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Short Research Communication Anti-Spike Antibody Response to COVISHIELD™ (SII-ChAdOx1 nCoV-19) Vaccine in Patients with B-Cell and Plasma Cell Malignancies and Hematopoietic Cell Transplantation Recipients

INTRODUCTION: There is limited data on the serologic antibody responses after the ChAdOx1 vaccine in patients with hematological malignancies and hematopoietic cell transplantation recipients. There is no data on the safety and efficacy of the Indian COVISHIELD™ vaccine in this population. METHODS:...

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Detalles Bibliográficos
Autores principales: Chopra, Madhu, Jain, Arihant, Chhabra, Sanjeev, Kaundal, Shaweta, Singh, Charanpreet, Jandial, Aditya, Prakash, Gaurav, Khadwal, Alka, Das, Chandan, Singh, Mini P, Das, Reena, Malhotra, Pankaj, Lad, Deepesh P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer India 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891427/
https://www.ncbi.nlm.nih.gov/pubmed/35261492
http://dx.doi.org/10.1007/s12288-022-01528-y
Descripción
Sumario:INTRODUCTION: There is limited data on the serologic antibody responses after the ChAdOx1 vaccine in patients with hematological malignancies and hematopoietic cell transplantation recipients. There is no data on the safety and efficacy of the Indian COVISHIELD™ vaccine in this population. METHODS: This study reports the anti-S antibody response to the COVISHIELD™ vaccine in a prospective cohort of patients with B-cell and plasma cell malignancies and HCT recipients at a single center. The quantitative antibodies to the SARS-CoV-2 S protein receptor-binding domain in human plasma were determined by the validated Roche Elecsys Anti-SARS-CoV-2 S kit. RESULTS: A total of 118 patients were included over the study period from April 2021 to August 2021. The seropositivity rate at baseline and after the first and second dose of the vaccine was 39%, 66%, and 79%, respectively (p < 0.0001). The seronegative cohort had a higher median age (65 vs. 60 years, p = 0.03), were more likely to be males (81% vs. 42%, p = 0.009), had a diagnosis of B-CLPD (100% vs. 42%, p < 0.001) and were more likely to be on ibrutinib therapy (56% vs. 15%, p = 0.001). CONCLUSIONS: This study confirms the safety and efficacy of the COVISHIELD™ vaccine in patients with hematological malignancies.