| Literature DB >> 35015688 |
Tanaya Shree1, Vishnu Shankar2, Julian J K Lohmeyer1, Debra K Czerwinski1, Joseph G Schroers-Martin1, Gladys M Rodriguez1, Sara Beygi1, Alyssa M Kanegai1, Karen S Corbelli1, Etelka Gabriel1, David M Kurtz1, Michael S Khodadoust1, Neel K Gupta1, Lauren S Maeda1, Ranjana H Advani1, Ash A Alizadeh1, Ronald Levy1.
Abstract
To obtain a deeper understanding of poor responses to COVID-19 vaccination in patients with lymphoma, we assessed blocking antibodies, total anti-spike IgG, and spike-specific memory B cells in the peripheral blood of 126 patients with lymphoma and 20 age-matched healthy controls 1 and 4 months after COVID-19 vaccination. Fifty-five percent of patients developed blocking antibodies postvaccination, compared with 100% of controls. When evaluating patients last treated from days to nearly 18 years prior to vaccination, time since last anti-CD20 was a significant independent predictor of vaccine response. None of 31 patients who had received anti-CD20 treatment within 6 months prior to vaccination developed blocking antibodies. In contrast, patients who initiated anti-CD20 treatment shortly after achieving a vaccine-induced antibody response tended to retain that response during treatment, suggesting a policy of immunizing prior to treatment whenever possible. SIGNIFICANCE: In a large cohort of patients with B-cell lymphoma, time since anti-CD20 treatment was an independent predictor of neutralizing antibody response to COVID-19 vaccination. Comparing patients who received anti-CD20 treatment before or after vaccination, we demonstrate that vaccinating first can generate an antibody response that endures through anti-CD20-containing treatment. This article is highlighted in the In This Issue feature, p. 85. ©2022 American Association for Cancer Research.Entities:
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Year: 2022 PMID: 35015688 DOI: 10.1158/2643-3230.BCD-21-0222
Source DB: PubMed Journal: Blood Cancer Discov ISSN: 2643-3230