Prf1 − / − mice exhibit increased immunopathology with prior CD8 T
cell memory secondary to immunization.
Not exact matches
When antigens such as viruses and vaccines enter the human body, germinal centers are produced within
secondary lymph nodes and
memory B
cells are then induced from germinal - center B
cells.
This is because
memory B
cells, which remember antigens in the primary immune response, are induced and respond faster in the
secondary exposure to bacteria or viruses and differentiate into antibody - producing
cells.
The phenotype of NP
cells generated ex vivo (Figure S8) closely resembles that of central
memory CD4 + T
cells found in vivo, which persist for years in
secondary lymphoid organs and can differentiate into effector
memory CD4 + T
cells [45].