Bayesian inference of antibody evolutionary dynamics using multitype branching processes

TL;DR

This paper introduces a Bayesian method to infer antibody evolutionary dynamics from limited data by modeling B-cell evolution as a multitype branching process, revealing a sigmoidal relationship between fitness and affinity.

Contribution

It develops a novel Bayesian framework with an efficient likelihood algorithm to infer fitness-affinity relationships from single-time-point antibody sequence data.

Findings

Recovered sigmoidal fitness-affinity relationship from simulated data.

Inferred that high-affinity B cells have over six times higher fitness.

Identified a sharp transition in fitness as affinity increases.

Abstract

When our immune system encounters foreign antigens (i.e., from pathogens), the B cells that produce our antibodies undergo a cyclic process of proliferation, mutation, and selection, improving their ability to bind to the specific antigen. Immunologists have recently developed powerful experimental techniques to investigate this process in mouse models. In one such experiment, mice are engineered with a monoclonal B-cell precursor and immunized with a model antigen. B cells are sampled from sacrificed mice after the immune response has progressed, and the mutated genetic loci encoding antibodies are sequenced. This experiment allows parallel replay of antibody evolution, but produces data at only one time point; we are unable to observe the evolutionary trajectories that lead to optimized antibody affinity in each mouse. To address this, we model antibody evolution as a multitype branching process and integrate over unobserved histories conditioned on phylogenetic signal in sequence data, leveraging parallel experimental replays for parameter inference. We infer the functional relationship between B-cell fitness and antigen binding affinity in a Bayesian framework, equipped with an efficient likelihood calculation algorithm and Markov chain Monte Carlo posterior approximation. In a simulation study, we demonstrate that a sigmoidal relationship between fitness and binding affinity can be recovered from realizations of the branching process. We then perform inference for experimental data from 52 replayed B-cell lineages sampled 15 days after immunization, yielding a total of 3,758 sampled B cells. The recovered sigmoidal curve indicates that the fitness of high-affinity B cells is over six times larger than that of low-affinity B cells, with a sharp transition from low to high fitness values as affinity increases.