| Literature DB >> 27571906 |
Dhiraj Kumar Singh1,2, Ved Prakash Dwivedi1,2, Anand Ranganathan1,2, William R Bishai3, Luc Van Kaer4, Gobardhan Das1.
Abstract
Tuberculosis is the oldest known infectious disease, yet there is no effective vaccine against adult pulmonary tuberculosis. Emerging evidence indicates that T-helper 1 and T-helper 17 cells play important roles in host protection against tuberculosis. However, tuberculosis vaccine efficacy in mice is critically dependent on the balance between antigen-specific central memory T (Tcm) and effector memory T (Tem) cells. Specifically, a high Tcm/Tem cell ratio is essential for optimal vaccine efficacy. Here, we show that inhibition of Kv1.3, a potassium channel preferentially expressed by Tem cells, by Clofazimine selectively expands Tcm cells during BCG vaccination. Furthermore, mice that received clofazimine after BCG vaccination exhibited significantly enhanced resistance against tuberculosis. This superior activity against tuberculosis could be adoptively transferred to naive, syngeneic mice by CD4+ T cells. Therefore, clofazimine enhances Tcm cell expansion, which in turn provides improved vaccine efficacy. Thus, Kv1.3 blockade is a promising approach for enhancing the efficacy of the BCG vaccine in humans.Entities:
Keywords: BCG vaccine; Kv1.3 potassium ion channel; Memory T cells; Mycobacterium tuberculosis; clofazimine
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Year: 2016 PMID: 27571906 DOI: 10.1093/infdis/jiw395
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226