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Mechanisms underlying vaccination protocols that may optimally elicit broadly neutralizing antibodies against highly mutable pathogens
- Source :
- Physical review. E. 103(5-1)
- Publication Year :
- 2020
-
Abstract
- Effective prophylactic vaccines usually induce the immune system to generate potent antibodies that can bind to an antigen and thus prevent it from infecting host cells. B cells produce antibodies by a Darwinian evolutionary process called affinity maturation (AM). During AM, the B cell population evolves in response to the antigen to produce antibodies that bind specifically and strongly to the antigen. Highly mutable pathogens pose a major challenge to the development of effective vaccines because antibodies that are effective against one strain of the virus may not protect against a mutant strain. Antibodies that can protect against diverse strains of a mutable pathogen have high “breadth” and are called broadly neutralizing antibodies (bnAbs). In spite of extensive studies, an effective vaccination strategy that can generate bnAbs in humans does not exist for any highly mutable pathogen. Here we study a minimal model to explore the mechanisms underlying how the selection forces imposed by antigens can be optimally chosen to guide AM to maximize the evolution of bnAbs. For logistical reasons, only a finite number of antigens can be administered in a finite number of vaccinations; that is, guiding the non-equilibrium dynamics of AM to produce bnAbs must be accomplished non-adiabatically. The time-varying Kullback-Leibler divergence (KLD) between the existing B cell population distribution and the fitness landscape imposed by antigens is a quantitative metric of the thermodynamic force acting on B cells. If this force is too small, adaptation is minimal. If the force is too large, contrary to expectations, adaptation is not faster; rather, the B cell population is extinguished for reasons that we describe. We define the conditions necessary for the force to be set optimally such that the flux of B cells from low to high breadth states is maximized. Even in this case we show why the dynamics of AM prevent perfect adaptation. If two shots of vaccination are allowed, the optimal protocol is characterized by a relatively low optimal KLD during the first shot that appropriately increases the diversity of the B cell population so that the surviving B cells have a high chance of evolving into bnAbs upon subsequently increasing the KLD during the second shot. Phylogenetic tree analysis further reveals the evolutionary pathways that lead to bnAbs. The connections between the mechanisms revealed by our analyses and recent simulation studies of bnAb evolution, the problem of generalist versus specialist evolution, and learning theory are discussed.
- Subjects :
- education.field_of_study
B-Lymphocytes
biology
Fitness landscape
Population
Vaccination
Computational biology
01 natural sciences
Virus
010305 fluids & plasmas
Affinity maturation
Immune system
medicine.anatomical_structure
Antigen
0103 physical sciences
biology.protein
medicine
Antibody
Adaptation
010306 general physics
education
B cell
Broadly Neutralizing Antibodies
Phylogeny
Subjects
Details
- ISSN :
- 24700053
- Volume :
- 103
- Issue :
- 5-1
- Database :
- OpenAIRE
- Journal :
- Physical review. E
- Accession number :
- edsair.doi.dedup.....eb46444df450894d9edd9fcc8df53420