Lyme disease, caused by infection with the spirochete Borrelia burgdorferi or closely related species, is the most common vector-borne disease in the United States, accounting for over 300,000 infections per year according to public health estimates. It is also one of the few infectious diseases that requires a two-step laboratory testing protocol, comprising a screening assay, typically ELISA, followed by a confirmatory immunoblot. This protocol is followed where the disease has progressed beyond the hallmark erythema migrans rash, or the rash cannot be identified, and symptoms or history suggest Lyme disease. The two-step protocol is a result of the poor specificity of most Lyme screening tests, which results in a high false positive rate. This in turn is due to the cross-reactive nature of many bacterial antigens, combined with the limitations of conventional ELISA immunochemistry. In principle, a confirmatory result must be obtained prior to initiating treatment, but in practice, the multi-day delay that is often incurred for this purpose leads to physicians frequently prescribing antibiotic treatment in the absence of definitive lab results. As the vast majority of the roughly three million annual Lyme tests in the U.S. are carried out on individuals who do not have Lyme disease, this practice leads to the unnecessary prescription and use of antibiotics, contributing to the growth of antibiotic resistance which has become a significant threat to public health. A first step test with significantly higher specificity would avoid the need for a second step test and enable clinicians to make informed treatment decisions in a timely manner, based on credible test results. This project is aimed at bringing about a significant change in medical practice by reducing Lyme testing from the current two-step process to a one-step process. To achieve this objective, we have developed a novel ELISA methodology for Lyme antibody detection that enables exceptionally high assay specificity. The test is based on well-established, highly specific and sensitive Borrelia antigens in a unique immunochemical format. The novel ELISA immunochemistry eliminates almost all non-specific reactivity, yielding results comparable in both sensitivity and specificity to those obtained with the conventional two-tier testing protocol. Consequently, this assay promises to deliver a one-step testing solution for Lyme disease, at a time when alternatives to the original two-step method are gaining legitimacy at the scientific as well as regulatory level. In this Phase I project, we will develop a prototype ELISA assay, proving feasibility by demonstrating sensitivity and specificity on retrospective samples comprising Lyme patients and controls, in comparison with two-tier testing results. In Phase II, we will complete development of a commercial product, carry out prospective and retrospective clinical studies and submit an application to FDA for in vitro diagnostic claims, allowing commercial launch upon approval.
Lyme disease, a bacterial infection which has become the most common vector-borne disease in the United States, poses a diagnostic challenge to clinicians and a threat of chronic illness to patients. The current paradigm for diagnosis of Lyme disease relies on a two-step laboratory- based testing approach. In this proposal, we intend to develop a simple and accurate one-step test for Lyme disease based on novel immunochemistry that can be carried out in an average, non-specialized laboratory, enabling faster diagnosis and consequently more appropriate treatment for patients.
