TB/Flu-06E

Stage of Development

Proof of Concept – Animal Model

Vaccine Platform

Viral Vector

Candidate Overview

The vaccine platform is based on the live influenza virus vector that is highly attenuated through alteration in NS1 protein function. This effect is achieved by the replacement of immunosuppressive C-terminal part of NS1 open reading frame with foreign sequences, encoding ESAT-6 antigen of M. tuberculosis. Importantly, viral vector itself acts as an adjuvant, stimulating the innate immune system.

Sponsor / Lead Developer: Smorodintsev Research Institute of Influenza, The Ministry of Health of the Russian Federation

Development partner(s): Saint-Petersburg State Research Institute of Phthisiopulmonology, The Ministry of Health of the Russian Federation,

Primary Indication: Immunotherapy / Shortening TB treatment

Other Indication(s): Prevention of TB recurrence

Target Population(s): Adolescents, Adults, People cured of active TB, People with active TB, People with MDR-TB, and People with Mtb infection

Target Route of Administration: Intranasal and Sublingual

Immune tissue localization: Lung, Lymph node, and Spleen

Immunological responses: T-cell

Preclinical Animal Models: Ferret, Guinea pig, and Mouse

Intended to elicit trained immunity: Yes

Additional Immunologic Response Information

HYPOTHESIZED
DEMONSTRATED
Immune ResponseT-cell
T-cell phenotypeCD4
CD8
T-cell functional profileIFN-γ
TNF-α
IL-17
Mycobacterial growth inhibition
Preferential immune tissue localizationLung
Lymph node
Spleen
Trained immunityYes