Franzese C

University of Missouri Hospital

2
Publications
1
h-index
(1 citations, 3 total works)

Research Topics

Food Allergy and Anaphylaxis Research (2)Xenotransplantation and immune response (2)Vector-borne infectious diseases (1)Allergic Rhinitis and Sensitization (1)Complement system in diseases (1)

Alpha-gal Syndrome Publications

α-Gal Syndrome in the South: Why We Need Treatment Trials, Not Just Tick Prevention.

Casterline BW, Franzese C, Park Y, McElroy JA
Southern medical journal •

α-Gal syndrome (AGS), a tick bite-associated allergy to mammalian meat, affects an estimated 450,000 Americans, with the highest prevalence concentrated in the US South and Southeast. The lone star tick (), ubiquitous across the region, transmits AGS sensitization, making reexposure nearly inevitable for outdoor workers and residents. Current management relies on dietary avoidance of mammalian products of an indeterminant length, a recommendation that is neither practical in a region where mammalian meat is central to cuisine and culture nor evidence based regarding duration or necessity. In the absence of treatment options, patients are turning to alternative interventions such as acupuncture protocols that lack validation from controlled trials. Meanwhile, oral immunotherapy has demonstrated safety and efficacy for other immunoglobulin E-mediated food allergies, and individual case reports suggest desensitization may be feasible for AGS syndrome. The US South, with its high disease burden, clinical expertise, and patient populations, is uniquely positioned to lead the rigorous phase 1 and phase 2 trials needed to develop evidence-based treatment alternatives. Without such research, patients have only dietary restriction as an evidence-based option and may seek purported treatments that lack rigorous validation.

Digital Health Solutions for Alpha-Gal Syndrome: A Scoping Review of Telemedicine Evidence and Applications.

Abadi AEZS, Becevic M, Dunaway L, Franzese C, Casterline BW
Missouri medicine •

Alpha-gal syndrome (AGS) is an emerging allergy initiated by tick bites that leads to delayed IgE-mediated hypersensitivity reactions to galactose-α-1,3-galactose (α-gal), a carbohydrate present in mammalian tissues. Symptoms are highly variable and include urticaria, gastrointestinal distress, and life-threatening anaphylaxis. Diagnosis relies on patient history and serological testing for α-gal-specific IgE antibodies. This scoping review, following PRISMA methodology, evaluates telemedicine for clinical management of AGS. The syndrome's characteristic delayed response pattern poses distinct challenges for standard allergy management protocols. Telehealth presents compelling solutions by enabling structured follow-up, remote data collection, and patient support, which is especially critical given that AGS is concentrated in geographic areas with limited specialist access and low provider familiarity. A case study of successful AGS desensitization using remotely monitored oral immunotherapy provides proof-of-principle for telemedicine's transformative potential. Integrating telehealth is a strategic approach to improve diagnosis, facilitate long-term management, and strengthen surveillance for this increasingly prevalent condition.