Abstract
Introduction. The new COVID-19 coronavirus infection makes treatment of patients with hematological pathologies more complicated, as well as worsens their prognosis. Therefore, pre-contact emergent prevention is important in this group of patients, for which the preparation of recombinant human monoclonal antibodies (AB) of IgGIk class Tixagevimab + Cilgavimab (Evusheld) has been approved.
Purpose. To study AB dynamics and duration to SARS-CoV-2 after Tixagevimab + Cilgavimab administration in patients with hematological pathologies, to determine the level of IgG class protective antibodies to SARS-CoV-2 S-protein and AB sufficient level to prevent COVID-19 infection.
Materials and methods. 44 patients with hematological diseases, who were treated in the hospital, were prescribed Evusheld as COVID-19 emergent protective agent. Out of these 44 patients, 29 (65.9%) had lymphomas, 11 (25%) – multiple myelomas, and 4 (9.1%) – acute leukemia. AB of IgG class to SARS-CoV-2 S-protein (quantitative method, BAU/ml) and AB of IgM class to SARS-CoV-2 S-and N-proteins (semi-quantitative method, coefficient of positivity) were studied.
Results and discussion. The studied parameters were analyzed before Evusheld administration , on days 3–7 and in 1, 3 and 6 months after it. Patients were divided into three groups depending on the protective AB level before Evusheld administration: first- AB of IgG class to SARS-CoV-2 S-protein less than 150 BAU/ml (36.4% of patients); second – sufficient level of protective antibodies from 150 to 550 BAU/ml ( 27.3% of patients ); third – AB of IgG class to SARS-CoV-2 S-protein more than 550 BAU/ml (36.4% of patients). The researchers found out that patients who survived COVID-19 or were vaccinated within six months have a higher level of IgG-class AB to SARS-CoV-2 S-protein. In the first month after preparation administration, 93.75% of patients had AB to SARS-CoV-2 IgG more than 2000 BAU/ml. The decrease of AB level was registered in three months after Evusheld administration. 7 (15.9%) patients fell ill with COVID-19 within one – two months after administration of the studied preparation. The overall mortality rate in the trial group was 18%.
Conclusion. Administration of the combined preparation Tixagevimab + Cilgavimab decreases the incidence of new corona virus infection in hematological patients. A proper immune response in hematological patients is achievable at the level of protective AB of IgG-class to S-protein more than 550 BAU/ml. Patients who survived new corona virus infection or who were vaccinated within six months have higher level of protective antibodies. Therefore, before Tixagevimab + Cilgavimab administration, it is necessary to assess the level of IgG-class AB to S-protein. After administration of combined Tixagevimab + Cilgavimab preparation, the level of IgG-class AB to S-protein should be monitored every three months.
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