from these sera. Therefore, it is not known whether or not there was live MERS virus in the serum, and the patients’ blood may not have been infectious <xref rid="bb0045" ref-type="bibr">[9]</xref>
. Although almost all MERS patients have severe clinical symptoms, atypical patients were found during the 2015 outbreak of South Korea. One individual had infection of MERS-CoV confirmed by real-time reverse-transcription PCR, but he had no symptoms in the following 4 days. However, it is worthy of note that each of the individuals tested were immunocompromised inpatients. Therefore, the findings are not directly related to risks among blood donors.</p>
<p id="p0080">In the document from AABB <xref rid="bb0175" ref-type="bibr">[35]</xref>
, it was noted that populations such as persons in close contact with a confirmed case, camel workers who were visiting or residing in the Middle East, and health care personnel during a nosocomial outbreak were at increased risk of MERS-CoV infection. Because detection of virus from blood was rare and MERS viral load was low, the FDA recommended some deferral criteria similar to the SARS epidemic: 14 days from last exposure or 14 days after arrival in the United States following travel/residence exposure, or 28 days after complete symptom resolution and cessation of a treatment.</p>
</sec>
<sec id="s0020"><label>4</label>
<title>SARS-CoV-2</title>
<p id="p0085">In December 2019, an unknown pneumonia rapidly spread in Wuhan, China, and most initial cases were related to source infection from a seafood wholesale market <xref rid="bb0180" ref-type="bibr">[36]</xref>
. Quickly, researchers sequenced and identified a new <italic>β</italic>
-coronavirus, the genome of which has 86.9% identity to a previously published bat SARS-like CoV genome (bat-SL-CoVZC45, MG772933.1) and is distinct from human SARS-CoV and MERS-CoV <xref rid="bb0080" ref-type="bibr">[16]</xref>
. Individuals with COVID-19 usually have a fever and lower respiratory tract symptoms, and the estimated incubation time is within 14 days.</p>
<p id="p0090">Limited data have shown that viral RNA could be detected in plasma or serum from COVID-19 patients. In the first 41 patients in the city of Wuhan, viremia was found in 6/41 (15%) patients. The median PCR cycle threshold value was 35.1 (95% CI: 34.7-35.1), suggesting a very low RNA concentration with no difference found between intensive care unit patients and patients with mild symptoms. Of note, 1 of 41 patients was positive for SARS-CoV-2 RNA but did not have a fever <xref rid="bb0005" ref-type="bibr">[1]</xref>
. A family cluster of COVID-19 was reported from Shenzhen, China, and it was found that serum from 1 of 6 patients in one family showed a weak positive result for SARS-CoV-2 RNA and a 10-year-old child was confirmed to be an asymptomatic carrier <xref rid="bb0185" ref-type="bibr">[37]</xref>
. With the virus spreading all over the world, reports from Vietnam <xref rid="bb0190" ref-type="bibr">[38]</xref>
, Germany <xref rid="bb0195" ref-type="bibr">[39]</xref>
, and the United States <xref rid="bb0200" ref-type="bibr">[40]</xref>
have described the clinical symptoms, diagnosis, and treatment of COVID-19. One controversial report suggested transmission by contact with an asymptomatic carrier in Germany <xref rid="bb0195" ref-type="bibr">[39]</xref>
: an individual from China attended business meetings in Germany and infected at least 2 business partners during the incubation period. This report suggested that, in contrast to SARS, COVID-19 patients might be infectious during an asymptomatic incubation period. However, in this report, the authors did not directly interview the Chinese traveler who later was found to have been symptomatic at the time of the contact. Moreover, the researchers did not detect viral RNA of samples taken from the index patient during the period of incubation.</p>
<p id="p0095">In January 2020, the European Center for Disease Prevention and Control (ECDC) <xref rid="bb0205" ref-type="bibr">[41]</xref>
and AABB <xref rid="bb0210" ref-type="bibr">[42]</xref>
published rapid risk assessments of the outbreak of SARS-CoV-2 and blood safety. ECDC implied a precautionary deferral of donation of blood and cells for 21 days after possible exposure to a confirmed patient or anyone who returned from Wuhan, China—applying the approach used for SARS-CoV and MERS-CoV. In addition, recovering confirmed COVID-19 patients should be deferred for at least 28 days after symptom resolution and completion of therapy <xref rid="bb0205" ref-type="bibr">[41]</xref>
. AABB updated their Web site to state that, considering the concern regarding SARS-CoV-2 and blood safety, they would continue to closely monitor the outbreak of respiratory illness. The AABB, FDA, and Centers for Disease Control and Prevention do not currently require any action on blood collection and testing because there are no data suggesting a risk of transfusion transmission of SARS-CoV-2 <xref rid="bb0210" ref-type="bibr">[42]</xref>
.</p>
<p id="p0100">As the infection continues to demand urgent attention in China and is being very closely monitored worldwide, the following points may be relevant to considerations regarding transfusion and organ transplantation: (1) viral RNA in plasma or serum could be detected in COVID-19 patients on the first 2 or 3 days after onset of symptoms; (2) most patients, especially younger adults who can donate blood, had milder symptoms than the older adults; (3) patients with no fever and asymptomatic carriers have been identified in China, which increase the possibility that a COVID-19 patient or virus carrier could donate blood; (4) the rate of infectivity of patients who are in the incubation period remains uncertain, and there are no data on the viral load in plasma, serum, or lymphocytes among individuals in the incubation period. Therefore, whether the risk of transfusion transmission of SARS-CoV-2 is higher than other coronaviruses, especially in endemic areas such as Wuhan, China, should be further explored as soon as possible. There still needs to be careful assessment on any measures regarding deferral of donors, screening for SARS-CoV-2 RNA, testing for virus-related antibodies, or use of pathogen-inactivated blood products.</p>
</sec>
<sec id="s0025"><label>5</label>
<title>Inactivation of Coronavirus in Blood Products</title>
<p id="p0105">Coronaviruses are enveloped, positive-sense, single-stranded RNA viruses. Usually, coronaviruses are vulnerable to acid-pH, basic-pH, and heat <xref rid="bb0215" ref-type="bibr">[43]</xref>
but seem to be more stable at 4°C <xref rid="bb0220" ref-type="bibr">[44]</xref>
. The infectious titer of virus did not show any significant reduction after 25 cycles of thawing and freezing <xref rid="bb0220" ref-type="bibr">[44]</xref>
. After the outbreak of SARS and MERS, a few studies investigated pathogen inactivation/reduction technologies (PRTs) based on in-house or commercial methods with the aim to decrease or completely eradicate the potential risk of transmission of coronaviruses via blood products or blood derivatives <xref rid="bb0225" ref-type="bibr">[45]</xref>
, <xref rid="bb0230" ref-type="bibr">[46]</xref>
, <xref rid="bb0235" ref-type="bibr">[47]</xref>
, <xref rid="bb0240" ref-type="bibr">[48]</xref>
, <xref rid="bb0245" ref-type="bibr">[49]</xref>
, <xref rid="bb0250" ref-type="bibr">[50]</xref>
, <xref rid="bb0255" ref-type="bibr">[51]</xref>
, <xref rid="bb0260" ref-type="bibr">[52]</xref>
, <xref rid="bb0265" ref-type="bibr">[53]</xref>
, <xref rid="bb0270" ref-type="bibr">[54]</xref>
. These studies are summarized in <xref rid="t0005" ref-type="table">Table 1</xref>
.<table-wrap position="float" id="t0005"><label>Table 1</label>
<caption><p>Different methods on inactivation of coronavirus in blood products and laboratory tissue culture</p>
</caption>
<alt-text id="al0005">Table 1</alt-text>
<table frame="hsides" rules="groups"><thead><tr><th>Methods</th>
<th>Commercial systems</th>
<th>Mechanism of action <xref rid="bb0280" ref-type="bibr">[56]</xref>
</th>
<th>SARS-CoV</th>
<th>MERS-CoV</th>
</tr>
</thead>
<tbody><tr><td rowspan="2">Heat</td>
<td rowspan="2">N/A</td>
<td rowspan="2">Denaturing the secondary structures of proteins</td>
<td>Products without cells<break></break>
56°C 20 min in serum<break></break>
65°C 10 min in serum<break></break>
60°C 25 min in 25% BSA solution <xref rid="bb0245" ref-type="bibr">[49]</xref>
</td>
<td rowspan="2">DMEM + 5% FBS<break></break>
56°C 25 min<break></break>
(reduction of 4 log<sub>10</sub>
TCID<sub>50</sub>
/mL) <xref rid="bb0265" ref-type="bibr">[53]</xref>
</td>
</tr>
<tr><td>Plasma products<break></break>
60°C 10 h <xref rid="bb0260" ref-type="bibr">[52]</xref>
</td>
</tr>
<tr><td rowspan="2">S/D treatments</td>
<td rowspan="2">Octaplas (Octapharma)</td>
<td rowspan="2">Disruption of lipid<break></break>
membranes</td>
<td>Products without cells<break></break>
2 h for TNBP/Triton X-100 in PBS or 10% BSA<break></break>
2 h for TNBP/Tween 80 in PBS or 10% BSA<break></break>
24 h for sodium cholate in 10% BSA <xref rid="bb0245" ref-type="bibr">[49]</xref>
</td>
<td rowspan="2">N/A</td>
</tr>
<tr><td>Products without cells<break></break>
30 min <break></break>
(reduction of >5.75±0.3 log<sub>10</sub>
TCID<sub>50</sub>
/mL) <xref rid="bb0250" ref-type="bibr">[50]</xref>
</td>
</tr>
<tr><td rowspan="2">Amotosalen + UV-A light</td>
<td rowspan="2">INTERCEPT Blood<break></break>
system for plasma<break></break>
and platelets (Cerus)</td>
<td rowspan="2">Amotosalen (S-59) intercalates into nucleic acid and induces covalent cross-linking upon UV-A exposure</td>
<td rowspan="2">MEM + 10% FBS<break></break>
(reduction of >5.8 log<sub>10</sub>
PFU/mL) <xref rid="bb0255" ref-type="bibr">[51]</xref>
</td>
<td>Platelet concentrate<break></break>
(reduction of 4·48 ± 0.3 log<sub>10</sub>
PFU/mL) <xref rid="bb0230" ref-type="bibr">[46]</xref>
</td>
</tr>
<tr><td>Fresh-frozen plasma<break></break>
(reduction of 4.67 ± 0.25 log<sub>10</sub>
PFU/mL) <xref rid="bb0235" ref-type="bibr">[47]</xref>
</td>
</tr>
<tr><td>Riboflavin + UV-B light</td>
<td>MIRASOL PRT<break></break>
system for plasma<break></break>
and platelets<break></break>
(Terumo)</td>
<td>Riboflavin associates with nucleic acids and mediates an oxygen-independent electron transfer upon UV exposure</td>
<td>N/A</td>
<td>reduction of >4.07 log<sub>10</sub>
PFU/mL<break></break>
for pooled plasma <break></break>
reduction of >4.42 log<sub>10</sub>
PFU/mL<break></break>
for individual donor plasma<xref rid="bb0270" ref-type="bibr">[54]</xref>
</td>
</tr>
<tr><td>UV-C light</td>
<td>THERAFLEX<break></break>
UV-Platelets (Macopharma)</td>
<td>UV-C directly interacts with nucleic acids, causing the formation of nucleotide dimers</td>
<td>Platelet concentrates<break></break>
(reduction of ≥3.4 log<sub>10</sub>
TCID<sub>50</sub>
/mL) <xref rid="bb0225" ref-type="bibr">[45]</xref>
</td>
<td>Platelet concentrates<break></break>
(reduction of ≥3.7 log<sub>10</sub>
TCID<sub>50</sub>
/mL) <xref rid="bb0240" ref-type="bibr">[48]</xref>
</td>
</tr>
<tr><td>Methylene blue + Visible light</td>
<td>THERAFEX MB<break></break>
(Macopharma)</td>
<td>MB intercalates into nucleic acid and mediates the formation of singlet oxygen upon illumination</td>
<td>Plasma<break></break>
(reduction of >3.1 log<sub>10</sub>
TCID<sub>50</sub>
/mL <xref rid="bb0225" ref-type="bibr">[45]</xref>
</td>
<td>Plasma<break></break>
(reduction of >3.3 log<sub>10</sub>
TCID<sub>50</sub>
/mL) <xref rid="bb0240" ref-type="bibr">[48]</xref>
</td>
</tr>
</tbody>
</table>
<table-wrap-foot><fn><p>BSA, bovine serum albumin; DMEM, Dulbecco modified Eagle medium; FBS, fetal bovine serum; MB, methylene blue; N/A, not available; PBS, phosphate-buffered saline; PFU, plaque-forming units; TNBP, tri-<italic>n</italic>
-butyl phosphate.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</p>
<p id="p0110">Generally, no single PRT is suitable for all blood products because some blood components are damaged by the PRT treatment <xref rid="bb0275" ref-type="bibr">[55]</xref>
, <xref rid="bb0280" ref-type="bibr">[56]</xref>
. In-house studies of methods to inactivate coronaviruses in plasma and platelet concentrates focused mainly on heat and solvent/detergent (S/D) treatment. Usually, 60°C for 15-30 minutes is enough for reduction of SARS-CoV from plasma without cells <xref rid="bb0245" ref-type="bibr">[49]</xref>
, and inactivation could be achieved by 60°C for 10 hours for plasma products <xref rid="bb0260" ref-type="bibr">[52]</xref>
. In the other study, heating at 56°C for 25 minutes could reduce more than 4 log<sub>10</sub>
TCID<sub>50</sub>
/mL of MERS virus <xref rid="bb0265" ref-type="bibr">[53]</xref>
. Because heating could denature protein in blood products, it could only be used in manufactured plasma-derived products. In addition, SARS-CoV was found to be sensitive to solvent and detergent, such as TNBP/Triton X-100, TNBP/Tween 80, and sodium cholate <xref rid="bb0245" ref-type="bibr">[49]</xref>
. After 30-minute treatment using S/D produced by Octaplas (Octapharma), the virus was reduced more than 5.75 ± 0.3 log<sub>10</sub>
TCID<sub>50</sub>
/mL <xref rid="bb0250" ref-type="bibr">[50]</xref>
.</p>
<p id="p0115">Illumination with different wavelengths also influenced activities of SARS and MERS virus in blood. Ultraviolet (UV)-A <xref rid="bb0230" ref-type="bibr">[46]</xref>
, <xref rid="bb0235" ref-type="bibr">[47]</xref>
, <xref rid="bb0255" ref-type="bibr">[51]</xref>
and UV-B light <xref rid="bb0270" ref-type="bibr">[54]</xref>
in the presence of amotosalen or riboflavin could inactivate the pathogens’ nucleic acids, whereas a third PRT method uses UV-C light only <xref rid="bb0225" ref-type="bibr">[45]</xref>
, <xref rid="bb0240" ref-type="bibr">[48]</xref>
. These commercial systems could reduce the activities of SARS and MERS virus in plasma or platelet concentrates to different degrees. Methylene blue plus visible light also has the ability to inactivate coronaviruses in plasma <xref rid="bb0225" ref-type="bibr">[45]</xref>
, <xref rid="bb0240" ref-type="bibr">[48]</xref>
. Cost remains a major administrative obstacle to PRT use <xref rid="bb0275" ref-type="bibr">[55]</xref>
. Therefore, whether or not these PRTs should be implemented in response to SARS-CoV-2depends on the severity and prevalence of COVID-19 in different regions and on the actual risk of transfusion transmission of SARS-CoV-2.</p>
</sec>
<sec id="s0030"><label>6</label>
<title>Conclusions</title>
<p id="p0120">Although coronaviruses cause primarily mild to severe respiratory infections, the potential for transmission by transfusion is worthy of consideration. In China, most of blood centers or blood banks have taken the following measures during the current outbreak: (1) taking body temperature before blood donation; (2) additional questions in the donor screening questionnaire regarding whether the donor or relatives have related symptoms, have traveled to areas with local transmission of SARS-CoV-2 (Wuhan or Hubei province) within 28 days, or are donors with high risk; (3) calling back all blood donors and asking the donors and their family about their current physical condition after donation; and (4) recalling untransfused blood products from infected donors <xref rid="bb0285" ref-type="bibr">[57]</xref>
. However, given the differences between SARS-CoV, MERS-CoV, and SARS-CoV-2, it is not known if the prior recommendations used for SARS and MERS are sufficient. We are facing many unknowns, and careful monitoring and further studies should continue. Stricter measures could be implemented if necessary, such as viral RNA and virus-related antibody screening of blood donations or use of PRT in some regions. As we know, the Wuhan Blood Center and all blood banks in Hubei province have started to test SARS-CoV-2 RNA from blood donations since February 10. Meanwhile, because coronaviruses RNA could be detected in plasma or lymphocytes, staff in blood centers and laboratories should improve biosafety protection during the epidemic. The coming months will provide an enormous amount of new information on SARS-CoV-2 and COVID-19—information which will allow us to make decisions regarding this new virus and public safety.</p>
</sec>
<sec id="s0035"><title>Funding</title>
<p id="p0125">This research did not receive any specific grant from funding agencies in the public, commercial, or not-for profit sectors.</p>
</sec>
<sec id="s0040"><title>Declarations of interest</title>
<p id="p0130">None.</p>
</sec>
</body>
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