|
Vol 48 No. 10: 909-922 |
[PDF] [Full Text] |
|
A subunit vaccine based on rH-NS induces protection against Mycobacterium tuberculosis infection by inducing the Th1 immune response and activating macrophages |
|
Yuan Liu1,
Suting Chen2,
Bowen Pan3,
Zhu Guan3,
Zhenjun Yang3,
Linfei Duan1 and
Hong Cai1,*
|
1State Key Laboratory of Protein and Plant Gene Research, College of Life Sciences, Peking University, Beijing 100871, China
2National Clinical Laboratory on Tuberculosis, Beijing Key Laboratory on Drug-Resistant Tuberculosis Research, Beijing Chest Hospital, Capital Medical University, Beijing Tuberculosis and Thoracic Tumor Institute, Beijing 101149, China
3State Key Laboratory of Natural and Biomimetic Drugs, Peking Universtiy Health Science Center, Beijing 100191, China
|
|
Abstract Mycobacterium tuberculosis (Mtb) is a Gram-positive pathogen which causes tuberculosis in both animals and humans. All tested rH-NS formulations induced a specific Th1 response, as indicated by increased production of interferon γ (IFN-γ) and interleukin 2 (IL-2) by lymphocytes in the spleen of mice which were immunized with rH-NS alone or with rH-NS and the adjuvant cyclic GMP-AMP (cGAMP). Serum from mice immunized with rH-NS with or without adjuvant also had higher levels of IL-12p40 and TNF-α, compared with those from control mice immunized with phosphate-buffered saline. Both vaccines increased protective efficacy in mice which were challenged with Mtb H37Rv, as measured by reduced relative CFU counts in the lungs. We found that rH-NS induced the production of TNF-α, IL-6, and IL-12p40, which relied on the activation of mitogen-activated protein kinases by stimulating the rapid phosphorylation of ERK1/2, p38, and JNK, and on the activation of transcription factor NF-κB in macrophages. Additionally, we also found that rH-NS could interact with TLR2 but not TLR4 in pull-down assays. The rH-NS-induced cytokine production from TLR2-silenced RAW264.7 cells was lower than that from BALB/c macrophages. Prolonged exposure (>24 h) of RAW264.7 cells to rH-NS resulted in a significant enhancement in IFN-γ-induced MHC II expression, which was not found in shTLR2-treated RAW264.7 cells. These results suggest that rH-NS is a TLR2 agonist which induces the production of cytokines by macrophages and up-regulates macrophage function.
|
|
Keywords tuberculosis; rH-NS antigen; vaccines; adjuvant; cytokines; APC function; TLR2
|
|
Received 2016-1-6
Accepted 2016-7-6
|
|
Funding This work was supported, in part, by the Seeding Grant for Medicine and Life Sciences of Peking University (No. 2014-MB-15).
|
|
* Correspondence address Tel: +86-10-62756077; Fax: +86-10-62754427; E-mail: [email protected]
|
|
Browse:277 |
|