4.6 Review

Developing New Anti-Tuberculosis Vaccines: Focus on Adjuvants

Journal

CELLS
Volume 10, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/cells10010078

Keywords

vaccines; adjuvants; infectious diseases; tuberculosis

Categories

Funding

  1. European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant [860325]
  2. Italian Ministry grant PRIN2017 [2017E44A9P]

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Tuberculosis is a major global health concern, and new vaccines are needed to overcome the limitations of the current BCG vaccine. The World Health Organization considers the development of new TB vaccines to be a top priority, with subunit vaccines being promising candidates that may require adjuvants to enhance their efficacy.
Tuberculosis (TB) is an infectious disease caused by Mycobacterium tuberculosis (Mtb) that sits in the top 10 leading causes of death in the world today and is the current leading cause of death among infectious diseases. Although there is a licensed vaccine against TB, the Mycobacterium bovis bacilli Calmette-Guerin (BCG) vaccine, it has several limitations, namely its high variability of efficacy in the population and low protection against pulmonary tuberculosis. New vaccines for TB are needed. The World Health Organization (WHO) considers the development and implementation of new TB vaccines to be a priority. Subunit vaccines are promising candidates since they can overcome safety concerns and optimize antigen targeting. Nevertheless, these vaccines need adjuvants in their formulation in order to increase immunogenicity, decrease the needed antigen dose, ensure a targeted delivery and optimize the antigens delivery and interaction with the immune cells. This review aims to focus on adjuvants being used in new formulations of TB vaccines, namely candidates already in clinical trials and others in preclinical development. Although no correlates of protection are defined, most research lines in the field of TB vaccination focus on T-helper 1 (Th1) type of response, namely polyfunctional CD4+ cells expressing simultaneously IFN-gamma, TNF-alpha, and IL-2 cytokines, and also Th17 responses. Accordingly, most of the adjuvants reviewed here are able to promote such responses. In the future, it might be advantageous to consider a wider array of immune parameters to better understand the role of adjuvants in TB immunity and establish correlates of protection.

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