Tuberculosis Clinical Trial
Official title:
Utilizing the Crosstalk Among Chicoric Acid, 13-Cis Retinoic Acid(Aerosolized), Minocycline and Vitamin D as a Potent Quadrate Therapy for Treating Patients With Multidrug-resistant TB and Patient With Both Multidrug-resistant TB and COVID-19
Utilizing the Crosstalk Among Chicoric Acid, 13-Cis Retinoic Acid(Aerosolized), Minocycline and Vitamin D as a Potent Quadrate Therapy for treating patients with Multidrug-resistant TB and patient with both Multidrug-resistant TB and COVID-19 . A double-edged sword Clinical Study I)Part of Tuberculosis Tuberculosis (TB) is a major infectious disease killer globally. It affected 10 million and killed 1.4 million people in 2019 alone. The predicted impact of the COVID-19 pandemic is an additional 190,000 TB deaths in 2020, and it is expected in the next 5 y that there will be up to a 20% increase in the global TB disease burden , stressing the critical need for new safe and effective drugs against Mycobacterium tuberculosis (Mtb). In addition, controlling multidrug-resistant TB (MDR-TB) presents a huge public health challenge . New drug discovery could require several years with no guarantee but repurposing established may be useful to treat patients with tuberculosis . Here we demonstrate that we could utilize the crosstalk among Chicoric Acid, 13-Cis Retinoic Acid, Minocycline , and vitamin D as a novel quadrate therapy against TB.Drug-resistant tuberculosis represents a global emergency, requiring new drugs. Recently Minocycline was found to be highly potent in laboratory strains of Mycobacterium TB, and 30 drug-sensitive and multidrug/extensively drug-resistant clinical strains were susceptible to clinically attainable dosages. The lung concentration-time profiles of a 7 mg/kg/day human-equivalent minocycline dosage yielded bacterial kill rates comparable to first-line antituberculosis drugs. Extracellular bacilli were destroyed directly by minocycline. Minocycline also killed intracellular bacilli indirectly through granzyme A-driven apoptosis. Furthermore, minocycline showed dose-dependent antiinflammatory effect, suggesting that it may protect tuberculosis patients against immunopathology. A study showed that M. tuberculosis induced the expression of indoleamine 2,3-dioxygenase (IDO), an enzyme involved in tryptophan catabolism, in macrophages and in the lungs of animals (mice and macaque) with active disease. In a macaque model of inhalation TB, suppression of IDO activity reduced bacterial burden, pathology, and clinical signs of TB disease, leading to increased host survival. This increased protection was accompanied by increased lung T cell proliferation, induction of inducible bronchus-associated lymphoid tissue and correlates of bacterial killing . A recent study showed that Minocycline-induced significantly inhibition of IDO expression. But Minocycline-induced inhibition of IDO expression is retinoid-dependent. The combined treatment with minocycline and retinol, however, resulted in a striking, statistically significant decrease in IDO. Co-treatment with minocycline and retinol again resulted in decreased TNF-α and IL-6 levels. A study showed that IL-6 inhibits IFN-γ induced autophagy in Mycobacterium (TB) H37Rv infected macrophages. As well as neutralization of endogenous IL-6 by anti-IL-6 antibody significantly enhances the IFN-γ mediated killing of the intracellular bacteria. Minocycline's anti-inflammatory effects are mediated through RAR signaling. Therefore, The combined treatment with minocycline and retinol is expected to effectively inhibit (TB) and its inflammatory complication, Fortunately, Retinoic Acid significantly inhibits the in vivo growth of M. tuberculosis and the development of tuberculosis. In addition to, 13-Cis RA and Chicoric Acid ( CA ) enhanced the cell surface expression of HLA-DR and CD14 molecules on U937 macrophages and prevented the growth of Mtb within macrophages. Moreover, 13-cis RA and CA, have increased NO generation compared to untreated control macrophages, significantly . Both drugs have a significant inhibitory effect on Mtb growth but CA at the highest concentration was more potent than 13-cis RA . Therefore we will use retinoic acid to induce the effect of Minocycline as well as its ability to inhibit tuberculosis in combination with CA .Recent data showed that Vitamin D support innate immune responses to Mycobacterium TB and Low vitamin D levels were associated with a 5-fold increased risk for progression to tuberculosis. Deficiency of vitamin D has long been implicated in activation of (TB) . Serum vitamin D in TB patients are lower than in healthy controls . Vitamin D has been found to speed up the clearance of (TB) bacteria from the lungs of people with multi-drug resistant TB, according to a study of 1,850 patients. It was showed that Vitamin D receptor (VDR) must form a heterodimer complex with retinoid X receptor (RXR) to regulate gene transcription. Retinol plays a crucial role in lung development and signaling the vitamin D pathway. 9-cis-retinoic acid, an active vitamin A metabolite and the ligand of RXR, assists VDR signaling and suppresses the degradation of circulating vitamin D.
Status | Not yet recruiting |
Enrollment | 250 |
Est. completion date | February 2022 |
Est. primary completion date | February 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Age above 18 up to 65 years - Microbiologically or histologically confirmed active tuberculosis as well as confirmed positive with COVID-19 - Clinically confirmed latent tuberculosis - Drug resistant MTb - Negative pregnancy test for 18-40 year-old females - Able to sign consent Exclusion Criteria: - HIV positive - Known intolerance of vitamin D - Sarcoidosis - Hyperparathyroidism or nephrolithiasis - Taking vitamin D or A supplementation in the two months preceding enrolment - Baseline serum corrected calcium >2.65 mmol/L - Current haemodialysis - Children, pregnant or breastfeeding individuals - Concomitant benzothiadiazine derivative, cardiac glycoside, carbamazepine, phenobarbital, phenytoin, primidone or long-term immunosuppressant therap - Extra-pulmonary or smear negative tuberculosis - Patients receiving steroids, cytotoxic drugs, post transplant or metastatic malignancy, or not expected to survive for the duration of ATT - Pregnant or lactating women - Active diarrhoea, indicating possible fat-soluble vitamin malabsorption. - Baseline Hypercalcemia >10.5 mg/dl - Concurrent use of cyclosporin, cisplatin, amfotericin B, cephalosporins, polymyxins and vancomycin. - History of adverse events on previous Minocycline or other tetracycline use (by spontaneous reporting nor by active questioning). - Depressive disorder - Body mass index less than 18 points or higher than 25 points - Contraindications for hormonal contraception or intrauterine device. - Autoimmune diseases A history of organ, bone marrow or hematopoietic stem cell transplantation - Patients receiving anti-hcv treatment - Permanent blindness in one eye - History of iritis, endophthalmitis, scleral inflammation or retinitis 15-90 days of retinal detachment or eye surgery |
Country | Name | City | State |
---|---|---|---|
Egypt | Kafr El-sheikh University | Cairo | Kafr El-sheikh |
Saudi Arabia | Ministry of health. First health cluster | Riyadh | Riaydh |
Lead Sponsor | Collaborator |
---|---|
Kafrelsheikh University | Ministry of Health, Saudi Arabia |
Egypt, Saudi Arabia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Time to first negative SARS-CoV-2 PCR in NP swap and Mycobacterium tuberculosis sputum culture | within 4 weeks | ||
Secondary | Sputum culture result (positive or negative)& COVID-19 PCR (positive or negative) | 2 weeks after therapy start date | ||
Secondary | Serum levels of CRP and ESR | one month | ||
Secondary | All cause mortality rate | one month | ||
Secondary | Absolute lymphocyte counts (CD4,CD8 and CD25+FOXP3+ Regulatory T) | one month | ||
Secondary | Measurement of cytokine (IFN-gamma and alpha , IL-6, IL-10, TNF-alpha, TGF-beta) levels produced in response to M. tb. | one month | ||
Secondary | Vitamin D status | Serum 25(OH)D concentrations | one month | |
Secondary | Retinoic acid status | Serum Retinoic acid concentrations | one month | |
Secondary | Minocycline status | Serum Minocycline concentrations | one month | |
Secondary | Serum indoleamine 2,3-dioxygenase (IDO) enzyme status | Serum indoleamine 2,3-dioxygenase (IDO) enzyme concentration | one month | |
Secondary | Chicoric Acid status | Serum Chicoric Acid concentrations | one month |
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