English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

Results During the acute phase of infection BLT mice rapidly mounted multiple HIV-1-specific CD8+ cellular immune responses against normally immunodominant human CD8 epitopes, with rapid and reproducible viral escape observed within epitopes that similarly tend to escape early in humans. CD8+ T cell responses and viral escape to these same epitopes was confirmed in mice reconstituted with distinct human tissue but expressing the same restricting HLA alleles. Importantly, in two independent groups of mice expressing HLA-B*57 we observed the rapid induction of CD8+ T-cell responses against a number of B*57-restricted responses at frequencies similar to those seen in humans, including the normally immunodominant B*57-IW9, -KF11 and -TW10 epitopes in Gag from which the virus failed to rapidly escape. As in humans, the presence of these conserved responses correlated with significantly greater control over early viral replication. Preliminary vaccine studies in BLT mice support the ability of conventional approaches to induce CD8+ T cell responses and suppress viral loads.

Rapid evolution of HIV-1 to functional CD8+ T-cell rResponses in humanized BLT mice