A Molecular Assay for Sensitive Detection of Pathogen-Specific T-Cells
2011

A New Test for Detecting T-Cells in Infections

Sample size: 69 publication 10 minutes Evidence: high

Author Information

Author(s): Kasprowicz Victoria O., Mitchell Jessica E., Chetty Shivan, Govender Pamla, Huang Kuan-Hsiang Gary, Fletcher Helen A., Webster Daniel P., Brown Sebastian, Kasmar Anne, Millington Kerry, Day Cheryl L., Mkhwanazi Nompumelelo, McClurg Cheryl, Chonco Fundisiwe, Lalvani Ajit, Walker Bruce D., Ndung'u Thumbi, Klenerman Paul

Primary Institution: Ragon Institute of MGH, MIT and Harvard, Harvard Medical School, Boston, Massachusetts, United States of America

Hypothesis

Can a novel qPCR assay improve the detection of pathogen-specific T cells in HIV co-infected patients?

Conclusion

The developed qPCR assay is a sensitive method for detecting MTB-specific T cells and can be performed on small blood samples.

Supporting Evidence

  • The qPCR assay showed a clear quantitative correlation with the traditional Elispot assay.
  • The assay was able to detect T cell responses at lower frequencies than the Elispot.
  • MIG and IP10 expression was significantly higher in fresh PBMC samples compared to frozen samples.
  • The assay can be performed on small blood samples, making it suitable for various clinical settings.

Takeaway

Researchers created a new test that can find specific immune cells in the blood, which helps diagnose infections like tuberculosis, even in people with HIV.

Methodology

The study involved developing a qPCR assay to measure MIG and IP10 expression in response to specific antigens in blood samples from HIV co-infected patients.

Limitations

The assay may not differentiate between latent TB infection and active TB disease.

Participant Demographics

Participants included HIV co-infected individuals with varying CD4 counts and both active and latent TB infections.

Statistical Information

P-Value

p<0.001

Statistical Significance

p<0.001

Digital Object Identifier (DOI)

10.1371/journal.pone.0020606

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication