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URL: https://pubmed.ncbi.nlm.nih.gov/30479379/

⇱ Models of immune selection for multi-locus antigenic diversity of pathogens - PubMed


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Abstract

It is well accepted that pathogens can evade recognition and elimination by the host immune system by varying their antigenic targets. Thus, it has become a truism that host immunity is a major driver and determinant of the antigenic diversity of pathogens. However, it remains puzzling how host immunity selects for antigenic diversity at the level of the pathogen population, given that hosts have acquired immune responses to multiple antigens of most pathogens - sometimes through multiple effectors of both humoral and cellular immunity. In this Opinion article, we address this puzzle and the related question of why pathogens often have diversity at multiple antigenic loci. Here, we describe five hypotheses to explain the polymorphism of multiple antigens in a single pathogen species and highlight research relevant to our current models of thinking about multi-locus antigenic diversity.

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Conflict of interest statement

Competing interests

M.L. has received consulting income/honoraria from Antigen Discovery, Pfizer, Merck and Affinivax, and has received institutional grant funding from Pfizer. The other authors declare no competing interests.

Figures

👁 Figure 1 |
Figure 1 |. Non-overlapping antigenic repertoires.
a | We consider three antigenic loci A, B and C, each of which has two variants, such that A1, A2, B1, C1 and C2 together comprise the antigenic space for the example pathogen. b | A host who has previously been infected by a pathogen of genotype A1B1C1 generates immune responses against A1, B1 and C1 antigens and is therefore immune to infection with any pathogen with a genotype carrying A1 or B1 or C1. Therefore, a host who has previously been infected by a pathogen of genotype A1B1C1 would be subsequently susceptible to only a pathogen expressing a different variant at each antigenic locus — namely, A2B2C2.
👁 Figure 2 |
Figure 2 |. Additive effects of host immunity.
a | We consider three antigenic loci A, B and C, each of which has two variants, such that A1, A2, B1, B2, C1 and C2 together comprise the antigenic space for the example pathogen. Sequence diversification of these loci increases the antigenic distance between strains, such that a pathogen of genotype A2B2C2, which is marked by antigenic diversity in all three loci, has the greatest antigenic distance from a pathogen of genotype A1B1C1. b | Increases in antigenic distance between strains incrementally increase the probability that a pathogen strain can infect a previously infected host. Although the relationship shown here between antigenic distance and probability of infection is linear, it could also be nonlinear as a result of a synergistic relationship between immune effectors such as antibodies, for example.
👁 Figure 3 |
Figure 3 |. Variation at one locus affects responses at other loci.
a | We consider three antigenic loci A, B and C. Locus A has two variants (A1 and A2), whereas loci B and C have a single variant each (B1 and C1, respectively). Therefore, A1, A2, B1 and C1 together comprise the antigenic space for the example pathogen. b | A host who has previously been infected by a pathogen of genotype A1B1C1 generates specific immunity against loci A1, B1 and C1, and is therefore immune to subsequent infection by a pathogen with the same genotype. Under the model of hypothesis 2, the single variable antigenic locus A with two variants (A1 and A2) could reduce the effectiveness of immunity against additional loci (locus B and locus C), thereby rendering the A1B1C1-immune host susceptible to any pathogen with a genotype containing A2, despite pre-existing immunity to loci B and C.

References

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