Antiphospholipid antibodies in convalescent plasma of donors recovered from mild COVID-19 infection

被引:0
作者
Blickstein, Dorit [1 ]
Izak, Marina [2 ]
Filipovich-Rimon, Talia [3 ]
Garach-Jehoshua, Osnat [3 ]
Rahimi-Levene, Naomi [4 ]
Shinar, Eilat [2 ]
Hamad, Ramzia Abu [5 ]
Bar-Chaim, Adina [6 ]
Koren-Michowitz, Maya [7 ]
机构
[1] Shamir Med Ctr, Dept Hematol, Beer Yaagov, Israel
[2] Magen David Adom Natl Blood Serv, Ramat Gan, Israel
[3] Shamir Med Ctr, Hematol Lab, Beer Yaagov, Israel
[4] Shamir Med Ctr, Blood Bank, Beer Yaagov, Israel
[5] Shamir Med Ctr, Clin Chem Lab, Beer Yaagov, Israel
[6] Shamir Med Ctr, Clin Labs, Beer Yaagov, Israel
[7] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
关键词
anti-N antibodies; antiphospholipid antibodies; anti-S antibodies; convalescent plasma; COVID-19; LUPUS ANTICOAGULANT; GUIDELINES; SOCIETY;
D O I
10.1111/vox.13439
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and Objectives: Passive immunization by the infusion of convalescent plasma (CP) obtained from patients who have recently recovered from COVID-19, thus having antibodies to severe acute respiratory syndrome coronavirus 2, is a potential strategy to reduce the severity of illness. A high prevalence of antiphospholipid antibodies (APLA) in patients with COVID-19 has been reported during the pandemic, raising a concern whether the use of CP could increase the risk of thrombosis in transfused patients. We aimed to evaluate the prevalence of APLA in COVID-19 CP (CCP) in order to assess the potential prothrombotic influence of transfused CCP to COVID-19 patients. Materials and Methods: We studied the prevalence of APLA in 122 CCP samples collected from healthy donors who recovered from mild-COVID-19 at two time periods: September 2020-January 2021 (defined as 'early period' samples) and April-May 2021 (defined as 'late period' samples). Thirty-four healthy subjects unexposed to COVID-19 were used as controls.Results APLA were present in 7 of 122 (6%) CCP samples. One donor had anti-beta 2-glycoprotein 1(anti-beta 2GP1) IgG, one had anti-beta 2GP1 IgM and five had lupus anticoagulant (LAC) using silica clotting time (SCT), all in 'late period' donors. In the control group, one subject had anti-beta 2GP1 IgG, two had LAC using dilute Russell viper venom time (dRVVT) and four had LAC SCT (both LAC SCT and LAC dRVVT in one subject). Conclusion: The low prevalence of APLA in CCP donors reassures the safety of CCP administration to patients with severe COVID-19.
引用
收藏
页码:517 / 522
页数:6
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