Tuberculosis
Conditions
Keywords
filariae, tuberculosis, BCG vaccination
Brief summary
Filarial nematodes modulate the host immune response to promote regulatory and T helper type 2 immune responses, which were shown to influence concomitant infections. Indeed, several studies showed that increased susceptibility and worsened disease course of HIV, tuberculosis (TB) and malaria in filarial endemic regions. Moreover, the investigators demonstrated that M. perstans infections polarize and suppress immune responses with likely consequences for concomitant infections and vaccine-induced protection. In addition, the investigators observed altered frequencies of natural killer and regulatory T and B cells in filarial and M. tuberculosis co-infected individuals and that M. perstans influences CD4+ T cell function and immune responses upon purified protein derivative antigen stimulation. Nevertheless, the consequences of manifestation of TB disease and influence on TB vaccination remains unknown. Thus, the trial aim to address two main questions with high clinical relevance: 1) Does filarial infection influence disease severity and recovery in tuberculosis patients? 2) Does filarial infection influence Bacille Calmette-Guérin (BCG)-induced protection against disease progression in vaccinated children?
Interventions
DRUGTB treatment according to national guidelines
National clinics in Cameroon will initiate TB treatment according to national guidelines upon positive TB diagnosis
Sponsors
University Hospital, Bonn
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
5 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Patient is older than 5 years old * Patient have BCG scare or get the BCG vaccination at birth * Patient had no previous treatment of, tuberculosis or with at least one of the study drugs i.e. isoniazid,rifampicin, pyraziamide, ethambutol * Patient have no history of hypersensitivity to rifampicin, or any of the above mentioned drugs * Patient is not on any medication likely to interact with the study medication * Patient have no history of or current clinical signs of ascites, jaundice, partial or complete deafness, myasthenia gravis, renal dysfunction (known or suspected), diabetes mellitus, and severe immune compromise (e.g., immunosuppressive drugs after organ transplant), or have no evidence of (previous) tuberculosis, Buruli ulcer or leprosy and no terminal illness (e.g., metastasized cancer) * Patient have no mental condition * Patient is able to take oral medication * Patient have no mental condition including addiction with substance abuse e.g. alcohol * Patient is willing to give informed pre-consent, and consent * In case the patient is below 18, the parents or legal guardians were informed and provide consent
Exclusion criteria
* Patient is younger than 5 years old * Patient have no BCG scare or miss the BCG vaccination at birth * Patient had previous treatment of, tuberculosis or with at least one of the study drugs i.e. isoniazid,rifampicin, pyraziamide, ethambutol * Patient have a history of hypersensitivity to rifampicin, or any of the above mentioned drugs * Patient is on any medication likely to interact with the study medication * Patient have a history of or current clinical signs of ascites, jaundice, partial or complete deafness, myasthenia gravis, renal dysfunction (known or suspected), diabetes mellitus, and severe immune compromise (e.g., immunosuppressive drugs after organ transplant), or evidence of (previous) tuberculosis, Buruli ulcer or leprosy; or terminal illness (e.g., metastasized cancer) * Patient have a mental condition including addiction with substance abuse e.g. alcohol likely to interfere with possibility to comply with study protocol * Patient is unable to take oral medication or having gastrointestinal disease likely to interfere with drug absorption * Patient have a mental condition including addiction with substance abuse e.g. alcohol likely to interfere with possibility to comply with study protocol * Patient is not willing to give informed pre-consent, and consent or withdrawal or consent * In case the patient is below 18, were the parents or legal guardians were not informed and did not provide consent
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Influence of filariae infection on TB disease outcome and BCG vaccination | 3 years | Does filarial infection influence tuberculosis disease severity and recovery under treatment and influence Bacille Calmette-Guérin (BCG)-induced protection against disease progression Parasitological diagnosis: * Blood smear for microfilaria detection using microscopy * DNA isolation from urine, blood and stool for helminth detection using LAMP and PCR technology * Helminth egg detection in urine and stool using Kato Katz technique * Skin snip for detection of Onchocerca volvulus infection TB diagnosis: * Chest radiography * Sputum smear and culture * GeneXpert * TST Test * Physical examination * Questionnaires to obtain medical, TB contact and treatment history |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Biomarkers for TB severity and BCG vaccination | 3 years | Decipher biomarker for TB disease severity and recovery under treatment and for prediction of BCG vaccine induced immune protection against development of TB Laboratory assessment: \- CFP10/ESAT6 in vitro and TB-TAM assay from peripheral whole blood using flow cytometry technology |
Countries
Cameroon
Contacts
Primary ContactSamuel Wanji, Prof. Dr.
Backup ContactManuel Ritter, Dr.
Outcome results
None listed