Abstract

There is increasing evidence supporting a role for antibodies in protection against tuberculosis (TB), with functional antibodies being described in the latent state of TB infection. Antibody avidity is an important determinant of antibody-mediated protection. This study characterised the avidity of antibodies against Ag85A, an immunodominant Mycobacterium tuberculosis (M.tb) antigen and constituent of several anti-TB vaccine candidates, in individuals of varied M.tb infection status. Avidity of Ag85A specific antibodies was measured in 30 uninfected controls, 34 individuals with latent TB infection (LTBI) and 75 active pulmonary TB (APTB) cases, employing the more commonly used chaotrope-based dissociation assays, and surface plasmon resonance (SPR). Chaotrope-based assays indicated that APTB was associated with a higher antibody avidity index compared to uninfected controls [adjusted geometric mean ratio (GMR): 1.641, 95% confidence interval (CI): 1.153, 2.337, p = 0.006, q = 0.018] and to individuals with LTBI [adjusted GMR: 1.604, 95% CI: 1.282, 2.006, p < 0.001, q <0.001]. SPR assays showed that APTB was associated with slower dissociation rates, an indication of higher avidity, compared to uninfected controls (adjusted GMR: 0.796, 95% CI: 0.681, 0.932, p = 0.004, q = 0.012) and there was also weak evidence of more avid antibodies in the LTBI compared to the uninfected controls (adjusted GMR: 0.871, 95% CI: 0.763, 0.994, p = 0.041, q = 0.123). We found no statistically significant differences in anti-Ag85A antibody avidity between the APTB and LTBI groups. This study shows that antibodies of increased avidity are generated against a principle vaccine antigen in M.tb infected individuals. It would be important to determine whether TB vaccines are able to elicit a similar response. Additionally, more research is needed to determine whether antibody avidity is important in protection against infection and disease.

Highlights

  • According to the WHO, tuberculosis (TB) was the leading cause of mortality from a single infectious microorganism in 2016 [1]

  • As part of the parent study, infection with malaria, cytomegalovirus and helminths and the presence of a Bacille Calmette–Guerin (BCG) scar was ascertained among the HHCs but due to the nature of the study, the same was not done in the active pulmonary TB (APTB) cases [32]

  • This is the first study to characterise the avidity of Mycobacterium specific antibodies in individuals of varied M.tb infection status using surface plasmon resonance (SPR) derived dissociation rates

Read more

Summary

Introduction

According to the WHO, tuberculosis (TB) was the leading cause of mortality from a single infectious microorganism in 2016 [1]. The exact mechanisms of BCG induced protection are still not known [6], the presence of interferon (IFN)-γ secreting T cells has been associated with a lower risk of TB in a study of BCG vaccinated infants [7]. This same study reported elevated levels of antibodies against the immunodominant secreted protein, Ag85A, in children who did not develop TB

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call