Humoral Immune Response in Hematooncological Patients and Health Care Workers Who Received SARS-CoV-2 Vaccinations.


Journal

JAMA oncology
ISSN: 2374-2445
Titre abrégé: JAMA Oncol
Pays: United States
ID NLM: 101652861

Informations de publication

Date de publication:
01 01 2022
Historique:
pubmed: 1 10 2021
medline: 29 1 2022
entrez: 30 9 2021
Statut: ppublish

Résumé

To our knowledge, little is known about antibody development after SARS-CoV-2 vaccination in immunocompromised individuals, such as patients with cancer. To determine whether hematooncological patients develop anti-SARS-CoV-2 antibodies after vaccination. This retrospective cohort study included 2 independent cohorts of patients who were treated for hematological and solid malignant tumors between October 2020 and May 2021, comprising 901 samples from 595 patients and 58 health care workers (HCWs). Serum samples were collected from patients who were treated at an academic center and a community hospital in a rural area and a control group of HCWs, all of whom received SARS-CoV-2 vaccination. Total anti-SARS-CoV-2 nucleocapsid (anti-NC) and antispike protein (anti-S) antibodies were measured retrospectively. In total, 595 patients (320 women [53.8%] and 275 men [46.2%]; median [range] age, 67 [19-96] years) and 58 HCWs (40 women [69.0%] and 18 men [31.0%]; median [range] age, 42 [24-60] years) were included. Previous SARS-CoV-2 infection was documented in 43 of 595 (7.2%), while anti-NC antibodies that suggested previous infections were observed in 49 of 573 evaluable patients (8.6%). In both cohorts, anti-S antibody levels were higher in fully vaccinated patients compared with patients who received 1 dose. After the first vaccination, patients with hematological cancer who received B cell-targeting agents had lower anti-S levels (median, 1.6 AU/mL; range: 0-17 244 AU/mL) than patients who received other therapies (median, 191.6 AU/mL; range, 0-40 000; P < .001) or patients with solid tumors (median, 246.4 AU/mL; range, 0-40 000 AU/mL; P < .001). Anti-S levels after the first vaccination differed according to ongoing antineoplastic treatment modalities, with the lowest median levels in patients who received chemotherapy alone (157.7 AU/mL; range, 0-40 000 AU/mL) or in combination with immunotherapy (118.7 AU/mL; range, 14.1-38 727 AU/mL) and the highest levels in patients with no ongoing antineoplastic treatment (median, 634.3 AU/mL; range, 0-40 000 AU/mL; P = .01). Antibody levels after full immunization were higher in HCWs (median, 2500 U/mL; range, 485-2500 U/mL) than in patients with cancer (median, 117.0 U/mL; range, 0-2500 U/mL; P < .001). In this cohort study of patients with hematooncological diseases and a control group of HCWs, anti-SARS-CoV-2 antibodies after vaccination could be detected in patients with cancer. Lower antibody levels compared with HCWs and differences in seroconversion in specific subgroups underscore the need for further studies on SARS-CoV-2 vaccination in patients with hematooncological disease.

Identifiants

pubmed: 34591965
pii: 2784649
doi: 10.1001/jamaoncol.2021.5437
pmc: PMC8485209
doi:

Substances chimiques

COVID-19 Vaccines 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

106-113

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Auteurs

Maximilian J Mair (MJ)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Julia M Berger (JM)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Anna S Berghoff (AS)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Angelika M Starzer (AM)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Gregor Ortmayr (G)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Hannah C Puhr (HC)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Ariane Steindl (A)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Thomas Perkmann (T)

Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.

Helmuth Haslacher (H)

Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.

Robert Strassl (R)

Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.

Selma Tobudic (S)

Division of Infectious Diseases and Tropical Medicine, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Wolfgang W Lamm (WW)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Markus Raderer (M)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Manfred Mitterer (M)

Hemato-Oncological Day Hospital Unit, Franz Tappeiner Hospital, Meran/Merano, Italy.

Thorsten Fuereder (T)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Dominic Fong (D)

Hemato-Oncological Day Hospital Unit, Franz Tappeiner Hospital, Meran/Merano, Italy.

Matthias Preusser (M)

Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

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Classifications MeSH