COVID-19 and humoral immune response in convalescent plasma donors in Pakistani cohort.

J. Hassan, Shahtaj Masood, N. Fatima, T. Khan, J. Akram, Faridoon Ahmad, Lubna Meraj, Ayesha Mahesar, Z. Malik, N. Sheikh, Irfan Ghafoor baig, M. Adil, Muhammad Asif, S. Maqsood, Mahjabeen Imam, Durenaz Jamal, Dilnasheen Safdar, T. Shamsi
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Abstract

Current COVID-19 pandemic has affected the entire globe. While there was no vaccine neither any specific treatment, investigational use of convalescent plasma has been explored in clinical trials. A prospective multicenter study of convalescent plasma was conducted. Donors were tested for total Anti-SARS-CoV-2 antibodies by electrochemiluminescence (ECLIA) and RT-PCR for COVID-19. Enzyme Linked Immunosorbent Assay (ELISA) was used to detect semi-quantitative and quantitative IgG anti-SARS-COV-2 antibodies. IgG Immunofluorescence-based lateral flow immunoassay (LFIA) was used to recheck seronegative donors. A total of 400 donors were enrolled. Twelve donors were SARS-CoV-2 positive by RT-PCR. Nine of 12 donors had developed SARS-CoV-2 IgG antibodies, while in 3 donors antibodies were not developed. A total of 70 donors (17.5%) were deferred due to seronegative status; 64 (16%) of them did not develop antibodies when plasma collection was planned. The IgG semiquantitative ELISA was positive in 282 and quantitative in 284 of 330 donors with a mean value of >1:160 and 44.10±39.22 IU/ml respectively. A total of 116 (29%) donors did not show IgG humoral response to COVID-19 even 28 days from the onset of illness. Subsequently, LFIA method was able to detect IgG antibodies in 20 of 48 (41.6%) seronegative donors and in 20 of 34 (58.8%) ECLIA positive ELISA negative donors. Viral RNA detection in recovered asymptomatic patients with concomitant IgG antibodies indicates recovery. Inability to detect antibodies by different testing kits may be due to their different antigenic targets or sensitivity. Significance of a positive COVID-19 RT-PCR in asymptomatic recovered patients is yet to be determined.
巴基斯坦队列恢复期血浆供者的COVID-19与体液免疫反应
当前,新冠肺炎疫情波及全球。虽然没有疫苗,也没有任何特定的治疗方法,但已经在临床试验中探索了恢复期血浆的研究性使用。对恢复期血浆进行了前瞻性多中心研究。通过电化学发光(ECLIA)和RT-PCR检测供体的COVID-19总抗sars - cov -2抗体。采用酶联免疫吸附试验(ELISA)检测半定量和定量IgG抗sars - cov -2抗体。IgG免疫荧光侧流免疫分析法(LFIA)用于复检血清阴性供者。总共登记了400名捐赠者。12名供体经RT-PCR检测为SARS-CoV-2阳性。12名献血者中有9人产生了SARS-CoV-2 IgG抗体,3名献血者没有产生抗体。共有70名献血者(17.5%)因血清状态阴性而被推迟;其中64例(16%)在计划收集血浆时未产生抗体。330例献血者中IgG半定量ELISA阳性282例,定量284例,平均值分别为>∶160和44.10±39.22 IU/ml。116名(29%)献血者在发病后28天内未表现出对COVID-19的IgG体液反应。随后,LFIA方法能够在48例血清阴性供者中的20例(41.6%)和34例ECLIA阳性ELISA阴性供者中的20例(58.8%)中检测到IgG抗体。在无症状的康复患者中检测病毒RNA并伴有IgG抗体提示康复。不同的检测试剂盒无法检测抗体可能是由于它们不同的抗原靶点或敏感性。COVID-19 RT-PCR在无症状康复患者中的阳性意义尚未确定。
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