Potentiation of Th1-type immune responses to Mycobacterium tuberculosis antigens in mice by cationic liposomes combined with de-O-acylated lipooligosaccharide

Ara Ko, Seo Ri Wui, Ji In Ryu, Yeon Jeong Lee, Do Thi Thu Hien, Inmoo Rhee, Sung Jae Shin, Shin Ae Park, Kwang Sung Kim, Yang Je Cho, Na Gyong Lee

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)


Tuberculosis (TB) is an infectious disease caused by Mycobacterium tuberculosis. Bacillus Calmette-Guérin (BCG) vaccine is the only TB vaccine currently available, but it is not sufficiently effective in preventing active pulmonary TB or adult infection. With the purpose of developing an improved vaccine against TB that can overcome the limitations of the current BCG vaccine, we investigated whether adjuvant formulations containing de-O-acylated lipooligosaccharide (dLOS) are capable of enhancing the immunogenicity and protective efficacy of TB subunit vaccines. The results revealed that the dLOS/dimethyl dioctadecyl ammonium bromide (DDA) adjuvant formulation significantly increased both humoral and Th1-type cellular responses to TB subunit vaccine that are composed of three antigens, Ag85A, ESAT-6, and HspX. The adjuvanted TB vaccine also effectively induced the Th1-type response in a BCG-primed mouse model, suggesting a potential as a booster vaccine. Finally, the dLOS/ DDA-adjuvanted TB vaccine showed protective efficacy against M. tuberculosis infection in vitro and in vivo. These data indicate that the dLOS/DDA adjuvant enhances the Th1-type immunity and protective efficacy of the TB subunit vaccine, suggesting that it would be a promising adjuvant candidate for the development of a booster vaccine.

Original languageEnglish
Pages (from-to)136-144
Number of pages9
JournalJournal of microbiology and biotechnology
Issue number1
Publication statusPublished - 2018 Jan

Bibliographical note

Funding Information:
We thank Prof. Eun-Kyeong Jo of Chungnam National University for kindly providing the M. tuberculosis BCG strain. This study was supported by a grant from the Technological Innovation R&D Program of Small and Medium Business Administration (No. S2052272) and a grant from the Korean Health Technology R&D Project, Ministry of Health & Welfare (No. HI14C2664).

Publisher Copyright:
© 2018 by The Korean Society for Microbiology and Biotechnology.

All Science Journal Classification (ASJC) codes

  • Biotechnology
  • Applied Microbiology and Biotechnology


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