TY - CHAP
T1 - In Silico Tools for Predicting Novel Epitopes
T2 - Methods and Protocols
AU - Quaglia, Carolina Barra
AU - Nilsson, Jonas Birkelund
AU - Saksager, Astrid
AU - Carri, Ibel
AU - Deleuran, Sebastian
AU - Garcia Alvarez, Heli M.
AU - Høie, Magnus Haraldson
AU - Li, Yuchen
AU - Clifford, Joakim Nøddeskov
AU - Wan, Yat-Tsai Richie
AU - Moreta, Lys Sanz
AU - Nielsen, Morten
PY - 2024
Y1 - 2024
N2 - Identifying antigens within a pathogen is a critical task to develop effective vaccines and diagnostic methods, as well as understanding the evolution and adaptation to host immune responses. Historically, antigenicity was studied with experiments that evaluate the immune response against selected fragments of pathogens. Using this approach, the scientific community has gathered abundant information regarding which pathogenic fragments are immunogenic. The systematic collection of this data has enabled unraveling many of the fundamental rules underlying the properties defining epitopes and immunogenicity, and has resulted in the creation of a large panel of immunologically relevant predictive (in silico) tools. The development and application of such tools have proven to accelerate the identification of novel epitopes within biomedical applications reducing experimental costs. This chapter introduces some basic concepts about MHC presentation, T cell and B cell epitopes, the experimental efforts to determine those, and focuses on state-of-the-art methods for epitope prediction, highlighting their strengths and limitations, and catering instructions for their rational use.
AB - Identifying antigens within a pathogen is a critical task to develop effective vaccines and diagnostic methods, as well as understanding the evolution and adaptation to host immune responses. Historically, antigenicity was studied with experiments that evaluate the immune response against selected fragments of pathogens. Using this approach, the scientific community has gathered abundant information regarding which pathogenic fragments are immunogenic. The systematic collection of this data has enabled unraveling many of the fundamental rules underlying the properties defining epitopes and immunogenicity, and has resulted in the creation of a large panel of immunologically relevant predictive (in silico) tools. The development and application of such tools have proven to accelerate the identification of novel epitopes within biomedical applications reducing experimental costs. This chapter introduces some basic concepts about MHC presentation, T cell and B cell epitopes, the experimental efforts to determine those, and focuses on state-of-the-art methods for epitope prediction, highlighting their strengths and limitations, and catering instructions for their rational use.
KW - MHC presentation
KW - T cell epitopes
KW - B cell epitopes
KW - Epitope prediction
KW - Immunogenicity prediction
U2 - 10.1007/978-1-0716-3890-3_17
DO - 10.1007/978-1-0716-3890-3_17
M3 - Book chapter
C2 - 38888783
SN - 978-1-0716-3889-7
VL - 2813
T3 - Methods in Molecular Biology
SP - 245
EP - 280
BT - Intracellular Pathogens
PB - Humana Press
ER -