Introduction
Tuberculosis (TB) is the leading cause of death in AIDS patients worldwide; the earliest opportunistic infection occurring in conjunction with HIV; an accelerant of HIV replication and immune system deterioration. Co-infection with Mycobacterium tuberculosis (Mtb) and HIV is an increasing global emergency. Little is known regarding the early events of Mtb infection in humans especially infants. There is an urgent need for a clinically relevant animal model that mimics TB disease in human children to better understand early immune responses, pathogenicity and disease progression in newborn/infants.
Methods
Aerosolized Mtb transmission was performed in neonatal macaques to mimic mother-to-child transmission and to: i. Characterize early TB-specific immune responses during acute Mtb-infection, ii. Investigate the dynamics of Mtb-specific T cell responses following early infection in infants; and, iii. Characterize the distribution and frequency of Mtb-specific responses in various host tissues. Six newborn macaques (6 weeks old) were infected via broncho or aerosol routes of infection with various Mtb doses (Erdman or Rh37rv strains). All clinical, immunologic, microbiologic, and pathologic events were assessed for 84 days post-infection.
Results
Gross pathological abnormalities were observed as early as 35 et 42 days post infection including Ghon complex formation and granulomas in the lung. Caseous granulomas were also observed in the lungs at these early time-points, reflecting strong initial responses. Using ELISPOT assays, we found that IL-12 production correlated with early Mtb infection lesions seen by routine thoracic radiographs. Flow cytometry revealed robust granzyme B productions by NK8/NK cells that increased over time and transient Perforin productions that peak at day 56. Mtb-specific T cells responses were also detected and increased IL-12 and MIP-1β production in PBMC, Spleen and LN collected day 84.
Conclusions
Overall, we successfully developed/optimized an aerosol neonatal macaque model that mimics clinical and bacteriological characteristics of early Mtb-infection as seen in human newborns/infants. This model represents a unique opportunity to characterize neonatal Mtb infection and, further understand all interactions between TB and HIV co-infection in pediatric AIDS and develop appropriate therapeutic interventions.
Author information
Authors and Affiliations
Rights and permissions
This article is published under an open access license. Please check the 'Copyright Information' section either on this page or in the PDF for details of this license and what re-use is permitted. If your intended use exceeds what is permitted by the license or if you are unable to locate the licence and re-use information, please contact the Rights and Permissions team.
About this article
Cite this article
Gauduin, MC., Cepeda, M., Salas, M. et al. Neonatal macaque model to study Mycobacterium tuberculosis infection in pediatric AIDS. BMC Infect Dis 14 (Suppl 2), O11 (2014). https://doi.org/10.1186/1471-2334-14-S2-O11
Published:
DOI: https://doi.org/10.1186/1471-2334-14-S2-O11