Post‐COVID immunity in patients with solid tumor or hematological malignancies treated with SARS‐CoV‐2 monoclonal antibodies

All mAB-treated patients with malignancies developed polyfunctional immunity humoral and T-cell immunity to SARS-CoV-2 even in the setting of B-cell deficiency. The evolution of this immunity, including new variant-specific antibodies, without secondary illnesses suggests that patients were protected from symptomatic re-infection, and mAB therapy did not blunt the development of host immunity. Future studies are warranted to better characterize immunologic memory over time with exposures to new viral variants, evaluate prolonged viral shedding and the continued use of appropriate mAB for infection in high-risk patients.

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Publication Details

Journal
Immunity Inflammation and Disease
Published
2024-12-01
DOI
https://doi.org/10.1002/iid3.70039
Citations
2
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
0.78

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article

Post‐COVID immunity in patients with solid tumor or hematological malignancies treated with SARS‐CoV‐2 monoclonal antibodies

Jyotsna Fuloria, John S. Schieffelin, Bronwyn M. Gunn, Gilberto Sabino‐Santos et al.
2 citations
Immunity Inflammation and Disease
SARS-CoV-2 and COVID-19 Research
0.78
article

Post‐COVID immunity in patients with solid tumor or hematological malignancies treated with SARS‐CoV‐2 monoclonal antibodies

Jyotsna Fuloria, John S. Schieffelin, Bronwyn M. Gunn, Gilberto Sabino‐Santos, Sinem Ulusan, Sruti Chandra, Elizabeth B. Norton, Lin Li, Bo Ning, Shuangyi Bai, Ye Hu, James E. Robinson, Debra Elliott, Cathryn Leggio, Sam Litwin, Ashley R. Smira, Najia Waheed, Anoli Karunathilake
article en
2 citations

Abstract

All mAB-treated patients with malignancies developed polyfunctional immunity humoral and T-cell immunity to SARS-CoV-2 even in the setting of B-cell deficiency. The evolution of this immunity, including new variant-specific antibodies, without secondary illnesses suggests that patients were protected from symptomatic re-infection, and mAB therapy did not blunt the development of host immunity. Future studies are warranted to better characterize immunologic memory over time with exposures to new viral variants, evaluate prolonged viral shedding and the continued use of appropriate mAB for infection in high-risk patients.

Immunity Inflammation and DiseaseVol. 12(12)
Tulane University (US), University Medical Center New Orleans (US), Washington State University (US)
Tulane University, National Institutes of Health, National Cancer Institute, National Institute of Allergy and Infectious Diseases
Good health and well-being
Openalex Percentile: Top 26%
SARS-CoV-2 and COVID-19 Research
0.78
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