Promising Cytokine Adjuvants for Enhancing Tuberculosis Vaccine Immunity.
Xuezhi CaoYang-Xin FuHua PengPublished in: Vaccines (2024)
Tuberculosis, caused by Mycobacterium tuberculosis ( M. tuberculosis ), remains a formidable global health challenge, affecting a substantial portion of the world's population. The current tuberculosis vaccine, bacille Calmette-Guérin (BCG), offers limited protection against pulmonary tuberculosis in adults, underscoring the critical need for innovative vaccination strategies. Cytokines are pivotal in modulating immune responses and have been explored as potential adjuvants to enhance vaccine efficacy. The strategic inclusion of cytokines as adjuvants in tuberculosis vaccines holds significant promise for augmenting vaccine-induced immune responses and strengthening protection against M. tuberculosis . This review delves into promising cytokines, such as Type I interferons (IFNs), Type II IFN, interleukins such as IL-2, IL-7, IL-15, IL-12, and IL-21, alongside the use of a granulocyte-macrophage colony-stimulating factor (GM-CSF) as an adjuvant, which has shown effectiveness in boosting immune responses and enhancing vaccine efficacy in tuberculosis models.
Keyphrases
- mycobacterium tuberculosis
- pulmonary tuberculosis
- immune response
- hiv aids
- global health
- randomized controlled trial
- systematic review
- dendritic cells
- emergency department
- early stage
- adverse drug
- human immunodeficiency virus
- oxidative stress
- antiretroviral therapy
- hepatitis c virus
- risk assessment
- muscle invasive bladder cancer