DEVELOPMENT OF SPECIFIC AIMS
This is often the most difficult part of a paper to write. It should be short, easy to understand and contain the essence of what you want to do. When developing these, start asking yourself:
Here is an example of some specific aims
The goal of this pilot study is to detect Mycobacterium tuberculosis (MTB) DNA in peripheral blood mononuclear cells (PBMCs) using a battery of automated, real-time, quantitative polymerase chain reaction (Q-PCR) screening assays in experimentally-infected guinea pigs and tuberculosis (TB) patients. The results should provide the foundation to design studies of the pathogenesis of early TB in guinea pigs and humans, as well as a strategy for mass screening for early active pulmonary TB in the community. The specific aims are:
AIM 1. Detect genes from MTB and its host in the blood of experimentally-infected guinea pigs using Q-PCR. We will evaluate the ability of Q-PCR to detect MTB DNA in the blood of experimentally-infected guinea pigs in the period following challenge during which a low level bacillemia is known to occur. Guinea pig host genes will also be detected and used to perform a relative quantification (burden) of MTB. The data from this well-established animal model of early TB infection will be used to standardize the assays for patients described in the second aim of this study.
AIM 2: Establish the feasibility of using the Q-PCR assay in PBMCs prospectively to distinguish active TB cases from non-infected healthy controls. The Q-PCR assays established for guinea pigs in Aim 1 will be adapted for use with human specimens. This preliminary study in human specimens will be done to establish the feasibility of identifying individuals with active TB disease through Q-PCR testing in PBMCs. A simple questionnaire will be administered to determine if individuals have co-morbidity with diabetes, a predisposing factor for TB disease. Blood from healthy individuals will be used as specificity controls.