ArticlemBio2026
Evasion of humoral immune responses by a key mutational region of the S2 subunit in PEDV variants.
Article in mBio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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14 authors.
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Abstract
Since 2010, millions of piglets have died from porcine epidemic diarrhea virus (PEDV) variant strains. Compared with classical strains, variants exhibit enhanced virulence and immune evasion capacity, rendering classical strain-based vaccines poorly effective. However, the critical mutants responsible for increased pathogenicity and immune evasion remain unclear. This study aims to identify the key mutations that drive humoral immune evasion in PEDV variants and to elucidate further the underlying molecular mechanisms. Cross-neutralization assays and recombinant virus screening identified the 894-993 amino acid (aa) mutation region of the S2 subunit as a key determinant of humoral immune evasion in variants. The challenge experiments in piglets demonstrated that the 894-993 aa mutation region plays a critical role in determining variants' virulence. Subsequent vaccination-challenge experiments further clarified the pivotal contribution of the 894-993 aa mutation region in the humoral immune evasion
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