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Durability of Immune Response to ChAdOx1-nCoV-19 Vaccine in Solid Cancer Patients Undergoing Anticancer Treatment
There are limited data available about the durability of the immune response after administration of the widely used adenovirus-vectored ChAdOx1-nCoV-19 vaccine in cancer patients. This prospective longitudinal observational study analyzed follow-up data of immunogenic responses 12 weeks after the s...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609471/ https://www.ncbi.nlm.nih.gov/pubmed/36298528 http://dx.doi.org/10.3390/vaccines10101662 |
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author | Wanchaijiraboon, Passakorn Teeyapun, Nattaya Pakvisal, Nussara Sainamthip, Panot Susiriwatananont, Thiti Zungsontiporn, Nicha Suntronwong, Nungruthai Vichaiwattana, Preeyaporn Klinsawat, Worata Wanlapakorn, Nasamon Tanasanvimon, Suebpong Sriuranpong, Virote Poovorawan, Yong Luangdilok, Sutima |
author_facet | Wanchaijiraboon, Passakorn Teeyapun, Nattaya Pakvisal, Nussara Sainamthip, Panot Susiriwatananont, Thiti Zungsontiporn, Nicha Suntronwong, Nungruthai Vichaiwattana, Preeyaporn Klinsawat, Worata Wanlapakorn, Nasamon Tanasanvimon, Suebpong Sriuranpong, Virote Poovorawan, Yong Luangdilok, Sutima |
author_sort | Wanchaijiraboon, Passakorn |
collection | PubMed |
description | There are limited data available about the durability of the immune response after administration of the widely used adenovirus-vectored ChAdOx1-nCoV-19 vaccine in cancer patients. This prospective longitudinal observational study analyzed follow-up data of immunogenic responses 12 weeks after the second dose of the ChAdOx1-nCoV-19 vaccine in 290 oncological patients compared to healthy controls. The study aimed to assess the persistence of the humoral immune response three months after the second dose, and omicron neutralization was also evaluated. Three months after completion of the second vaccine dose, the geometric mean titer of SARS-CoV-2 binding total Ig statistically decreased by 42% compared to those at 4 weeks, and was lower than that of the healthy control. Six percent of patients became seronegative for anti-RBD total Ig. Only 5% (2 of 40 samples) tested positive for surrogate neutralization against SAR-CoV-2 Omicron BA.2. Across different therapy types, a waning in immunogenicity was observed within three months after the second dose of the ChAdOx1 nCoV-19 vaccine, rendering it insufficient at that point to protect against the SAR-CoV-2 Omicron BA.2 variant. |
format | Online Article Text |
id | pubmed-9609471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96094712022-10-28 Durability of Immune Response to ChAdOx1-nCoV-19 Vaccine in Solid Cancer Patients Undergoing Anticancer Treatment Wanchaijiraboon, Passakorn Teeyapun, Nattaya Pakvisal, Nussara Sainamthip, Panot Susiriwatananont, Thiti Zungsontiporn, Nicha Suntronwong, Nungruthai Vichaiwattana, Preeyaporn Klinsawat, Worata Wanlapakorn, Nasamon Tanasanvimon, Suebpong Sriuranpong, Virote Poovorawan, Yong Luangdilok, Sutima Vaccines (Basel) Article There are limited data available about the durability of the immune response after administration of the widely used adenovirus-vectored ChAdOx1-nCoV-19 vaccine in cancer patients. This prospective longitudinal observational study analyzed follow-up data of immunogenic responses 12 weeks after the second dose of the ChAdOx1-nCoV-19 vaccine in 290 oncological patients compared to healthy controls. The study aimed to assess the persistence of the humoral immune response three months after the second dose, and omicron neutralization was also evaluated. Three months after completion of the second vaccine dose, the geometric mean titer of SARS-CoV-2 binding total Ig statistically decreased by 42% compared to those at 4 weeks, and was lower than that of the healthy control. Six percent of patients became seronegative for anti-RBD total Ig. Only 5% (2 of 40 samples) tested positive for surrogate neutralization against SAR-CoV-2 Omicron BA.2. Across different therapy types, a waning in immunogenicity was observed within three months after the second dose of the ChAdOx1 nCoV-19 vaccine, rendering it insufficient at that point to protect against the SAR-CoV-2 Omicron BA.2 variant. MDPI 2022-10-05 /pmc/articles/PMC9609471/ /pubmed/36298528 http://dx.doi.org/10.3390/vaccines10101662 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wanchaijiraboon, Passakorn Teeyapun, Nattaya Pakvisal, Nussara Sainamthip, Panot Susiriwatananont, Thiti Zungsontiporn, Nicha Suntronwong, Nungruthai Vichaiwattana, Preeyaporn Klinsawat, Worata Wanlapakorn, Nasamon Tanasanvimon, Suebpong Sriuranpong, Virote Poovorawan, Yong Luangdilok, Sutima Durability of Immune Response to ChAdOx1-nCoV-19 Vaccine in Solid Cancer Patients Undergoing Anticancer Treatment |
title | Durability of Immune Response to ChAdOx1-nCoV-19 Vaccine in Solid Cancer Patients Undergoing Anticancer Treatment |
title_full | Durability of Immune Response to ChAdOx1-nCoV-19 Vaccine in Solid Cancer Patients Undergoing Anticancer Treatment |
title_fullStr | Durability of Immune Response to ChAdOx1-nCoV-19 Vaccine in Solid Cancer Patients Undergoing Anticancer Treatment |
title_full_unstemmed | Durability of Immune Response to ChAdOx1-nCoV-19 Vaccine in Solid Cancer Patients Undergoing Anticancer Treatment |
title_short | Durability of Immune Response to ChAdOx1-nCoV-19 Vaccine in Solid Cancer Patients Undergoing Anticancer Treatment |
title_sort | durability of immune response to chadox1-ncov-19 vaccine in solid cancer patients undergoing anticancer treatment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609471/ https://www.ncbi.nlm.nih.gov/pubmed/36298528 http://dx.doi.org/10.3390/vaccines10101662 |
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