Progress Update on STING Agonists as Vaccine Adjuvants

Low antigen immunogenicity poses a significant challenge in vaccine development, often leading to inadequate immune responses and reduced vaccine efficacy. Therefore, the discovery of potent immune-enhancing adjuvants is crucial. STING (stimulator of interferon genes) agonists are a promising class...

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Main Authors: Yanru Shen, Weijin Huang, Jianhui Nie, Li Zhang
Format: Article
Language:English
Published: MDPI AG 2025-03-01
Series:Vaccines
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Online Access:https://www.mdpi.com/2076-393X/13/4/371
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author Yanru Shen
Weijin Huang
Jianhui Nie
Li Zhang
author_facet Yanru Shen
Weijin Huang
Jianhui Nie
Li Zhang
author_sort Yanru Shen
collection DOAJ
description Low antigen immunogenicity poses a significant challenge in vaccine development, often leading to inadequate immune responses and reduced vaccine efficacy. Therefore, the discovery of potent immune-enhancing adjuvants is crucial. STING (stimulator of interferon genes) agonists are a promising class of adjuvants which have been identified in various immune cells and are activated in response to DNA fragments, triggering a broad range of type-I interferon-dependent immune responses. Integrating STING agonists with vaccine components is an ideal strategy to bolster vaccine-induced immunity to infections and cancer cells. Several STING agonists are currently under investigation in preclinical studies and clinical trials; however, some have shown limited efficacy, while others exhibit off-target effects. To ensure safety, they are typically delivered with carriers that exhibit high biocompatibility and insolubility. In this review, we present the latest research on natural and synthetic STING agonists that have been effectively used in vaccine development, and summarize their application in adjuvant preventive and therapeutic vaccines. Additionally, we discuss the safety of STING agonists as vaccine adjuvants by reviewing potential delivery strategies. Overall, incorporating STING agonists into vaccine formulations represents a significant advancement in vaccine research with the potential to significantly enhance immune responses and improve vaccine efficacy. However, ongoing research is still required to identify the most effective and safe delivery strategies for STING agonists, as well as to evaluate their long-term safety and efficacy in clinical trials.
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spelling doaj-art-3fadd02c355b4bb48e9e9b3dc0d9fdce2025-08-20T02:18:21ZengMDPI AGVaccines2076-393X2025-03-0113437110.3390/vaccines13040371Progress Update on STING Agonists as Vaccine AdjuvantsYanru Shen0Weijin Huang1Jianhui Nie2Li Zhang3Division of HIV/AIDS and Sex-Transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC), Beijing 102629, ChinaDivision of HIV/AIDS and Sex-Transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC), Beijing 102629, ChinaDivision of HIV/AIDS and Sex-Transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC), Beijing 102629, ChinaDivision of HIV/AIDS and Sex-Transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC), Beijing 102629, ChinaLow antigen immunogenicity poses a significant challenge in vaccine development, often leading to inadequate immune responses and reduced vaccine efficacy. Therefore, the discovery of potent immune-enhancing adjuvants is crucial. STING (stimulator of interferon genes) agonists are a promising class of adjuvants which have been identified in various immune cells and are activated in response to DNA fragments, triggering a broad range of type-I interferon-dependent immune responses. Integrating STING agonists with vaccine components is an ideal strategy to bolster vaccine-induced immunity to infections and cancer cells. Several STING agonists are currently under investigation in preclinical studies and clinical trials; however, some have shown limited efficacy, while others exhibit off-target effects. To ensure safety, they are typically delivered with carriers that exhibit high biocompatibility and insolubility. In this review, we present the latest research on natural and synthetic STING agonists that have been effectively used in vaccine development, and summarize their application in adjuvant preventive and therapeutic vaccines. Additionally, we discuss the safety of STING agonists as vaccine adjuvants by reviewing potential delivery strategies. Overall, incorporating STING agonists into vaccine formulations represents a significant advancement in vaccine research with the potential to significantly enhance immune responses and improve vaccine efficacy. However, ongoing research is still required to identify the most effective and safe delivery strategies for STING agonists, as well as to evaluate their long-term safety and efficacy in clinical trials.https://www.mdpi.com/2076-393X/13/4/371STINGSTING agonistsvaccine adjuvantsinfectious diseasescancer
spellingShingle Yanru Shen
Weijin Huang
Jianhui Nie
Li Zhang
Progress Update on STING Agonists as Vaccine Adjuvants
Vaccines
STING
STING agonists
vaccine adjuvants
infectious diseases
cancer
title Progress Update on STING Agonists as Vaccine Adjuvants
title_full Progress Update on STING Agonists as Vaccine Adjuvants
title_fullStr Progress Update on STING Agonists as Vaccine Adjuvants
title_full_unstemmed Progress Update on STING Agonists as Vaccine Adjuvants
title_short Progress Update on STING Agonists as Vaccine Adjuvants
title_sort progress update on sting agonists as vaccine adjuvants
topic STING
STING agonists
vaccine adjuvants
infectious diseases
cancer
url https://www.mdpi.com/2076-393X/13/4/371
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AT lizhang progressupdateonstingagonistsasvaccineadjuvants