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Impact of HIV Infection on Latent Tuberculosis (TB) Among Patients With HIV-TB Co-Infection
This study is not yet open for participant recruitment.
Verified by All India Institute of Medical Sciences, New Delhi, June 2008
Sponsors and Collaborators: All India Institute of Medical Sciences, New Delhi
Indian Council of Medical Research
Ministry of Science and Technology, India
Information provided by: All India Institute of Medical Sciences, New Delhi
ClinicalTrials.gov Identifier: NCT00692809
  Purpose

HIV induced altered representation and function of regulatory T cell subsets (NKT and Treg cells) impair the protective T cell response against M.tuberculosis and disrupts LTBI, thus facilitates faster progression and development of severe forms of clinical TB in HIV-TB co-infection.


Condition
Latent Tuberculosis Infection
HIV Infections
Tuberculosis

MedlinePlus related topics: AIDS Tuberculosis
Drug Information available for: Interferons Interferon gamma-1b
U.S. FDA Resources
Study Type: Observational
Study Design: Prospective
Official Title: Impact of HIV Infection on Latent TB Among Patients With HIV-TB Co-Infection

Further study details as provided by All India Institute of Medical Sciences, New Delhi:

Primary Outcome Measures:
  • Precise component(s) of T cell response against M.tuberculosis compromised by HIV infection which leads to the development of severe forms of clinical tuberculosis. [ Time Frame: 5 months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Elucidation of critical events of the cellular and molecular interactions that would be useful for developing newer therapeutic strategies and vaccination. [ Time Frame: 5 months ] [ Designated as safety issue: No ]

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 180
Study Start Date: July 2008
Estimated Study Completion Date: March 2010
Estimated Primary Completion Date: March 2010 (Final data collection date for primary outcome measure)
Groups/Cohorts
1
HIV+ve+LTBI (n=100)
2
HIV+ve+clinical TB (n=50)
3
HIV-ve+clinical TB (n=15)
4
Normal control (n=15)

Detailed Description:

During the natural course of HIV disease, emergence of opportunistic infection not only imposes morbidity on HIV-TB co-infected patients, but also facilitates viral replication causing faster disease progression. Tuberculosis, being the commonest among the opportunistic infections among HIV infected persons deserves special attention. Moreover, disruption of latency of TB infection (LTBI) with development of more severe clinical forms at relatively early stage of HIV disease when CD4 count still remains above 300/ul, makes TB a unique opportunistic infection and negatively influence the outcome of dual infection.This is suggestive of impairment of some critical immune function involving relatively less frequent fine T cell subsets with functional hierarchy over bulk T cells, so as to weaken the immune containment of LTBI resulting in reactivation of M. tuberculosis and manifestation of severe forms of TB.HIV has recently been reported to preferentially infect, destroy and incapacitate two key immune-regulatory T cell subsets, namely NKT and Treg cells.Therefore, studying them along the course of HIV disease and impact of their changes on the function of effector T cells directed against M.tuberculosis is important.

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

HIV+ve+LTBI HIV+ve+clinical TB HIV-ve+clinical TB Normal control

Criteria

Inclusion Criteria:

HIV infected +LTBI group:

  • Patient of either sex between 18-65 years of age
  • All the patients should be HIV ELISA test positive irrespective of CD4 count and presence of other opportunistic infections Antiretroviral drug naive HIV patients
  • No past history of TB
  • Patients should be either tuberculin test positive (> 5mm) or interferon gamma release assay positive
  • Written informed consent to participate in the study given by participants or legal guardian
  • Patients able to comply with instructions and come back for a regular follow up

HIV infected + Clinical TB group:

  • Patient of either sex between 18-65 years of age
  • All the patients should be HIV ELISA test positive irrespective of CD4 count and presence of other opportunistic infections
  • In PTB group, patient should be two sputum smear positive out of three consecutive samples
  • In EPTB group, diagnosis of TB will be:

    • Definitive -Culture confirmed
    • Probable -Histopathological or radiological -Clinical features and response to anti TB treatment (ATT)
    • Possible TB -Clinical feature and response to anti TB treatment (ATT)
  • Written informed consent to participate in the study given by participants or legal guardian
  • Patients able to comply with instructions and come back for a regular follow up

HIV negative Clinical TB group:

  • Patients of either sex between 18-65 years of age who are permanent resident of Delhi
  • All patients should be HIV ELISA negative
  • In PTB group, patients should be two sputum smear positive (at least 1+) out of three consecutive samples
  • In EPTB group, diagnosis of TB will be:

    • Definitive -Culture-confirmed
    • Probable -Histopathological or radiological -Clinical features and response to anti-TB treatment (ATT)
    • Possible TB -Clinical features and response to anti-TB treatment (ATT)
  • Written informed consent to participate in the study given by participants or legal guardian
  • Patients able to comply with instructions and come back for a regular follow up

Normal controls:

  • Persons of either sex between 18-65 years of age who are permanent resident of Delhi
  • Written informed consent to participate in the study given by participants or legal guardian
  • Person should not have past history of TB

    • Mantoux test negative (< 10mm)
    • Chest-X-ray normal
    • Hemogram normal
  • Renal and liver functions normal
  • Hepatitis viral markers normal
  • No clinical evidence of malnutrition
  • HIV ELISA negative

Exclusion Criteria:

HIV infected +LTBI group:

  • Pregnant and lactating females
  • Patients who are getting steroid therapy
  • Transplant patients, diabetes mellitus or malignancy, chronic renal failure or liver diseases
  • Currently receiving cytotoxic therapy, or have received it within the last 3 months
  • Terminally ill as per treating clinician's judgment
  • Patient from outside Delhi and migrants

HIV infected + Clinical TB group:

  • Category II and multidrug-resistant pulmonary tuberculosis
  • Pregnant and lactating females
  • Patients who are getting steroid therapy
  • Transplant patients, diabetes mellitus or malignancy, chronic renal failure or liver diseases
  • Currently receiving cytotoxic therapy, or have received it within the last 3 months
  • Terminally ill patient as per treating clinician's judgment
  • Patients from outside Delhi and migrants

HIV negative Clinical TB group:

  • Category II and multi drug-resistant pulmonary tuberculosis
  • Patients who are getting steroid therapy
  • Transplant patients, diabetes mellitus or malignancy, chronic renal failure or liver disease
  • Currently receiving cytotoxic therapy, or have received it within the last 3 months
  • Terminally ill patient as per treating clinician's judgment
  • Patients unwilling to comply with the study procedures or those with history of alcohol or drug abuse

Normal controls:

  • Transplant patients, diabetes mellitus or malignancy
  • Patients unwilling to comply with the study procedures or those with history of alcohol or drug abuse
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00692809

Contacts
Contact: Surendra K Sharma, M.D., Ph.D 26594415 surensk@gmail.com

Locations
India, Delhi
All India Institute of Medical Sciences
New Delhi, Delhi, India, 110608
Sponsors and Collaborators
All India Institute of Medical Sciences, New Delhi
Indian Council of Medical Research
Ministry of Science and Technology, India
Investigators
Principal Investigator: Surendra K Sharma, M.D., Ph.D All India Institute of Medical Sciences, New Delhi
  More Information

Responsible Party: All India Institute of Medical Sciences ( Dr. S.K. Sharma, Professor & Head )
Study ID Numbers: SKS/LTBI/07
Study First Received: June 5, 2008
Last Updated: June 9, 2008
ClinicalTrials.gov Identifier: NCT00692809  
Health Authority: India: Institutional Review Board

Keywords provided by All India Institute of Medical Sciences, New Delhi:
Latent tuberculosis infection
Human immunodeficiency virus
Tuberculosis
Natural Killer T Cells
Invariant Natural Killer T Cells
Regulatory T cells
Interferon-gamma

Study placed in the following topic categories:
Bacterial Infections
Sexually Transmitted Diseases, Viral
Interferon Type II
Acquired Immunodeficiency Syndrome
Interferons
Immunologic Deficiency Syndromes
Virus Diseases
Gram-Positive Bacterial Infections
HIV Infections
Sexually Transmitted Diseases
Mycobacterium Infections
Tuberculosis
Retroviridae Infections
Interferon-gamma, Recombinant

Additional relevant MeSH terms:
Communicable Diseases
RNA Virus Infections
Slow Virus Diseases
Immune System Diseases
Lentivirus Infections
Infection
Actinomycetales Infections

ClinicalTrials.gov processed this record on January 16, 2009