Neutralizing Antibody Response following a Third Dose of the mRNA-1273 Vaccine among Cancer Patients
Authors:
- Christopher W. DukesCDChristopher W. Dukes
- Marine PotezMPMarine Potez
- Jeffrey LancetJLJeffrey Lancet
- Barbara J. KuterBKBarbara J. Kuter
- Junmin WhitingJWJunmin Whiting
- Qianxing MoQMQianxing Mo
- Brett LeavBLBrett Leav
- Haixing WangHWHaixing Wang
- Julie S. VanasJVJulie S. Vanas
- Christopher L. CubittCCChristopher L. Cubitt
- Kimberly Isaacs-SorianoKIKimberly Isaacs-Soriano
- Kayoko KennedyKKKayoko Kennedy
Open Access
Abstract
Cancer patients are at an increased risk of morbidity and mortality from SARS-CoV-2 infection and have a decreased immune response to vaccination. We conducted a study measuring both the neutralizing and total antibodies in cancer patients following a third dose of the mRNA-1273 COVID-19 vaccine. Immune responses were measured with an enzyme-linked immunosorbent assay (ELISA) and neutralization assays. Kruskal–Wallis tests were used to evaluate the association between patient characteristics and neutralization geometric mean titers (GMTs), and paired t-tests were used to compare the GMTs between different timepoints. Spearman correlation coefficients were calculated to determine the correlation between total antibody and neutralization GMTs. Among 238 adults diagnosed with cancer, a third dose of mRNA-1273 resulted in a 37-fold increase in neutralization GMT 28 days post-vaccination and maintained a 14.6-fold increase at 6 months. Patients with solid tumors or lymphoid cancer had the highest and lowest neutralization GMTs, respectively, at both 28 days and 6 months post-dose 3. While total antibody GMTs in lymphoid patients continued to increase, other cancer types showed decreases in titers between 28 days and 6 months post-dose 3. A strong correlation (p < 0.001) was found between total antibody and neutralization GMTs. The third dose of mRNA-1273 was able to elicit a robust neutralizing antibody response in cancer patients, which remained for 6 months after administration. Lymphoid cancer patients can benefit most from this third dose, as it was shown to continue to increase total antibody GMTs 6 months after vaccination.Keywords
Funding Information
- Moderna, Inc.
This publication has 33 references indexed in Scilit:
- Effectiveness of mRNA BNT162b2 COVID-19 vaccine up to 6 months in a large integrated health system in the USA: a retrospective cohort studyThe Lancet, 2021
- Antibody response to SARS-CoV-2 vaccines in patients with hematologic malignanciesCancer Cell, 2021
- Seroconversion rates following COVID-19 vaccination among patients with cancerCancer Cell, 2021
- Evaluation of Seropositivity Following BNT162b2 Messenger RNA Vaccination for SARS-CoV-2 in Patients Undergoing Treatment for CancerJAMA Oncology, 2021
- Suboptimal Response to Coronavirus Disease 2019 Messenger RNA Vaccines in Patients With Hematologic Malignancies: A Need for Vigilance in the Postmasking EraOpen Forum Infectious Diseases, 2021
- Safety and immunogenicity of one versus two doses of the COVID-19 vaccine BNT162b2 for patients with cancer: interim analysis of a prospective observational studyThe Lancet Oncology, 2021
- Low neutralizing antibody responses against SARS-CoV-2 in older patients with myeloma after the first BNT162b2 vaccine doseBlood, 2021
- Efficacy of the BNT162b2 mRNA COVID-19 vaccine in patients with chronic lymphocytic leukemiaBlood, 2021
- Effect of Bruton tyrosine kinase inhibitor on efficacy of adjuvanted recombinant hepatitis B and zoster vaccinesBlood, 2021
- Age-related differences in humoral and cellular immune responses after primary immunisation: indications for stratified vaccination schedulesScientific Reports, 2018