Official Title
Phase I/II Multicenter Trial of Lentiviral Minigene Vaccine (LV-SMENP) of Covid-19 Coronavirus
Brief Summary

In December 2019, viral pneumonia caused by a novel beta-coronavirus (Covid-19) broke out in Wuhan, China. Some patients rapidly progressed and suffered severe acute respiratory failure and died, making it imperative to develop a safe and effective vaccine to treat and prevent severe Covid-19 pneumonia. Based on detailed analysis of the viral genome and search for potential immunogenic targets, a synthetic minigene has been engineered based on conserved domains of the viral structural proteins and a polyprotein protease. The infection of Covid-19 is mediated through binding of the Spike protein to the ACEII receptor, and the viral replication depends on molecular mechanisms of all of these viral proteins. This trial proposes to develop and test innovative Covid-19 minigenes engineered based on multiple viral genes, using an efficient lentiviral vector system (NHP/TYF) to express viral proteins and immune modulatory genes to modify dendritic cells (DCs) and to activate T cells. In this study, the safety and efficacy of this LV vaccine (LV-SMENP) will be investigated.

Detailed Description

Background: The 2019 discovered new coronavirus, Covid-19, is an enveloped positive strand
single strand RNA virus. The number of Covid-19 infected people has increased rapidly and WHO
has warned that the spread of Covid-19 may soon become pandemic and have disastrous outcomes.
Covid-19 could pose a serious threat to human health and global economy. There is no vaccine
available or clinically approved antiviral therapy as yet. This study aims to evaluate the
safety and efficacy of treating Covid-19 infections with a novel lentiviral based DC and T
cell vaccines.

Objective: Primary study objectives: Injection and infusion of LV-SMENP DC and
antigen-specific cytotoxic T cell vaccines to healthy volunteers and Covid-19 infected
patients to evaluate the safety.

Secondary study objectives: To evaluate the anti- Covid-19 efficacy of the LV-SMENP DC and
antigen-specific cytotoxic T cell vaccines.

Design:

1. Based on the genomic sequence of the new coronavirus Covid-19, select conserved and
critical structural and protease protein domains to engineer lentiviral SMENP minigenes
to express Covid-19 antigens.

2. LV-SMENP-DC vaccine is made by modifying DC with lentivirus vectors expressing Covid-19
minigene SMENP and immune modulatory genes. CTLs will be activated by LV-DC presenting
Covid-19 specific antigens.

3. LV-DC vaccine and antigen-specific CTLs are prepared in 7~21 days. Subject will receive
total 5x10^6 cells of LV-DC vaccine and 1x10^8 antigen-specific CTLs via sub-cutaneous
injection and IV infusion, respectively. Patients are followed weekly for one month
after the infusion, monthly for 3 months, and then every 3 months until the trial ends.

Recruiting
Pathogen Infection Covid-19 Infection

Biological: Injection and infusion of LV-SMENP-DC vaccine and antigen-specific CTLs

Patients will receive approximately 5x10^6 LV-DC vaccine and 1x10^8 CTLs via sub-cutaneous injections and iv infusions, respectively.

Eligibility Criteria

Inclusion Criteria:

- Laboratory (RT-PCR) confirmed Covid-19 infection in throat swab and/or sputum and/or
lower respiratory tract samples;

- The interval between the onset of symptoms and randomized is within 7 days. The onset
of symptoms is mainly based on fever. If there is no fever, cough or other related
symptoms can be used;

- White blood cells ≥ 3,500 / μl, lymphocytes ≥ 750 / μl;

- Human immunodeficiency virus (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV)
or tuberculosis (TB) test is negative;

- Sign the Informed Consent Form on a voluntary basis;

Exclusion Criteria:

- Subject infected with HCV (HCV antibody positive), HBV (HBsAg positive), HIV (HIV
antibody positive), or HTLV (HTLV antibody positive).

- Subject is albumin-intolerant.

- Subject with life expectancy less than 4 weeks.

- Subject participated in other investigational somatic cell therapies within past 30
days.

- Subject with positive pregnancy test result.

- Researchers consider unsuitable.

Eligibility Gender
All
Eligibility Age
Minimum: 6 Months ~ Maximum: 80 Years
Countries
China
Locations

Shenzhen Geno-immune Medical Institute
Shenzhen, Guangdong, China

Shenzhen Second People's Hospital
Shenzhen, Guangdong, China

Shenzhen Third People's Hospital
Shenzhen, Guangdong, China

Contacts

Lung-Ji Chang, PhD
+86(755)8672 5195
c@szgimi.org

Lung-Ji Chang, PhD, Principal Investigator
Shenzhen Geno-Immune Medical Institute

Shenzhen Geno-Immune Medical Institute
NCT Number
Keywords
Lentiviral vector
LV-DC vaccine
Covid-19 CTL
MeSH Terms
COVID-19