Multiple cross‐reactivities amongst antigens of <i>Plasmodium falciparum</i> impair the development of protective immunity against malaria

Robin F. Anders

Parasite Immunology · 1986 · 229 citations · 44 references

Concepts

TL;DR

Malaria parasite antigens contain short tandem repeats that encode immunodominant epitopes, with some antigens having one or multiple repeat blocks that are often conserved yet degenerate. The study aims to determine whether cross‑reactivity among repeat epitopes impairs the maturation of high‑affinity antibodies in malaria. The authors propose that cross‑reactive epitopes retain a large fraction of somatically mutated B cells during clonal expansion, disrupting normal affinity maturation. They observed extensive cross‑reactions among epitopes from related repeats, spanning different repeat blocks within a single antigen or across distinct antigens.

Abstract

Summary The majority of protein antigens of the malaria parasite Plasmodium falciparum contain short sequences that are extensively repeated in tandem arrays. Some antigens contain a single block of repeats whereas in other antigens there may be two or more blocks of related repeats. The repetitive sequences in an individual antigen may be highly conserved but more usually there is some degeneracy which occasionally is extensive. The repetitive sequences encode immunodominant epitopes to which much of the antibody response in malaria is directed. Recently, we have found that there are extensive cross‐reactions amongst the epitopes encoded by related repetitive sequences. These cross‐reactions may involve different blocks of repeats in the one antigen or repetitive sequences in different antigens. It is proposed that these cross‐reactions interfere with the normal maturation of a high affinity antibody response in malaria by causing an abnormally high proportion of somatically‐mutated B cells to be preserved during clonal expansion.

References

44