4.5 Article

Isotype-specific outcomes in Fc gamma receptor targeting of PspA using fusion proteins as a vaccination strategy against Streptococcus pneumoniae infection

期刊

VACCINE
卷 38, 期 35, 页码 5634-5646

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2020.06.067

关键词

Vaccine; Streptococcus pneumoniae; Mucosa; Fc receptors

资金

  1. Department of Biological Sciences at Seton Hall University

向作者/读者索取更多资源

Streptococcus pneumoniae (Spn) remains a considerable threat to public health despite the availability of antibiotics and polysaccharide conjugate vaccines. The lack of mucosal immunity in addition to capsular polysaccharide diversity, has proved to be problematic in developing a universal vaccine against Spn. Targeting antigen to Fc receptors is an attractive way to augment both innate and adaptive immunity against mucosal pathogens, by promoting interactions with activating Fc gamma receptors (Fc gamma R) that mediate diverse immunomodulatory functions. The effect of targeting Fc gamma R is highly influenced by the IgG subclass, which bares differential affinities for activating and inhibitory Fc gamma R. In the current study we demonstrate targeting activating Fc gamma R with fusion proteins consisting of PspA and IgG2a Fc enhance PspA-specific immune responses, and effectively protect against mucosal Spn challenge. Specifically, targeting PspA to Fc gamma R polarized alveolar macrophage to the AM1 phenotype and increased conventional dendritic cell subsets in the lung in addition to augmenting Th1 cytokines and PspA-specific IgG and IgA. In contrast, fusion proteins consisting of PspA fused to the IgG1 Fc provided minimal benefit over administration of PspA alone, as a result of interaction with the inhibitory Fc gamma RIIB. Protective efficacy of the IgG1 fusion protein was significantly enhanced in animals deficient for Fc gamma RIIB accompanied by increased B cell maturation and proliferation levels in these animals. These studies demonstrate Fc gamma R targeting is an effective strategy for inducing potent cellular and humoral responses via mucosal immunization with Fc fusion proteins, however, careful consideration of the Fc region utilized is required since Fc isotype subclass heavily influenced immunization induced effector functions and survival against lethal Spn challenge. Fc-engineering with specific attention to Fc gamma RIIB engagement presents a valuable vaccine strategy for protecting against Spn infection. (C) 2020 The Author(s). Published by Elsevier Ltd.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据