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Abstract For many years, researchers have emphasized the production of high-affinity specific antibodies by hosts during viral infections. However, this has made it challenging for immunologists to systematically evaluate the initiation mechanisms of humoral immunity in specific immune responses. Employing mathematical modeling, we have systematically investigated the dynamic changes of the entire antibody atlas in response to exogenous antigenic stimuli, including viral infections. Our study reveals that the host’s antibody atlas is reshaped during viral infection, not through the proliferation of individual antibody types, but rather through the proliferation of antibody pools with strong binding activity. Moreover, we observe a contraction in pools of antibodies with low binding activity. We have identified the crucial role of self-antigens in maintaining antibody persistence, which can effectively explain the organism’s lifelong protection against pathogens that are less prone to mutation. Using this model, we further explore the mechanisms underlying original antigenic sin and elucidate the specific practical applications of this model. This research transcends the limitations of mere mathematical parameter fitting, as we endeavor to elucidate the complex humoral immune processes using physical mechanisms as a foundation. Our work contributes to a renewed understanding of the antibody elicitation process in specific immune responses.
Xu et al. (Thu,) studied this question.