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Antibody Response to COVID-19 mRNA Vaccine in Patients With Lung Cancer After Primary Immunization and Booster: Reactivity to the SARS-CoV-2 WT Virus and Omicron Variant.
Valanparambil, Rajesh M; Carlisle, Jennifer; Linderman, Susanne L; Akthar, Akil; Millett, Ralph Linwood; Lai, Lilin; Chang, Andres; McCook-Veal, Ashley A; Switchenko, Jeffrey; Nasti, Tahseen H; Saini, Manpreet; Wieland, Andreas; Manning, Kelly E; Ellis, Madison; Moore, Kathryn M; Foster, Stephanie L; Floyd, Katharine; Davis-Gardner, Meredith E; Edara, Venkata-Viswanadh; Patel, Mit; Steur, Conor; Nooka, Ajay K; Green, Felicia; Johns, Margaret A; O'Brein, Fiona; Shanmugasundaram, Uma; Zarnitsyna, Veronika I; Ahmed, Hasan; Nyhoff, Lindsay E; Mantus, Grace; Garett, Michael; Edupuganti, Srilatha; Behra, Madhusmita; Antia, Rustom; Wrammert, Jens; Suthar, Mehul S; Dhodapkar, Madhav V; Ramalingam, Suresh; Ahmed, Rafi.
  • Valanparambil RM; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
  • Carlisle J; Department of Microbiology and Immunology, Emory University, Atlanta, GA.
  • Linderman SL; Winship Cancer Institute, Atlanta, GA.
  • Akthar A; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
  • Millett RL; Department of Microbiology and Immunology, Emory University, Atlanta, GA.
  • Lai L; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
  • Chang A; Department of Microbiology and Immunology, Emory University, Atlanta, GA.
  • McCook-Veal AA; Winship Cancer Institute, Atlanta, GA.
  • Switchenko J; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
  • Nasti TH; Yerkes National Primate Center, Atlanta, GA.
  • Saini M; Center for Childhood Infections and Vaccines of Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
  • Wieland A; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
  • Manning KE; Department of Microbiology and Immunology, Emory University, Atlanta, GA.
  • Ellis M; Winship Cancer Institute, Atlanta, GA.
  • Moore KM; Department of Hematology and Medical Oncology, Emory University, Atlanta, GA.
  • Foster SL; Biostatistics Shared Resource, Winship Cancer Institute, Emory University, Atlanta, GA.
  • Floyd K; Department of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA.
  • Davis-Gardner ME; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
  • Edara VV; Department of Microbiology and Immunology, Emory University, Atlanta, GA.
  • Patel M; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
  • Steur C; Department of Microbiology and Immunology, Emory University, Atlanta, GA.
  • Nooka AK; ICGEB-Emory Vaccine Centre, International Centre for Genetic Engineering and Biotechnology (ICGEB), New Delhi, India.
  • Green F; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
  • Johns MA; Department of Microbiology and Immunology, Emory University, Atlanta, GA.
  • O'Brein F; Department of Otolaryngology, The Ohio State University, Columbus, OH.
  • Shanmugasundaram U; Pelotonia Institute for Immuno-Oncology, The Ohio State University, Columbus, OH.
  • Zarnitsyna VI; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
  • Ahmed H; Yerkes National Primate Center, Atlanta, GA.
  • Nyhoff LE; Center for Childhood Infections and Vaccines of Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
  • Mantus G; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
  • Garett M; Yerkes National Primate Center, Atlanta, GA.
  • Edupuganti S; Center for Childhood Infections and Vaccines of Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
  • Behra M; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
  • Antia R; Yerkes National Primate Center, Atlanta, GA.
  • Wrammert J; Center for Childhood Infections and Vaccines of Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
  • Suthar MS; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
  • Dhodapkar MV; Yerkes National Primate Center, Atlanta, GA.
  • Ramalingam S; Center for Childhood Infections and Vaccines of Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
  • Ahmed R; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
J Clin Oncol ; 40(33): 3808-3816, 2022 Nov 20.
Article in English | MEDLINE | ID: covidwho-2117954
ABSTRACT

PURPOSE:

To examine COVID-19 mRNA vaccine-induced binding and neutralizing antibody responses in patients with non-small-cell lung cancer (NSCLC) to SARS-CoV-2 614D (wild type [WT]) strain and variants of concern after the primary 2-dose and booster vaccination.

METHODS:

Eighty-two patients with NSCLC and 53 healthy volunteers who received SARS-CoV-2 mRNA vaccines were included in the study. Blood was collected longitudinally, and SARS-CoV-2-specific binding and neutralizing antibody responses were evaluated by Meso Scale Discovery assay and live virus Focus Reduction Neutralization Assay, respectively.

RESULTS:

A majority of patients with NSCLC generated binding and neutralizing antibody titers comparable with the healthy vaccinees after mRNA vaccination, but a subset of patients with NSCLC (25%) made poor responses, resulting in overall lower (six- to seven-fold) titers compared with the healthy cohort (P = < .0001). Although patients age > 70 years had lower immunoglobulin G titers (P = < .01), patients receiving programmed death-1 monotherapy, chemotherapy, or a combination of both did not have a significant impact on the antibody response. Neutralizing antibody titers to the B.1.617.2 (Delta), B.1.351 (Beta), and in particular, B.1.1.529 (Omicron) variants were significantly lower (P = < .0001) compared with the 614D (WT) strain. Booster vaccination led to a significant increase (P = .0001) in the binding and neutralizing antibody titers to the WT and Omicron variant. However, 2-4 months after the booster, we observed a five- to seven-fold decrease in neutralizing titers to WT and Omicron viruses.

CONCLUSION:

A subset of patients with NSCLC responded poorly to the SARS-CoV-2 mRNA vaccination and had low neutralizing antibodies to the B.1.1.529 Omicron variant. Booster vaccination increased binding and neutralizing antibody titers to Omicron, but antibody titers declined after 3 months. These data highlight the concern for patients with cancer given the rapid spread of SARS-CoV-2 Omicron variant.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: Carcinoma, Non-Small-Cell Lung / COVID-19 / Lung Neoplasms Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Aged / Humans Language: English Journal: J Clin Oncol Year: 2022 Document Type: Article Affiliation country: JCO.21.02986

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Carcinoma, Non-Small-Cell Lung / COVID-19 / Lung Neoplasms Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Aged / Humans Language: English Journal: J Clin Oncol Year: 2022 Document Type: Article Affiliation country: JCO.21.02986