TY - JOUR
T1 - Integrated antibody and cellular immunity monitoring are required for assessment of the long term protection that will be essential for effective next generation vaccine development
AU - Paramithiotis, Eustache
AU - Varaklis, Christophe
AU - Pillet, Stephane
AU - Shafiani, Shahin
AU - Lancelotta, Mary Pat
AU - Steinhubl, Steve
AU - Sugden, Scott
AU - Clutter, Matt
AU - Montamat-Sicotte, Damien
AU - Chermak, Todd
AU - Crawford, Stephanie Y.
AU - Lambert, Bruce L.
AU - Mattison, John
AU - Murphy, Robert L.
N1 - Publisher Copyright:
Copyright © 2023 Paramithiotis, Varaklis, Pillet, Shafiani, Lancelotta, Steinhubl, Sugden, Clutter, Montamat-Sicotte, Chermak, Crawford, Lambert, Mattison and Murphy.
PY - 2023
Y1 - 2023
N2 - The COVID pandemic exposed the critical role T cells play in initial immunity, the establishment and maintenance of long term protection, and of durable responsiveness against novel viral variants. A growing body of evidence indicates that adding measures of cellular immunity will fill an important knowledge gap in vaccine clinical trials, likely leading to improvements in the effectiveness of the next generation vaccines against current and emerging variants. In depth cellular immune monitoring in Phase II trials, particularly for high risk populations such as the elderly or immune compromised, should result in better understanding of the dynamics and requirements for establishing effective long term protection. Such analyses can result in cellular immunity correlates that can then be deployed in Phase III studies using appropriate, scalable technologies. Measures of cellular immunity are less established than antibodies as correlates of clinical immunity, and some misconceptions persist about cellular immune monitoring usefulness, cost, complexity, feasibility, and scalability. We outline the currently available cellular immunity assays, review their readiness for use in clinical trials, their logistical requirements, and the type of information each assay generates. The objective is to provide a reliable source of information that could be leveraged to develop a rational approach for comprehensive immune monitoring during vaccine development.
AB - The COVID pandemic exposed the critical role T cells play in initial immunity, the establishment and maintenance of long term protection, and of durable responsiveness against novel viral variants. A growing body of evidence indicates that adding measures of cellular immunity will fill an important knowledge gap in vaccine clinical trials, likely leading to improvements in the effectiveness of the next generation vaccines against current and emerging variants. In depth cellular immune monitoring in Phase II trials, particularly for high risk populations such as the elderly or immune compromised, should result in better understanding of the dynamics and requirements for establishing effective long term protection. Such analyses can result in cellular immunity correlates that can then be deployed in Phase III studies using appropriate, scalable technologies. Measures of cellular immunity are less established than antibodies as correlates of clinical immunity, and some misconceptions persist about cellular immune monitoring usefulness, cost, complexity, feasibility, and scalability. We outline the currently available cellular immunity assays, review their readiness for use in clinical trials, their logistical requirements, and the type of information each assay generates. The objective is to provide a reliable source of information that could be leveraged to develop a rational approach for comprehensive immune monitoring during vaccine development.
KW - COVID
KW - COVID-19
KW - antibody
KW - cellular immunity
KW - vaccine development
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U2 - 10.3389/fimmu.2023.1166059
DO - 10.3389/fimmu.2023.1166059
M3 - Review article
C2 - 38077383
AN - SCOPUS:85178963370
SN - 1664-3224
VL - 14
JO - Frontiers in immunology
JF - Frontiers in immunology
M1 - 1166059
ER -