TY - JOUR
T1 - Boosting of Waned Humoral and Cellular Responses to SARS-CoV-2 Variants of Concern Among Patients with Cancer
AU - McKenzie, Duncan R
AU - Graham, Rosalind
AU - Lechmere, Thomas
AU - Domingo-Vila, Clara
AU - Alaguthurai, Thanussuyah
AU - Arman, Celeste
AU - Pollock, Emily
AU - Gousis, Charalampos
AU - Kakkassery, Helen
AU - Carpenter, Esme
AU - Kurshan, Ashwini
AU - Vidler, Jennifer
AU - Kulasekararaj, Austin
AU - Patten, Piers
AU - North, Bernard V
AU - Tree, Timothy
AU - Doores, Katie J
AU - Hayday, Adrian C
AU - Irshad, Sheeba
PY - 2022/11/17
Y1 - 2022/11/17
N2 - This study offers longitudinal insight into the impact of three SARS-CoV-2 vaccinations on humoral and cellular immunity in patients with solid cancers, patients with hematologic malignancies, and persons without cancer. For all cohorts, virus-neutralizing immunity was significantly depleted over a period of up to 9 months following the second vaccine dose, the one striking exception being IL2 production by SARS-CoV-2 antigen-specific T cells. Immunity was restored by the third vaccine dose, except in a substantial number of patients with hematologic malignancy, for whom both cancer type and treatment schedule were associated with nonresponse. Thus, whereas most patients with myelodysplastic syndrome were conspicuously good responders, some patients with other hematologic malignancies receiving cancer therapies within 2 weeks of vaccination showed no seroconversion despite three vaccine doses. Moreover, SARS-CoV-2 exposure during the course of the study neither prevented immunity waning, even in healthy controls, nor guaranteed vaccine responsiveness. These data offer real-world human immunologic insights that can inform health policy for patients with cancer.
AB - This study offers longitudinal insight into the impact of three SARS-CoV-2 vaccinations on humoral and cellular immunity in patients with solid cancers, patients with hematologic malignancies, and persons without cancer. For all cohorts, virus-neutralizing immunity was significantly depleted over a period of up to 9 months following the second vaccine dose, the one striking exception being IL2 production by SARS-CoV-2 antigen-specific T cells. Immunity was restored by the third vaccine dose, except in a substantial number of patients with hematologic malignancy, for whom both cancer type and treatment schedule were associated with nonresponse. Thus, whereas most patients with myelodysplastic syndrome were conspicuously good responders, some patients with other hematologic malignancies receiving cancer therapies within 2 weeks of vaccination showed no seroconversion despite three vaccine doses. Moreover, SARS-CoV-2 exposure during the course of the study neither prevented immunity waning, even in healthy controls, nor guaranteed vaccine responsiveness. These data offer real-world human immunologic insights that can inform health policy for patients with cancer.
KW - Humans
KW - SARS-CoV-2/genetics
KW - COVID-19
KW - Neoplasms
KW - Hematologic Neoplasms
U2 - 10.1158/2767-9764.CRC-22-0298
DO - 10.1158/2767-9764.CRC-22-0298
M3 - Article
C2 - 36824220
SN - 2767-9764
VL - 2
SP - 1449
EP - 1461
JO - Cancer research communications
JF - Cancer research communications
IS - 11
ER -