Screening for Potential Adjuvants Administered by the Pulmonary Route for Tuberculosis Vaccines

Journal Title: The AAPS Journal - Year 2009, Vol 11, Issue 1

Abstract

Tuberculosis (TB) infects one third of the world’s population, and new infections occur at a rate of 1/s. Better vaccines are needed than the live mycobacterium Bacille Calmette-Guérin (BCG). Alveolar macrophages (AMΦs) play a central role in pulmonary manifestations of TB. Targeting immunomodulators to AMΦs, the first line of defense against Mycobacterium tuberculosis (Mtb), may initiate a potent cell-mediated immune response. Muramyl dipeptide (MDP) and trehalose dibehenate (TDB) have elicited strong immune response when delivered to the lungs as aerosols. AMΦs show toxicity in response to some immunomodulators. The objective of this work was to screen the immunomodulators MDP and/or TDB encapsulated in microparticles (MPs) and to evaluate certain indicators of toxicity in human AMΦ-like cells. Poly(lactide-co-glycolide) (PLGA) MPs containing MDP and/or TDB were prepared by spray-drying. The morphology, particle size distribution, and immunomodulator encapsulation efficiency of MPs were examined. THP-1 cells were exposed to these MPs for 24 h and characteristics of cell morphology, tumor necrosis factor-alpha (TNF-α) release, lactate dehydrogenase (LDH), N-acetyl-β-d -glucosaminidase (NAG) and alkaline phosphatase (ALP) activity in AMΦ culture supernatants were measured. MTT assay was used to assess the viability of cells. Spray-drying produced low-density MPs having volume median diameters between 4 and 6 μm as measured by laser diffraction and projected area diameter between 3 and 5 μm calculated by microscopy. More TNF-α was produced by THP-1 cells exposed to MPs composed of PLGA-MDP or PLGA alone than PLGA-TDB. LDH release following exposure to MPs of PLGA-MDP and PLGA alone was greater than controls. NAG release was higher following exposure to MPs of PLGA alone or PLGA-MDP 0.1% than PLGA-TDB (0.1% and 1.0%). Cells remained viable after exposure to MPs as per MTT assay. PLGA-MDP MPs demonstrated statistically elevated indicators of biochemical responses in cell culture compared to PLGA-TDB MPs, but the extent of their potential to elicit adverse effects in vivo must be studied independently.

Authors and Affiliations

Chenchen Wang, Pavan Muttil, Dongmei Lu, Adela Ayulia Beltran-Torres, Lucila Garcia-Contreras, Anthony J. Hickey

Keywords

Related Articles

Commentary: Where and how could biomarkers be used in 2016

Since the beginning of the human genome project there has been considerable speculation about how this resource and the knowledge creation it enabled would change therapeutic discovery, development, and delivery. As the...

Kinetic modeling of plasmid DNA degradation in rat plasma

A major obstacle in gene delivery is the transport of intact plasmid DNA (pDNA) to target sites. We sought to investigate the kinetic processes underlying the degradation of pDNA in a rat plasma model, as this is one of...

Elucidation of Arctigenin Pharmacokinetics After Intravenous and Oral Administrations in Rats: Integration of In Vitro and In Vivo Findings via Semi-mechanistic Pharmacokinetic Modeling

The online version of this article (doi:10.1208/s12248-014-9664-x) contains supplementary material, which is available to authorized users.

Bioanalytical Approaches to Quantify “Total” and “Free” Therapeutic Antibodies and Their Targets: Technical Challenges and PK/PD Applications Over the Course of Drug Development

The predominant driver of bioanalysis in supporting drug development is the intended use of the data. Ligand-binding assays (LBA) are widely used for the analysis of protein biotherapeutics and target ligands (L) to supp...

Pharmacodynamic Model of Parathyroid Hormone Modulation by a Negative Allosteric Modulator of the Calcium-Sensing Receptor

In this study, a pharmacodynamic model is developed, based on calcium–parathyroid hormone (PTH) homeostasis, which describes the concentration–effect relationship of a negative allosteric modulator of the...

Download PDF file
  • EP ID EP681449
  • DOI  10.1208/s12248-009-9089-0
  • Views 71
  • Downloads 0

How To Cite

Chenchen Wang, Pavan Muttil, Dongmei Lu, Adela Ayulia Beltran-Torres, Lucila Garcia-Contreras, Anthony J. Hickey (2009). Screening for Potential Adjuvants Administered by the Pulmonary Route for Tuberculosis Vaccines. The AAPS Journal, 11(1), -. https://europub.co.uk/articles/-A-681449